PubMed Health⌕ Search

PubMed · 8295952

Individual behavioral differences and ethanol consumption in Wistar rats.

Abstract

The aim of this study was to determine if inherent differences in the behavioral measures between individual Wistar male rats influence the level of ethanol consumption. We addressed this question by searching for differences in ethanol intake that an individual animal develops. Measures of ethanol intake were then correlated with the outcome of various behavioral tests. Our results indicate that individual variations of behavioral reactivity may be associated with the predisposition to develop high ethanol intake. Animals with delayed habituation to a novel environment, enhanced locomotor activity during testing in the open field after initial habituation, and excessive locomotor inhibition after administration of 0.07 mg/kg dose of apomorphine, are predisposed to develop high ethanol intake in a free-choice condition. Measures of activity in the forced swim test, apomorphine-induced stereotypy, hypothermia, and locomotor stimulation could not predict a propensity to acquire high ethanol preference. It is suggested that individual differences in the acquisition of high ethanol intake may be influenced, at least partially, by the differences in the sensitivity of brain dopaminergic neurotransmission.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

A Bisaga, W Kostowski. 1993. Individual behavioral differences and ethanol consumption in Wistar rats.. https://doi.org/10.1016/0031-9384(93)90336-e

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

FGF21 suppresses alcohol consumption through an amygdalo-striatal circuit.

Excessive alcohol consumption is a major health and social issue in our society. Pharmacologic administration of the endocrine hormone fibroblast growth factor 21 (FGF21) suppresses alcohol consumption through actions in the brain in rodents, and genome-wide association studies have identified single nucleotide polymorphisms in genes involved with FGF21 signaling as being associated with increased alcohol consumption in humans. However, the neural circuit(s) through which FGF21 signals to suppress alcohol consumption are unknown, as are its effects on alcohol consumption in higher organisms. Here, we demonstrate that administration of an FGF21 analog to alcohol-preferring non-human primates reduces alcohol intake by 50%. Further, we reveal that FGF21 suppresses alcohol consumption through a projection-specific subpopulation of KLB-expressing neurons in the basolateral amygdala. Our results illustrate how FGF21 suppresses alcohol consumption through a specific population of neurons in the brain and demonstrate its therapeutic potential in non-human primate models of excessive alcohol consumption.

Alcohol Drinking↗

Alcohol intake and colorectal cancer risk: a dose-response meta-analysis of published cohort studies.

The epidemiologic evidence support that alcohol intake might be associated with increased colorectal cancer risk. However, the results by anatomic site in the large bowel are inconsistent. We conducted a meta-analysis of prospective cohort studies published between 1990 and June 2005 on the relationship between alcohol intake and colon and rectal cancer. We quantified associations with colon and rectal cancer using meta-analysis of relative risk (RR) associated to the highest versus the lowest category of alcohol intake and meta-analysis of study-specific dose-response slopes using fixed or random effect models depending on the heterogeneity of effects among studies. Sixteen prospective cohort studies including more than 6,300 patients with colorectal cancer were eligible for inclusion. High alcohol intake was significantly associated with increased risk of colon (RR = 1.50; 95% CI = 1.25, 1.79) and rectal cancer (RR = 1.63; 95% CI = 1.35, 1.97) when comparing the highest with the lowest category of alcohol intake, equivalent to a 15% increase of risk of colon or rectal cancer for an increase of 100 g of alcohol intake per week. The relationship did not differ significantly by anatomical site (colon, rectum). Using meta-regression analysis, we identified geographical area where the study was conducted as a possible source of between-study heterogeneity of effects among studies. Lifestyle recommendations for prevention of colorectal cancer should consider limiting alcohol intake.

Alcohol Drinking↗