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短期吡啶斯的明治疗对静息和运动大鼠肌肉影响的研究。

Study of muscular effects of short-term pyridostigmine treatment in resting and exercising rats.

作者信息

Hubert M, Lison D

机构信息

AsIAT, Laboratory of Medical Toxicology, Vilvoorde, Belgium.

出版信息

Hum Exp Toxicol. 1995 Jan;14(1):49-54. doi: 10.1177/096032719501400110.

Abstract
  1. Pyridostigmine (PYR) pretreatment is used by the military to obtain 20-30% whole blood acetylcholinesterase (AChE) inhibition in order to enhance the effectiveness of the standard therapeutic regimen for poisoning by an organophosphate anticholinesterase agent. The present study was undertaken to investigate in a rat model the potential muscle damage produced by this pretreatment when given alone or combined with physical exercise. 2. Grip strength and biochemical measurements, i.e. serum creatine phosphokinase (CPK) activity and creatine urinary excretion rate, together with histological studies, were performed in resting animals during a period of 14 days of PYR administration in a dose producing 20-30% whole blood acetylcholinesterase inhibition. No evidence was found of a deleterious effect of this treatment on the skeletal muscle. 3. In contrast, following physical exercise, the same treatment significantly exacerbated the biochemical changes reflecting a loss of integrity in skeletal muscles, namely, increased CPK and urinary creatine excretion rate. The significance of this observation remains to be clarified.
摘要
  1. 军方采用吡啶斯的明(PYR)预处理,使全血乙酰胆碱酯酶(AChE)受到20%-30%的抑制,以提高有机磷酸酯类抗胆碱酯酶剂中毒标准治疗方案的疗效。本研究旨在通过大鼠模型,探究单独给予该预处理或联合体育锻炼时可能产生的肌肉损伤。2. 在给予能使全血乙酰胆碱酯酶受到20%-30%抑制剂量的PYR的14天期间,对静息状态的动物进行握力及生化指标测定,即血清肌酸磷酸激酶(CPK)活性和尿肌酸排泄率,并进行组织学研究。未发现该治疗对骨骼肌有有害作用。3. 相比之下,体育锻炼后,相同治疗显著加剧了反映骨骼肌完整性丧失的生化变化,即CPK升高和尿肌酸排泄率增加。这一观察结果的意义尚待阐明。

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