Seipin Deficiency Leads to Energy Dyshomeostasis via Inducing Hypothalamic Neuroinflammation and Aberrant Expression of Neuropeptides

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Wenli Cui, Hong Chen, Lingfeng Lei, Wenru Wang, Kah-Leong Lim, Chengwu Zhang, Li Lu
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Abstract

Seipin is a key regulator of lipid metabolism, the deficiency of which leads to severe lipodystrophy. Hypothalamus is the pivotal center of brain that modulates appetite and energy homeostasis, where Seipin is abundantly expressed. Whether and how Seipin deficiency leads to systemic metabolic disorders via hypothalamus-involved energy metabolism dysregulation remains to be elucidated. In the present study, we demonstrated that Seipin-deficiency induced hypothalamic inflammation, reduction of anorexigenic pro-opiomelanocortin (POMC), and elevation of orexigenic agonist-related peptide (AgRP). Importantly, administration of rosiglitazone, a thiazolidinedione antidiabetic agent, rescued POMC and AgRP expression, suppressed hypothalamic inflammation, and restored energy homeostasis in Seipin knockout mice. Our findings offer crucial insights into the mechanism of Seipin deficiency-associated energy imbalance and indicates that rosiglitazone could serve as potential intervening agent towards metabolic disorders linked to Seipin.

Abstract Image

塞品基因缺陷通过诱导下丘脑神经炎症和神经肽的异常表达导致能量失衡
塞品(Seipin)是脂质代谢的关键调节因子,缺乏它会导致严重的脂肪营养不良。下丘脑是大脑调节食欲和能量平衡的关键中枢,塞品在下丘脑中大量表达。塞品缺乏是否以及如何通过下丘脑参与的能量代谢失调导致全身性代谢紊乱仍有待阐明。在本研究中,我们证实 Seipin 缺乏会诱发下丘脑炎症、促厌食原绒毛膜促皮质素(POMC)减少和促厌激动剂相关肽(AgRP)升高。重要的是,服用噻唑烷二酮类抗糖尿病药物罗格列酮能挽救POMC和AgRP的表达,抑制下丘脑炎症,并恢复塞品基因敲除小鼠的能量平衡。我们的研究结果为了解塞品缺乏相关能量失衡的机制提供了重要见解,并表明罗格列酮可作为潜在的干预药物,用于治疗与塞品相关的代谢紊乱。
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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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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