Oriowo M A, Bevan J A
J Cardiovasc Pharmacol. 1987 Jul;10(1):76-81. doi: 10.1097/00005344-198707000-00011.
Histamine H1 and H2 receptors in the rabbit isolated ovarian artery and vein were studied. Histamine (10(-6)-3 X 10(-4) M) and 2-thiazolylethylamine (2ThEA) (10(-5)-3 X 10(-4)) concentration dependently caused contraction of both vessels. The -log EC50 for the artery was 5.20 +/- 0.13 and 4.48 +/- 0.01, and for the vein it was, 5.50 +/- 0.10 and 5.10 +/- 0.27, respectively. Metiamide (10(-5) M) significantly potentiated histamine-induced but not 2ThEA-induced contractions. The pA2 for antagonism by mepyramine against histamine and 2ThEA was 8.80 +/- 0.20 (slope = 0.73) and 9.02 +/- 0.11 (slope = 0.74) in the artery and 9.50 +/- 0.30 (slope = 1.0 +/- 0.2) and 9.00 +/- 0.20 (slope = 1.0 +/- 0.1) in the vein. Histamine and impromidine concentration dependently relaxed the contracted ovarian artery and vein. Impromidine was 300-fold and sixfold more potent than histamine in the artery and vein, respectively. The relaxant potency of histamine was the same in both vessels. The relaxations were antagonized by metiamide (10(-5) M). The KB against histamine and impromidine was similar in both vessels. These results indicate that functional histamine H1 and H2 receptors exist in the ovarian artery and vein. The possible relevance of this to the proposed role of histamine in ovulation is discussed.
对兔离体卵巢动脉和静脉中的组胺H1和H2受体进行了研究。组胺(10⁻⁶ - 3×10⁻⁴ M)和2-噻唑基乙胺(2ThEA)(10⁻⁵ - 3×10⁻⁴)浓度依赖性地引起两种血管收缩。动脉的-log EC50分别为5.20±0.13和4.48±0.01,静脉的-log EC50分别为5.50±0.10和5.10±0.27。甲硫咪特(10⁻⁵ M)显著增强组胺诱导的收缩,但不增强2ThEA诱导的收缩。在动脉中,美吡拉敏对组胺和2ThEA拮抗作用的pA2分别为8.80±0.20(斜率 = 0.73)和9.02±0.11(斜率 = 0.74),在静脉中分别为9.50±0.30(斜率 = 1.0±0.2)和9.00±0.20(斜率 = 1.0±0.1)。组胺和英普咪定浓度依赖性地使收缩的卵巢动脉和静脉舒张。英普咪定在动脉和静脉中的效力分别比组胺强300倍和6倍。组胺在两种血管中的舒张效力相同。这些舒张作用被甲硫咪特(10⁻⁵ M)拮抗。两种血管中对组胺和英普咪定的KB相似。这些结果表明,卵巢动脉和静脉中存在功能性组胺H1和H2受体。讨论了这与组胺在排卵中所提出作用的可能相关性。