Abstract |
Ghrelin was first identified as an endogenous ligand of the growth hormone secretagogue receptor (GHSR) in 1999, with the function of stimulating the release of growth hormone (GH), while nesfatin-1 was identified in 2006. Both peptides are secreted by the same kind of endocrine cells, X/A-like cells in the stomach. Compared with ghrelin, nesfatin-1 exerts opposite effects on energy metabolism, glucose metabolism, gastrointestinal functions and regulation of blood pressure, but exerts similar effects on anti- inflammation and neuroprotection. Up to now, nesfatin-1 remains as an orphan ligand because its receptor has not been identified. Several studies have shown the effects of nesfatin-1 are dependent on the receptor of ghrelin. We herein compare the effects of nesfatin-1 and ghrelin in several aspects and explore the possibility of their interactions.
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Authors | Xi Chen, Jing Dong, Qian Jiao, Xixun Du, Mingxia Bi, Hong Jiang |
Journal | Cellular and molecular life sciences : CMLS
(Cell Mol Life Sci)
Vol. 79
Issue 3
Pg. 169
(Mar 03 2022)
ISSN: 1420-9071 [Electronic] Switzerland |
PMID | 35239020
(Publication Type: Journal Article, Review)
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Copyright | © 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG. |
Chemical References |
- GHRL protein, human
- Ghrelin
- NUCB2 protein, human
- Nucleobindins
|
Topics |
- Animals
- Diabetes Mellitus
(metabolism)
- Ghrelin
(metabolism)
- Humans
- Nucleobindins
(metabolism)
|