Balaraman V, Kullama L K, Easa D, Robillard J E, Hashiro G M, Nakamura K T
Department of Pediatrics, Kapiolani Medical Center for Women and Children, Honolulu, Hawaii 96826.
Pediatr Res. 1990 Apr;27(4 Pt 1):392-5. doi: 10.1203/00006450-199004000-00013.
Sodium nitroprusside (SNP), a nonreceptor mediated stimulant of soluble guanylate cyclase, and atrial natriuretic factor, a receptor-dependent stimulator of particulate guanylate cyclase, mediate relaxation responses by increasing intracellular cGMP. This in vitro study was designed to compare the ontogeny of relaxation responses to SNP and atrial natriuretic factor in the guinea pig thoracic aorta. Aortic rings from fetuses at 55-60 d gestation (term = 68 d), 1- to 3-d-old newborn, and 12-wk-old adult Hartley guinea pigs were mounted in an organ bath, bathed in Kreb's solution, and connected to a force-displacement transducer to measure isometric tension. Relaxation responses to SNP and atriopeptin III were studied with the vessels at optimal resting tension and after preconstriction with an EC85 concentration of norepinephrine. SNP-mediated relaxation showed a significant increase in sensitivity with development among the three age groups (p less than 0.05). Methylene blue, an inhibitor of soluble guanylate cyclase, produced no inhibition of relaxation to SNP in fetal aortae, significantly decreased responses along the straight portion of the concentration-response curve in newborn aortae (p less than 0.05), and significantly shifted the concentration-response curve to the right (p less than 0.05) in adult aortae; but did not prevent vessels from relaxing almost 100% in any age group. However, atriopeptin III-mediated responses were similar in the three age groups and were unaffected by methylene blue. These results suggest that 1) sensitivity to SNP increases with age from fetal through adult life; 2) relaxation mediated by atriopeptin III is similar during development; 3) methylene blue does not affect SNP mediated relaxation in fetuses but progressively decreases sensitivity to SNP in newborns and adults; and 4) methylene blue does not affect atriopeptin III-mediated relaxation in any age group.
硝普钠(SNP)是一种非受体介导的可溶性鸟苷酸环化酶刺激剂,心房利钠因子是一种受体依赖性颗粒鸟苷酸环化酶刺激剂,二者均通过增加细胞内环磷酸鸟苷(cGMP)来介导舒张反应。本体外研究旨在比较豚鼠胸主动脉对SNP和心房利钠因子舒张反应的个体发生情况。取自妊娠55 - 60天(足月为68天)的胎儿、出生1 - 3天的新生儿以及12周龄成年Hartley豚鼠的主动脉环,安装在器官浴槽中,置于克雷布斯溶液中,并连接到力 - 位移换能器以测量等长张力。在血管处于最佳静息张力时以及用85%效能浓度的去甲肾上腺素预收缩后,研究对SNP和心房肽III的舒张反应。在三个年龄组中,SNP介导的舒张反应敏感性随发育显著增加(p < 0.05)。可溶性鸟苷酸环化酶抑制剂亚甲蓝对胎儿主动脉对SNP的舒张反应无抑制作用,使新生儿主动脉浓度 - 反应曲线直线部分的反应显著降低(p < 0.05),并使成年主动脉浓度 - 反应曲线显著右移(p < 0.05);但在任何年龄组中均未阻止血管几乎完全舒张。然而,心房肽III介导的反应在三个年龄组中相似,且不受亚甲蓝影响。这些结果表明:1)从胎儿到成年,对SNP的敏感性随年龄增加;2)心房肽III介导的舒张在发育过程中相似;3)亚甲蓝不影响胎儿中SNP介导的舒张,但逐渐降低新生儿和成年人对SNP的敏感性;4)亚甲蓝在任何年龄组中均不影响心房肽III介导的舒张。