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从概念基础到瘦素的发现。

From the conceptual basis to the discovery of leptin.

机构信息

Université Pierre et Marie Curie, UPMC Paris 6, Faculté de Médecine, Paris 75012, France.

出版信息

Biochimie. 2012 Oct;94(10):2065-8. doi: 10.1016/j.biochi.2012.06.028. Epub 2012 Jul 4.

Abstract

Two years ago, the Lasker Award was shared by Douglas Coleman and Jeffrey Friedman for their discovery of leptin, a hormone that exerts a key role in the central regulation of appetite and body weight. Douglas Coleman is recognized as the researcher who raised the hypothesis and predicted that a circulating satiety factor was lacking in the ob/ob mouse, and predicted that this factor acted at the hypothalamic level to modulate food intake. After three decades, in an attempt to identify the genes that were mutated in the ob/ob mouse, Jeffrey Friedman found that the ob gene encodes a protein hormone that reverses obesity and other abnormalities of this genetic rodent model of obesity. This discovery was a landmark event in physiology, and revolutionized our understanding of energy homeostasis. This short review aims to summarize the main steps that lead to the identification of leptin, the product of the ob gene.

摘要

两年前,道格拉斯·科尔曼(Douglas Coleman)和杰弗里·弗里德曼(Jeffrey Friedman)因发现瘦素(leptin)而共同获得拉斯克奖(Lasker Award)。瘦素是一种激素,在中枢调控食欲和体重方面发挥着关键作用。道格拉斯·科尔曼(Douglas Coleman)被公认为提出假说并预测在肥胖(ob/ob)小鼠中存在循环饱食因子缺失的研究人员,他还预测这种因子在下丘脑水平发挥作用,以调节食物摄入。三十年后,杰弗里·弗里德曼(Jeffrey Friedman)试图确定肥胖(ob/ob)小鼠中突变的基因,发现 ob 基因编码一种蛋白激素,该激素可逆转肥胖症和这种遗传性肥胖症啮齿动物模型的其他异常。这一发现是生理学上的一个里程碑事件,彻底改变了我们对能量平衡的理解。这篇简短的综述旨在总结鉴定 ob 基因产物瘦素的主要步骤。

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