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裙带菜富含多酚的组分改善高脂饮食喂养小鼠的非酒精性脂肪性肝病

Polyphenol-Rich Fraction of Ecklonia cava Improves Nonalcoholic Fatty Liver Disease in High Fat Diet-Fed Mice.

作者信息

Park Eun-Young, Choi Hojung, Yoon Ji-Young, Lee In-Young, Seo Youngwan, Moon Hong-Seop, Hwang Jong-Hee, Jun Hee-Sook

机构信息

College of Pharmacy, Mokpo National University, Muan-gun, Jeonnam 58554, Korea.

College of Pharmacy, Gachon Institute of Pharmaceutical Science, Gachon University, Yeonsu-gu, Incheon 21999, Korea.

出版信息

Mar Drugs. 2015 Nov 12;13(11):6866-83. doi: 10.3390/md13116866.

DOI:10.3390/md13116866
PMID:26569269
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4663557/
Abstract

Ecklonia cava (E. cava; CA) is an edible brown alga with beneficial effects in diabetes via regulation of various metabolic processes such as lipogenesis, lipolysis, inflammation, and the antioxidant defense system in liver and adipose tissue. We investigated the effect of the polyphenol-rich fraction of E. cava produced from Gijang (G-CA) on nonalcoholic fatty liver disease (NAFLD) in high-fat diet (HFD)-fed mice. C57BL6 mice were fed a HFD for six weeks and then the HFD group was administered 300 mg/kg of G-CA extracts by oral intubation for 10 weeks. Body weight, fat mass, and serum biochemical parameters were reduced by G-CA extract treatment. MRI/MRS analysis showed that liver fat and liver volume in HFD-induced obese mice were reduced by G-CA extract treatment. Further, we analyzed hepatic gene expression related to inflammation and lipid metabolism. The mRNA expression levels of inflammatory cytokines and hepatic lipogenesis-related genes were decreased in G-CA-treated HFD mice. The mRNA expression levels of cholesterol 7 alpha-hydroxylase 1 (CYP7A1), the key enzyme in bile acid synthesis, were dramatically increased by G-CA treatment in HFD mice. We suggest that G-CA treatment ameliorated hepatic steatosis by inhibiting inflammation and improving lipid metabolism.

摘要

海蕴是一种可食用的褐藻,通过调节各种代谢过程,如肝脏和脂肪组织中的脂肪生成、脂肪分解、炎症和抗氧化防御系统,对糖尿病具有有益作用。我们研究了产自巨济的海蕴富含多酚的部分(G-CA)对高脂饮食(HFD)喂养小鼠的非酒精性脂肪性肝病(NAFLD)的影响。C57BL6小鼠接受高脂饮食六周,然后对高脂饮食组通过口服灌胃给予300mg/kg的G-CA提取物,持续10周。G-CA提取物处理降低了体重、脂肪量和血清生化参数。MRI/MRS分析表明,G-CA提取物处理降低了高脂饮食诱导的肥胖小鼠的肝脏脂肪和肝脏体积。此外,我们分析了与炎症和脂质代谢相关的肝脏基因表达。在G-CA处理的高脂饮食小鼠中,炎症细胞因子和肝脏脂肪生成相关基因的mRNA表达水平降低。在高脂饮食小鼠中,G-CA处理显著增加了胆汁酸合成关键酶胆固醇7α-羟化酶1(CYP7A1)的mRNA表达水平。我们认为,G-CA处理通过抑制炎症和改善脂质代谢改善了肝脏脂肪变性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/dbe97fa38465/marinedrugs-13-06866-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/ed8585fa16d2/marinedrugs-13-06866-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/02e987fd8404/marinedrugs-13-06866-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/74625afeb45b/marinedrugs-13-06866-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/843ca8035b37/marinedrugs-13-06866-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/dbe97fa38465/marinedrugs-13-06866-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/ed8585fa16d2/marinedrugs-13-06866-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/02e987fd8404/marinedrugs-13-06866-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/74625afeb45b/marinedrugs-13-06866-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/843ca8035b37/marinedrugs-13-06866-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964c/4663557/dbe97fa38465/marinedrugs-13-06866-g005a.jpg

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