Lee C, Durant N N, Au E, Katz R L
Anesthesiology. 1981 Jan;54(1):61-5. doi: 10.1097/00000542-198101000-00012.
Dantrolene sodium, a muscle relaxant, does not have a clinically useful antagonist. The present study was undertaken to test the efficacies of germine monoacetate, 4-aminopyridine, neostigmine, and calcium chloride as possible agents for the reversal of the direct skeletal muscle depression produced by dantrolene sodium in the cat anesthetized with alpha-chloralose. Depression of the indirectly elicited twitch responses (0.1 Hz) of the tibialis anterior muscle by 25, 50, 75 and 84 per cent was produced by dantrolene, 0.16, 0.36, 0.88 and 1.13 mg/kg respectively; spontaneous recovery of twitch tension during the subsequent 30 min was negligible. After the 30-min observation period had elapsed, one of the reversal agents under study was given (iv) in divided doses at intervals of 10 min (five cats for each agent). Germine monoacetate (2 X 0.5 mg/kg) immediately reversed the dantrolene-induced twitch depression, with an over-shoot that persisted for an hour. 4-Aminopyridine (4 X 0.5 mg/kg) caused a steady but incomplete reversal to 17 per cent depression, 30 min after the last dose. Neostigmine (4 X 0.04 mg/kg) caused an immediate, but transient, reversal of the twitch depression, with overshoot. Calcium chloride (4 X 10 mg/kg) was without effect. It is concluded that germine monoacetate is the drug of choice for reversal of the muscle depression produced by dantrolene sodium in the cat.
丹曲林钠是一种肌肉松弛剂,没有临床上有用的拮抗剂。本研究旨在测试氧化孪胺、4-氨基吡啶、新斯的明和氯化钙作为可能的药物,用于逆转在α-氯醛糖麻醉的猫中由丹曲林钠引起的直接骨骼肌抑制。丹曲林分别以0.16、0.36、0.88和1.13mg/kg的剂量使胫前肌间接诱发的抽搐反应(0.1Hz)抑制25%、50%、75%和84%;在随后的30分钟内抽搐张力的自发恢复可忽略不计。在30分钟的观察期过后,以10分钟的间隔分剂量静脉注射(iv)一种正在研究的逆转剂(每种药物五只猫)。氧化孪胺(2×0.5mg/kg)立即逆转了丹曲林引起的抽搐抑制,并有持续一小时的超射现象。4-氨基吡啶(4×0.5mg/kg)在最后一剂后30分钟导致稳定但不完全的逆转,抑制率为17%。新斯的明(4×0.04mg/kg)引起抽搐抑制的立即但短暂的逆转,并伴有超射现象。氯化钙(4×10mg/kg)无效。得出的结论是,氧化孪胺是逆转猫中由丹曲林钠引起的肌肉抑制的首选药物。