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首页> 外文期刊>Hypertension in pregnancy: Official journal of the International Society for the Study of Hypertension in Pregnancy >Adrenomedullin requires an intact nitric oxide system to function as an endogenous vasodilator in rat gestation.
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Adrenomedullin requires an intact nitric oxide system to function as an endogenous vasodilator in rat gestation.

机译:肾上腺髓质素需要完整的一氧化氮系统才能在大鼠妊娠中起内源性血管扩张剂的作用。

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摘要

OBJECTIVE: We hypothesize that administration of adrenomedullin (AM), an endogenous vasodilator, will ameliorate the hypertension and growth restriction associated with chronic nitric oxide inhibition induced by l-omega nitro-l-arginine methyl ester (l-NAME) infusion in pregnant rats. METHODS: Osmotic minipumps were inserted on day 14 of gestation to deliver continuously either AM, l-NAME, AM+l-NAME, or vehicle control. Systolic blood pressure was recorded daily in pregnant rats. Pregnant rats were either sacrificed on gestational days 15, 16, 17, 18, or 22, or they were allowed to deliver at term. The placentas from all of the treated groups were fixed for 24 hr in Bouin solution, sectioned, processed, embedded in paraffin, and stained with hematoxylin and eosin. The placentas were graded for the quality of fetal vessel development in the labyrinth. RESULTS: Systolic blood pressure was increased in AM+l-NAME-treated rats. The animals that delivered in the AM+l-NAME group exhibited decreased pup weight(l-NAME and AM+l-NAME, 5.2+/-0.1 compared with 6.4+/-0.1 g for both AM and controls, p<0.001) and increased pup mortality (AM+l-NAME, 44.4% compared with 16.7% in l-NAME, 0% in AM and 3.1% in controls, p<0.001 AM+l-NAME compared with controls). Increased decidual necrosis, necrosis in the labyrinth, and deficient fetal vessel development in the labyrinth was identified in the placentas treated with AM+l-NAME. CONCLUSIONS: Addition of the endogenous vasodilator AM to an l-NAME-induced state of chronic NO inhibition did not ameliorate hypertension and growth restriction.
机译:目的:我们假设内源性血管扩张药肾上腺髓质素(AM)的使用将减轻妊娠大鼠输注l-ω-硝基-l-精氨酸甲酯(l-NAME)诱导的慢性一氧化氮抑制相关的高血压和生长受限。方法:在妊娠的第14天插入渗透性微型泵,以连续递送AM,I-NAME,AM + 1-I或媒介物对照。每天记录妊娠大鼠的收缩压。在妊娠第15、16、17、18或22天处死怀孕的大鼠,或者允许它们在足月分娩。将所有治疗组的胎盘在Bouin溶液中固定24小时,切片,加工,包埋在石蜡中,并用苏木精和曙红染色。胎盘根据迷宫中胎儿血管发育的质量进行分级。结果:AM + 1-NAME处理的大鼠的收缩压升高。在AM + 1-NAME组中分娩的动物表现出降低的幼犬体重(1-NAME和AM + 1-NAME,为5.2 +/- 0.1,而AM和对照组均为6.4 +/- 0.1 g,p <0.001)并增加幼仔死亡率(AM + 1-NAME,44.4%,而I-NAME为16.7%,AM为0%,对照组为3.1%,与对照组相比,p <0.001 AM + 1-NAME)。在用AM + 1-NAME处理过的胎盘中,发现蜕膜坏死增加,迷路坏死和迷路胎儿血管发育不足。结论:将内源性血管舒张剂AM加到l-NAME诱导的慢性NO抑制状态不能改善高血压和生长受限。

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