Kasé Y, Matsumoto Y, Takahama K, Miyata T, Hitoshi T, Hirotsu I, Okano Y
Arzneimittelforschung. 1983;33(7):947-52.
The sites of antitussive action of dl-1,2,9,10-tetramethoxy-6a,alpha-aporphine phosphate (dl-glaucine phosphate, DL-832) were studied. It was assumed from the following results that DL-832 acts on the cough center per se. a) When DL-832 was given by the routes leading to the brain stem such as the vertebral artery and the cerebello-medullary cistern, far smaller doses were sufficient to obtain the same effect as that by i.v. administration. b) DL-832 showed neither effect on the afferent pathway for cough reflex nor influence on pulmonary stretch receptors. c) It exhibited practically no influence on the efferent pathways for cough reflex, that is, that for innervating respiratory muscle movement as well as that for controlling bronchial muscle tone. d) Decerebration exerted no influence on the antitussive effect. e) DL-832 definitely depressed the potentials of both the recurrent and internal intercostal nerves evoked by the superior laryngeal nerve stimulation. f) In deafferentated and decerebrate cats, DL-832 rather increased the spontaneous discharges of the phrenic nerve, whereas codeine decreased them.
研究了dl-1,2,9,10-四甲氧基-6a,α-阿朴啡磷酸盐(dl-青藤碱磷酸盐,DL-832)的镇咳作用部位。从以下结果推测DL-832本身作用于咳嗽中枢。a)当通过椎动脉和小脑延髓池等通向脑干的途径给予DL-832时,所需剂量远小于静脉注射给药以获得相同效果时的剂量。b)DL-832对咳嗽反射的传入途径无作用,对肺牵张感受器也无影响。c)它对咳嗽反射的传出途径实际上无影响,即对支配呼吸肌运动的传出途径以及控制支气管肌张力的传出途径均无影响。d)去大脑对镇咳作用无影响。e)DL-832能明确抑制由喉上神经刺激诱发的肋间神经和肋间内神经的电位。f)在去传入神经和去大脑的猫中,DL-832反而增加膈神经的自发放电,而可待因则使其减少。