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提取物通过改善脂肪组织和骨骼肌中的线粒体功能来提高能量消耗。

Extract Enhances Energy Expenditure via Improving Mitochondrial Function in Adipose Tissue and Skeletal Muscle.

机构信息

Division of Food Functionality Research, Korea Food Research Institute, Wanju-gun, Jeonbuk 55365, Korea.

Department of Food Biotechnology, University of Science and Technology, Daejeon 34113, Korea.

出版信息

Nutrients. 2020 Feb 7;12(2):431. doi: 10.3390/nu12020431.

Abstract

Withania somnifera (WS), commonly known as ashwagandha, possesses diverse biological functions. WS root has mainly been used as an herbal medicine to treat anxiety and was recently reported to have an anti-obesity effect, however, the mechanisms underlying its action remain to be explored. We hypothesized that WS exerts its anti-obesity effect by enhancing energy expenditure through improving the mitochondrial function of brown/beige adipocytes and skeletal muscle. Male C57BL/6J mice were fed a high-fat diet (HFD) containing 0.25% or 0.5% WS 70% ethanol extract (WSE) for 10 weeks. WSE (0.5%) supplementation significantly suppressed the increases in body weight and serum lipids, and lipid accumulation in the liver and adipose tissue induced by HFD. WSE supplementation increased oxygen consumption and enhanced mitochondrial activity in brown fat and skeletal muscle in the HFD-fed mice. In addition, it promoted browning of subcutaneous fat by increasing mitochondrial uncoupling protein 1 (UCP1) expression. Withaferin A (WFA), a major compound of WS, enhanced the differentiation of pre-adipocytes into beige adipocytes and oxygen consumption in C2C12 murine myoblasts. These results suggest that WSE ameliorates diet-induced obesity by enhancing energy expenditure via promoting mitochondrial function in adipose tissue and skeletal muscle, and WFA is a key regulator in this function.

摘要

睡茄(Withania somnifera),俗称 Ashwagandha,具有多种生物学功能。睡茄根主要被用作草药来治疗焦虑症,最近有报道称其具有抗肥胖作用,但作用机制仍有待探索。我们假设睡茄通过改善棕色/米色脂肪细胞和骨骼肌的线粒体功能来增强能量消耗,从而发挥其抗肥胖作用。雄性 C57BL/6J 小鼠喂食含有 0.25%或 0.5%睡茄 70%乙醇提取物(WSE)的高脂肪饮食(HFD)10 周。WSE(0.5%)补充显著抑制了 HFD 诱导的体重和血清脂质增加,以及肝脏和脂肪组织中的脂质积累。WSE 补充增加了 HFD 喂养小鼠棕色脂肪和骨骼肌中的耗氧量和增强了线粒体活性。此外,它通过增加解偶联蛋白 1(UCP1)的表达促进皮下脂肪的褐色化。WS 的主要化合物,醉茄内酯 A(WFA),促进前脂肪细胞向米色脂肪细胞分化,并增加 C2C12 鼠成肌细胞的耗氧量。这些结果表明,WSE 通过促进脂肪组织和骨骼肌中线粒体功能来改善饮食诱导的肥胖,而 WFA 是该功能的关键调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3d2/7071232/ea5afcfd825f/nutrients-12-00431-g001.jpg

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