Everitt B J, Fuxe K, Hökfelt F T, Jonsson G
J Comp Physiol Psychol. 1975 Aug;89(6):556-72. doi: 10.1037/h0077430.
The involvement of indole- and catecholamines in the hormonal regulation of sexual receptivity has been investigated in ovariectomized female rats. Drugs that reduce 5-hydroxytryptamine, dopamine, and adrenaline or increase noradrenaline neurotransmission tended to facilitate the occurrence of estrous behavior in estrogen-treated females, and drugs having opposite effects tended to inhibit receptivity induced by estrogen and progesterone. Estrogen decreased noradrenaline turnover in cortex and brain stem; progesterone enhanced this effect in brain stem but prevented it in cortex. Both hormones tended to block noradrenaline uptake in hypothalamus in vitro. In a schedule used to induce receptivity, estrogen accelerated serotonin turnover, an effect prevented by progesterone. Thus a number of monoamines may be involved in the control by hormones of estrous behavior. Furthermore, hormones affect both amine turnover and uptake mechanisms.
已在切除卵巢的雌性大鼠中研究了吲哚胺和儿茶酚胺在性接受激素调节中的作用。降低5-羟色胺、多巴胺和肾上腺素或增加去甲肾上腺素神经传递的药物往往会促进雌激素处理的雌性大鼠发情行为的发生,而具有相反作用的药物则往往会抑制雌激素和孕酮诱导的性接受。雌激素降低了皮质和脑干中的去甲肾上腺素周转率;孕酮增强了脑干中的这种作用,但在皮质中则阻止了这种作用。两种激素在体外都倾向于阻断下丘脑对去甲肾上腺素的摄取。在用于诱导性接受的方案中,雌激素加速了血清素周转率,孕酮可阻止这种作用。因此,许多单胺可能参与了激素对发情行为的控制。此外,激素会影响胺的周转率和摄取机制。