Female gonadal hormones, mild restraint, and male preference.

The partner preference paradigm was used to test the hypothesis that mild restraint reduced sexual motivation of female rats. Ovariectomized rats were primed with 10 pg estradiol benzoate or estradiol benzoate and 500 microg progesterone. Additional rats were injected with sesame seed oil. These three groups of rats (oil-oil, estradiol benzoate-oil, or estradiol benzoate-progesterone; OO, EO, EP) were placed for 10 min in an arena, the ends of which enclosed either a sexually active male or an ovariectomized, unprimed female. Time spent near the sexually active male relative to time spent near either stimulus animal was used as the index of male preference. As expected, hormonal treatment significantly increased male preference. After this first 10 min interval, females were returned to the home cage or restrained for 5 min in a Decapicone. Thereafter, male preference was recorded for another 10 min. Consistent with the first 10 min period, EP rats spent significantly more time near the male than did OO rats while EO rats were intermediate. There was no effect of restraint, but there was a significant increase in self-grooming. These findings contrast with previous studies and allow the suggestion that a brief, mild restraint fails to influence the female's sexual motivation. The implications of these findings are discussed.

GABAA-5-HT1A receptor interaction in the mediobasal hypothalamus.

Both serotonin (5-HT) and gamma-aminobutyric acid (GABA) modulate female rat lordosis behavior and appear to interact in their control of the behavior. The current experiments were designed to investigate the interaction between these two neurotransmitters in sexually receptive female rats. Ovariectomized female rats, with bilateral cannulae directed toward the ventromedial nucleus of the hypothalamus (VMN), were hormonally primed with 10 microg estradiol benzoate and 500 microg progesterone. Sexual behavior was examined after intracranial infusion with 200 ng (+/-)-8-hydroxy 2-(di-n-propylamino)tetralin (8-OH-DPAT), 25 ng (5-aminomethyl-3-hydroxyisoxazole)hydrobromide (muscimol), 10 ng bicuculline or a combination of the drugs. As expected, 8-OH-DPAT reduced lordosis behavior and muscimol attenuated this inhibition in a bicuculline-sensitive manner. Muscimol alone also reduced lordosis behavior. These findings contrast with several reports that muscimol facilitates lordosis behavior of suboptimally hormonally primed female rats. The current outcome is discussed in terms of procedural differences between the present experiment and earlier studies. It is suggested that muscimol may enhance lordosis responding in suboptimally hormonally primed rats by activation of GABAA receptors located dorsal to the VMN. In contrast, activation of receptors located more ventrally within the mediobasal hypothalamus (MBH) may inhibit the behavior of rats that are already sexually receptive.