Neuropeptide W: An Anorectic Peptide Regulated by Leptin and Metabolic State

Author:

Date Yukari1,Mondal Muhtashan S.2,Kageyama Haruaki3,Ghamari-Langroudi Masoud4,Takenoya Fumiko3,Yamaguchi Hideki2,Shimomura Yukio5,Mori Masaaki6,Murakami Noboru7,Shioda Seiji3,Cone Roger D.8,Nakazato Masamitsu2

Affiliation:

1. Frontier Science Research Center (Y.D.), University of Miyazaki, Miyazaki 889-1692, Japan

2. Neurology, Respirology, Endocrinology, and Metabolism (M.S.M., H.Y., M.N.), Department of Internal Medicine, Miyazaki Medical College, University of Miyazaki, Miyazaki 889-1692, Japan

3. Department of Anatomy (H.K, F.T., S.S.), Showa University School of Medicine, Tokyo 142-8555, Japan

4. The Center for the Study of Weight Regulation (M.G.-L.), Oregon Health and Science University, Portland, Oregon 97239-3098

5. Frontier Research Laboratories (Y.S.), Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Ibaraki 300-4293, Japan

6. Pharmacology Research Laboratories I (M.M.), Pharmaceutical Research Division, Takeda Pharmaceutical Company Ltd., Osaka 532-8686, Japan

7. Department of Veterinary Physiology (N.M.), Faculty of Agriculture, University of Miyazaki, Miyazaki 889-2192, Japan

8. Department of Molecular Physiology and Biophysics (R.D.C.), Vanderbilt University Medical Center, Nashville, Tennessee 37232

Abstract

Neuropeptide W (NPW) is an anorectic peptide produced in the brain. Here, we showed that NPW was present in several hypothalamic nuclei, including the paraventricular hypothalamic nucleus, ventromedial hypothalamic nucleus, lateral hypothalamus, and hypothalamic arcuate nucleus. NPW expression was significantly up-regulated in leptin-deficient ob/ob and leptin receptor-deficient db/db mice. The increase in NPW expression in ob/ob mice was abrogated to control levels after leptin replacement. Leptin induced suppressors of cytokine signaling-3 after phosphorylation of signal transducer and activator of transcription-3 in NPW-expressing neurons. In addition, we demonstrated that NPW reduces feeding via the melanocortin-4-receptor signaling pathway. We also showed that NPW activates proopiomelanocortin and inhibits neuropeptide Y neurons using loose-patch extracellular recording of these neurons identified by promoter-driven green fluorescent protein expression. This study indicates that NPW may play an important role in the regulation of feeding and energy metabolism under the conditions of leptin insufficiency.

Publisher

The Endocrine Society

Subject

Endocrinology

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