Related Experiment Video
Updated: Mar 26, 2026

Identification and Dissection of Diverse Mouse Adipose Depots
Published on: July 11, 2019
New adipokines.
Bruno Fève1, Claire Bastard2, Soraya Fellahi3
1UMR_S 938 CDR-Saint-Antoine, faculté de médecine, Sorbonne Universities UPMC Paris 6, 27, rue de Chaligny, 75012 Paris, France; University Hospital ICAN Institute, 75013 Paris, France; Endocrinology, Saint-Antoine Hospital, AP-HP, 75012 Paris, France.
Adipose tissue secretes adipokines that regulate metabolism. This review highlights three newly discovered adipokines—apelin, FGF21, and NRG4—as promising targets for obesity-related metabolic disorders.
Area of Science:
- Endocrinology and Metabolism
- Molecular Biology
- Physiology
Background:
- Adipose tissue functions as an endocrine organ, secreting numerous adipokines.
- Adipokines regulate key physiological processes including glucose and lipid metabolism, inflammation, and angiogenesis.
- Leptin and adiponectin are well-studied adipokines involved in energy metabolism.
Purpose of the Study:
- To review the roles of three recently discovered adipokines: apelin, fibroblast growth factor-21 (FGF21), and neuroregulin-4 (NRG4).
- To highlight their emerging importance in metabolic regulation.
- To discuss their potential as therapeutic targets for obesity-associated metabolic disorders.
Main Methods:
- Literature review of recent experimental and clinical data.
- Focus on the discovery and functional characterization of apelin, FGF21, and NRG4.
- Analysis of their involvement in metabolic pathways.
Main Results:
- Apelin, FGF21, and NRG4 are identified as key adipokines with significant metabolic functions.
- These adipokines influence glucose homeostasis, lipid metabolism, and energy balance.
- Emerging data link these adipokines to various metabolic disorders.
Conclusions:
- Apelin, FGF21, and NRG4 represent a new generation of adipokines with critical roles in metabolism.
- These adipokines hold significant promise as therapeutic targets for managing obesity and related metabolic diseases.
- Further research into their mechanisms of action is warranted.
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