Reduced efficacy of 8-OH-DPAT's inhibition of lordosis behavior by prior estrogen treatment

被引:15
|
作者
Trevino, A [1 ]
Wolf, A [1 ]
Jackson, A [1 ]
Price, T [1 ]
Uphouse, L [1 ]
机构
[1] Texas Womans Univ, Dept Biol, Denton, TX 76204 USA
关键词
5-HT1A receptors; serotonin; sexual behavior; hormones;
D O I
10.1006/hbeh.1999.1515
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The effects of bilateral VMN infusion with the 5-HT1A receptor agonist, (+/-)-8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; 200, 1000, or 2000 ng), on lordosis behavior were examined in hormonally primed ovariectomized rats. When rats were given a single injection with 25 mu g estradiol benzoate followed 48 h later with 500 mu g progesterone, inhibition of lordosis behavior was evident at all doses of 8-OH-DPAT. However, when rats were treated with 25 mu g estradiol benzoate followed 7 days later with a second injection of 25 mu g estradiol benzoate and then progesterone, none of the doses of 8-OH-DPAT effectively inhibited lordosis behavior. In some rats, cannulae were located near the most rostral portion of the VMN. In these rats, there was no effect of the second estrogen treatment on the response to 8-OH-DPAT. Therefore, a second experiment was performed to specifically evaluate the effects of two estradiol benzoate treatments on the response to bilateral 8-OH-DPAT infusion in the rostral VMN. In contrast to the reduced effectiveness of the 8-OH-DPAT infusion in the mid to caudal VMN in rats given two injections with estradiol benzoate, 2000 ng 8-OH-DPAT continued to effectively inhibit lordosis behavior following the 5-HT1A receptor agonist's infusion into the more rostral areas. These findings are discussed in relation to earlier studies in which the potency, but not the efficacy, of 8-OHDPAT was reduced following systemic treatment with the 5-HT1A receptor agonist. (C) 1999 Academic Press.
引用
收藏
页码:215 / 223
页数:9
相关论文
共 50 条