Dipartimento di Scienze Fisiologiche, Viale G. B. Morgagni 63, 50134 Florence, Italy.
J Appl Physiol (1985). 2010 Oct;109(4):1002-10. doi: 10.1152/japplphysiol.00406.2010. Epub 2010 Jul 22.
We have previously shown that the caudal nucleus tractus solitarii is a site of action of some antitussive drugs and that the caudal ventral respiratory group (cVRG) region has a crucial role in determining both the expiratory and inspiratory components of the cough motor pattern. These findings led us to suggest that the cVRG region, and possibly other neural substrates involved in cough regulation, may be sites of action of antitussive drugs. To address this issue, we investigated changes in baseline respiratory activity and cough responses to tracheobronchial mechanical stimulation following microinjections (30-50 nl) of some antitussive drugs into the cVRG of pentobarbital-anesthetized, spontaneously breathing rabbits. [D-Ala(2),N-Me-Phe(4),Gly(5)-ol]-enkephalin (DAMGO) and baclofen at the lower concentrations (0.5 mM and 0.1 mM, respectively) decreased cough number, peak abdominal activity, and peak tracheal pressure and increased cough-related total cycle duration (Tt). At the higher concentrations (5 mM and 1 mM, respectively), both drugs abolished the cough reflex. DAMGO and baclofen also affected baseline respiratory activity. Both drugs reduced peak abdominal activity, while only DAMGO increased Tt, owing to increases in expiratory time. The neurokinin-1 (NK(1)) receptor antagonist CP-99,994 (10 mM) decreased cough number, peak abdominal activity, and peak tracheal pressure, without affecting baseline respiration. The NK(2) receptor antagonist MEN 10376 (5 mM) had no effect. The results indicate that the cVRG is a site of action of some antitussive agents and support the hypothesis that several neural substrates involved in cough regulation may share this characteristic.
我们之前已经证明,孤束核尾端是一些镇咳药的作用部位,而尾端腹侧呼吸群(cVRG)区域在确定咳嗽运动模式的呼气和吸气成分方面起着至关重要的作用。这些发现使我们认为,cVRG 区域,以及可能涉及咳嗽调节的其他神经基质,可能是镇咳药的作用部位。为了解决这个问题,我们研究了戊巴比妥麻醉、自主呼吸的兔子经尾端腹侧呼吸群内微量注射(30-50nl)一些镇咳药后,基础呼吸活动和对气管支气管机械刺激的咳嗽反应的变化。[D-Ala(2),N-Me-Phe(4),Gly(5)-ol]-脑啡肽(DAMGO)和巴氯芬在较低浓度(分别为 0.5mM 和 0.1mM)时,减少咳嗽次数、腹侧活动峰值和气管压力峰值,并增加咳嗽相关总周期时间(Tt)。在较高浓度(分别为 5mM 和 1mM)时,两种药物均消除了咳嗽反射。DAMGO 和巴氯芬还影响基础呼吸活动。两种药物均降低腹侧活动峰值,而只有 DAMGO 增加 Tt,这是由于呼气时间增加所致。神经激肽-1(NK(1))受体拮抗剂 CP-99,994(10mM)减少咳嗽次数、腹侧活动峰值和气管压力峰值,但不影响基础呼吸。NK(2)受体拮抗剂 MEN 10376(5mM)则没有影响。结果表明,尾端腹侧呼吸群是一些镇咳药的作用部位,并支持这样的假设,即几个参与咳嗽调节的神经基质可能具有这种特性。