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[硫酸异帕米星(HAPA-B)与其他氨基糖苷类抗生素相比的神经肌肉阻滞活性]

[The neuromuscular blocking activity of isepamicin sulfate (HAPA-B) compared with other aminoglycoside antibiotics].

作者信息

Shinoda Y, Mochizuki D, Hokonohara T, Takayanagi N

出版信息

Jpn J Antibiot. 1987 Jan;40(1):136-44.

PMID:3586326
Abstract

Effects of isepamicin sulfate (HAPA-B), a new aminoglycoside antibiotic, on the neuromuscular transmission were studied in rats and compared with those of amikacin (AMK) or other aminoglycoside antibiotics. The HAPA-B, as well as other aminoglycoside antibiotics, depressed the twitch response of diaphragm to phrenic nerve stimulation in vitro. The depression effects of different drugs were compared and graded in the order of strengths of blocking action as: netilmicin (NTL) greater than gentamicin (GM) greater than streptomycin (SM) greater than kanamycin (KM) greater than AMK greater than HAPA-B. The IC50 (concentration which inhibited the response by 50%) of HAPA-B was 3.6 X 10(-3) g/ml. The neuromuscular blockade produced by HAPA-B was reversed by CaCl2, KCl or caffeine but not by neostigmine. D-Tubocurarine or MgCl2 augmented the neuromuscular effects of HAPA-B. Intramuscular (400 mg/kg) and intravenous (100 mg/kg) injections of HAPA-B did not affect the twitch response of gastrocnemius muscle to sciatic nerve stimulation in situ. Intravenous injection of 200 mg/kg caused death in some rats and depression of the twitch response in others. Intravenous AMK produced no significant effect on the twitch response at 50 mg/kg and caused death at 100 mg/kg. GM and SM caused death or significant degree of depression of the twitch response at intravenous doses of 50 mg/kg. In experiments of intravenous drug infusion for 60 minutes, the twitch response was depressed by HAPA-B at 400 mg/kg/hr and by AMK at 200 and 400 mg/kg/hr. In conclusion, HAPA-B has a neuromuscular blocking action presumably at the nerve terminal. However, its action was the weakest among the aminoglycoside antibiotics tested.

摘要

研究了新型氨基糖苷类抗生素硫酸异帕米星(HAPA - B)对大鼠神经肌肉传递的影响,并与阿米卡星(AMK)或其他氨基糖苷类抗生素进行比较。HAPA - B以及其他氨基糖苷类抗生素在体外均能抑制膈神经刺激引起的膈肌抽搐反应。比较了不同药物的抑制作用,并按阻断作用强度顺序分级为:奈替米星(NTL)>庆大霉素(GM)>链霉素(SM)>卡那霉素(KM)>AMK>HAPA - B。HAPA - B的半数抑制浓度(IC50,即抑制反应50%时的浓度)为3.6×10⁻³g/ml。HAPA - B产生的神经肌肉阻滞可被氯化钙、氯化钾或咖啡因逆转,但不能被新斯的明逆转。筒箭毒碱或氯化镁可增强HAPA - B的神经肌肉作用。肌肉注射(400mg/kg)和静脉注射(100mg/kg)HAPA - B对原位腓肠肌对坐骨神经刺激的抽搐反应无影响。静脉注射200mg/kg可导致部分大鼠死亡,其他大鼠的抽搐反应受到抑制。静脉注射50mg/kg的AMK对抽搐反应无显著影响,100mg/kg时可导致死亡。静脉注射剂量为50mg/kg时,GM和SM可导致死亡或抽搐反应明显受抑制。在静脉输注药物60分钟的实验中,HAPA - B以400mg/kg/hr的速度输注、AMK以200和400mg/kg/hr的速度输注时,抽搐反应均受到抑制。总之,HAPA - B可能在神经末梢具有神经肌肉阻断作用。然而,在所测试的氨基糖苷类抗生素中,其作用最弱。

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