Berghem L, Bergman U, Schildt B, Sörbo B
Br J Anaesth. 1980 Jun;52(6):597-601. doi: 10.1093/bja/52.6.597.
The plasma concentrations of atropine following i.v. or i.m. administration to surgical patients were determined by radioimmunoassay. When atropine sulphate 1 mg was given i.v. there was a rapid initial removal of the drug from the circulation in the first 10 min; thereafter the plasma concentration decreased more slowly. Atropine i.m. was rapidly absorbed with peak concentrations occurring at 30 min following injection. The plasma atropine concentration then decreased slowly, probably because of uptake of atropine by muscarinic cholinergic receptors. The chronotropic effect of atropine appeared to correspond to the concentration in plasma following i.m. administration. We conclude that i.m. atropine, as a premedication, should be given not later than 30 min before induction of anaesthesia.
通过放射免疫分析法测定了手术患者静脉注射或肌肉注射阿托品后的血浆浓度。静脉注射1毫克硫酸阿托品时,药物在最初10分钟内迅速从循环中清除;此后血浆浓度下降得更慢。肌肉注射阿托品吸收迅速,注射后30分钟达到峰值浓度。然后血浆阿托品浓度缓慢下降,可能是因为毒蕈碱胆碱能受体摄取了阿托品。阿托品的变时作用似乎与肌肉注射后的血浆浓度相对应。我们得出结论,作为术前用药,肌肉注射阿托品应在麻醉诱导前不迟于30分钟给予。