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新斯的明诱导大鼠骨骼肌强直性收缩减弱。

Decreased tetanic contracture of rat skeletal muscle induced by pyridostigmine.

作者信息

Anderson R J, Chamberlain W L, Roesner M, Dacko C, Robertson D G

出版信息

J Toxicol Environ Health. 1986;18(2):221-30. doi: 10.1080/15287398609530863.

Abstract

The purpose of this study was to compare the effects of various regimens of pyridostigmine administration on the contractile strength of skeletal muscle. Rats were exposed to pyridostigmine according to 3 dosing schedules: 2 mg/kg ip daily, 5 mg/kg X d by sc infusion, and 25 mg/kg X d by sc infusion. After 1, 4, 10, and 20 d of exposure, measurements were made of muscle tension during tetanic stimulation, and of muscle mass, erythrocyte acetylcholinesterase activity, and body weight. Pyridostigmine produced a dose-dependent decrement in the contracture generated during tetanic stimulation. Peak effect was observed after 4 d of exposure but remained depressed after 20 d. The magnitude of the decrement correlated with the frequency of the tetanic stimulation (from 20 to 100 Hz). Muscle tension at the end of the tetanic stimulus was affected to a greater extent than the initial tension. The 25-mg/kg infusion of pyridostigmine significantly depressed erythrocyte acetylcholinesterase activity throughout the study and also decreased body weight on d 1-4. No change in muscle mass was observed in any treatment group. These results show that pyridostigmine exposure results in decrements in skeletal muscle contracture that are dose-dependent, frequency-dependent, and time-dependent. The effect is probably not the result of muscle wasting and does not correlate well with erythrocyte acetylcholinesterase inhibition. The results are consistent with effects of pyridostigmine, both presynaptically and postsynaptically, at the neuromuscular junction that affect neurotransmitter release and receptor responsiveness.

摘要

本研究的目的是比较不同给药方案的吡啶斯的明对骨骼肌收缩力的影响。大鼠按照3种给药方案接受吡啶斯的明:每日腹腔注射2 mg/kg,皮下输注5 mg/kg×d,皮下输注25 mg/kg×d。在暴露1、4、10和20天后,测量强直刺激期间的肌肉张力、肌肉质量、红细胞乙酰胆碱酯酶活性和体重。吡啶斯的明使强直刺激期间产生的挛缩呈剂量依赖性降低。在暴露4天后观察到峰值效应,但在20天后仍保持降低。降低幅度与强直刺激频率(从20至100 Hz)相关。强直刺激结束时的肌肉张力比初始张力受到的影响更大。在整个研究过程中,25 mg/kg输注吡啶斯的明显著降低红细胞乙酰胆碱酯酶活性,并且在第1 - 4天还降低体重。在任何治疗组中均未观察到肌肉质量的变化。这些结果表明,暴露于吡啶斯的明会导致骨骼肌挛缩降低,且呈剂量依赖性、频率依赖性和时间依赖性。这种效应可能不是肌肉萎缩的结果,并且与红细胞乙酰胆碱酯酶抑制没有很好的相关性。这些结果与吡啶斯的明在神经肌肉接头处的突触前和突触后作用一致,其影响神经递质释放和受体反应性。

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