Rastogi S K, Puri J N, Sinha J N, Bhargava K P
Psychopharmacology (Berl). 1979 Oct;65(2):215-7. doi: 10.1007/BF00433052.
Atropine sulphate (10 mg/kg IP) afforded 90% protection against clonic convulsions induced by standard doses of metrazol (80 mg/kg SC) in mice, whereas atropine methonitrate (10 mg/kg IP) did not offer any protection. Furthermore, physostigmine (1 mg/kg IP) caused recurrence of convulsions in atropinzed metrazol-treated mice and converted the subconvulsive dose of metrazol (40 mg/kg SC) into a 100% convulsive dose. However, neostigmine (1 mg/kg IP) did not antagonize the protection afforded by atropine sulphate against metrazol. The results of the study suggest an involvement of central cholinergic mechanisms in metrazol-induced convulsions.
硫酸阿托品(腹腔注射10毫克/千克)对标准剂量(皮下注射80毫克/千克)戊四氮诱导的小鼠阵挛性惊厥提供了90%的保护作用,而硝酸甲阿托品(腹腔注射10毫克/千克)则未提供任何保护。此外,毒扁豆碱(腹腔注射1毫克/千克)使经阿托品处理的戊四氮治疗小鼠惊厥复发,并将戊四氮的亚惊厥剂量(皮下注射40毫克/千克)转变为100%惊厥剂量。然而,新斯的明(腹腔注射1毫克/千克)并未拮抗硫酸阿托品对戊四氮的保护作用。该研究结果提示中枢胆碱能机制参与了戊四氮诱导的惊厥。