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呼吸道病毒感染对内皮素-1诱导的小鼠气管胆碱能神经介导收缩增强作用的影响。

Influence of respiratory tract viral infection on endothelin-1-induced potentiation of cholinergic nerve-mediated contraction in mouse trachea.

作者信息

Carr M J, Goldie R G, Henry P J

机构信息

Department of Pharmacology, University of Western Australia, Nedlands.

出版信息

Br J Pharmacol. 1996 Nov;119(5):891-8. doi: 10.1111/j.1476-5381.1996.tb15756.x.

Abstract
  1. This study examined the influence of respiratory tract infection with influenza A/PR-8/34 virus on endothelin receptor-mediated modulation of contraction induced by stimulation of cholinergic nerves in mouse isolated trachea. 2. The ETB receptor-selective agonist, sarafotoxin S6c (30 nM) induced large transient contractions (118 +/- 5% Cmax, n = 13; where Cmax is the contraction induced by 10 microM carbachol) of isolated tracheal segments from control mice. The peak contractile response to 30 nM sarafotoxin S6c was significantly lower in preparations from virus-inoculated mice at day 2 (57 +/- 8% Cmax, n = 3, P < 0.05) and 4 post-inoculation (90 +/- 8% Cmax, n = 9, P < 0.05), consistent with virus-induced attentuation of the ETB receptor-effector system linked to airway smooth muscle contraction. The mean peak contraction to 30 nM sarafotoxin S6c of preparations from virus-inoculated mice at day 8 post-inoculation (94 +/- 17% Cmax, n = 4) was not significantly different from that of control. 3. Electrical field stimulation (EFS; 90 V, 0.5 ms duration, 10 s train, 0.1-30 Hz) of preparations from control and virus-inoculated mice, caused contractions that were abolished by 0.1 microM atropine or 3 microM tetrodotoxin, indicating that these responses were mediated by neuronally released acetylcholine. Sarafotoxin S6c markedly potentiated contractions induced by a standard stimulus (0.3 Hz, every 3 min) in tracheal segments from control and virus-inoculated mice. In tracheal tissue from control mice, 30 nM sarafotoxin S6c significantly increased a standard EFS-induced contraction of 24 +/- 4% Cmax by a further 24 +/- 3% Cmax (i.e. 2 fold increase, n = 11). Sarafotoxin S6c (30 nM) also markedly potentiated standard EFS-induced contractions in preparations from virus-inoculated mice at day 2 (17 +/- 2% Cmax, n = 3), day 4 (17 +/- 5% Cmax, n = 9) and day 8 (26 +/- 5% Cmax, n = 4) post-inoculation. The level of potentiation of EFS-induced contractions in preparations from virus-inoculated mice was similar to that in tissue from control mice at days, 2, 4 and 8 post-inoculation. In contrast, sarafotoxin S6c (30 nM) did not enhance contractile responses of tracheal segments from control and virus-inoculated mice to exogenously applied acetylcholine (n = 3). 4. Endothelin-1 (1 nM) caused similar potentiations of standard EFS-induced contractions in tracheal segments from control (13 +/- 2% Cmax, n = 23) and virus-inoculated mice at day 2 (13 +/- 1% Cmax, n = 5), day 4 (16 +/- 5% Cmax, n = 6), and day 8 (13 +/- 3% Cmax, n = 8) post-inoculation. In contrast, 1 nM endothelin-1 did not enhance contractile responses of tracheal segments from control and virus-inoculated mice to exogenously applied acetylcholine (n = 4). Neither the ETA receptor-selective antagonist, BQ-123 (3 microM) nor the ETB receptor-selective antagonist, BQ-788 (1 microM) alone had any significant inhibitory effect on endothelin-1-induced potentiations of tracheal segments from control or virus-inoculated mice at days 2, 4 and 8 post-inoculation. However, simultaneous pre-incubation with BQ-123 (3 microM) and BQ-788 (1 microM) prevented endothelin-1-evoked potentiations, indicative of a role for both ETA and ETB receptors in this system. 5. These data clearly demonstrate that respiratory tract viral infection attenuated the function of the postjunctional ETB receptor-effector system linked directly to airway smooth muscle contraction. However, the function of prejunctional ETA and ETB receptor-effector systems linked to augmentation of cholinergic nerve-mediated airway smooth muscle contraction remained unaffected during respiratory tract viral infection in mice.
摘要
  1. 本研究检测了甲型流感病毒A/PR - 8/34感染呼吸道对小鼠离体气管中内皮素受体介导的胆碱能神经刺激所致收缩调节的影响。2. ETB受体选择性激动剂沙拉新(30 nM)可引起对照小鼠离体气管节段产生大幅度的瞬时收缩(118±5% Cmax,n = 13;其中Cmax是由10 μM卡巴胆碱诱导的收缩)。在接种病毒后第2天(57±8% Cmax,n = 3,P < 0.05)和第4天(90±8% Cmax,n = 9,P < 0.05),病毒接种小鼠标本对30 nM沙拉新的收缩峰值反应显著降低,这与病毒诱导的与气道平滑肌收缩相关的ETB受体 - 效应器系统减弱一致。接种病毒后第8天,病毒接种小鼠标本对30 nM沙拉新的平均收缩峰值(94±17% Cmax,n = 4)与对照无显著差异。3. 对对照小鼠和病毒接种小鼠的标本进行电场刺激(EFS;90 V,0.5 ms持续时间,10 s串刺激,0.1 - 30 Hz),引起的收缩可被0.1 μM阿托品或3 μM河豚毒素消除,表明这些反应是由神经释放的乙酰胆碱介导的。沙拉新显著增强了对照小鼠和病毒接种小鼠气管节段由标准刺激(0.3 Hz,每3分钟一次)诱导的收缩。在对照小鼠的气管组织中,30 nM沙拉新使标准EFS诱导的24±4% Cmax收缩进一步显著增加24±3% Cmax(即增加2倍,n = 11)。沙拉新(30 nM)在接种病毒后第2天(17±2% Cmax,n = 3)、第4天(17±5% Cmax,n = 9)和第8天(26±5% Cmax,n = 4)也显著增强了病毒接种小鼠标本中标准EFS诱导的收缩。接种病毒后第2天至第8天,病毒接种小鼠标本中EFS诱导收缩的增强水平与对照小鼠组织相似。相比之下,30 nM沙拉新并未增强对照小鼠和病毒接种小鼠气管节段对外源性乙酰胆碱的收缩反应(n = 3)。4. 内皮素 - 1(1 nM)在对照小鼠(13±2% Cmax,n = 23)以及接种病毒后第2天(13±1% Cmax,n = 5)、第4天(16±5% Cmax,n = 6)和第8天(!3±3% Cmax,n = 8)的病毒接种小鼠的气管节段中,对标准EFS诱导的收缩产生相似的增强作用。相比之下,1 nM内皮素 - 1并未增强对照小鼠和病毒接种小鼠气管节段对外源性乙酰胆碱的收缩反应(n = 4)。ETA受体选择性拮抗剂BQ - 123(3 μM)和ETB受体选择性拮抗剂BQ - 788(1 μM)单独对接种病毒后第2天、第4天和第8天的对照或病毒接种小鼠气管节段中内皮素 - 1诱导的增强作用均无显著抑制作用。然而,同时用BQ - 123(3 μM)和BQ - 788(1 μM)预孵育可阻止内皮素 - 1诱发的增强作用,表明ETA和ETB受体在该系统中均起作用。5. 这些数据清楚地表明,呼吸道病毒感染减弱了直接与气道平滑肌收缩相关的节后ETB受体 - 效应器系统的功能。然而,在小鼠呼吸道病毒感染期间,与胆碱能神经介导的气道平滑肌收缩增强相关的节前ETA和ETB受体 - 效应器系统的功能未受影响。

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