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新生羔羊硝普钠诱导低血压期间的血浆血管加压素、肾素和儿茶酚胺

Plasma vasopressin, renin and catecholamines during nitroprusside-induced hypotension in the newborn lamb.

作者信息

Zubrow A B, Daniel S S, Stark R I, Husain M K, James L S

机构信息

Medical College of Pediatrics, Philadelphia, Pennsylvania.

出版信息

J Perinat Med. 1989;17(4):271-7. doi: 10.1515/jpme.1989.17.4.271.

DOI:10.1515/jpme.1989.17.4.271
PMID:2696775
Abstract

The circulating levels of vasopressin, catecholamines and renin activity before, during and following a 10-20% fall in mean arterial blood pressure induced by sodium nitroprusside were measured in six chronically catheterized lambs during the first week of life. No significant changes in pHa, PaO2, PaCO2, Plasma sodium or osmolality were observed during or following the infusion of sodium nitroprusside at an average of 12 g.kg-1.min-1 (table I). However, the fall in blood pressure at the end of 60 minutes infusion, was associated with significant increases in the plasma levels of vasopressin from a control value of 2.4 +/- 0.57 to a maximum of 35.1 +/- 16.3 pg/ml (p = .002), renin activity from 6.7 +/- 1.56 to 27.4 +/- 11.44 ng.ml-1.hr-1 (p = .003), and catecholamines from 189.3 +/- 42.15 to 543.3 +/- 100.52 pg.ml-1 (p = .0001). The increase in vasopressin is lower, while that of PRA was higher and catecholamines similar to those found in the ewe. Plasma renin activity (PRA) and catecholamine levels remained elevated for at least 30 minutes following the end of the infusion while the mean blood pressure rose significantly above control levels and remained elevated for twenty minutes. We speculate that the persistent elevated levels of vasoactive mediators are responsible for the prolonged rebound hypertension following the cessation of the nitroprusside infusion and is the result of an immaturity of either a feedback process or metabolism of the vasoactive mediators or a combination of both mechanisms. This rebound hypertension could have adverse effects particularly in the very immature neonate.

摘要

在出生后第一周,对6只长期插管的羔羊进行了测量,观察硝普钠使平均动脉血压下降10%-20%之前、期间及之后血管加压素、儿茶酚胺和肾素活性的循环水平。在以平均12μg·kg⁻¹·min⁻¹的速度输注硝普钠期间及之后,未观察到动脉血pH值、动脉血氧分压、动脉血二氧化碳分压、血浆钠或渗透压有显著变化(表I)。然而,输注60分钟结束时血压下降,同时血管加压素血浆水平从对照值2.4±0.57显著升高至最高35.1±16.3pg/ml(p = 0.002),肾素活性从6.7±1.56升高至27.4±11.44ng·ml⁻¹·hr⁻¹(p = 0.003),儿茶酚胺从189.3±42.15升高至543.3±100.52pg/ml(p = 0.0001)。血管加压素的升高幅度较小,而血浆肾素活性(PRA)的升高幅度较大,儿茶酚胺的升高情况与母羊相似。输注结束后至少30分钟,血浆肾素活性(PRA)和儿茶酚胺水平仍保持升高,而平均血压显著高于对照水平并持续升高20分钟。我们推测,血管活性介质水平持续升高是硝普钠输注停止后出现长时间反弹性高血压的原因,这是反馈过程或血管活性介质代谢不成熟或两者机制共同作用的结果。这种反弹性高血压可能会产生不良影响,尤其是对极不成熟的新生儿。

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