LACK OF EFFECTS OF 5-HT3 ANTAGONISTS ON NORMAL AND MORPHINE-ATTENUATED SEXUAL BEHAVIORS IN FEMALE AND MALE-RATS
被引:11
作者:
TANCO, SA
论文数: 0引用数: 0
h-index: 0
机构:Department of Psychology, University of British Columbia, Vancouver, V6T 1Z4, Britisch Columbia
TANCO, SA
WATSON, NV
论文数: 0引用数: 0
h-index: 0
机构:Department of Psychology, University of British Columbia, Vancouver, V6T 1Z4, Britisch Columbia
WATSON, NV
GORZALKA, BB
论文数: 0引用数: 0
h-index: 0
机构:Department of Psychology, University of British Columbia, Vancouver, V6T 1Z4, Britisch Columbia
GORZALKA, BB
机构:
[1] Department of Psychology, University of British Columbia, Vancouver, V6T 1Z4, Britisch Columbia
来源:
EXPERIENTIA
|
1993年
/
49卷
/
03期
关键词:
SEXUAL BEHAVIOR;
SEROTONIN;
5-HT;
5-HT3;
RECEPTORS;
ANTAGONISTS;
OPIOIDS;
RATS;
D O I:
10.1007/BF01923532
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Although 5-HT1 and 5-HT2 receptor activity is known to influence copulation, the effects of 5-HT3 receptor-selective drugs on sexual activity have yet to be systematically studied. The following experiments investigated the effects of the 5-HT3-selective antagonists MDL 72222, ondansetron and ICS 205-930 on female sexual behaviour; male rats were studied using ondansetron and granisetron. These compounds influenced neither male nor female copulatory behaviours, suggesting that 5-HT3 receptors contribute little to the modulation of sexual activity. 5-HT3 receptor antagonists block certain opioid-induced behaviours and opioids selectively inhibit sexual behaviours; therefore, the ability of ondansetron and ICS 205-930 to modify morphine-attenuated copulatory activity was also tested. While morphine inhibited copulation, 5-HT3 antagonists failed to reverse the effects.