Ohbayashi H, Suito H, Takagi K
Second Department of Internal Medicine, Nagoya University School of Medicine, Japan.
Eur J Pharmacol. 1998 Apr 3;346(1):55-64. doi: 10.1016/s0014-2999(98)00014-4.
We compared the effects of natriuretic peptides on antigen-induced bronchoconstriction and airway microvascular leakage in sensitized guinea pigs. Anesthetized male guinea pigs, ventilated via a tracheal cannula, were placed in a plethysmograph to measure pulmonary mechanics for 10 min after challenge with 1 mg/kg of ovalbumin, and then Evans blue dye was extravasated into airway tissue in order to indicate and evaluate microvascular leakage. Three separate intravenous pretreatments using atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), and C-type natriuretic peptide (CNP) significantly inhibited the ovalbumin-induced bronchoconstriction and microvascular leakage in a dose-dependent manner. These inhibitory effects were mimicked by 8-bromoguanosine 3',5'-cyclic monophosphate. We showed that the rank order of inhibitory potencies, which were mediated by cyclic guanosine 3',5'-monophosphate, was BNP > or = ANP > or = CNP. These results gave us some clues for the clinical application of the natriuretic peptides.
我们比较了利钠肽对致敏豚鼠抗原诱导的支气管收缩和气道微血管渗漏的影响。经气管插管通气的麻醉雄性豚鼠,在用1mg/kg卵清蛋白激发后,置于体积描记器中测量肺力学10分钟,然后将伊文思蓝染料渗入气道组织以指示和评估微血管渗漏。分别使用心房利钠肽(ANP)、脑利钠肽(BNP)和C型利钠肽(CNP)进行三次静脉预处理,以剂量依赖方式显著抑制了卵清蛋白诱导的支气管收缩和微血管渗漏。这些抑制作用可被8-溴鸟苷3',5'-环一磷酸模拟。我们发现,由环鸟苷3',5'-单磷酸介导的抑制效力顺序为BNP≥ANP≥CNP。这些结果为利钠肽的临床应用提供了一些线索。