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The crosstalk between fibroblast growth factor 21 (FGF21) system and substance use
Tammy Wang1,2, Ryan E Tyler1, Oyenike Ilaka1,3
1Clinical Psychoneuroendocrinology and Neuropsychopharmacology Section, Translational Addiction Medicine Branch, National Institute on Drug Abuse Intramural Research Program and National Institute on Alcohol Abuse and Alcoholism Division of Intramural Clinical and Biological Research, National Institutes of Health, Baltimore, MD, USA.
Fibroblast growth factor 21 (FGF21) plays a key role in regulating alcohol consumption, showing an inverse relationship with alcohol use disorder (AUD). Understanding this liver-brain axis hormone may lead to new treatments for AUD.
Area of Science:
- Neuroscience
- Endocrinology
- Addiction Medicine
Background:
- Substance use disorders (SUDs), including alcohol use disorder (AUD), disrupt central and peripheral nervous system communication.
- Fibroblast growth factor 21 (FGF21), a hormone regulating energy homeostasis, influences alcohol and other substance use.
- The liver-brain axis involvement in AUD pathogenesis requires further investigation.
Purpose of the Study:
- To explore the association between FGF21 and SUDs through a scoping review.
- To elucidate the relationship between FGF21, alcohol consumption, and other substance use.
Main Methods:
- Scoping review of existing literature.
- Analysis of studies investigating FGF21 levels in relation to alcohol and substance use.
- Examination of molecular pathways modulated by FGF21.
Main Results:
- An inverse relationship exists between FGF21 levels and alcohol consumption: increased FGF21 reduces intake, while suppressed FGF21 enhances it.
- Alcohol elevates hepatic FGF21 production, which signals the brain to decrease alcohol intake.
- FGF21 activation protects against alcohol-induced hepatic fat accumulation, oxidative stress, and inflammation.
Conclusions:
- FGF21 exhibits a bidirectional association with alcohol consumption.
- The FGF21 system presents a potential therapeutic target for AUD and alcohol-associated liver disease.
- Further research into FGF21-based pharmacotherapies is warranted.
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