首页> 外文期刊>Pathology International >Japanese herbal medicines shosaikoto, inchinkoto, and juzentaihoto inhibit high-fat diet-induced nonalcoholic steatohepatitis in db/db mice.
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Japanese herbal medicines shosaikoto, inchinkoto, and juzentaihoto inhibit high-fat diet-induced nonalcoholic steatohepatitis in db/db mice.

机译:日本草药shosaikoto,inchinkoto和juzentaihoto抑制高脂饮食诱发的db / db小鼠非酒精性脂肪性肝炎。

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Few studies have investigated the effects of Japanese herbal medicines on nonalcoholic fatty liver disease (NAFLD)onalcoholic steatohepatitis (NASH). To the best of our knowledge, only one study has examined whether high-fat (HF) diet-fed db/db mice are appropriate animal models of NASH. We investigated the effects of four types of Japanese herbal medicines (shosaikoto (TJ-9), inchinkoto (TJ-135), juzentaihoto (TJ-48), and keishibukuryogan (TJ-25)) on hepatic lesions of HF diet-fed db/db mice. Db/db mice were divided into six groups: control diet (control); HF diet (HF); and HF diet supplemented with TJ-9, TJ-135, TJ-48, or TJ-25 (TJ-9, TJ-135, TJ-48, and TJ-25, respectively). Mice were killed after 6 weeks of treatment, and biochemical and pathological analyses were performed. Mice in the HF group consistently developed histopathological features consistent with definite NASH, and marked necroinflammation occurred. Serum alanine aminotransferase levels in the TJ-9, TJ-135, and TJ-48 groups were significantly improved compared with those in the HF group. With regard to liver histology, TJ-9 and TJ-48 significantly improved lobular inflammation, and TJ-135 significantly improved ballooning degeneration. We have shown that HF diet-fed db/db mice are animal models that correctly recapitulate the histopathology of human NASH and that TJ-9, TJ-135, and TJ-48 inhibit necroinflammatory activity in this model.
机译:很少有研究调查日本草药对非酒精性脂肪肝疾病(NAFLD)/非酒精性脂肪性肝炎(NASH)的影响。据我们所知,只有一项研究检查了高脂(HF)饮食的db / db小鼠是否是NASH的合适动物模型。我们调查了四种类型的日本草药(绍萨科托(TJ-9),inchinkoto(TJ-135),juzentaihoto(TJ-48)和keishibukuryogan(TJ-25))对高脂饮食喂养的肝损害的影响/ db鼠标。 Db / db小鼠分为六组:对照饮食(对照); HF饮食(HF);和含TJ-9,TJ-135,TJ-48或TJ-25(分别为TJ-9,TJ-135,TJ-48和TJ-25)的HF饮食。治疗6周后杀死小鼠,并进行生化和病理分析。 HF组的小鼠始终具有与明确的NASH一致的组织病理学特征,并出现明显的坏死性炎症。与HF组相比,TJ-9,TJ-135和TJ-48组的血清丙氨酸氨基转移酶水平显着提高。就肝脏组织学而言,TJ-9和TJ-48显着改善了小叶炎症,TJ-135显着改善了球囊变性。我们已经表明,HF饮食喂养的db / db小鼠是能够正确概括人类NASH的组织病理学的动物模型,并且TJ-9,TJ-135和TJ-48在该模型中抑制了坏死性炎症活动。

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