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致炎瘦素。

Incendiary Leptin.

机构信息

International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.

CIMUS, University of Santiago de Compostela-Instituto de Investigación Sanitaria, 15782 Santiago de Compostela, Spain.

出版信息

Nutrients. 2020 Feb 13;12(2):472. doi: 10.3390/nu12020472.

Abstract

Leptin is a hormone released by adipose tissue that plays a key role in the control of energy homeostasis through its binding to leptin receptors (LepR), mainly expressed in the hypothalamus. Most scientific evidence points to leptin's satiating effect being due to its dual capacity to promote the expression of anorexigenic neuropeptides and to reduce orexigenic expression in the hypothalamus. However, it has also been demonstrated that leptin can stimulate (i) thermogenesis in brown adipose tissue (BAT) and (ii) the browning of white adipose tissue (WAT). Since the demonstration of the importance of BAT in humans 10 years ago, its study has aroused great interest, mainly in the improvement of obesity-associated metabolic disorders through the induction of thermogenesis. Consequently, several strategies targeting BAT activation (mainly in rodent models) have demonstrated great potential to improve hyperlipidemias, hepatic steatosis, insulin resistance and weight gain, leading to an overall healthier metabolic profile. Here, we review the potential therapeutic ability of leptin to correct obesity and other metabolic disorders, not only through its satiating effect, but by also utilizing its thermogenic properties.

摘要

瘦素是一种由脂肪组织释放的激素,通过与瘦素受体(LepR)结合,在能量平衡的控制中发挥关键作用,瘦素受体主要在下丘脑表达。大多数科学证据表明,瘦素的饱腹感效应是由于其双重能力,既能促进厌食神经肽的表达,又能减少下丘脑的食欲肽表达。然而,也有研究表明,瘦素可以刺激(i)棕色脂肪组织(BAT)的产热和(ii)白色脂肪组织(WAT)的褐色化。自从 10 年前证明 BAT 在人类中的重要性以来,它的研究引起了极大的兴趣,主要是通过诱导产热来改善与肥胖相关的代谢紊乱。因此,针对 BAT 激活的几种策略(主要在啮齿动物模型中)已经证明了在改善高脂血症、肝脂肪变性、胰岛素抵抗和体重增加方面具有巨大的潜力,从而导致整体代谢特征更加健康。在这里,我们回顾了瘦素纠正肥胖和其他代谢紊乱的潜在治疗能力,不仅通过其饱腹感效应,还利用其产热特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd31/7071158/517d76a98be3/nutrients-12-00472-g001.jpg

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