Delaunois A, Gustin P, Ansay M
Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Université de Liège, Belgium.
Fundam Clin Pharmacol. 1995;9(5):450-7. doi: 10.1111/j.1472-8206.1995.tb00520.x.
The pharmacological mechanisms involved in the substance P (SP)-induced pulmonary oedema were studied in isolated perfused rabbit lungs. Substance P induced a dose-dependent increase in the capillary filtration coefficient (Kf,c), responsible for oedema. Atropine, hemicholinium-3 and ruthenium red pretreatment partly protected the lungs against SP effects, while tetrodotoxin and hexamethonium did not significantly modify them. (+/-)CP96,345, a NK1 receptor antagonist, completely inhibited the SP-induced increase in the Kf,c. Like SP, acetylcholine (ACh) and capsaicin also increased the Kf,c. Atropine and (+/-)CP96,345 completely blocked the oedema induced by both drugs. Tetrodotoxin and ruthenium red strongly inhibited the response to capsaicin and acetylcholine. It was concluded that SP-induced pulmonary oedema is in part mediated by a stimulating action on cholinergic efferent nerves, with subsequent release of endogenous acetylcholine. Acetylcholine can, in turn, stimulate the release of SP from excitatory non adrenergic, non cholinergic nerves. The effects induced by capsaicin and exogenous acetylcholine, thus endogenous SP, involve tetrodotoxin-sensitive mechanisms, while those produced by exogenous SP are tetrodotoxin-resistant.
在离体灌注兔肺中研究了P物质(SP)诱导肺水肿的药理机制。P物质使负责水肿的毛细血管滤过系数(Kf,c)呈剂量依赖性增加。阿托品、半胱氨酸-3和钌红预处理可部分保护肺免受SP的影响,而河豚毒素和六甲铵则无明显作用。NK1受体拮抗剂(±)CP96,345完全抑制了SP诱导的Kf,c增加。与SP一样,乙酰胆碱(ACh)和辣椒素也增加了Kf,c。阿托品和(±)CP96,345完全阻断了这两种药物诱导的水肿。河豚毒素和钌红强烈抑制对辣椒素和乙酰胆碱的反应。得出的结论是,SP诱导的肺水肿部分是由对胆碱能传出神经的刺激作用介导的,随后内源性乙酰胆碱释放。反过来,乙酰胆碱可刺激兴奋性非肾上腺素能、非胆碱能神经释放SP。辣椒素和外源性乙酰胆碱(即内源性SP)诱导的效应涉及河豚毒素敏感机制,而外源性SP产生的效应则对河豚毒素有抗性。