Day: January 5, 2025

10 Quirkiest Male Anime Love Interests, Ranked  CBR
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The expose published by Michael Hauser Tov on Friday in Haaretz Hebrew revealed how the plan to overthrow Israel’s legal system was formulated and implemented.

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Three altcoins are in the spotlight this week, with Fartcoin (FARTCOIN), SPX6900 (SPX), and Ethena (ENA) delivering impressive performances. FARTCOIN, a rising star in the meme coin space, surged 67% in the past seven days, hitting new all-time highs and securing its place as the fifth-largest meme coin on Solana.
SPX also reached a new all-time high with a market cap of $1.22 billion, climbing 63% this week, despite a slight dip in trading volume. Ethena (ENA), meanwhile, gained 37% following the release of its 2025 roadmap.
Fartcoin (FARTCOIN)
FARTCOIN, first launched on Pump.fun, now has a $1.4 billion market cap and surged 67% in the past seven days. The coin has consistently hit new all-time highs over recent weeks, solidifying its position as the fifth-largest meme coin on Solana.
Its EMA lines remain bullish, signaling potential for continued upward momentum. If the uptrend persists, FARTCOIN could test the $1.61 resistance, and a breakout could push the price to $1.7 or even $1.8.

FARTCOIN Price Analysis. Source: TradingView
However, if the support at $1.299 fails to hold, a sharp correction could ensue, potentially driving the price down to $0.92 and below the $1 mark.
SPX6900 (SPX)
SPX has achieved a new all-time high, with its market cap reaching $1.22 billion, placing it among the top 100 largest altcoins. The coin has surged 63% over the last seven days, showcasing strong bullish momentum despite a 27% drop in trading volume over the past 24 hours.
SPX Price Analysis. Source: TradingView
If the uptrend continues, SPX could rise further to test resistance levels at $1.40 and potentially $1.50 for the first time. However, if the trend reverses, SPX could retest its closest strong support at $0.93.
A break below this level could trigger further declines, pushing the price down to $0.819 or even $0.615.
Ethena (ENA)
Ethena, an Ethereum-based platform building a synthetic dollar, has emerged as one of the top-performing altcoins this week, with its price surging 37% in the last seven days.
The announcement of its 2025 roadmap, which includes a Telegram payments app and plans for TradFi adoption, has fueled significant investor interest.
ENA Price Analysis. Source: TradingView
With a market cap of $3.77 billion, ENA is now just 19% below its previous all-time high. If the uptrend persists, ENA could break the $1.32 resistance and move closer to testing its all-time high of $1.50.
However, if momentum fades, ENA may retest the $1.12 support level, and a failure to hold that could push the price down to $1.01.

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Background: Inflammatory bowel disease (IBD) is a refractory inflammatory disorder of the intestine, which is probably triggered by dysfunction of the intestinal epithelial barrier. Secretory leukocyte protease inhibitor (SLPI) secreted by colon epithelial cells protects against intestinal inflammation by exerting anti-protease and anti-microbial activities. Daikenchuto (DKT) is one of the most commonly prescribed Japanese traditional herbal medicines for various digestive diseases. Although several animal studies have revealed that DKT exerts anti-inflammatory effects, its detailed molecular mechanism is unclear. This study aimed to clarify the anti-inflammatory mechanism of DKT using a murine colitis model, and to evaluate its potential as a therapeutic agent for IBD.
Methods: Experimental colitis was induced in wild-type (WT) mice and SLPI-deficient (KO) mice by dextran sulfate sodium (DSS) after oral administration of DKT. The resultant clinical symptoms, histological changes, and pro-inflammatory cytokine levels in the colon were assessed. Expression of SLPI in the colon was detected by Western blotting and immunohistochemistry. Composition of the gut microbiota was analyzed by 16S rRNA metagenome sequencing and intestinal metabolites were measured by gas chromatography-mass spectrometry analysis. Intestinal epithelial barrier function was assessed by oral administration of FITC-dextran and immunostaining of tight junction proteins (TJPs).
Results: Oral administration of DKT increased the number of butyrate-producing bacteria, such as Parabacteroides, Allobaculum, and Akkermansia, enhanced the levels of short-chain fatty acids, including butyrate, in the colon, induced SLPI expression, and ameliorated DSS-induced colitis in WT mice. We found that mouse colon carcinoma cell line treatment with either DKT or butyrate significantly enhanced the expression of SLPI. Moreover, supplementation of DKT protected the intestinal epithelial barrier with augmented expression of TJPs in WT mice, but not in KO mice. Finally, the composition of the gut microbiota was changed by DKT in WT mice, but not in KO mice, suggesting that DKT alters the colonic bacterial community in an SLPI-dependent manner.
Conclusion: These results indicate that DKT exerts anti-inflammatory effects on the intestinal epithelial barrier by SLPI induction, due, at least in part, to increased butyrate-producing bacteria and enhanced butyrate levels in the colon. These results provide insight into the mechanism of the therapeutic effects of DKT on IBD.
Inflammatory bowel disease (IBD), including ulcerative colitis (UC) and Crohn’s disease (CD), is a recurrent inflammatory disorder of the gastrointestinal tract that occurs in young people. It is recognized as a global health problem because the incidence and prevalence of IBD are rapidly increasing worldwide (1, 2). However, the pathogenesis of IBD remains largely unknown, and no fundamental treatment has been developed for it. In recent years, molecular targeted drugs targeting various cytokines, integrins, and Janus kinase (JAK) have been developed to treat patients with refractory IBD with an inadequate response to existing therapies, such as 5-aminosalicylic acids, immunomodulators, and corticosteroids (3). While these drugs are effective in treating refractory IBD, their immunosuppressive side effects and the high cost of these agents are problematic. Therefore, new therapeutic drugs for IBD with high safety and cost-effectiveness are desired (4).
Daikenchuto (DKT), a Japanese traditional herbal medicine (Kampo medicine), is one of the most commonly prescribed herbal medicines for patients with gastrointestinal disorders, such as constipation and intestinal obstruction. While Kampo medicine was introduced in ancient China and developed uniquely as a traditional medicine in Japan, it is also used in Western countries due to its effectiveness and high safety profile (5, 6). Although the mode of action of DKT was unknown for a long time, a comprehensive analysis of its pharmacological properties has been conducted at component and molecular levels since the 2000s. DKT consists of an aqueous extract powder prepared from a mixture of Zingiberis rhizoma (Ginger), Zanthoxyli fructus (Japanese pepper), Panax ginseng (Ginseng radix), and maltose. DKT has the effects of increasing intestinal blood flow, improving gastrointestinal motility, and inhibiting fibrosis (7–9). In fact, several clinical trials have demonstrated the preventive effect of DKT on intestinal obstruction after abdominal surgery (10, 11). In addition, several animal studies have demonstrated that DKT exerts anti-inflammatory effects (12–14). Moreover, dietary administration of DKT is known to alter the composition of the gut microbiota in mice, suggesting that DKT acts on the host’s immune system by affecting the gut microbiota (15, 16). Shi et al. reported that DKT ameliorates acute experimental colitis by altering gut microbial composition and increasing propionate acids (17). However, the precise mechanisms of its anti-inflammatory effects and the regulatory function of the intestinal microbiota remain largely unclear.
Secretory leukocyte protease inhibitor (SLPI) is an endogenous serine protease inhibitor secreted by glandular tissue that antagonizes neutrophil proteases, such as neutrophil elastase (NE) and cathepsin G (18). Previous studies using SLPI-deficient mice (SLPI^-/-) have shown the tissue protective effects of SLPI through anti-protease activity in the skin, lung, and colon (19–21). SLPI has also been reported to have antimicrobial activity (22), suggesting that it regulates the gut microbiota by acting as an antimicrobial peptide in the intestine.
The purpose of this study was to elucidate the anti-inflammatory mechanism of DKT and potential involvement of SLPI using a murine colitis model. Here, we showed that oral administration of DKT induced the expression of SLPI, in association with an increase in the number of butyric acid-producing bacteria in the colon of mice, and administration of DKT ameliorated the disease severity of DSS-induced colitis in an SLPI-dependent manner. These results provide insight into the possible mechanisms of the therapeutic effects of DKT on IBD.
To examine the efficacy of DKT on intestinal inflammation, we first compared the disease severity of DSS-induced colitis with and without DKT in wild-type (WT) mice. We prepared the following four experimental groups: a normal water and diet group (DW), normal water and DKT diet group (DW+DKT), a DSS-induced colitis group (DSS), and a DSS-induced colitis with DKT treatment group (DSS+DKT) (Figure 1A). Based on the study group, mice were given a normal diet or a 3.6% DKT diet for 21 days, followed by 2% DSS for 5 days, as appropriate. Although the body weight of the DW and DW+DKT groups increased slightly, both DSS and DSS+DKT groups demonstrated weight loss, diarrhea, and bloody feces. As shown in Figures 1B, C, however, the weight loss and colitis symptoms in DSS+DKT mice were significantly suppressed on day 7 compared to the DSS group. It is generally accepted that a decrease in colon length in DSS-treated mice is associated with the severity of inflammation and fibrosis in experimental colitis (23). Colon length in the DSS+DKT group was significantly longer than that in the DSS group (Figure 1D). Histological analysis showed that severe crypt loss and inflammatory cell infiltration in the colonic mucosa were seen in the DSS group, while these symptoms were significantly milder in the DSS+DKT group (Figures 1E, F). Furthermore, mRNA levels of IL-1β, IL-6, IL-17A, and IFN-γ were significantly up-regulated in the colon of the DSS group compared to the control DW group. The expression levels of these pro-inflammatory cytokines in the colon were significantly suppressed in the DSS+DKT group compared to the DSS group (Figure 1G). These results indicate that DKT treatment ameliorates DSS-induced colon inflammation in WT mice.
Figure 1. DKT ameliorates DSS-induced colon inflammation in wild-type (WT) mice. (A) Experimental schematic: a normal water and diet group (DW), normal water and DKT diet group (DW+DKT), DSS-induced colitis group (DSS), and DSS-induced colitis with DKT treatment group (DSS+DKT) were created using C57BL/6N mice. (B) Changes in body weight in WT mice were monitored for seven days after DSS treatment (n = 5 in each group). (C) Clinical symptoms of DSS-induced colitis were determined by the disease activity index (DAI) (n = 5 in each group). (D) Colon length was measured on day 7 (n = 5 in each group). (E) The distal colon was excised on day 7, sectioned, and stained with H&E. Scale bars represent 100 μm. (F) Histological scores were evaluated on day 7 (n = 5 in each group) (G) mRNA expression levels of the indicated pro-inflammatory cytokines were determined by quantitative RT-PCR (n = 5 in each group). Statistical analysis was performed using one-way ANOVA followed by Tukey’s multiple comparisons test. *: P < 0.05 and ***: P < 0.001.
To clarify the protective mechanisms of DKT in the intestine, we examined whether DKT induces colon protective molecules, such as antimicrobial peptides or protease inhibitors. CMT93 cells, a colon carcinoma cell line, were cultured for 24 hours in the presence or absence of DKT extract powder (DKT-E), and mRNA expression was examined. As shown in Figure 2A, mRNA expression of SLPI was significantly increased in CMT93 cells treated with DKT-E compared to that in untreated control cells, which was more pronounced than other protease inhibitors, including β-defensin, regenerating islet-derived protein IIIγ (Reg-IIIγ), and lactoferrin or protease inhibitors, such as serine protease inhibitor A3N (SerpinA3N) and serine peptidase inhibitor kazal type 4 (Spink4). We previously reported that lipopolysaccharide (LPS) stimulation induces SLPI expression (21) (Figure 2B, left), which depends on the TLR signaling pathway through TRAF6, since CMT93 cells lacking TRAF6 failed to induce SLPI (Figure 2B right). Interestingly, however, induction of SLPI expression by DKT-E treatment, albeit weaker than that induced by LPS (Figure 2B, left), occurred even in the absence of TRAF6 (Figure 2B, right), suggesting that DKT-E induces SLPI from intestinal epithelial cells in a TLR ligand-independent manner. Since the gut microbiota is an important factor in the severity of colitis (24), we performed 16S rRNA metagenome sequencing analysis of stool samples of mice treated with DKT. In the gut microbiota composition profile, the abundance of beneficial bacteria, such as Parabacteroides, Allobaculum, and Akkermansia, were increased at the genus level in WT mice after treatment with DKT (day 0) (Figures 2C, D). Since these species of bacteria are known to produce short chain fatty acids (SCFAs), we next analyzed SCFAs in fecal samples using GC/MS. As expected, dietary DKT increased SCFAs, including butyrate, propionate and acetate in fecal samples (Figure 2E). Notably, butyrate, a major gut microbiome-derived SCFA, was significantly higher in WT mice treated with DKT. Recent studies have demonstrated that butyrate might exert beneficial effects on barrier integrity by inducing endogenous antimicrobial peptides (25). Interestingly, the expression of SLPI mRNA in CMT93 cells was significantly increased after 24 hours of butyrate treatment compared to that in untreated control cells in vitro (Figure 2F). Similarly, oral supplementation of butyrate slightly, but not significantly, increased SLPI expression in the mice colon (Supplementary Figure 1A). These results suggest that DKT enhances SLPI expression directly in the colon, as well as indirectly by modulating the gut microbiota and increasing butyrate production.
Figure 2. DKT alters the gut environment and induces SLPI in intestinal epithelial cells. (A) Quantitative RT-PCR analysis of the mRNA expression of SLPI and other antimicrobial peptides or protease inhibitors in DKT extract powder (DKT-E)-treated CMT93 cells. Cells were treated with DKT-E (1 mg/mL) for 24 hours. Relative mRNA expression of the indicated genes in CMT93 cells treated with DKT-E is shown as the fold-increase compared to untreated control cells (CONT). Graphs show the mean ± SEM (n = 6). (B) Quantitative RT-PCR analysis of the mRNA expression of SLPI in CMT93 and TRAF6-deficient CMT93 cells (CMT93ΔTRAF6). Cells were treated with DKT-E (1 mg/mL) or LPS (3 μg/mL) for 24 hours, or were left untreated (CONT). Graphs show the mean ± SEM (n = 3). (C) Fecal samples from mice fed a normal diet (DW) or DKT diet (DW+DKT) for 21 days (on day 0) were subjected to 16S rRNA metagenome sequencing to examine the composition of the gut microbiota. The relative abundance of bacterial genera is shown. Each bar shows relative bacterial abundance in individual mice (n = 5 in each group). (D) Relative bacterial abundance is shown at the genus level. Data are presented as the mean ± SEM (WT: n = 5, WT+DKT: n = 5) (E) The relative concentrations of the indicated SCFAs in murine feces before (Day -21) and after (Day 0) DKT administration. Stool samples from the same mice were analyzed by GC/MS. (F) CMT93 cells were stimulated with sodium butyrate (1 mM) for 24 hours. Relative mRNA expression of SLPI is shown. Statistical analysis was performed using one-way ANOVA followed by Tukey’s multiple comparisons test or student’s t test. Data are expressed as the mean ± SEM (n = 5 in each group). *: P < 0.05, **: P < 0.01, ***: P < 0.001, ****: P < 0.0001, and NS, not significant.
Next, we prepared the following four experimental groups to check the expression of SLPI in vivo: WT mice on a normal diet (WT-CON), WT mice on a DKT diet (WT-DKT), SLPI^-/- mice on a normal diet (KO-CON), and SLPI^-/- mice on a DKT diet (KO-DKT). After 28 days of feeding, SLPI mRNA levels were significantly enhanced in the colon of WT-DKT mice, but not in KO-DKT mice (Figure 3A). In agreement with this finding, SLPI protein was clearly detected in the colon of DKT-treated WT mice by Western blotting (Figure 3B). Furthermore, we investigated the localization of SLPI by immunohistochemistry. SLPI expression was not observed in colon of mice given normal diet (WT-CON), while SLPI expression was observed in goblet cells of the colon of mice treated with DKT (WT-DKT) (Supplementary Figure 1B). These results indicate that DKT induces SLPI production.
Figure 3. Induction of SLPI is required for the suppressive effect of DKT on DSS-induced colitis. (A) Quantitative RT-PCR analysis of the mRNA expression of SLPI in the colon of mice after the treatment of DKT. Graphs show the mean ± SEM (n = 3-4). (B) SLPI protein in colonic tissues of WT and KO mice with (+) and without (-) DKT. SLPI was detected by Western blotting. (C) Experimental schematic: WT and SLPI^-/- (KO) mice were administered DSS after pre-feeding with a normal diet (DSS) or a DKT diet (DSS+DKT). (D) Body weight changes in WT and SLPI^-/- mice were monitored after DSS treatment (WT-DSS group: n = 10, WT-DSS+DKT group: n = 10, KO-DSS group: n = 7, KO-DSS+DKT group: n = 8). (E) Clinical symptoms of DSS-induced colitis in WT (n = 10) and SLPI^-/- mice (n = 9) were determined by the DAI (F, G). Colon length was compared between DSS-treated WT and SLPI^-/- mice on day 7 (WT-DSS group: n = 10, WT-DSS+DKT group: n = 10, KO-DSS group: n = 7, KO-DSS+DKT group: n = 8). Data from two different experiments are presented together. Statistical analysis was performed using one-way ANOVA followed by Tukey’s multiple comparisons test. Data represent the mean ± SEM. *: P < 0.05 and **: P < 0.01. N.S, not significant.
To clarify the role of SLPI in the suppressive effect of DKT on DSS-induced colitis, we next evaluated the effect of DKT on DSS-induced colitis in WT and SLPI^-/- mice. Diet-incorporated DKT was administered from 21 days prior to DSS treatment to the end of the experiment. We prepared the following four experimental groups: WT mice on a normal diet (WT-DSS), WT mice on a DKT diet (WT-DSS+DKT), SLPI^-/- mice on a normal diet (KO-DSS), and SLPI^-/- mice on a DKT diet (KO-DSS+DKT) (Figure 3C). DSS-treated mice continued to experience a decrease in body weight from day 5 of DSS administration to the end of the experiment. Oral DKT administration significantly suppressed weight loss in WT mice, although it failed to do so in SLPI^-/- mice (Figure 3D). The same was true for the DAI. DKT treatment reduced DAI scores in WT mice, but not in SLPI^-/- mice (Figure 3E). Moreover, DSS-treated mice displayed a reduction in colon length and grossly thickened walls, which was clearly suppressed by DKT in WT mice, but not in SLPI^-/- mice (Figures 3F, G). These results suggest that DKT attenuates the severity of DSS-induced colitis in an SLPI-dependent manner.
Next, we examined histopathological changes in DSS-induced colitis and the efficacy of DKT and found that loss of crypts, submucosal infiltration of inflammatory cells, and ulceration were observed in all groups except the WT-DSS+DKT group (Figure 4A). Numerous neutrophils with a segmented nucleus with 2-5 lobes were seen to infiltrate the submucosa (Figure 4A, lowest panel). In addition, the histological score was significantly lower in the WT-DSS+DKT group than the WT-DSS group (Figure 4B). On the other hand, there were no significant differences between the KO-DSS and KO-DSS+DKT groups. We next assessed the mRNA expression levels of pro-inflammatory cytokines in colonic tissue. mRNA levels of IL-6, IL-17A, and IL-23p19 were significantly up-regulated in the colon of DSS-treated WT and SLPI^-/- mice as compared to untreated mice. The expression levels of pro-inflammatory cytokines in the colon of DSS-treated WT mice were significantly suppressed by DKT treatment, while no suppression was observed in SLPI^-/- mice (Figure 4C). Consistent with neutrophil infiltration, MPO activity was increased by DSS treatment, which was significantly suppressed by the administration of DKT in WT mice (Figure 4D). These data indicate that treatment with DKT ameliorates the inflammatory changes induced by DSS in WT mice in an SLPI-dependent manner.
Figure 4. DKT treatment ameliorates DSS-induced intestinal inflammation in WT mice, but not in SLPI^-/- mice. (A) H&E staining of DSS-induced colitis in WT and SLPI^-/- mice treated with DKT (DKT +) or left untreated (DKT -). A higher magnification image of the rectangle in the left panel is shown in the lowest panel. The scale bar represents 100 μm (upper panels) and 10 μm (lowest panel), respectively. (B) Graph showing the histological score (WT-DSS group: n = 10, WT-DSS+DKT group: n = 10, KO-DSS group: n = 7, KO-DSS+DKT group: n = 8). (C) The mRNA expression level of pro-inflammatory cytokines was determined by quantitative RT-PCR (WT: n = 5 in each group; SLPI^-/-: n = 6-8 in each group). (D) Neutrophil activity was measured by MPO assay (WT-DW: n = 5, WT-DW+DKT: n = 5, WT-DSS: n = 5, WT-DSS+DKT: n = 6, KO-DW: n = 6, KO-DW+DKT: n = 6, KO-DSS: n = 5, and KO-DSS+DKT: n = 5). Statistical analysis was performed using one-way ANOVA followed by Tukey’s multiple comparisons test. Results are expressed as the mean ± SEM. *: P < 0.05, **: P < 0.01, and NS, not significant.
The intestinal epithelial barrier is essential for intestinal homeostasis, and its dysfunction is implicated in the development of gut inflammation (26). We next examined intestinal epithelial permeability to assess the effects of DKT on the intestinal epithelial barrier in the context of DSS-induced colitis. Mice were given FITC-dextran orally, and intestinal permeability was evaluated by assessing serum FITC-dextran fluorescence levels. Serum FITC-dextran fluorescence levels were comparable at baseline in both DSS and DSS+DKT groups on day 3 because no inflammation was observed in either group (data not shown), indicating that the effect of DKT on the intestinal epithelial barrier function is limited in the early stage of colonic inflammation. On day 7, serum FITC-dextran fluorescence levels were significantly increased in DSS-treated mice compared with untreated mice (Figure 5A). Pre-treatment with DKT significantly suppressed serum FITC-dextran fluorescence levels to the levels seen in intact WT mice. In contrast, DKT treatment exhibited little inhibitory effects in SLPI^-/- mice (Figure 5A). Tight junction proteins (TJPs) are also important components of the intestinal epithelial barrier (27). Therefore, we examined the expression of occludin and ZO-1 proteins in the colon using immunohistochemistry, and found a decrease in their expression in the DSS-treated group compared to the DSS-untreated group (Figure 5B). Interestingly, pretreatment with DKT increased the expression of occludin and ZO-1 in DSS-treated WT mice, but not in the KO group (Figure 5B). These results indicate that DKT protects the intestinal epithelial barrier by maintaining TJPs in WT mice in an SLPI-dependent manner. Since neutrophil proteases are known to disrupt the intestinal epithelial barrier, we next evaluated the activity of neutrophil elastase (NE), a specific target of SLPI, in each mouse. NE activities in the colon were increased by DSS treatment, which was attenuated by DKT treatment in WT mice (Figure 5C). On the other hand, the suppressive effect was not seen in SLPI^-/- mice. These data suggest that DKT suppresses NE activity in neutrophils via the protease-inhibitory activity of SLPI.
Figure 5. DKT protects the intestinal epithelial barrier by suppression of neutrophil protease in WT mice, but not SLPI^-/- mice. (A) WT and SLPI^-/- mice under the indicated treatment were given FITC-dextran orally, and blood samples were collected 4 hours later. The graph shows FITC-dextran levels in serum in the different groups, determined by fluorescence intensity. Data from two different experiments are presented together. (WT-DW: n = 5, WT-DW+DKT: n = 3, WT-DSS: n = 10, WT-DSS+DKT: n = 4, KO-DW: n = 5, KO-DW+DKT: n = 5, KO-DSS: n = 5, and KO-DSS+DKT: n = 4). (B) Expressions of occludin and ZO-1 in the colon tissues from mice under the indicated treatment were detected by immunohistochemistry (×200). Scale bars:100 μm (C) Colonic NE activity was measured by NE assay (WT-DW: n = 10, WT-DW+DKT: n = 10, WT-DSS: n = 10, WT-DSS+DKT: n = 12, KO-DW: n = 6, KO-DW+DKT: n = 6, KO-DSS: n = 5, and KO-DSS+DKT: n = 5). Data from two different experiments are presented together. Data were analyzed by one-way ANOVA followed by Tukey’s multiple comparisons test, and are presented as the mean ± SEM. *: P < 0.05, **: P < 0.01, and NS, not significant.
To investigate the impact of DKT and SLPI on the gut microbiota, we analyzed the composition of the gut microbiota by 16S rRNA metagenome sequencing of fecal samples. To assimilate the gut microbiota in a steady state, WT mice and SLPI^-/- mice were co-housed for several weeks prior to the experiment. 16S rRNA genes were sequenced and principal coordinate analysis (PCoA) plots were generated by QIIME 1.9.0 from MiSeq data. In WT mice, PCoA plots showed that each group formed a cluster of different intestinal flora after treatment with DKT in unweighted UniFrac distances (Figure 6A). On the other hand, PCoA plots showed that there was no obvious separation in SLPI^-/- mice with DKT treatment (Figure 6B). There was no significant difference in the profile of the gut microbiota in both WT and SLPI^-/- mice at the phylum level before administration of DKT (day -21) (Supplementary Figure 2A). However, after the DKT treatment (day 0), the abundance of beneficial bacteria, such as Parabacteroides, Allobaculum, and Akkermansia, was significantly increased at the genus level in WT mice, while there were no significant changes in these bacteria in SLPI^-/- mice (Figure 6C). These data indicate that DKT might alter the colonic bacterial community in an SLPI-dependent manner.
Figure 6. DKT alters the gut microbiota in an SLPI-dependent manner. (A, B) Visualization of principal coordinates analysis (PCoA) of unweighted UniFrac distances, to show differences in bacterial composition in WT (A) and SLPI^-/- mice (B). Each point represents the fecal bacterial microbiota in a single sample. (C) Relative bacterial abundance is shown at the genus level. Data are presented as the mean ± SEM (WT: n = 5 in each group; SLPI^-/-: n = 4 in each group) *: P < 0.05, **: P < 0.01, and NS, not significant. (D) Schematic model for the mechanism of DKT in suppressing colitis, whereby DKT induces SLPI, which in turn increases beneficial bacteria, such as Parabacteroides, Allobaculum, and Akkermansia, which produce butyric acid and further induce SLPI. SLPI inhibits neutrophil elastase activity and butyric acid enhances intestinal epithelial proliferation.
We next analyzed the composition of the gut microbiota in mice with colitis (day 7). Alpha diversity analysis revealed that DSS treatment reduced microbial diversity in fecal samples from both WT and SLPI^-/- mice (Supplementary Figure 2B). DKT suppressed the reduction of alpha diversity by DSS treatment in WT mice, but not in SLPI^-/- mice (Supplementary Figure 2B). In beta diversity analysis, PCoA plots were not clearly separated after DSS treatment regardless of dietary DKT intake (Supplementary Figure 3A). Genus-level profiling showed that DSS treatment increased the relative abundance of Turicibacter, also known as colitogenic bacteria, in both WT and SLPI^-/- mice, and no significant effect of DKT was observed (Supplementary Figure 3B). Moreover, there were no significant changes in the gut microbiota at the genus level between DKT treated and untreated groups of DSS-treated mice (day 7), probably due to limited activity of DKT under DSS-induced inflammation in the colon (Supplementary Figure 4).
In the present study, we showed that SLPI, directly induced by DKT in the colon, as well as indirectly by modulating the gut microbiota and increasing butyrate production, alleviates DSS-induced colitis by protecting the intestinal epithelial barrier. Our findings delineate the molecular mechanisms by which DKT ameliorates IBD.
IBD, such as CD and UC, is characterized by chronic relapsing inflammation of the intestine. Although the precise mechanism of IBD remains unclear, dysfunction of the intestinal epithelial barrier is crucial for the development and perpetuation of IBD (26). Once the intestinal barrier function is disrupted by genetic or environmental factors, bacterial antigens in the intestinal tract come into contact with immune cells, leading to unwanted immune reactions and an excessive recruitment of neutrophils to sites of inflammation (28, 29). Eventually, the intestinal epithelium is further damaged by the neutrophil proteases released from neutrophils (30). Thus, neutrophil proteases must be strictly controlled to ensure the integrity of the intestinal epithelial barrier.
DKT, a traditional Japanese herbal medicine, has been shown to increase intestinal blood flow and improve intestinal propulsive motility, as well as to have anti-inflammatory effects in experimental models. For example, Matsunaga et al. revealed that DKT attenuated DSS-induced colitis by enhancing the anti-inflammatory cytokine IL-10 (13). Furthermore, Li et al. have reported that DKT reduces methotrexate-induced small intestinal inflammation by stimulating cell proliferation and protecting the intestinal barrier (12). In the present study, we found that SLPI was induced by DKT in a colon carcinoma cell line in vitro, and in the colon of mice in vivo (Figures 2, 3; Supplementary Figure 1B). SLPI is an endogenous serine protease inhibitor expressed at mucosal surfaces, mainly by epithelial cells (31). We previously showed that the protease inhibitory activity of SLPI prevents the intestinal epithelial barrier dysfunction caused by excessive NE activity in DSS-induced colitis (21). Thus, SLPI maintains homeostasis of the intestinal barrier by preventing tissue destruction and regulating the threshold of inflammatory immune responses in the intestine. In this study, we revealed that administration of DKT attenuates DSS-induced colitis in WT mice, but not in SLPI^-/- mice (Figure 3). In particular, increased permeability of the epithelium caused by DSS treatment was suppressed by DKT in an SLPI-dependent manner (Figure 5A). This is probably partly due to the fact that DKT administration maintained the expression of the adhesion molecules, occludin and ZO-1, under DSS-induced inflammation in the colon of WT mice, but not in SLPI^-/- mice (Figure 5B). These results indicate that DKT attenuates DSS-induced colitis by protecting the intestinal epithelial barrier in an SLPI-dependent manner. Infiltration of neutrophils into the mucosal tissue is a hallmark of colitis activity. Subsequently, neutrophil proteases, such as NE, derived from neutrophils damage the gut epithelium, resulting in increased permeability (30). Given the protease inhibitory activity of SLPI, it is likely that administration of DKT might inhibit the activity of NE that is enhanced by DSS-induced colitis. As expected, the activity of MPO, an indicator of neutrophil activation, and NE activity were decreased by DKT treatment in WT mice, but not in SLPI^-/- mice (Figures 4D, 5C). These results suggest that DKT exerts protective effects against colitis due, at least in part, to induction of anti-protease protein SLPI in the colon.
Interactions between various natural compounds or diets and the gut microbiota are known to alter intestinal permeability and the severity of colitis in mice (32, 33). DKT, a combination of four natural herbs, has been reported to alter the microbiota composition in mice in a dose-dependent manner (16). Long-term dietary DKT increases the abundance of a number of bacteria that produce SCFAs, including butyrate, propionate, and acetate (15). On the other hand, SLPI is known to have broad spectrum antimicrobial activity against enteric pathogens, including Gram-positive and -negative bacteria and fungi (34). We, therefore, explored the possible involvement of DKT and SLPI in the regulation of the gut microbiota composition, and its effect on DSS-induced colitis. In the principal coordinates analysis, the composition of the gut microbiota was clearly separated between pre- and post-DKT treatment of mice in the presence of SLPI (Figure 6A). In particular, administration of DKT increased the relative abundance of the beneficial bacteria, Parabacteroides, Allobaculum, and Akkermansia at the genus level (Figure 6C). These changes were only seen in WT mice, suggesting that DKT might alter the gut microbiota composition in an SLPI-dependent manner. SLPI has been known to have not only an inhibitory property against serine proteases but also an antimicrobial property against Gram-negative bacteria in vitro (34). It has been reported that deficiency of certain antimicrobial peptides can alter the occupancy of specific commensal bacteria and change the composition of the intestinal microbiota (35). Therefore, the lack of SLPI may influence to certain commensal bacteria in the gut. In addition, it has been reported that DKT increases IL-22 following ILC3 induction (17) and that IL-22 increases certain commensal intestinal bacteria (Akkermansia) by induction of antimicrobial peptides (36). Thus, SLPI induced by DKT, may control the growth of specific commensal bacteria such as Akkermansia through its antimicrobial activity. However, the precise mechanism has not yet been elucidated in this study, and is a subject for future research.
Parabacteroides spp., core members of the human gut microbiota, have a close relationship with host health due to its physiological characteristics on carbohydrate metabolism and secreting SCFAs (37). A previous animal study has reported that oral administration of Parabacteroides distasonis and its cellular components attenuate experimental colitis through the reduction of pro-inflammatory cytokines and increase in the number of regulatory T cells in the colon (38). Allobaculum spp., known as a butyric acid producer, is a newly identified IBD-associated bacteria that is thought to be closely associated with the host epithelial barrier (39, 40). Akkermansia spp. reportedly ameliorate the symptoms of DSS-induced colitis through the upregulation of NLPR3 (41). Moreover, Akkermansia species enhance the function of the intestinal epithelial barrier by producing mucin and TJPs in intestinal epithelial cells (42, 43). Since the initial gut microbiota has a profound influence on DSS-induced colitis (44), greater abundance of beneficial bacteria, such as Parabacteroides, Allobaculum, and Akkermansia, by treatment with DKT might reduce the susceptibility to DSS-induced colitis. Moreover, these bacteria are known to produce butyric acid (39, 45, 46), which is consistent with our observation that DKT treatment increased both, the relative abundance of these bacteria (Figure 6C) and the amount of butyric acid in the colon (Figure 2D). Interestingly, butyrate enhanced the expression of SLPI in a colon carcinoma cell line in vitro (Figure 2E), suggesting that DKT increases butyrate-producing bacteria via induction of SLPI expression, which forms a positive feedback loop whereby butyrate induces further SLPI expression (Figure 6D). In addition, the expression of SLPI was not increased by DKT treatment in antibiotics-treated mice (Supplementary Figure 3C), suggesting that gut microbiota is required for the proper induction of SLPI. In other word, DKT directly induces SLPI from intestinal epithelial cells in vitro, but requires the presence of intestinal bacteria for the proper induction of SLPI in vivo. SCFAs, such as butyric acid, are known to enhance epithelial integrity by enhancing intestinal cell proliferation (47) and modulating TJP expression (48, 49), suggesting that increased butyric acid contributes to ameliorating DSS-induced colitis.
We found that abundance of the genus Turicibacter, known to correlate positively with the development of IBD (50), was increased by DSS treatment in the presence of SLPI, while DKT treatment failed to inhibit its growth (Supplementary Figure 3B). These results indicate that the effect of DKT on the gut microbiota composition is limited to bacterial species.
Although the present findings provide insight into the mechanism of the colon protective effect of DKT via induction of SLPI, the precise signaling pathways by which DKT induces SLPI remain unclear. In general, herbal medicines consist of multiple plant extracts containing several constituents, which are often believed to work together synergistically (51). The pharmacological effects of DKT were not analyzed at the component level in this study. Therefore, determining the biological components of DKT that induce SLPI and modulate the gut microbiota would be of interest for future research.
In conclusion, DKT exerts a protective effect against DSS-induced colitis, in which SLPI promotes prebiotic effects by reshaping the gut microbiota and increasing butyrate-producing bacteria, while enhancing the integrity of the intestinal epithelial barrier through protease inhibitory activity. Therefore, our findings shed new light on the mechanism of the therapeutic effect of DKT on IBD.
Daikenchuto (DKT, TJ-100) was obtained from Tsumura & Co. (Ibaraki, Japan). DKT consists of an herbal medicinal extract powder (DKT-E) and maltose (ratio 1.25 g to 10 g, respectively). DKT-E was prepared by spray-drying a hot-water extract mixture containing the following three crude drugs/herbs in the proportions mentioned in parentheses: Zanthoxyli fructus (Japanese pepper) (2.0), Zingiberis rhizoma (Ginger) (5.0), and Panax ginseng (Ginseng radix) (3.0). DKT was included in PicoLab rodent diet 20 (Land O’ Lakes, Inc., Arden Hills, MN, USA), at 36 g DKT/kg of diet (3.6% wt/wt) (Oriental Yeast Co., Ltd., Tokyo, Japan). The dosage of DKT was based on a previous animal experiment (16) and the human equivalent dosage was adjusted to the mouse dosage based on the animal’s surface area (52). Ampicillin and vancomycin were purchased from Wako (Osaka, Japan).
CMT93, a mouse colon carcinoma cell line, was purchased from ECACC (Salisbury, UK). CMT93 cells were cultured in Dulbecco’s modified Eagle medium (DMEM) containing 10% FCS, 2 mM L-Alanyl-L-glutamine (Nacalai tesque), 100 U/mL penicillin, and 100 μg/mL streptomycin (Nacalai tesque, Kyoto, Japan). We established TNF receptor-associated factor 6 (TRAF6) knockout (KO) CMT93 cells using the CRISPR-Cas9 genome editing system. Briefly, a single guide RNA targeting TRAF6 (5’-GGAGGACAAGGTTGCCGAAA-3’) was cloned into a Cas9-expressing plasmid (pSpCas9(BB)-2A-Puro (PX459); addgene plasmid #48139), and the plasmid was transfected into CMT93 cells, and then subsequently cloned after a 2-day treatment with 2 μg/mL puromycine. DKT-E was suspended in distilled water, sterilized by boiling at 95°C, passed through a 0.45 μm filter, and then added to CMT93 cells at final concentrations of 330 or 1000 μg/mL. In addition, CMT93 cells were treated with 1 mM sodium butyrate (Wako Pure Chemical Industries, Ltd., Kyoto, Japan) or stimulated with 3 μg/mL of LPS (Sigma-Aldrich, St. Louis, MO, USA) for 24 hours. The cells were then harvested and total RNA was extracted using TRI Reagent^® (Sigma-Aldrich, St. Louis, MO, USA) for performing quantitative RT-PCR analysis.
Seven-week-old female C57BL/6 mice were purchased from Japan SLC (Hamamatsu, Japan). SLPI^-/- mice, as described previously (20), were backcrossed with C57BL/6 inbred mice more than 10 times. Mice were maintained in a specific pathogen-free facility under conditions of constant temperature (24 ± 1°C), humidity (50 – 60%), and a 12-hour light-dark cycle with free access to food and water. All experiments using these mice were approved by and performed according to the guidelines of the Oita University Animal Ethics Committee (approval number: 180901A). This study adheres to standards articulated in the ARRIVE guidelines.
A 28-day protocol was designed and mice were fed a normal diet or a 3.6% DKT diet during this protocol period (day -21 to 7). To induce colitis, mice were administered 2% Dextran Sulfate Sodium Salt (DSS) – Colitis Grade (36,000-50,000 MW) (MP Biomedicals, Irvine, CA, USA) in drinking water for 5 days (days 1-5), followed by normal water for 2 days (days 6-7). Their body weight and disease activity index (DAI) were monitored daily. DAI scores were determined according to a previous report (53) as follows: body weight loss (0: no loss; 1: 1-5%; 2: 5-10%; 3: 10-20%; 4: >20% loss), stool consistency (0: normal; 2: loose stools; 3: mud stools; 4: diarrhea), and bleeding per rectum (0: no blood; 2: visual pellet bleeding; 3: blood around anus; 4: gross bleeding).
Mice were sacrificed by cervical dislocation on day 28 and their large intestine was removed. After measuring the length of the colon, the distal parts of the colon were stained with hematoxylin and eosin (H&E). The severity of DSS-induced colitis was evaluated using distal colon sections by a modified histological scoring system (54) as follows: epithelial cell damage (0: no damage; 1: focal loss of goblet cells; 2: diffuse loss of goblet cells; 3: focal loss of crypts; 4: diffuse loss of crypts), cell infiltration (0: no increase; 1: around the base of the crypts; 2: along the muscularis mucosal layer; 3: mucosal layer; 4: mucosal and submucosal layer), ulcer (0: no ulcer; 1: focal erosion; 2: diffuse shallow ulcer on the epithelial surface or focal ulcer in the mucosal layer; 3: diffuse ulcer involving the entire mucosal layer). Immunohistochemistry was performed using 2 μm sections of paraffin-embedded colon tissue. We used primary antibodies against occludin (Abcam, Cambridge, UK), ZO-1 (Gene Tex, Irvine, CA, USA), and SLPI (R&D Biosystems, Minneapolis, MN, USA). DAKO EnVision™+ (Rabbit) (Agilent Technologies) was used as a secondary antibody. Sections were subsequently counterstained with hematoxylin. All histological evaluations were performed in a blind fashion.
Metabolites in the cecal contents were analyzed by GC/MS-TQ8040 (Shimazu, Kyoto, Japan) with a BPX-5 column (30 m × 0.25 mm i.d.; film thickness 1.00 μm, Trajan Scientific and Medical, Vic., Australia) for SCFAs, as described previously (55). Mass spectrum peaks were detected using the GC/MS solution software (Shimazu), and the retention time correction of peaks was performed based on the retention time of a standard alkane series mixture (C9 to C33). Metabolites were identified by the Smart Metabolites Database (Shimazu), which contains multiple reaction monitoring transitions for 12 metabolites commonly found in biological samples for BPX-5. Raw data have been deposited at figshare with DOI: 10.6084/m9.figshare.26212430.
The bacterial genomic DNA was isolated using the standard protocol with some modifications (56). DNA from mouse feces was extracted using a phenol/chloroform/isoamyl alcohol method. Preparation of the 16S rRNA gene metagenome library for MiSeq (Illumina, Inc., San Diego, CA, USA) was performed according to the manufacturer’s protocol. Briefly, 10 ng of the DNA template was amplified using an Advantage-HF 2 PCR kit (Takara Bio Inc., Shiga, Japan) with universal primers for the 16S rRNA v3-v4 region (forward primer: 5’ TCGTCGGCAGCGTCAGATGTGTATAAGAGACAGCCTACGGGNGGCWGCAG 3’, reverse primer: 5’ GTCTCGTGGGCTCGGAGATGTGTATAAGAGACAGGACTACHVGGGTATCTAATCC 3’). Subsequently, index sequences for each sample were added to both ends of the purified PCR fragments. The concentrations of each amplicon were measured by the Quant-iT PicoGreen dsDNA Assay Kit (Thermo Fisher Scientific, Inc.) and mixed equally. The library was applied to MiSeq Reagent Kit v3 (Illumina, Inc.) and the sequence was determined using the manufacturer’s standard protocol. Sequence data were processed as follows using the 16S rRNA sequence analysis pipeline, QIIME 1.9.0 (57). Initially, both sequence reads were joined and sequences with a Phred quality score below 20 were removed. Chimera elimination by Usearch was performed to remove contaminated sequences. Open reference OTU picking was performed against Greengenes 13_8 97% OTU representative sequences. A summary of taxonomy in each sample was obtained using the script ‘summarize_taxonomy_through_plots.py’ in QIIME 1.9.0. Raw data have been deposited at figshare with DOI: 10.6084/m9.figshare.26241974.
Mice were fasted for 4 hours and administered FITC-dextran (4 kDa MW, 0.6 mg/g body weight) (Sigma-Aldrich) by oral gavage. Four hours later, blood samples were collected and the fluorescence intensity of serum FITC at 485/528 nm wavelength was measured using a microplate reader (Infinite 200 PRO, TECAN, Männedorf, Switzerland).
MPO activity was determined in colon tissues. Briefly, the colon tissues were homogenized in 500 μL of potassium phosphate buffer (pH 6.0) containing 0.5% hexadecyltrimethylammonium bromide (HTAB) (Sigma-Aldrich). Then, the samples were centrifuged at 14,600 rpm for 15 min at 4°C. Thereafter, 7 μL of the supernatant was mixed with 200 μL of O-dianisidine/Buffer solution, and absorbance readings at 450 nm were assessed every minute for 30 minutes. Colonic NE activity was measured using a Neutrophil Elastase Activity Assay Kit, Fluorometric (Abcam), according to the manufacturer’s instructions. The colon tissues were homogenized in 500 μL of HTAB buffer and then incubated with substrate in reaction buffer. Fluorescence was determined using a microplate reader at 380/500 nm wavelength every 3 minutes for 30 minutes.
Total proteins in the colons were subjected to SDS-PAGE. The separated protein on a PVDF membrane (Millipore, Darmstadt, Germany) was incubated with primary antibody against SLPI (1: 1000; R&D Biosystems) overnight at 4°C, followed by secondary antibody conjugated with horseradish peroxidase, and visualized with the ECL Western blotting analysis system (GE Healthcare, Piscataway, NJ, USA). Levels of SLPI were measured by quantification of the band intensities with ImageQuant TL software (Roche Diagnosis, Rotkreuz, Switzerland).
Total RNA from the colon was extracted using TRI Reagent^®, purified using a PureLink RNA Mini Kit (Thermo Fisher Scientific Inc.) and then reverse-transcribed using a Verso cDNA Synthesis Kit (Thermo Fisher Scientific Inc.). Quantitative RT-PCR was performed using a real-time PCR machine (LightCycler 96, Roche Diagnostics) with a KAPA SYBR FAST qPCR Kit (Kapa Biosystems, Wilmington, MA, USA). The relative mRNA levels were normalized to β-actin, and data were analyzed by LightCycler software (Roche Diagnostics). The sequences of primers used in this study are shown in Table 1.
Table 1. Primer sequences used for polymerase chain reaction in this study.
All data are presented as the mean ± SEM. Differences between two groups were analyzed by Student’s t test. Multiple comparisons were analyzed by one-way ANOVA followed by Tukey’s multiple comparisons test. Alpha and beta diversity analyses in fecal samples were calculated using QIIME 1.9.0. Univariate analysis between two groups was performed with the Mann-Whitney U test using GraphPad Prism7 software (GraphPad Software, San Diego, CA, USA). The graphs were visualized by Excel Software and GraphPad Prism 7 software. P values less than 0.05 were considered statistically significant in all experiments. In the figures, *: P < 0.05, **: P < 0.01, ***: P < 0.001, and ****: P < 0.0001.
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
The animal study was approved by Oita University Animal Ethics Committee (approval number: 180901A). The study was conducted in accordance with the local legislation and institutional requirements.
SO: Writing – original draft, Writing – review & editing. AS: Investigation, Writing – review & editing. YKu: Formal analysis, Writing – review & editing. KI: Formal analysis, Writing – review & editing. NK: Writing – review & editing, Funding acquisition. NS: Funding acquisition, Writing – review & editing. TC: Writing – review & editing. YKa: Writing – review & editing. YS: Writing – review & editing. SE: Writing – review & editing. SA: Writing – review & editing. KMi: Writing – review & editing. SI: Investigation, Writing – review & editing. MN: Investigation, Writing – review & editing. KMu: Funding acquisition, Writing – review & editing. KT: Writing – review & editing. TK: Conceptualization, Funding acquisition, Writing – review & editing.
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Nakatomi Foundation (to NS); Oita University President’s Strategic Discretionary Fund (to SO, NK, YKa); Research Grant and the Grant for Joint Research Project of the Research Institute for Microbial Diseases, Osaka University (to TK); Four Seasons Ladies Clinic Research Grant (to TK); Tsumura & Co (to KMu); and the Japan Society for the Promotion of Science {grant numbers (20K16028 and 23K16304 [to SO]), (20K16499 [to NS]), (22K20860 [to YKa]), (24K12629 [to NK]), and (21K07984 [to TK])}. This study received funding from Tsumura & Co. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
We thank Ms. Mami Koya (Oita University) for excellent technical assistance.
Authors SI and MN were employed by the company Tsumura & Co.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The authors declare that this study received funding from Tsumura & Co. The funder had the following involvement in the study: analysis of the gut microbiota.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2024.1457562/full#supplementary-material
Supplementary Figure 1 | (A) Quantitative RT-PCR analysis of the mRNA expression of SLPI in the colon of mice after oral butyrate supplementation. Graphs show the mean ± SEM (n = 5). (B) Immunohistochemistry of SLPI in the colon tissues from WT mice treated with normal or DKT diet for 28 days (upper panel: WT-CON, middle panel: WT-DKT). A higher magnification image of the rectangle in the middle panel is shown in the lowest panel. The scale bar represents 50 μm (upper and middle panels) and 10 μm (lowest panel).
Supplementary Figure 2 | (A) Fecal samples from mice before the DKT treatment (on day -21) were subjected to 16S rRNA metagenome sequencing to examine the composition of the gut microbiota. The relative abundance of bacteria at a phylum level is shown. Each bar shows relative bacterial abundance in individual mice (WT mice: n = 10, SLPI-/- mice: n = 8). (B) Alpha diversity of the gut microbiota is shown. Data are presented as the mean ± SEM (WT: n = 5, SLPI-/-: n = 4 in each group). *: P < 0.05 and NS, not significant.
Supplementary Figure 3 | (A) Visualization of principal coordinates analysis (PCoA) of unweighted UniFrac distances showing differences in bacterial composition. Each point represents the fecal bacterial microbiota in a single sample. (B) The relative abundance of Turicibacter is shown. Data are presented as the mean ± SEM (WT: n = 5 in each group; SLPI-/-: n = 4 in each group). (C) 1 g/L ampicillin and 0.5 g/L vancomycin were administered in drinking water for seven days to eliminate bacteria in the intestine. Quantitative RT-PCR analysis of the mRNA expression of SLPI in the colon of antibiotics-treated WT mice after the treatment of normal diet (antibiotic group) or DKT diet (antibiotic + DKT group). Graphs show the mean ± SEM (n = 4). NS, not significant.
Supplementary Figure 4 | Fecal samples from mice fed a normal diet or DKT diet for 21 days following DSS treatment for 7 days (on day 7) were subjected to 16S rRNA metagenome sequencing to examine the composition of the gut microbiota. The relative abundance of bacterial genera is shown. Each bar shows relative bacterial abundance in individual mice (WT: n = 5 in each group; SLPI-/-: n = 4 in each group).
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Keywords: Daikenchuto (DKT), SLPI, DSS-induced colitis, inflammatory bowel disease (IBD), butyric acid, Parabacteroides, Allobaculum, Akkermansia
Citation: Ozaka S, Sonoda A, Kudo Y, Ito K, Kamiyama N, Sachi N, Chalalai T, Kagoshima Y, Soga Y, Ekronarongchai S, Ariki S, Mizukami K, Ishizawa S, Nishiyama M, Murakami K, Takeda K and Kobayashi T (2024) Daikenchuto, a Japanese herbal medicine, ameliorates experimental colitis in a murine model by inducing secretory leukocyte protease inhibitor and modulating the gut microbiota. Front. Immunol. 15:1457562. doi: 10.3389/fimmu.2024.1457562
Received: 01 July 2024; Accepted: 07 October 2024;
Published: 25 October 2024.
Edited by:
Reviewed by:
Copyright © 2024 Ozaka, Sonoda, Kudo, Ito, Kamiyama, Sachi, Chalalai, Kagoshima, Soga, Ekronarongchai, Ariki, Mizukami, Ishizawa, Nishiyama, Murakami, Takeda and Kobayashi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Takashi Kobayashi, dGFrYXNoaWtAb2l0YS11LmFjLmpw
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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Elon Musk’s global influence campaign: What it means for politics  New Zealand Herald
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Werewolves have been one of the most popular creatures in pop culture since the 1940s, with dozens of masterpieces revolving around them.
By Marco Vito Oddo
Universal Pictures is set to unleash a new take on one of its most iconic monsters with Wolf Man, arriving in theaters on January 17, 2025. Helmed by The Invisible Man’s director Leigh Whannell and starring Christopher Abbott and Julia Garner, this modern reimagining follows a family man named Blake who becomes infected with lycanthropy after a werewolf attack at his inherited farmhouse. The premise promises a fresh perspective on the werewolf genre while honoring the horror elements that made the 1941 original a classic. As we await this new interpretation of the Wolf Man story, the time is ripe to look back at some of the greatest werewolf films that have shaped the genre.
From groundbreaking classics to modern masterpieces, these movies showcase the evolution of werewolf cinema and its ability to explore complex themes through the lens of supernatural horror. Here are the seven best werewolf movies to watch before Wolf Man:
While technically a TV special rather than a feature film, Werewolf by Night earns its place as a werewolf feature through its masterful homage to classic horror. Following the death of monster hunter Ulysses Bloodstone, elite warriors gather to compete for the powerful Bloodstone relic. Among them is Jack Russell (Gael García Bernal), who harbors a secret: he’s a werewolf trying to save his captured friend Ted, aka the Man-Thing. Allying with Ulysses’ estranged daughter Elsa (Laura Donnelly), Jack must navigate a deadly game while concealing his true nature.
Director Michael Giacchino’s black-and-white presentation and atmospheric storytelling make this hour-long special feel like a lost Universal monster movie, complete with practical effects and Gothic imagery. Even better, Werewolf at Night is a standalone story that can be enjoyed without any previous knowledge of the MCU. Upon release, the special became the top-streamed program, with critics praising its departure from typical MCU fare and its commitment to horror elements. Its success proved that werewolf stories could work within the superhero genre while maintaining their horror roots.
Before diving into this influential classic, it’s worth noting that every werewolf movie that followed owes a debt to Universal’s original masterpiece, which literally set the rules for how international cinema handles lycanthropy. Wolf Man follows Larry Talbot (Lon Chaney Jr.), who returns to his ancestral Welsh home following his brother’s death. After being bitten by a wolf while saving a local girl, Larry learns from a Romani woman that he’s now cursed to become a werewolf. What follows is a tragic tale of transformation, murder, and ultimately death at the hands of his own father.
The film’s exploration of the beast within man resonated deeply with audiences, while Chaney’s sympathetic performance elevated the material beyond simple monster movie fare. Critics have consistently praised the film, maintaining a 91% approval rating on Rotten Tomatoes. Its influence can still be felt today, from establishing werewolf mythology – silver as a weakness, complete moon transformations – to its psychological exploration of man’s dual nature. These elements are referenced in Leigh Whannell’s upcoming reboot, which aims to maintain the original’s focus on psychological horror.
Joe Dante’s pioneering werewolf film follows Karen White (Dee Wallace), a TV news anchor traumatized after a violent encounter with serial killer Eddie Quist (Robert Picardo). Her therapist, Dr. George Waggner (Patrick Macnee), recommends she recover at “the Colony,” a secluded resort. However, this seemingly peaceful retreat harbors dark secrets, as Karen discovers the residents are all werewolves, including her supposedly dead attacker, Eddie, and, eventually, her own husband, Bill.
The film’s groundbreaking transformation effects by Rob Bottin helped revitalize the werewolf genre in the 1980s. Critics praised its clever mix of horror and satire, with Dante masterfully balancing genuine scares with social commentary. The shocking finale, where Karen transforms on live television before being killed with silver bullets, remains one of horror cinema’s most memorable moments. While The Howling spawned numerous sequels, none matched the original’s impact or critical success.
Neil Marshall’s directorial debut combines military action with werewolf horror to create a unique and intense experience. The story follows a squad of British soldiers besieged by a pack of werewolves on a training exercise in the Scottish Highlands. Led by Sergeant Harry Wells (Sean Pertwee), the soldiers take refuge in an abandoned farmhouse, leading to a night of brutal survival horror.
Dog Soldiers earned praise for its intense action sequences and effective blend of genres. What makes the movie feel so refreshing is its focus on delivering unhinged fun without all the philosophical discussion other werewolf movies bring. The film won the Brussels International Festival of Fantasy Film’s Golden Raven award and helped revitalize British horror cinema. Its influence can be seen in subsequent military horror films, while its practical effects and tense atmosphere have earned it a strong cult following.
Most likely the least movie on this list, Good Manners is a Brazilian dark fantasy that expertly weaves social commentary with supernatural horror. The story follows Clara (Isabél Zuaa), a live-in nanny for Ana (Marjorie Estiano), a wealthy pregnant woman with mysterious nocturnal habits. Their relationship grows intimate, but everything changes when Ana dies giving birth to a werewolf child. Clara decides to raise the boy, Joel (Miguel Lobo), as her own, leading to a unique exploration of motherhood, class dynamics, and identity.
Good Manners received widespread critical acclaim, with critics praising its bold genre-blending approach and thoughtful exploration of social issues through a horror lens. In addition, directors Juliana Rojas and Marco Dutra create a visually striking film that subverts traditional werewolf movie expectations while delivering genuine emotional depth. Even though Brazilian cinema doesn’t have much space outside the country, Good Manners is one of the best werewolf movies ever.
John Landis’s horror-comedy masterpiece follows American tourists David Kessler (David Naughton) and Jack Goodman (Griffin Dunne) as they encounter a werewolf on the Yorkshire moors. After Jack’s death and David’s transformation, the film becomes a unique blend of genuine horror and dark humor, with David haunted by his decomposing friend’s ghost while falling in love with nurse Alex Price (Jenny Agutter).
The film’s revolutionary werewolf transformation scene, created by makeup artist Rick Baker, won the first-ever Academy Award for Best Makeup and set a new standard for practical effects in horror. An American Werewolf in London is rightfully celebrated for its perfect balance of horror and humor, strong performances, and an unforgettable soundtrack featuring moon-themed songs. Its influence extends beyond horror, inspiring countless filmmakers in their approach to practical effects and genre-blending storytelling.
This Canadian horror film brilliantly uses lycanthropy as a metaphor for female adolescence. Sisters Ginger (Katharine Isabelle) and Brigitte Fitzgerald (Emily Perkins) share a fascination with death and isolation from their peers. When Ginger is bitten by a werewolf, her transformation becomes intertwined with her entrance into womanhood, creating a powerful allegory for the changes and challenges of puberty.
Since its release, Ginger Snaps has developed a strong cult following, particularly among female horror fans, with good reason. Ginger Snaps‘ intelligent script, dark humor, and the compelling performances of Emily Perkins and Katharine Isabelle as the Fitzgerald sisters are reasons enough for this movie to be on anyone’s radar. However, Ginger Snaps has also used horror to tell a story from a female perspective before feminist horror became popular. While initially overlooked upon release, Ginger Snaps has since been recognized for its feminist themes and unique approach to the werewolf genre, earning the love it always deserved.
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01/04/2025 Sharon Swanepoel Police and Fire, Top News 0
MONROE, GA (Jan. 4, 2025) – Monroe Police Department Chief R.V. Watts reports that MPD responded to a call at the Monroe Airport located at 535 Towler Street today and arrived to find the body of a woman in a vehicle parked in front of the airport gate. She was the sole occupant of the vehicle and allegedly died as a result of a self-inflicted gunshot wound.
The victim has been identified at Deborah Williams, 66, of Cumming, Ga.
The Athens Georgia Bureau of Investigation Office was called in to assist and has taken over the case. MPD report that it is an open and active investigation and anyone with information is asked to contact Special Agent Kelsey Ward of the GBI at 1-706-542-7903.
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Cyclone State wins an allowance optional claiming race at Aqueduct Racetrack
Races like the Jerome Stakes are considered preps for the Kentucky Derby (G1).
But they are actually more of a test to see if a newly turned 3-year-old has what it takes to be a successful runner in longer and richer races in the new year.
"With these new 3-year-olds you want building blocks," trainer Chad Summers said.
Summers trains the Iowa-bred Cyclone State  who will make his stakes debut in the Jan. 4 $150,000 Jerome for 3-year-olds at Aqueduct Racetrack after a pair of sharp victories over the track at the same mile distance as Saturday's stakes.
"He's accomplished what he needed to in the last two starts and since then he continues to take steps forward," Summers said. "He's been working phenomenally."
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Owned by Al Gold's Gold Square, George Messina, and Michael Lee, Cyclone State found his groove in his fourth career start when Summers entered him as a main-track-only entrant in a Sept. 28 maiden turf race at the Big A.
When Mother Nature washed out grass racing, Cyclone State faced four rivals in the one-turn mile test after finishing sixth at 1 1/16 miles in a turf race in his previous try and sixth and fourth in a pair of dirt sprints before that.
After sitting a few lengths off the pace in those losses, he grabbed a four-length lead on the backstretch before settling for a runner-up finish by a length to Aviator Gui , who would subsequently finish second in the Remsen Stakes (G2).
After that, the son of McKinzie   bred by H. Allen Poindexter cruised to front-running maiden and allowance wins to earn his spot in the Jerome where there figures to be a lively early pace.
"When we saw how much speed was nominated to the Jerome, we decided to switch it up a little bit and we worked him behind horses to see if he can do that," Summers said. "He was able to overcome that and get the bullet for the work (five furlongs in 1:01.21 at the Belmont training track Dec. 27) but he also did it the right way with (jockey Luis Rivera Jr.) aboard. You want to learn more about him when he's taking dirt and things like that. I think we have a good Plan A, but we'll go to Plan B, C, or D depending on how the race shakes out."
Cyclone State, who has earned $125,750, was bought for $70,000 by Joe Hardoon on behalf of the ownership group from the Wynnstay Sales consignment at the 2023 Keeneland September Yearling Sale.
The field of eight will be chasing a total of 21 Kentucky Derby qualifying points, distributed in a 10-5-3-2-1 manner to the top five finishers.
David Hughes' Studlydoright  already has two qualifying points after finishing fourth in the Dec. 7 Remsen Stakes at 1 1/8 miles.

A Nyquist   colt trained by John Robb, the Maryland-bred already has wins in the Nashua and Tremont stakes and was second in the Sanford Stakes (G3) at Saratoga Race Course.
The top contenders also include a pair from trainer Rick Dutrow in Black Type Thoroughbreds, Swinbank Stables, Breeder Judy Hicks, and Scott Rice's McAfee  (Cloud Computing ), who is a half brother to leading Horse of the Year candidate Thorpedo Anna  and was beaten a head in a Nov. 24 starter race at Churchill Downs, and FMQ Stables' Ican  (Preservationist ), who was second by 2 3/4 lengths to Cyclone State in a Dec. 6 allowance optional claimer.

Al and Bill Ulwelling's Mansetti , a Canadian-bred son of Collected   trained by Kevin Attard, will make his dirt debut after winning the Clarendon Stakes on Woodbine's all weather track.

Entries: Jerome S.

Aqueduct Racetrack, Saturday, January 04, 2025, Race 8

• STK
• 1m
• Dirt
• $150,000
• 3 yo
• 3:39 PM (local)

PP	Horse	Jockey	Wgt	Trainer	M/L
1	1Enduring Spirit (KY)	Sofia Vives	118	Jose M. Jimenez	30/1
2	2Mansetti (ON)	Sahin Civaci	120	Kevin Attard	10/1
3	3Ican (KY)	Manuel Franco	118	Richard E. Dutrow, Jr.	8/1
4	4Omaha Omaha (VA)	Raul E. Mena	120	Michael E. Gorham	8/1
5	5Georgia Magic (KY)	Romero Ramsay Maragh	118	Raymond Handal	10/1
6	6Cyclone State (IA)	Luis R. Rivera, Jr.	120	Chad Summers	7/2
7	7Studlydoright (MD)	Xavier Perez	123	John J. Robb	5/2
8	8McAfee (KY)	Jose Antonio Gomez	118	Richard E. Dutrow, Jr.	2/1

Aqueduct Racetrack, Saturday, January 04, 2025, Race 8
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Coming off a 3-0 shutout win in Vancouver, the Nashville Predators play the Calgary Flames on Saturday at the Scotiabank Saddledome.
Juuse Saros made 27 saves for his fourth shutout of the season and Steven Stamkos scored his 12th goal to lead the Predators to their first win of 2025 on Friday. The Predators remain in seventh place in the Central Division, three points ahead of the Chicago Blackhawks.
Nashville (12-20-7, 31 points) also saw the debut of forward Ozzy Wiesblatt and the return of defenseman Spencer Stastney. Lineup changes were needed due to injuries to Adam Wilsby, Jeremy Lauzon, Tommy Novak and Cole Smith.
Calgary (18-13-7, 43 points) is in fifth place in the Pacific Division, having lost 5-3 to the Utah Hockey Club on Thursday. Goal scoring has been an issue for the Flames – they rank 26th in the NHL in goals per game (2.66). Jonathan Huberdeau leads the Flames with 16 goals and 13 assists.
The Flames will start either Dustin Wolf or Dan Vladar in net, while the Predators will likely turn to Justus Annunen on the second half of a back-to-back.
The Nashville Predators vs. Calgary Flames game will be televised by FanDuel Sports Network South with streaming available via FUBO and ESPN+ (outside of the Nashville TV market).
Odds according to BetMGM on Saturday, Jan. 4
All times Central; Games on FanDuel Sports Network South unless otherwise noted
Record: 12-20-7, 31 points
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