Hybbinette J C, Mercke U
Acta Otolaryngol. 1982 May-Jun;93(5-6):465-73. doi: 10.3109/00016488209130906.
The effect on the mucociliary (m.c.) activity of the parasympathomimetic drug methacholine and its antagonist atropine was studied with the aid of a newly developed animal test model, designed for evaluating the effect of pharmacological substances on the m.c. wave frequency. Methacholine i.a. (0.01-2 micrograms/kg) was found to give a dose-dependent acceleration of the m.c. wave frequency, and the threshold dose 0.03 +/- 0.02 (+/- S.D.) micrograms/kg is suggested to be within physiological limits. The anticholinergic drug atropine i.a. (0.05-0.5 mg/kg) did not influence the basal m.c. wave frequency, but a dose of 0.2 mg/kg reduced or abolished the responses to methacholine (0.05-2 micrograms/kg). These results indicate that the basal m.c. activity functions independently of parasympathetic activity in anesthetized animals, that parasympathomimetic drugs influence the m.c. activity and that the effects of these drugs can be reduced or blocked by atropine.
借助一种新开发的动物试验模型,研究了拟副交感神经药物乙酰甲胆碱及其拮抗剂阿托品对黏液纤毛(m.c.)活性的影响,该模型旨在评估药理物质对m.c.波频率的影响。腹腔注射乙酰甲胆碱(0.01 - 2微克/千克)可使m.c.波频率呈剂量依赖性加快,建议阈剂量0.03±0.02(±标准差)微克/千克在生理范围内。腹腔注射抗胆碱能药物阿托品(0.05 - 0.5毫克/千克)不影响基础m.c.波频率,但0.2毫克/千克的剂量可降低或消除对乙酰甲胆碱(0.05 - 2微克/千克)的反应。这些结果表明,在麻醉动物中,基础m.c.活性独立于副交感神经活动发挥作用,拟副交感神经药物影响m.c.活性,且这些药物的作用可被阿托品降低或阻断。