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Sensitivity of Hypocretin System to Chronic Alcohol Exposure: A Human and Animal Study.

Authors :
McGregor, Ronald
Matzeu, Alessandra
Thannickal, Thomas C.
Wu, Frank
Cornford, Marcia
Martin-Fardon, Rémi
Siegel, Jerome M.
Source :
Neuroscience. Jul2023, Vol. 522, p1-10. 10p.
Publication Year :
2023

Abstract

• Fewer hypocretin neurons are found in humans with alcohol use disorder. • Smaller size of hypocretin, MCH neurons and activation of microglia was detected. • No changes were observed in the histamine cell group in this same human population. • Rats exposed to alcohol do not show changes hypocretin, MCH or microglia. • Factors secondary to AUD might be responsible for the changes in humans. Human heroin addicts and mice administered morphine for a 2 week period show a greatly increased number of hypothalamic hypocretin (Hcrt or orexin) producing neurons with a concomitant reduction in Hcrt cell size. Male rats addicted to cocaine similarly show an increased number of detectable Hcrt neurons. These findings led us to hypothesize that humans with alcohol use disorder (AUD) would show similar changes. We now report that humans with AUD have a decreased number and size of detectable Hcrt neurons. In addition, the intermingled melanin concentrating hormone (MCH) neurons are reduced in size. We saw no change in the size and number of tuberomammillary histamine neurons in AUD. Within the Hcrt/MCH neuronal field we found that microglia cell size was increased in AUD brains. In contrast, male rats with 2 week alcohol exposure, sufficient to elicit withdrawal symptoms, show no change in the number or size of Hcrt, MCH and histamine neurons, and no change in the size of microglia. The present study indicates major differences between the response of Hcrt neurons to opioids and that to alcohol in human subjects with a history of substance abuse. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03064522
Volume :
522
Database :
Academic Search Index
Journal :
Neuroscience
Publication Type :
Academic Journal
Accession number :
164582814
Full Text :
https://doi.org/10.1016/j.neuroscience.2023.04.018