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羊肚菌多糖对非酒精性脂肪性肝病小鼠的肝保护作用与AMPK/Sirt1信号通路的激活有关。

Hepatoprotective effects of polysaccharide from Morchella esculenta are associated with activation of the AMPK/Sirt1 signaling pathway in mice with NAFLD.

作者信息

Wang Dandan, Zhang Menglian, Zhang Yaowen, Yin Zequn, Zhang Shuang, Zhao Zhiwei, Duan Yajun

机构信息

School of Pharmacy, Anhui University of Chinese Medicine, Hefei, Anhui 230011, China; College of Food and Biological Engineering, Hefei University of Technology, Hefei, Anhui 230601, China.

School of Pharmacy, Anhui University of Chinese Medicine, Hefei, Anhui 230011, China.

出版信息

Int J Biol Macromol. 2025 Apr;301:140444. doi: 10.1016/j.ijbiomac.2025.140444. Epub 2025 Jan 28.

Abstract

The functional food application of edible fungus polysaccharides has been widely studied based on their variety of potential pharmacological activities. However, the hepatoprotective effects and mechanisms of Morchella esculenta polysaccharide against nonalcoholic fatty liver disease (NAFLD) remain unknown. A high-fat diet (HFD) fed C57BL/6 J mice for 8 weeks was employed to establish NAFLD with simple steatosis, methionine choline deficiency (MCD) diet for 4 weeks induced hepatic steatohepatitis and fibrosis. The M. esculenta polysaccharide (MCP) or saline was administered intragastrically. MCP markedly reduced hepatic and serum triglyceride (TG) and cholesterol contents in HFD-fed mice. Moreover, treatment with MCP ameliorated nonalcoholic steatohepatitis (NASH) progression in MCD-fed mice, as evidenced by ameliorated hepatic steatosis, inflammatory response, and fibrosis. Mechanistically, MCP suppressed the expression of lipogenic genes and inflammatory cytokines and upregulated peroxisome proliferator-activated receptor (PPAR)-α expression to induce fatty acid β-oxidation. These beneficial effects were attributed to activating the AMP-activated kinase (AMPK)/Sirtuin 1 (Sirt1) signaling pathway. Therefore, we provided evidence that MCP might be an effective dietary supplement to ameliorate NAFLD.

摘要

基于食用菌多糖的多种潜在药理活性,其在功能性食品中的应用已得到广泛研究。然而,羊肚菌多糖对非酒精性脂肪性肝病(NAFLD)的肝脏保护作用及其机制尚不清楚。采用高脂饮食(HFD)喂养C57BL/6 J小鼠8周以建立单纯性脂肪变性的NAFLD,采用蛋氨酸胆碱缺乏(MCD)饮食4周诱导肝脂肪性肝炎和肝纤维化。将羊肚菌多糖(MCP)或生理盐水灌胃给药。MCP显著降低了HFD喂养小鼠的肝脏和血清甘油三酯(TG)及胆固醇含量。此外,MCP治疗改善了MCD喂养小鼠的非酒精性脂肪性肝炎(NASH)进展,表现为肝脏脂肪变性、炎症反应和纤维化减轻。机制上,MCP抑制了生脂基因和炎性细胞因子的表达,并上调过氧化物酶体增殖物激活受体(PPAR)-α表达以诱导脂肪酸β-氧化。这些有益作用归因于激活了AMP激活的蛋白激酶(AMPK)/沉默信息调节因子1(Sirt1)信号通路。因此,我们提供了证据表明MCP可能是改善NAFLD的一种有效膳食补充剂。

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