Bytautiene Egle, Vedernikov Yuri P, Saade George R, Romero Roberto, Garfield Robert E
Department of Obstetrics & Gynecology, Division of Reproductive Sciences, The University of Texas Medical Branch, Galveston 77555-1062, USA.
Am J Obstet Gynecol. 2002 Mar;186(3):438-45. doi: 10.1067/mob.2002.120488.
The purpose of this study was to investigate the effect of endogenous mast cell degranulation on the contractility of isolated cervical strips from nonpregnant and pregnant guinea pigs.
Longitudinal cervical strips from nonpregnant and pregnant (mid and term) guinea pigs were used for isometric tension recording. Responses to the mast cell degranulating agent, compound 48/80, were compared in the absence or presence of different inhibitors and receptor antagonists. Concentration-response curves were obtained to histamine and 5-hydroxytryptamine in strips that were incubated with antagonists or solvent.
Compound 48/80 and histamine significantly increased contractility of cervical strips in all 3 groups of animals. The inhibitor of mast cell degranulation significantly reduced responses to compound 48/80 and histamine-1 receptor antagonist reduced responses to histamine in all 3 groups. Histamine-1 receptor antagonist significantly inhibited responses to compound 48/80 in nonpregnant and mid pregnant guinea pigs. Histamine-2 receptor antagonist did not alter responses to compound 48/80 nor to histamine. The receptor antagonist 5-hydroxytryptamine-2 significantly inhibited cervical contractility that was induced by compound 48/80 in tissues from mid pregnant and term pregnant guinea pigs. Lipoxygenase inhibitor was effective in mid pregnant guinea pigs. Cyclooxygenase inhibitor, 5-hydroxytryptamine, and a combination of lipoxygenase and cyclooxygenase inhibitors had no effect on cervical contractility.
The degranulation of mast cells releases histamine and other mediators that stimulate cervical contractility through histamine-1 receptors. Cervical infiltration and modulation of contractility by mast cells may play an important physiologic and/or pathologic role in the control of cervical function during pregnancy.
本研究旨在探讨内源性肥大细胞脱颗粒对未孕和孕豚鼠离体子宫颈条收缩性的影响。
使用未孕和孕(中期和晚期)豚鼠的纵向子宫颈条进行等长张力记录。在不存在或存在不同抑制剂和受体拮抗剂的情况下,比较对肥大细胞脱颗粒剂化合物48/80的反应。在与拮抗剂或溶剂孵育的条带中获得组胺和5-羟色胺的浓度-反应曲线。
化合物48/80和组胺显著增加了所有3组动物子宫颈条的收缩性。肥大细胞脱颗粒抑制剂显著降低了对化合物48/80的反应,组胺-1受体拮抗剂降低了所有3组对组胺的反应。组胺-1受体拮抗剂显著抑制未孕和孕中期豚鼠对化合物48/80的反应。组胺-2受体拮抗剂未改变对化合物48/80或组胺的反应。5-羟色胺-2受体拮抗剂显著抑制孕中期和孕晚期豚鼠组织中化合物48/80诱导的子宫颈收缩。脂氧合酶抑制剂在孕中期豚鼠中有效。环氧化酶抑制剂、5-羟色胺以及脂氧合酶和环氧化酶抑制剂的组合对子宫颈收缩性无影响。
肥大细胞脱颗粒释放组胺和其他介质,这些介质通过组胺-1受体刺激子宫颈收缩。肥大细胞对子宫颈的浸润和收缩性调节可能在妊娠期间子宫颈功能的控制中发挥重要的生理和/或病理作用。