催产素舒张血管的作用及其机制

Effect of oxytocin on vascular dilation and its mechanism

  • 摘要: 目的 观察催产素(OT)的血管舒张作用并探讨其可能机制。方法 采用大鼠离体血管功能实验装置,描记张力变化,血管按随机数表分组,每组6枚血管环,分别保留或去除内皮,各阻断剂预处理30min之后做OT舒张曲线。结果 OT不能舒张苯肾上腺素(PE)预收缩的内皮完整非孕大鼠血管环。而OT(0.1U-3.2U)浓度依赖性地舒张苯肾上腺素(PE)预收缩的内皮完整或去除内皮的大鼠胸主动脉环。一氧化氮合成酶抑制剂亚硝基左旋精氨酸甲酯(L-NAME)可抑制PE诱导的血管舒张作用(P<0.01);环氧合酶抑制剂吲哚美辛(Indo)对PE诱导的血管舒张作用无影响。钾通道阻断剂四乙胺(TEA)3mmol/L预处理可减弱OT对内皮完好血管的舒张效应。OT对PE诱导的血管舒张作用与Ca2+浓度无关。结论 OT具有舒张孕鼠血管作用,其机制与NO-cGMP途径和血管平滑肌钾通道有关。

     

    Abstract: Objective To study the effect of oxytocin(OT) on vascular dilation and its mechanism. Methods Changes in vascular ring tension were observed with an in vitro vascular function experimental device.Blood vessels were taken from 6 rats of each group with their endothelium removed or preserved.OT dilating curves were plotted after the blood vessels were pretreated for 30min. Results OT could not dilate the vascular rings in endothelium of pregnant rats pretreated with phenylephrine(PE).The OT(0.1U-3.2U) dilated the thoracic aorta ring of rats with their endothelium preserved or removed in a PE concentration-dependent manner.Nitro-L-arginine methyl ester(L-NAME),a nitric oxide synthase inhibitor,showed an inhibitory effect on vascular dilation induced by PE(P<0.01).Indomethacin(Indo),a cyclooxygenase inhibitor,had no effect on vascular dilation induced by PE.Pretreatment with 3mmol/L of non-selective K+ channel blocker(TEA) could decrease the effect of OT on vascular dilation.The effect of OT on vascular dilation induced by PE was not related with the Ca2+ concentration. Conclusion OT can dilate the blood vessels in rats.Its mechanism is related with NO-cGMP and potassium channels in smooth muscle of blood vessels.

     

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