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Central mechanisms of adiposity in adult female mice with androgen excess
Author(s) -
Nohara Kazunari,
Laque Amanda,
Allard Camille,
Münzberg Heike,
MauvaisJarvis Franck
Publication year - 2014
Publication title -
obesity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.438
H-Index - 199
eISSN - 1930-739X
pISSN - 1930-7381
DOI - 10.1002/oby.20719
Subject(s) - endocrinology , medicine , proopiomelanocortin , androgen , leptin , adipose tissue , androgen receptor , anorectic , arcuate nucleus , downregulation and upregulation , energy homeostasis , hypothalamus , dihydrotestosterone , melanocortin , agonist , chemistry , receptor , obesity , hormone , body weight , prostate cancer , cancer , biochemistry , gene
Objective Androgen excess in women is associated with visceral adiposity. However, little is known on the mechanism through which androgen promotes visceral fat accumulation. Methods To address this issue, female mice to chronic androgen excess using 5α‐dihydrotestosterone (DHT) and studied the regulation of energy homeostasis was exposed. Results DHT induced a leptin failure to decrease body weight associated with visceral adiposity but without alterations in leptin anorectic action. This paralleled leptin's failure to upregulate brown adipose tissue expression of uncoupling protein‐1 , associated with decreased energy expenditure (EE). DHT decreased hypothalamic proopiomelanocortin ( pomc ) mRNA expression and increased POMC intensity in neuronal bodies of the arcuate nucleus while simultaneously decreasing the intensity of POMC projections to the dorsomedial hypothalamus (DMH). This was associated with a failure of the melanocortin 4 receptor agonist melanotan‐II to suppress body weight. Conclusion Taken together, these data indicate that androgen excess promotes visceral adiposity with reduced POMC neuronal innervation in the DMH, reduced EE but without hyperphagia.