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Inhibitory Effects of Japanese Herbal Medicines Sho-saiko-to and Juzen-taiho-to on Nonalcoholic Steatohepatitis in Mice

机译:日本草药Sho-saiko-to和Juzen-taiho-to对小鼠非酒精性脂肪性肝炎的抑制作用

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摘要

Although Japanese herbal medicines (JHMs) are widely used in Japan, only a few studies have investigated their effects on nonalcoholic steatohepatitis (NASH). In the present study, we examined the effect of 4 kinds of JHMs [sho-saiko-to (TJ-9), inchin-ko-to (TJ-135), juzen-taiho-to (TJ-48), and keishi-bukuryo-gan (TJ-25)] on a mouse model of NASH. Db/db mice were divided into 6 groups: control diet (control), methionine- and choline-deficient diet (MCD), and MCD diet supplemented with TJ-9, TJ-135, TJ-48, and TJ-25 (TJ-9, TJ-135, TJ-48, and TJ-25, respectively). All mice were sacrificed after 4 weeks of treatment, and biochemical, pathological, and molecular analyses were performed. Serum alanine aminotransferase levels and liver histology, including necroinflammation and fibrosis, were significantly alleviated in the TJ-9 and TJ-48 groups compared with the MCD group. The expression level of transforming growth factor (TGF)-β1 mRNA in the liver was significantly suppressed by TJ-48. Although the differences were not statistically significant, the expression levels of tumor necrosis factor (TNF)-α and interleukin (IL)-6 were lower, and those of peroxisome proliferators-activated receptor (PPAR)γ were higher in the TJ-9 and/or TJ-48 groups than in the MCD group. Similarly, even though the results were not statistically significant, malondialdehyde levels in liver tissues were lower in the TJ-9 and TJ-48 groups than in the MCD group. We showed that JHMs, especially TJ-9 and TJ-48, inhibited the necroinflammation and fibrosis in the liver of a mouse model of NASH, even though the mechanisms were not fully elucidated. Further studies are needed in the future to investigate the possibility of clinical application of these medicines in the treatment for NASH.
机译:尽管日本草药(JHMs)在日本已广泛使用,但只有少数研究调查了它们对非酒精性脂肪性肝炎(NASH)的影响。在本研究中,我们研究了4种JHM的作用[sho-saiko-to(TJ-9),inchin-ko-to(TJ-135),juzen-taiho-to(TJ-48)和keishi -bukuryo-gan(TJ-25)]在NASH的小鼠模型上。 db / db小鼠分为6组:对照饮食(对照),蛋氨酸和胆碱缺乏饮食(MCD)以及补充TJ-9,TJ-135,TJ-48和TJ-25(TJ -9,TJ-135,TJ-48和TJ-25)。治疗4周后处死所有小鼠,并进行生化,病理和分子分析。与MCD组相比,TJ-9和TJ-48组的血清丙氨酸氨基转移酶水平和肝脏组织学(包括坏死性炎症和纤维化)明显减轻。 TJ-48可显着抑制肝脏中转化生长因子(TGF)-β1mRNA的表达水平。尽管差异无统计学意义,但在TJ-9和TJ-9中,肿瘤坏死因子(TNF)-α和白介素(IL)-6的表达水平较低,过氧化物酶体增殖物激活受体(PPAR)γ的表达水平较高。 /或TJ-48组,而不是MCD组。同样,即使结果没有统计学意义,TJ-9和TJ-48组的肝组织中丙二醛水平也低于MCD组。我们显示JHMs,尤其是TJ-9和TJ-48,可抑制NASH小鼠模型肝脏的坏死性炎症和纤维化,即使其机理尚未完全阐明。未来需要进一步的研究,以研究这些药物在NASH治疗中的临床应用可能性。

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