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过氧化物酶体增殖物激活受体:脂质生理学中的一种核受体信号通路。

Peroxisome proliferator-activated receptors: a nuclear receptor signaling pathway in lipid physiology.

作者信息

Lemberger T, Desvergne B, Wahli W

机构信息

Institut de Biologie Animale, Université de Lausanne, Switzerland.

出版信息

Annu Rev Cell Dev Biol. 1996;12:335-63. doi: 10.1146/annurev.cellbio.12.1.335.

Abstract

Peroxisome proliferator-activated receptors (PPARs) are lipid-activated transcription factors that belong to the steroid/thyroid/retinoic acid receptor superfamily. All their characterized target genes encode proteins that participate in lipid homeostasis. The recent finding that antidiabetic thiazolidinediones and adipogenic prostanoids are ligands of one of the PPARs reveals a novel signaling pathway that directly links these compounds to processes involved in glucose homeostasis and lipid metabolism including adipocyte differentiation. A detailed understanding of this pathway could designate PPARs as targets for the development of novel efficient treatments for several metabolic disorders.

摘要

过氧化物酶体增殖物激活受体(PPARs)是脂质激活的转录因子,属于类固醇/甲状腺/视黄酸受体超家族。它们所有已被鉴定的靶基因都编码参与脂质稳态的蛋白质。最近发现抗糖尿病噻唑烷二酮类药物和促脂肪生成的前列腺素是其中一种PPAR的配体,这揭示了一条新的信号通路,该通路将这些化合物与包括脂肪细胞分化在内的葡萄糖稳态和脂质代谢过程直接联系起来。对这条通路的详细了解可能会将PPARs指定为开发几种代谢紊乱新有效治疗方法的靶点。

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