Nagase T, Aoki T, Matsui H, Ohga E, Katayama H, Teramoto S, Matsuse T, Fukuchi Y, Ouchi Y
Department of Geriatrics, Faculty of Medicine, University of Tokyo, Japan.
Can J Physiol Pharmacol. 1997 Dec;75(12):1369-74.
Endothelin (ET) 1, a 21 amino acid constrictor peptide, is one of the most potent agonists of airway smooth muscle and acts on two different receptors, i.e., ETA and ETB receptors. Recently, it has been shown that there are species and organ differences in physiological roles of each ET receptor. In rats, however, the physiological roles of ET receptors remain to be clarified. We questioned whether ET-1 might affect airway and lung tissue via different ET receptor subtypes in rats. To answer this question, we investigated the effects of ET-1 on lung behaviour in anesthetized, open-chested, mechanically ventilated (f = 1 Hz, VT = 9 mL/kg, PEEP = 3 cmH2O (1 cmH2O = 98.1 Pa)) rats in the absence or the presence of ETA and ETB selective antagonists, i.e., BQ-123 and BQ-788, respectively. Using alveolar capsules, we calculated lung elastance (EL), resistance of lung (RL), tissue (Rti), and airway (Raw), and hysteresivity (eta = 2 pifRti/EL) under control conditions and after intravenous administration of ET-1 (10(-8) mol/kg). ET-1 induced significant increases in RL, Rti, Raw, EL, and eta. BQ-123 did not affect ET-1 induced constriction, while BQ-788 significantly reduced delta RL, delta Rti, delta Raw, delta EL during ET-1 induced constriction. The effects of the combination of BQ-123 and BQ-788 were not different compared with BQ-788. Eta was not affected by BQ-123 and BQ-788. These data suggest that ETB, but not ETA, receptors may have significant physiological roles in rat lungs in response to ET-1.
内皮素(ET)-1是一种由21个氨基酸组成的缩血管肽,是气道平滑肌最有效的激动剂之一,作用于两种不同的受体,即ETA和ETB受体。最近的研究表明,每种ET受体的生理作用存在种属和器官差异。然而,在大鼠中,ET受体的生理作用仍有待阐明。我们质疑ET-1是否可能通过大鼠不同的ET受体亚型影响气道和肺组织。为了回答这个问题,我们研究了在麻醉、开胸、机械通气(频率f = 1 Hz,潮气量VT = 9 mL/kg,呼气末正压PEEP = 3 cmH2O(1 cmH2O = 98.1 Pa))的大鼠中,在不存在或存在ETA和ETB选择性拮抗剂(分别为BQ-123和BQ-788)的情况下,ET-1对肺功能的影响。使用肺泡囊,我们计算了对照条件下以及静脉注射ET-1(10(-8) mol/kg)后肺弹性(EL)、肺阻力(RL)、组织阻力(Rti)、气道阻力(Raw)和滞后性(η = 2πfRti/EL)。ET-1导致RL、Rti、Raw、EL和η显著增加。BQ-123不影响ET-1诱导的收缩,而BQ-788在ET-1诱导收缩期间显著降低ΔRL、ΔRti、ΔRaw、ΔEL。BQ-123和BQ-788联合使用的效果与BQ-788相比无差异。η不受BQ-123和BQ-788的影响。这些数据表明,ETB而非ETA受体可能在大鼠肺对ET-1的反应中具有重要的生理作用。