NPY Deficiency Prevents Postmenopausal Adiposity by Augmenting Estradiol-Mediated Browning

Author:

Park Seongjoon1,Nayantai Erkhembayar2,Komatsu Toshimitsu1,Hayashi Hiroko1,Mori Ryoichi1,Shimokawa Isao1

Affiliation:

1. Department of Pathology, Nagasaki University School of Medicine, Graduate School of Biomedical Sciences, Japan

2. Department of Physiology, School of Biomedicine, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia

Abstract

Abstract The orexigenic hormone neuropeptide Y (NPY) plays a pivotal role in the peripheral regulation of fat metabolism. However, the mechanisms underlying the effects of sex on NPY function have not been extensively analyzed. In this study, we examined the effects of NPY deficiency on fat metabolism in male and female mice. Body weight was slightly decreased, whereas white adipose tissue (WAT) mass was significantly decreased as the thermogenic program was upregulated in NPY-/- female mice compared with that in wild-type mice; these factors were not altered in response to NPY deficiency in male mice. Moreover, lack of NPY resulted in an increase in luteinizing hormone (LH) expression in the pituitary gland, with concomitant activation of the estradiol-mediated thermogenic program in inguinal WAT, and alleviated age-related modification of adiposity in female mice. Taken together, these data revealed a novel intracellular mechanism of NPY in the regulation of fat metabolism and highlighted the sexual dimorphism of NPY as a promising target for drug development to reduce postmenopausal adiposity.

Funder

Japan Society for the Promotion of Science

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Ageing

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