Okatani Y, Watanabe K, Wakatsuki A, Tamura S, Sagara Y
Department of Obstetrics and Gynecology, Kochi Medical School, Japan.
Acta Obstet Gynecol Scand. 1998 Oct;77(9):883-8.
While nitric oxide (NO) has been demonstrated to regulate vascular tone, superoxide (O2-) may also have an important role in regulating tension in the human fetoplacental vasculature. We therefore evaluate the effects of O2- and peroxynitrite (ONOO-) on vascular tension in isolated human umbilical arteries.
Helical sections of umbilical arteries were obtained from healthy pregnant women who were delivered between weeks 37 and 39 of gestation. Changes in maximal potassium chloride (KCl)-induced tension were measured in umbilical artery segments with intact endothelium.
We found that hypoxanthine plus xanthine oxidase significantly potentiated vascular tension, and that this effect was suppressed by pretreatment with L(NG)-monomethyl arginine (LNMA). Pretreatment with hypoxanthine plus xanthine oxidase, however, significantly inhibited the relaxation induced by the calcium ionophore A23187. 3-morpholinosydomine (SIN-1), which releases O2- and NO simultaneously produced a significant dose-dependent relaxation of vascular tension, which pretreatment with hemoglobin did not affect SIN-1-induced relaxation. Pretreatment with methylene blue significantly attenuated, while pretreatment with superoxide dismutase (SOD) significantly potentiated this effect.
These findings suggest that O2- potentiates vascular tension in human umbilical artery, in part, by suppressing NO synthesis in the endothelium. The vasorelaxation by exogenously generated ONOO suggests that this moiety has biological relevance in vasoregulation of the human umbilical artery.
虽然一氧化氮(NO)已被证明可调节血管张力,但超氧阴离子(O2-)在调节人胎盘血管张力方面可能也起着重要作用。因此,我们评估了O2-和过氧亚硝酸盐(ONOO-)对离体人脐动脉血管张力的影响。
从妊娠37至39周分娩的健康孕妇获取脐动脉螺旋切片。在具有完整内皮的脐动脉节段中测量最大氯化钾(KCl)诱导的张力变化。
我们发现次黄嘌呤加黄嘌呤氧化酶可显著增强血管张力,且该作用可被L(NG)-单甲基精氨酸(LNMA)预处理所抑制。然而,次黄嘌呤加黄嘌呤氧化酶预处理可显著抑制钙离子载体A23187诱导的舒张。3-吗啉代 sydomine(SIN-1)可同时释放O2-和NO,产生显著的剂量依赖性血管张力舒张,血红蛋白预处理并不影响SIN-1诱导的舒张。亚甲蓝预处理可显著减弱该作用,而过氧化物歧化酶(SOD)预处理则可显著增强此作用。
这些发现表明,O2-部分通过抑制内皮细胞中NO的合成来增强人脐动脉的血管张力。外源性生成的ONOO-引起的血管舒张表明该部分在人脐动脉血管调节中具有生物学相关性。