The Role of Leptin in Maintaining Plasma Glucose During Starvation.

Rachel J Perry, Gerald I Shulman
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Abstract

For 20 years it has been known that concentrations of leptin, a hormone produced by the white adipose tissue (WAT) largely in proportion to body fat, drops precipitously with starvation, particularly in lean humans and animals. The role of leptin to suppress the thyroid and reproductive axes during a prolonged fast has been well defined; however, the impact of leptin on metabolic regulation has been incompletely understood. However emerging evidence suggests that, in starvation, hypoleptinemia increases activity of the hypothalamic-pituitary-adrenal axis, promoting WAT lipolysis, increasing hepatic acetyl-CoA concentrations, and maintaining euglycemia. In addition, leptin may be largely responsible for mediating a shift from a reliance upon glucose metabolism (absorption and glycogenolysis) to fat metabolism (lipolysis increasing gluconeogenesis) which preserves substrates for the brain, heart, and other critical organs. In this way a leptin-mediated glucose-fatty acid cycle appears to maintain glycemia and permit survival in starvation.

瘦素在饥饿时维持血浆葡萄糖的作用
20 年来,人们一直知道瘦素是一种由白色脂肪组织(WAT)分泌的激素,其浓度主要与身体脂肪成比例,在饥饿时会急剧下降,尤其是在瘦人和动物体内。瘦素在长期禁食期间抑制甲状腺和生殖轴的作用已被明确定义;然而,瘦素对新陈代谢调节的影响却一直未被完全理解。不过,新的证据表明,在饥饿状态下,低瘦素血症会增加下丘脑-垂体-肾上腺轴的活性,促进WAT脂肪分解,增加肝脏乙酰-CoA浓度,维持优生。此外,瘦素还可能在很大程度上促使人们从依赖葡萄糖代谢(吸收和糖原分解)转向脂肪代谢(脂肪分解增加葡萄糖生成),从而为大脑、心脏和其他重要器官保留底物。通过这种方式,瘦素介导的葡萄糖-脂肪酸循环似乎可以维持血糖,使人们在饥饿状态下得以生存。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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