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Mechanisms by which Thiazolidinediones Enhance Insulin Action
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Mechanisms by which Thiazolidinediones Enhance Insulin Action

Mauricio J Reginato and Mitchell A Lazar
Trends in Endocrinology & Metabolism, v 10(1)
1999
PMID: 10322388
url
https://doi.org/10.1016/s1043-2760(98)00110-6View
Published, Version of Record (VoR) Open
url
https://doi.org/10.1016/S1043-2760(98)00110-6View
Published, Version of Record (VoR) Open

Abstract

adipose diabetes insulin nuclear receptors PPAR thiazolidinediones
Thiazolidinediones (TZDs) are an exciting new class of insulin-sensitizing drugs being used currently for the treatment of non-insulin-dependent diabetes mellitus. The molecular target of these compounds is thought to be the nuclear hormone receptor, peroxisome proliferator-activated receptor γ (PPARγ). PPARγ is expressed predominantly in adipose tissue, yet a major site of TZD-responsive glucose disposal is skeletal muscle. Potential explanations for this paradox are discussed in this review.

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Web of Science research areas
Endocrinology & Metabolism
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