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西施舌寡肽对高脂饮食诱导的小鼠非酒精性脂肪肝的保护作用。

Protective Effect of Meretrix meretrix Oligopeptides on High-Fat-Diet-Induced Non-Alcoholic Fatty Liver Disease in Mice.

机构信息

School of Food Science and Pharmacy, Zhejiang Provincial Key Engineering Technology Research Center of Marine Biomedical Products, Zhejiang Ocean University, Zhoushan 316000, China.

Zhejiang Provincial Key Engineering Technology Research Center of Marine Biomedical Products, Zhejiang Ocean University Donghai Science and Technology College, Zhoushan 316000, China.

出版信息

Mar Drugs. 2018 Jan 23;16(2):39. doi: 10.3390/md16020039.

DOI:10.3390/md16020039
PMID:29360762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5852467/
Abstract

The present study investigated the effects of MMO ( oligopeptides) on mice fed a high-fat diet. Mice were fed either a normal control diet (NC) or a high-fat diet (HFD) without or with MMO (50 mg/kg or 250 mg/kg) for four weeks. Levels of ALT, AST, liver tissue GSH-Px, and SOD activities, MDA levels were measured using commercially available kits; HE staining was performed to analyze pathologic changes of the liver; a TEM assay was performed to measure the ultrastructural alterations of the mitochondria, and Western blotting was performed to detect the expression of gene proteins related to lipid metabolism, inflammation, and liver apoptosis. After six weeks, body weight, ALT, AST, and MDA levels were significantly increased, and GSH-Px levels and SOD activities were significantly decreased in the HFD control group compared with the NC group. Consumption of the HFD compared with the NC caused fatty liver abnormal mitochondria with loss of cristae, intramitochondrial granules, and a swollen and rarefied matrix. Administration of MMO significantly decreased body weight gain, and ALT, AST, and MDA levels; increased SOD activity and GSH-Px levels; alleviated fatty liver steatosis; decreased the early apoptosis population; downregulated SREBP-1c, Bax, Caspase-9, Caspase-3, TNF-α, and NF-κB protein levels; and upregulated PPAR-α, Bcl-2, and AMPK-α, compared with the HFD control group. MMO exhibited protective effects in mice with NAFLD by regulating the NF-κB anti-inflammation signaling pathways to inhibit inflammation, regulate AMPK-α, PPAR-α and SREBP-1c to improve lipid metabolism disorder, and regulate Bcl-2/Bax anti-apoptosis signaling pathways to prevent liver cell apoptosis. These results suggest that dietary supplementation with MMO ameliorates high-fat-diet-induced NAFLD.

摘要

本研究旨在探讨 MMO(寡肽)对高脂饮食喂养小鼠的影响。将小鼠分为正常对照组(NC)、高脂饮食组(HFD)和 HFD 加不同剂量 MMO 组(50mg/kg 和 250mg/kg),每组 10 只,分别给予相应饲料喂养 4 周。采用试剂盒检测 ALT、AST、肝组织 GSH-Px、SOD 活性及 MDA 含量;HE 染色观察肝组织病理变化;透射电镜观察线粒体超微结构改变;Western blot 检测与脂代谢、炎症和肝凋亡相关的基因蛋白表达。6 周后,与 NC 组相比,HFD 对照组小鼠体重、ALT、AST 及 MDA 水平显著升高,GSH-Px 水平及 SOD 活性显著降低。与 NC 组相比,HFD 组导致小鼠发生脂肪肝,线粒体出现嵴缺失、基质颗粒减少、基质稀疏等超微结构改变。MMO 干预可显著降低 HFD 组小鼠体重、ALT、AST 及 MDA 水平,提高 SOD 活性和 GSH-Px 水平,减轻肝脂肪变性,减少早期凋亡细胞数量,下调 SREBP-1c、Bax、Caspase-9、Caspase-3、TNF-α 和 NF-κB 蛋白表达,上调 PPAR-α、Bcl-2 和 AMPK-α 蛋白表达。MMO 通过调控 NF-κB 炎症信号通路抑制炎症,调节 AMPK-α、PPAR-α 和 SREBP-1c 改善脂质代谢紊乱,调节 Bcl-2/Bax 抗凋亡信号通路防止肝细胞凋亡,对 HFD 诱导的非酒精性脂肪性肝病具有保护作用。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d325/5852467/ffaca27f570a/marinedrugs-16-00039-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d325/5852467/b6236c5dee4a/marinedrugs-16-00039-g008a.jpg

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