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狭叶越桔叶提取物改善高脂饮食诱导的大鼠脂质异常及脂质代谢基因调控。

Sasa quelpaertensis leaf extract improves high fat diet-induced lipid abnormalities and regulation of lipid metabolism genes in rats.

作者信息

Kim Jina, Kim Yoo-Sun, Lee Hyun Ah, Lim Ji Ye, Kim Mina, Kwon Oran, Ko Hee-Chul, Kim Se-Jae, Shin Jae-Ho, Kim Yuri

机构信息

1 Department of Nutritional Science and Food Management, Ewha Womans University , Seoul, Korea.

出版信息

J Med Food. 2014 May;17(5):571-81. doi: 10.1089/jmf.2013.2916. Epub 2014 Apr 16.

Abstract

Sasa quelpaertensis is a bamboo leaf that is only grown on Jeju Island in South Korea. It is used as a bamboo tea that is consumed for therapeutic purposes, particularly for its anti-diabetic, diuretic, and anti-inflammatory effects. This study investigated the effect of S. quelpaertensis leaf extract (SQE) on high fat-induced lipid abnormalities and regulation of lipid metabolism-related gene expressions in rats. SQE supplementation significantly decreased the levels of plasma triglycerides, total cholesterol, and low-density lipoprotein cholesterol as well as the atherogenic index. SQE restored levels of plasma high-density lipoprotein cholesterol, which were lowered by a high fat diet. Plasma and cardiac resistin levels were also significantly decreased by SQE supplementation. In adipose tissue, mRNA levels of CAAT/enhancer-binding protein β (C/EBPβ) were suppressed in the SQE group. SQE supplementation decreased the accumulation of lipid droplets, inflammatory cell infiltrations, levels of triglycerides, and total lipids in the liver and effectively down-regulated expression of sterol regulatory element binding protein-1 (SREBP-1), fatty acid synthetase (FAS), and uncoupling protein 2 (UCP-2). These results suggest that SQE may be a potential treatment for high fat-related disorders by improving lipid profiles and modulating lipid metabolism.

摘要

狭叶苦竹是一种仅生长在韩国济州岛的竹叶。它被用作一种竹叶茶,用于治疗目的,特别是因其具有抗糖尿病、利尿和抗炎作用。本研究调查了狭叶苦竹叶提取物(SQE)对高脂诱导的大鼠脂质异常及脂质代谢相关基因表达调控的影响。补充SQE显著降低了血浆甘油三酯、总胆固醇和低密度脂蛋白胆固醇水平以及动脉粥样硬化指数。SQE恢复了因高脂饮食而降低的血浆高密度脂蛋白胆固醇水平。补充SQE还显著降低了血浆和心脏抵抗素水平。在脂肪组织中,SQE组中CAAT/增强子结合蛋白β(C/EBPβ)的mRNA水平受到抑制。补充SQE减少了肝脏中脂滴的积累、炎症细胞浸润、甘油三酯水平和总脂质,并有效下调了固醇调节元件结合蛋白-1(SREBP-1)、脂肪酸合成酶(FAS)和解偶联蛋白2(UCP-2)的表达。这些结果表明,SQE可能通过改善脂质谱和调节脂质代谢成为治疗高脂相关疾病的潜在药物。

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