Literature DB >> 3786361

Effects of restraint stress on voluntary ethanol intake and ulcer proliferation in rats.

G E Rockman, A Hall, G B Glavin.   

Abstract

The present study examined the effect of exposure to a schedule of predictable restraint stress on voluntary ethanol consumption and ulcer proliferation in rats. Following ethanol screening rats were divided into high, medium and low ethanol consuming groups on the basis of daily ethanol intake (g/kg/day) and exposed to daily 1 hr restraint stress for 10 consecutive days. Voluntary ethanol consumption was monitored both during the stress period and for an additional 25 days post-stress. Stomach pathology was assessed on days 1, 5 and 10 of the stress period as well as at the conclusion of the post-stress period. Results indicated a differential effect of stress on ethanol intake in that high ethanol preferring rats consumed less ethanol in the first 5 days of the post-stress period as compared to non-stressed controls. In contrast, the medium ethanol preferring group drank more ethanol than controls during days 1-5 of the post-stress period. Ethanol consumption for the low ethanol groups did not change during the entire experiment. Stomach pathology data revealed no ulcer formation in the stressed groups during the stress period. At the end of the post-stress period, however, stressed animals exhibited a significantly greater ulcer severity (mean cumulative ulcer length) and ulcer frequency (mean number of ulcers per rat) than non-stressed groups. Stomach pathology for ethanol consuming groups did not differ from controls, indicating that ethanol did not, by itself, affect ulcer development.

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Year:  1986        PMID: 3786361     DOI: 10.1016/0091-3057(86)90089-4

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  6 in total

1.  The protective effects of the melanocortin receptor (MCR) agonist, melanotan-II (MTII), against binge-like ethanol drinking are facilitated by deletion of the MC3 receptor in mice.

Authors:  J J Olney; G M Sprow; M Navarro; T E Thiele
Journal:  Neuropeptides       Date:  2013-11-15       Impact factor: 3.286

2.  The Role of Orexin Signaling in the Ventral Tegmental Area and Central Amygdala in Modulating Binge-Like Ethanol Drinking Behavior.

Authors:  Jeffrey J Olney; Montserrat Navarro; Todd E Thiele
Journal:  Alcohol Clin Exp Res       Date:  2017-02-09       Impact factor: 3.455

Review 3.  Effects of stress on alcohol drinking: a review of animal studies.

Authors:  Howard C Becker; Marcelo F Lopez; Tamara L Doremus-Fitzwater
Journal:  Psychopharmacology (Berl)       Date:  2011-08-18       Impact factor: 4.530

4.  Neuropeptide Y (NPY)-induced reductions in alcohol intake during continuous access and following alcohol deprivation are not altered by restraint stress in alcohol-preferring (P) rats.

Authors:  Megan L Bertholomey; Angela N Henderson; Nancy E Badia-Elder; Robert B Stewart
Journal:  Pharmacol Biochem Behav       Date:  2010-10-16       Impact factor: 3.533

Review 5.  Stress modulation of drug self-administration: implications for addiction comorbidity with post-traumatic stress disorder.

Authors:  Marian L Logrip; Eric P Zorrilla; George F Koob
Journal:  Neuropharmacology       Date:  2011-07-19       Impact factor: 5.250

6.  Effects of chronic swim stress on EtOH-related behaviors in C57BL/6J, DBA/2J and BALB/cByJ mice.

Authors:  Janel M Boyce-Rustay; Alicia L Janos; Andrew Holmes
Journal:  Behav Brain Res       Date:  2007-08-02       Impact factor: 3.332

  6 in total

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