Yanaura S, Kitagawa H, Hosokawa T, Misawa M
Nihon Yakurigaku Zasshi. 1982 Jul;80(1):43-50.
Antitussive and respiratory effects of three newly synthesized methanobenzazonine derivatives and their d- and l-isomers were investigated to understand the relationship between the cough and respiratory centers. Antitussive effects were evaluated with the PEC (puncture electrode-induced cough) method in conscious d-, dl-, and l-ST-2123; d-, dl-, and l-ST-2121 into the right carotid artery at a dose range of 0.2-0.8 mg caused no effect on respiration. dl-ST-2121 at 0.4 to 0.8 mg and l-ST-2121 at 0.2 to 0.8 mg depressed respiration dose-dependently. Codeine (0.2-0.8 mg) depressed respiration slightly. Morphine (0.2-0.8 mg) depressed respiration more strongly. All the methanobenzazonine derivatives used, when given intraperitoneally, showed antitussive potencies that were 1/3-1/2 the potency of codeine. The antitussive potencies of the d-, dl-, and l-isomers of the three derivatives used were discussed on the bases of chemical structures and drug receptors. These results provide evidence of a discrepancy between the cough and respiratory centers in the brain stem.
研究了三种新合成的甲苄azonine衍生物及其d-和l-异构体的镇咳和呼吸作用,以了解咳嗽中枢与呼吸中枢之间的关系。采用PEC(穿刺电极诱发咳嗽)法在清醒的d-、dl-和l-ST-2123中评估镇咳作用;将d-、dl-和l-ST-2121以0.2-0.8mg的剂量范围注入右颈动脉对呼吸无影响。0.4至0.8mg的dl-ST-2121和0.2至0.8mg的l-ST-2121呈剂量依赖性抑制呼吸。可待因(0.2-0.8mg)轻微抑制呼吸。吗啡(0.2-0.8mg)更强烈地抑制呼吸。所有腹腔注射的甲苄azonine衍生物的镇咳效力均为可待因的1/3-1/2。根据化学结构和药物受体讨论了所使用的三种衍生物的d-、dl-和l-异构体的镇咳效力。这些结果为脑干中咳嗽中枢与呼吸中枢之间的差异提供了证据。