Melatonin induces browning of inguinal white adipose tissue in Zucker diabetic fatty rats

褪黑素 内科学 内分泌学 白色脂肪组织 脂肪组织 褐色脂肪组织 H&E染色 产热 生物 医学 免疫组织化学
作者
Aroa Jiménez‐Aranda,Gumersindo Fernández‐Vázquez,Daniel Campos,Mohamed Tassi,Lourdes Velasco‐Perez,Dun‐Xian Tan,Rüssel J. Reiter,Ahmad Agil
出处
期刊:Journal of Pineal Research [Wiley]
卷期号:55 (4): 416-423 被引量:178
标识
DOI:10.1111/jpi.12089
摘要

Abstract Melatonin limits obesity in rodents without affecting food intake and activity, suggesting a thermogenic effect. Identification of brown fat ( beige/brite ) in white adipose tissue ( WAT ) prompted us to investigate whether melatonin is a brown‐fat inducer. We used Zücker diabetic fatty ( ZDF ) rats, a model of obesity‐related type 2 diabetes and a strain in which melatonin reduces obesity and improves their metabolic profiles. At 5 wk of age, ZDF rats and lean littermates ( ZL ) were subdivided into two groups, each composed of four rats: control and those treated with oral melatonin in the drinking water (10 mg/kg/day) for 6 wk. Melatonin induced browning of inguinal WAT in both ZDF and ZL rats. Hematoxylin–eosin staining showed patches of brown‐like adipocytes in inguinal WAT in ZDF rats and also increased the amounts in ZL animals. Inguinal skin temperature was similar in untreated lean and obese rats. Melatonin increased inguinal temperature by 1.36 ± 0.02°C in ZL and by 0.55 ± 0.04°C in ZDF rats and sensitized the thermogenic effect of acute cold exposure in both groups. Melatonin increased the amounts of thermogenic proteins, uncoupling protein 1 ( UCP 1) (by ~2‐fold, P < 0.01) and PGC ‐1α (by 25%, P < 0.05) in extracts from beige inguinal areas in ZL rats. Melatonin also induced measurable amounts of UCP 1 and stimulated by ~2‐fold the levels of PGC ‐1α in ZDF animals. Locomotor activity and circulating irisin levels were not affected by melatonin. These results demonstrate that chronic oral melatonin drives WAT into a brown‐fat‐like function in ZDF rats. This may contribute to melatonin′s control of body weight and its metabolic benefits.
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