Literature DB >> 10814546

Volitional ethanol consumption affects overall serotonin metabolism in Syrian golden hamsters (Mesocricetus auratus).

W M Keung1, L Kunze, D J Li, O Lazo.   

Abstract

Methods were established for the determination of serotonin (5-HT)(1) metabolites 5-hydroxyindole-3-acetic acid (5-HIAA) and 5-hydroxytryptophol (5-HTOL) in the urine of Syrian golden hamsters (Mesocricetus auratus) and used to study the effect of volitional ethanol consumption on overall 5-HT metabolism in this ethanol-preferring rodent. The basal levels of 5-HIAA and 5-HTOL in 24-h urine of ethanol-naive hamsters were 300 +/- 101 and 4.96 +/- 1. 06 nmol (n = 8), respectively. Given free choice between water and a 15% ethanol solution, these hamsters chose to consume increasing amounts of ethanol. The increase was accompanied by a concomitant decrease in urine 5-HIAA and increase in urine 5-HTOL, indicating that volitional ethanol intake diverted part of the 5-HT metabolic flux from an oxidative into a reductive pathway. In a separate experiment, the amounts of ethanol consumed by and blood ethanol concentrations attained in ethanol-drinking golden hamsters were determined at 5 different time intervals between 6 PM and 7 AM when most feeding activities occurred. Except in the first hour after lights were turned off, ethanol was consumed at a relatively even pace throughout the night (2-3 g/kg/3 h) and blood ethanol levels were maintained at the low mM range which rarely exceeded 2 mM. These results suggest that the biochemical pathway that catalyzes 5-HT metabolism is extremely sensitive to ethanol and can play an important role in mediating the reported clinically beneficial action of a low concentration of ethanol during alcohol detoxification. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10814546     DOI: 10.1006/bbrc.2000.2718

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  6 in total

1.  Clozapine reconstructed: Haloperidol's ability to reduce alcohol intake in the Syrian golden hamster can be enhanced through noradrenergic modulation by desipramine and idazoxan.

Authors:  Jibran Y Khokhar; David T Chau; Ree Dawson; Alan I Green
Journal:  Drug Alcohol Depend       Date:  2015-04-22       Impact factor: 4.492

2.  Role of caloric homeostasis and reward in alcohol intake in Syrian golden hamsters.

Authors:  Danielle Gulick; Alan I Green
Journal:  Physiol Behav       Date:  2010-08-03

3.  Clozapine chronically suppresses alcohol drinking in Syrian golden hamsters.

Authors:  David T Chau; Danielle Gulick; Haiyi Xie; Ree Dawson; Alan I Green
Journal:  Neuropharmacology       Date:  2009-11-04       Impact factor: 5.250

4.  Effects of iloperidone, combined with desipramine, on alcohol drinking in the Syrian golden hamster.

Authors:  Jibran Y Khokhar; Alan I Green
Journal:  Neuropharmacology       Date:  2016-01-12       Impact factor: 5.250

5.  Desipramine enhances the ability of paliperidone to decrease alcohol drinking.

Authors:  David T Chau; Jibran Y Khokhar; Danielle Gulick; Ree Dawson; Alan I Green
Journal:  J Psychiatr Res       Date:  2015-07-18       Impact factor: 4.791

6.  Desipramine enhances the ability of risperidone to decrease alcohol intake in the Syrian golden hamster.

Authors:  Danielle Gulick; David T Chau; Jibran Y Khokhar; Ree Dawson; Alan I Green
Journal:  Psychiatry Res       Date:  2014-05-04       Impact factor: 3.222

  6 in total

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