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Heal the heart through gut (hormone) ghrelin: a potential player to combat heart failure

机译:通过肠道(激素)Ghrelin治愈心脏:潜在的球员来打击心力衰竭

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摘要

Ghrelin, a small peptide hormone (28 aa), secreted mainly by X/A-like cells of gastric mucosa, is also locally produced in cardiomyocytes. Being an orexigenic factor (appetite stimulant), it promotes release of growth hormone (GH) and exerts diverse physiological functions, viz. regulation of energy balance, glucose, and/or fat metabolism for body weight maintenance. Interestingly, administration of exogenous ghrelin significantly improves cardiac functions in CVD patients as well as experimental animal models of heart failure. Ghrelin ameliorates pathophysiological condition of the heart in myocardial infarction, cardiac hypertrophy, fibrosis, cachexia, and ischemia reperfusion injury. This peptide also exerts significant impact at the level of vasculature leading to lowering high blood pressure and reversal of endothelial dysfunction and atherosclerosis. However, the molecular mechanism of actions elucidating the healing effects of ghrelin on the cardiovascular system is still a matter of conjecture. Some experimental data indicate its beneficial effects via complex cellular cross talks between autonomic nervous system and cardiovascular cells, some other suggest more direct receptor-mediated molecular actions via autophagy or ionotropic regulation and interfering with apoptotic and inflammatory pathways of cardiomyocytes and vascular endothelial cells. Here, in this review, we summarise available recent data to encourage more research to find the missing links of unknown ghrelin receptor-mediated pathways as we see ghrelin as a future novel therapy in cardiovascular protection.
机译:Ghrelin是一种小肽激素(28AA),主要由胃粘膜的X/a样细胞分泌,也在心肌细胞中局部产生。作为一种促食欲因子(食欲刺激剂),它促进生长激素(GH)的释放,并发挥多种生理功能,即。调节能量平衡、葡萄糖和/或脂肪代谢以维持体重。有趣的是,服用外源性生长激素释放肽可显著改善CVD患者和心衰实验动物模型的心功能。Ghrelin可改善心肌梗死、心肌肥厚、纤维化、恶病质和缺血再灌注损伤时的心脏病理生理状况。这种肽在脉管系统水平上也发挥重要作用,从而降低高血压,逆转内皮功能障碍和动脉粥样硬化。然而,阐明ghrelin对心血管系统愈合作用的分子机制仍然是一个猜测。一些实验数据表明,其有益作用是通过自主神经系统和心血管细胞之间复杂的细胞交叉对话实现的,另一些实验数据表明,其更直接的受体介导分子作用是通过自噬或离子调节实现的,并干扰心肌细胞和血管内皮细胞的凋亡和炎症途径。在这篇综述中,我们总结了现有的最新数据,以鼓励更多的研究发现未知的ghrelin受体介导途径的缺失环节,因为我们认为ghrelin是心血管保护的未来新疗法。

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