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长期运动通过诱导多食肥胖小鼠枯否细胞表型变化预防非酒精性脂肪性肝炎。

Prevention of non-alcoholic steatohepatitis by long-term exercise via the induction of phenotypic changes in Kupffer cells of hyperphagic obese mice.

机构信息

Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba-shi, Ibaraki, Japan.

Faculty of Human Care, Department of Acupuncture and Moxibustion, Teikyo Heisei University, Toshima-ku, Tokyo, Japan.

出版信息

Physiol Rep. 2021 May;9(9):e14859. doi: 10.14814/phy2.14859.

Abstract

Exercise ameliorates nonalcoholic fatty liver disease (NAFLD) by inducing phenotypic changes in Kupffer cells (KCs). p62/Sqstm1-knockout (p62-KO) mice develop NAFLD alongside hyperphagia-induced obesity. We evaluated (1) the effects of long-term exercise on the foreign-body phagocytic capacity of KCs, their surface marker expression, and the production of steroid hormones in p62-KO mice; and (2) whether long-term exercise prevented the development of non-alcoholic steatohepatitis (NASH) in p62-KO mice fed a high-fat diet (HFD). In experiment 1, 30-week-old male p62-KO mice were allocated to resting (p62-KO-Rest) or exercise (p62-KO-Ex) groups, and the latter performed long-term exercise over 4 weeks. Then, the phenotype of their KCs was compared to that of p62-KO-Rest and wild-type (WT) mice. In experiment 2, 5-week-old male p62-KO mice that were fed a HFD performed long-term exercise over 12 weeks. In experiment 1, the phagocytic capacity of KCs and the proportion of CD68-positive cells were lower in the p62-KO-Rest group than in the WT group, but they increased with long-term exercise. The percentage of CD11b-positive KCs was higher in the p62-KO-Rest group than in the WT group, but lower in the p62-KO-Ex group. The circulating dehydroepiandrosterone (DHEA) concentration was higher in p62-KO-Ex mice than in p62-KO-Rest mice. In experiment 2, the body mass and composition of the p62-KO-Rest and p62-KO-Ex groups were similar, but the hepatomegaly, hepatic inflammation, and fibrosis were less marked in p62-KO-Ex mice. The DHEA concentration was higher in p62-KO-Ex mice than in WT or p62-KO-Rest mice. Thus, long-term exercise restores the impaired phagocytic capacity of KCs in NAFLD obese mice, potentially through greater DHEA production, and prevents the development of NASH by ameliorating hepatic inflammation and fibrogenesis. These results suggest a molecular mechanism for the beneficial effect of exercise in the management of patients with NAFLD.

摘要

运动通过诱导库普弗细胞(KCs)表型改变来改善非酒精性脂肪性肝病(NAFLD)。p62/Sqstm1 敲除(p62-KO)小鼠在肥胖症的同时发展为非酒精性脂肪肝。我们评估了(1)长期运动对 p62-KO 小鼠 KC 的吞噬能力、表面标志物表达和类固醇激素产生的影响;以及(2)长期运动是否能防止 p62-KO 高脂饮食(HFD)喂养的小鼠发生非酒精性脂肪性肝炎(NASH)。在实验 1 中,将 30 周龄雄性 p62-KO 小鼠分为休息组(p62-KO-Rest)或运动组(p62-KO-Ex),后者进行了 4 周的长期运动。然后,比较了它们的 KC 表型与 p62-KO-Rest 和野生型(WT)小鼠的表型。在实验 2 中,5 周龄雄性 p62-KO 高脂饮食喂养的小鼠进行了 12 周的长期运动。在实验 1 中,p62-KO-Rest 组 KC 的吞噬能力和 CD68 阳性细胞的比例低于 WT 组,但随着长期运动而增加。p62-KO-Rest 组 CD11b 阳性 KC 的比例高于 WT 组,但 p62-KO-Ex 组的比例较低。p62-KO-Ex 小鼠的循环脱氢表雄酮(DHEA)浓度高于 p62-KO-Rest 小鼠。在实验 2 中,p62-KO-Rest 和 p62-KO-Ex 组的体重和组成相似,但 p62-KO-Ex 组的肝肿大、肝炎症和纤维化程度较轻。p62-KO-Ex 小鼠的 DHEA 浓度高于 WT 或 p62-KO-Rest 小鼠。因此,长期运动恢复了肥胖 NAFLD 小鼠受损的 KC 吞噬能力,可能是通过增加 DHEA 产生,改善肝炎症和纤维化,从而防止 NASH 的发生。这些结果提示了运动对 NAFLD 患者管理有益作用的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75cd/8123550/a5ba1064b9ae/PHY2-9-e14859-g005.jpg

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