Bytautiene Egle, Vedernikov Yuri P, Saade George R, Romero Roberto, Garfield Robert E
Division of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, Tex 77555, USA.
Am J Obstet Gynecol. 2003 Mar;188(3):774-8. doi: 10.1067/mob.2003.162.
To enhance our understanding of the uterotonic effect of histamine, we compared the effects of histamine on spontaneous phasic and tonic contractile activity of uterine strips from term pregnant nonlaboring women.
Longitudinal uterine strips were used from the lower uterine segment of term pregnant nonlaboring women undergoing elective cesarean section. The concentration-response relationship to histamine (10(-8) to 10(-4) mol/L) was determined in spontaneously contracting strips or in strips contracted tonically with a protein kinase C activator (-)-indolactam V in the presence of H(1) receptor antagonist (S[+]-chlorpheniramine maleate), H(2) receptor antagonist (cimetidine), or solvent.
Histamine increased spontaneous phasic myometrial contractions in a concentration-dependent manner. H(1), but not H(2), receptor antagonist significantly attenuated the response to histamine. Histamine significantly reduced tonic contractions of uterine strips induced by indolactam V. H(1) histamine receptor antagonist abolished relaxation, whereas H(2) histamine receptor antagonist had no effect.
Histamine increases spontaneous, but inhibits tonic, contractions of uterine strips from term pregnant nonlaboring women. Both effects are mediated through activation of H(1) receptors.
为了增强我们对组胺子宫收缩作用的理解,我们比较了组胺对足月妊娠未临产妇女子宫肌条自发的节律性和强直性收缩活动的影响。
使用接受择期剖宫产的足月妊娠未临产妇女子宫下段的纵行子宫肌条。在自发收缩的肌条中,或在存在H(1)受体拮抗剂(S[+]-马来酸氯苯那敏)、H(2)受体拮抗剂(西咪替丁)或溶剂的情况下,用蛋白激酶C激活剂(-)-吲哚内酰胺V使肌条强直性收缩,测定对组胺(10(-8)至10(-4)mol/L)的浓度-反应关系。
组胺以浓度依赖性方式增加子宫肌层自发的节律性收缩。H(1)受体拮抗剂而非H(2)受体拮抗剂显著减弱对组胺的反应。组胺显著降低吲哚内酰胺V诱导的子宫肌条强直性收缩。H(1)组胺受体拮抗剂消除松弛作用,而H(2)组胺受体拮抗剂无作用。
组胺增加足月妊娠未临产妇女子宫肌条的自发收缩,但抑制强直性收缩。两种作用均通过H(1)受体的激活介导。