Regulation of Pancreatic β-Cell Function by the NPY System

Author:

Yang Chieh-Hsin1,Onda Danise-Ann1,Oakhill Jonathan S123,Scott John W134,Galic Sandra12,Loh Kim12ORCID

Affiliation:

1. St. Vincent’s Institute of Medical Research, Fitzroy, VIC 3065, Australia

2. Department of Medicine, University of Melbourne, Parkville, VIC 3010, Australia

3. Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, VIC 3000, Australia

4. The Florey Institute of Neuroscience and Mental Health, Parkville, VIC 3010, Australia

Abstract

Abstract The neuropeptide Y (NPY) system has been recognized as one of the most critical molecules in the regulation of energy homeostasis and glucose metabolism. Abnormal levels of NPY have been shown to contribute to the development of metabolic disorders including obesity, cardiovascular diseases, and diabetes. NPY centrally promotes feeding and reduces energy expenditure, while the other family members, peptide YY (PYY) and pancreatic polypeptide (PP), mediate satiety. New evidence has uncovered additional functions for these peptides that go beyond energy expenditure and appetite regulation, indicating a more extensive function in controlling other physiological functions. In this review, we will discuss the role of the NPY system in the regulation of pancreatic β-cell function and its therapeutic implications for diabetes.

Funder

National Health and Medical Research Council

Publisher

The Endocrine Society

Subject

Endocrinology

Reference62 articles.

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