Feldt-Rasmussen B F, Gefke K, Mosbech H, Hanel H K
Br J Anaesth. 1985 Feb;57(2):204-7. doi: 10.1093/bja/57.2.204.
Pyridostigmine 0.143 mg kg-1 (maximum 10 mg) and atropine 0.0143 mg kg-1 (maximum 1 mg) were administered i.v. to six healthy male volunteers. Peripheral venous blood samples were drawn for measurement of serum cholinesterase activity. Maximum inhibition of the enzyme was found 5 min after injection with a decrease to 27 +/- 5% (mean +/- SEM) of the original activity. Forced expiratory volume in the first 1s (FEV1) was measured at fixed time intervals for 90 min. No decrease in FEV1 was observed; on the contrary, there was a small increase. We conclude that atropine effectively antagonizes the muscarinic side-effects of pyridostigmine on bronchial smooth muscle tone and bronchial secretions, when administered in clinical doses to normal human subjects.
向6名健康男性志愿者静脉注射溴吡斯的明0.143毫克/千克(最大剂量10毫克)和阿托品0.0143毫克/千克(最大剂量1毫克)。采集外周静脉血样本以测量血清胆碱酯酶活性。注射后5分钟发现该酶受到最大抑制,活性降至原始活性的27±5%(平均值±标准误)。在90分钟内按固定时间间隔测量第1秒用力呼气量(FEV1)。未观察到FEV1下降;相反,有小幅增加。我们得出结论,当以临床剂量给予正常人类受试者时,阿托品可有效拮抗溴吡斯的明对支气管平滑肌张力和支气管分泌物的毒蕈碱样副作用。