Gender differences in the effects of ethanol on C57BL/6 mice

The influence of gender on the stimulatory and depressant effects of ethanol was examined in C57BL/6 (C57) mice. In Experiment 1, locomotor activity was assessed in young (2-month-old) male and female mice injected intraperitoneally (IP) with stimulatory (1.5 g/kg) or depressant (2.5 g/kg) doses of...

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Veröffentlicht in:Alcohol (Fayetteville, N.Y.) N.Y.), 1992-05, Vol.9 (3), p.257-260
Hauptverfasser: Middaugh, Lawrence D., Frackelton, William F., Boggan, William O., Onofrio, Amy, Shepherd, Cindy L.
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container_issue 3
container_start_page 257
container_title Alcohol (Fayetteville, N.Y.)
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creator Middaugh, Lawrence D.
Frackelton, William F.
Boggan, William O.
Onofrio, Amy
Shepherd, Cindy L.
description The influence of gender on the stimulatory and depressant effects of ethanol was examined in C57BL/6 (C57) mice. In Experiment 1, locomotor activity was assessed in young (2-month-old) male and female mice injected intraperitoneally (IP) with stimulatory (1.5 g/kg) or depressant (2.5 g/kg) doses of ethanol. Both the stimulatory and the depressive effects of ethanol were greater in young male than female C57 mice, and the gender difference was unrelated to blood ethanol concentration (BEC). In Experiment 2, older (9-month-old) male and female mice were given ethanol (2.5 g/kg) either by IP injection or gavage to determine if the gender differences in BEC and ethanol effects observed in the first experiment depended upon the route of ethanol administration. In this experiment, ethanol reduced locomotor activity more in males than females whether given by gavage or IP injection, and the males had higher BECs than females at the time of testing. Thus, the differences in the behavioral effects of ethanol appeared to be related to BEC. The greater depressive effect of ethanol on older male mice in this experiment is consistent with an earlier report of prolonged ethanol-hypnosis in older male C57 mice. Therefore, differences in BEC could account for the gender differences in the behavioral effects of ethanol on older but not young mice. The gender difference in BEC of mice obtained in the present and earlier reports is opposite to that reported for humans. Although the present study does not clarify what accounts for this species difference, it eliminates the route of administration as a plausible explanation, and establishes that females were less affected than males to either the stimulatory or the depressive effects of ethanol.
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In Experiment 1, locomotor activity was assessed in young (2-month-old) male and female mice injected intraperitoneally (IP) with stimulatory (1.5 g/kg) or depressant (2.5 g/kg) doses of ethanol. Both the stimulatory and the depressive effects of ethanol were greater in young male than female C57 mice, and the gender difference was unrelated to blood ethanol concentration (BEC). In Experiment 2, older (9-month-old) male and female mice were given ethanol (2.5 g/kg) either by IP injection or gavage to determine if the gender differences in BEC and ethanol effects observed in the first experiment depended upon the route of ethanol administration. In this experiment, ethanol reduced locomotor activity more in males than females whether given by gavage or IP injection, and the males had higher BECs than females at the time of testing. Thus, the differences in the behavioral effects of ethanol appeared to be related to BEC. The greater depressive effect of ethanol on older male mice in this experiment is consistent with an earlier report of prolonged ethanol-hypnosis in older male C57 mice. Therefore, differences in BEC could account for the gender differences in the behavioral effects of ethanol on older but not young mice. The gender difference in BEC of mice obtained in the present and earlier reports is opposite to that reported for humans. 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In Experiment 1, locomotor activity was assessed in young (2-month-old) male and female mice injected intraperitoneally (IP) with stimulatory (1.5 g/kg) or depressant (2.5 g/kg) doses of ethanol. Both the stimulatory and the depressive effects of ethanol were greater in young male than female C57 mice, and the gender difference was unrelated to blood ethanol concentration (BEC). In Experiment 2, older (9-month-old) male and female mice were given ethanol (2.5 g/kg) either by IP injection or gavage to determine if the gender differences in BEC and ethanol effects observed in the first experiment depended upon the route of ethanol administration. In this experiment, ethanol reduced locomotor activity more in males than females whether given by gavage or IP injection, and the males had higher BECs than females at the time of testing. Thus, the differences in the behavioral effects of ethanol appeared to be related to BEC. The greater depressive effect of ethanol on older male mice in this experiment is consistent with an earlier report of prolonged ethanol-hypnosis in older male C57 mice. Therefore, differences in BEC could account for the gender differences in the behavioral effects of ethanol on older but not young mice. The gender difference in BEC of mice obtained in the present and earlier reports is opposite to that reported for humans. 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The greater depressive effect of ethanol on older male mice in this experiment is consistent with an earlier report of prolonged ethanol-hypnosis in older male C57 mice. Therefore, differences in BEC could account for the gender differences in the behavioral effects of ethanol on older but not young mice. The gender difference in BEC of mice obtained in the present and earlier reports is opposite to that reported for humans. Although the present study does not clarify what accounts for this species difference, it eliminates the route of administration as a plausible explanation, and establishes that females were less affected than males to either the stimulatory or the depressive effects of ethanol.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>1605893</pmid><doi>10.1016/0741-8329(92)90062-F</doi><tpages>4</tpages></addata></record>
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identifier ISSN: 0741-8329
ispartof Alcohol (Fayetteville, N.Y.), 1992-05, Vol.9 (3), p.257-260
issn 0741-8329
1873-6823
language eng
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source Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE
subjects Alcoholism and acute alcohol poisoning
Animals
Biological and medical sciences
C57 mice
Dose-Response Relationship, Drug
Ethanol
Ethanol - blood
Ethanol - pharmacology
Female
Gender differences
Locomotor activity
Male
Medical sciences
Mice
Mice, Inbred C57BL
Motor Activity - drug effects
Pharmaceutical Vehicles
Sex Characteristics
Toxicology
title Gender differences in the effects of ethanol on C57BL/6 mice
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