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瘦素逆转1型糖尿病的多效性急性和慢性效应

Pleotropic Acute and Chronic Effects of Leptin to Reverse Type 1 Diabetes.

作者信息

Perry Rachel J

机构信息

Department of Internal Medicine, Yale University, New Haven, CT 06510.

出版信息

Postdoc J. 2017 Jan;5(1):3-11. doi: 10.14304/surya.jpr.v5n1.2.

Abstract

Recent studies have demonstrated that leptin can prolong life chronically in rats with poorly-controlled type 1 diabetes (T1D). Multiple explanations have been proposed to explain leptin's chronic antihyperglycemic effect, including suppression of glucagon release and/or signaling, reductions in hyperphagia and ectopic lipid content, and improvements in insulin sensitivity; it is leptin's ability to reduce plasma glucose relies on all of these effects. In addition, leptin reverses hyperglycemia and diabetic ketoacidosis (DKA) acutely, within 6 hours of leptin infusion, by suppressing hypothalamic-pituitary-adrenal (HPA) axis activity in insulinopenic rats. Thus current evidence suggests that leptin's acute, insulin-independent effect to reverse DKA by suppressing HPA axis activity occurs through a different mechanism from its chronic, pleotropic, insulin-dependent effect to reverse hyperglycemia and prolong survival in rodents with T1D. Leptin may therefore represent an attractive therapeutic target to improve glycemic control in humans with poorly-controlled T1D.

摘要

最近的研究表明,瘦素可以长期延长1型糖尿病(T1D)控制不佳的大鼠的寿命。人们提出了多种解释来阐述瘦素的慢性抗高血糖作用,包括抑制胰高血糖素释放和/或信号传导、减少食欲过盛和异位脂质含量,以及改善胰岛素敏感性;瘦素降低血糖的能力依赖于所有这些作用。此外,在胰岛素缺乏的大鼠中,通过抑制下丘脑-垂体-肾上腺(HPA)轴活性,瘦素在输注6小时内可迅速逆转高血糖和糖尿病酮症酸中毒(DKA)。因此,目前的证据表明,瘦素通过抑制HPA轴活性来逆转DKA的急性、不依赖胰岛素的作用,其发生机制与它在T1D啮齿动物中逆转高血糖和延长生存期的慢性、多效性、依赖胰岛素的作用不同。因此,瘦素可能是改善T1D控制不佳的人类血糖控制的一个有吸引力的治疗靶点。

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本文引用的文献

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