Goldstein B D
Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta 30912-2300.
Toxicol Lett. 1991 Jul;57(2):139-46. doi: 10.1016/0378-4274(91)90140-2.
The acute effects of the organophosphorus acetylcholinesterase inhibitor, soman, was studied on spinal cord reflexes in the spinal cord transected cat. It was found that doses of 10 micrograms/kg significantly altered the monosynaptic and dorsal root reflexes by causing an initial depression lasting about 20 min followed by a later facilitation lasting over 3 h. A higher dose of soman (20 micrograms/kg) caused the initial depression but did not produce the later facilitation. Cholinergic antagonists were used to determine whether these changes were related to inhibition of acetylcholinesterase or whether they were non-specific. It was found that mecamylamine blocked the depression and the facilitation while atropine depressed the spinal cord potentials. These data show that acute administration of 10 micrograms/kg soman produces specific effects on spinal cord reflexes which could be characterized as resulting from inhibition of acetylcholinesterase similar to the carbamate inhibitor, physostigmine.
研究了有机磷乙酰胆碱酯酶抑制剂梭曼对脊髓横断猫脊髓反射的急性作用。结果发现,10微克/千克的剂量会显著改变单突触反射和背根反射,先是出现持续约20分钟的初始抑制,随后是持续超过3小时的后期易化。更高剂量的梭曼(20微克/千克)会引起初始抑制,但不会产生后期易化。使用胆碱能拮抗剂来确定这些变化是与乙酰胆碱酯酶的抑制有关,还是非特异性的。结果发现,美加明可阻断抑制和易化,而阿托品会降低脊髓电位。这些数据表明,急性给予10微克/千克的梭曼会对脊髓反射产生特定作用,其特征可能是由于乙酰胆碱酯酶受到抑制,类似于氨基甲酸酯抑制剂毒扁豆碱的作用。