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钙信号通路:肥胖调控中的关键通路。

Calcium Signaling Pathways: Key Pathways in the Regulation of Obesity.

机构信息

College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China.

出版信息

Int J Mol Sci. 2019 Jun 5;20(11):2768. doi: 10.3390/ijms20112768.

Abstract

Nowadays, high epidemic obesity-triggered hypertension and diabetes seriously damage social public health. There is now a general consensus that the body's fat content exceeding a certain threshold can lead to obesity. Calcium ion is one of the most abundant ions in the human body. A large number of studies have shown that calcium signaling could play a major role in increasing energy consumption by enhancing the metabolism and the differentiation of adipocytes and reducing food intake through regulating neuronal excitability, thereby effectively decreasing the occurrence of obesity. In this paper, we review multiple calcium signaling pathways, including the IP3 (inositol 1,4,5-trisphosphate)-Ca (calcium ion) pathway, the p38-MAPK (mitogen-activated protein kinase) pathway, and the calmodulin binding pathway, which are involved in biological clock, intestinal microbial activity, and nerve excitability to regulate food intake, metabolism, and differentiation of adipocytes in mammals, resulting in the improvement of obesity.

摘要

如今,高发的肥胖引发的高血压和糖尿病严重损害了社会公共健康。人们普遍认为,人体脂肪含量超过一定阈值会导致肥胖。钙离子是人体内最丰富的离子之一。大量研究表明,钙信号可以通过增强代谢和脂肪细胞的分化来增加能量消耗,通过调节神经元兴奋性来减少食物摄入,从而有效减少肥胖的发生。在本文中,我们综述了多种钙信号通路,包括 IP3(肌醇 1,4,5-三磷酸)-Ca(钙离子)通路、p38-MAPK(丝裂原活化蛋白激酶)通路和钙调蛋白结合通路,这些通路参与生物钟、肠道微生物活性和神经兴奋性的调节,以控制哺乳动物的食物摄入、代谢和脂肪细胞的分化,从而改善肥胖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8681/6600289/2303083ab3d8/ijms-20-02768-g001.jpg

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