Donoso A O, Broitman S T
Psychopharmacology (Berl). 1979;66(3):251-5. doi: 10.1007/BF00428315.
Intraventricular administration of alpha-hydrazinohistidine, a histamine synthesis inhibitor, at different doses and times before testing produced a significant decrease of lordotic responses and sexual receptivity in ovariectomized estrogen plus progesterone-primed female rats. The H1-antihistamines pyrilamine and chlorfeniramine and the H2-antihistamine metiamide, injected in the lateral ventricle, significantly decreased the lordosis quotient but did not modify receptivity; antihistamine-injected rats showed no soliciting behavior. Exploratory activity was decreased by both alpha-hydrazinohistidine and metiamide but not by the H1-antihistamines. It is concluded that treatments which either deplete histamine or block their receptors can alter female copulatory responsiveness. The mechanism of this antihistamine effect appears to be unrelated to that of other side effects, such as motor impairment, sedation, or local anesthesia.
在测试前不同时间给予组胺合成抑制剂α-肼基组氨酸进行脑室内给药,可使切除卵巢并用雌激素加孕酮预处理的雌性大鼠的脊柱前凸反应和性接受能力显著降低。向侧脑室注射H1-抗组胺药吡苄明和氯苯那敏以及H2-抗组胺药甲硫米特,可显著降低脊柱前凸商数,但不改变接受能力;注射抗组胺药的大鼠未表现出求偶行为。α-肼基组氨酸和甲硫米特均可降低探索活动,但H1-抗组胺药则无此作用。结论是,耗尽组胺或阻断其受体的治疗均可改变雌性交配反应性。这种抗组胺作用的机制似乎与其他副作用,如运动障碍、镇静或局部麻醉的机制无关。