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磷酸双(对硝基苯)酯(BNPP)对麻醉作用的延长

Prolongation of anesthetic action by BNPP (bis-[p-nitrophenyl] phosphate).

作者信息

Boyce J R, Wright F J, Cervenko F W, Pietak S P, Faulkner S

出版信息

Anesthesiology. 1976 Dec;45(6):629-34. doi: 10.1097/00000542-197612000-00006.

Abstract

Bis-[p-nitrophenyl] phosphate, BNPP, an enzyme inhibitor of the organophosphate class, has been used to inhibit the enzyme, carboxylic ester hydrolase EC 3.1.1.1. Esterases play a major role in the rapid metabolism of propanidid in vivo; in fact, the short duration of action of this intravenous anesthetic agent is due to this rapid hydrolysis. The duration of anesthesia with propanidid alone in healthy mongrel dogs was 10.1 +/- 2.1 (SEM) minutes. When the dogs were pretreated with BNPP, propanidid anesthesia time was prolonged to 38.2 +/- 7.9 (SEM) minutes. Measurements of serum propanidid concentration demonstrated that prolonged high levels of propanidid were associated with the extended anesthesia time. Therefore, BNPP can significantly alter the anesthetic action of propanidid by inhibition of the enzyme system responsible for the rapid hydrolysis of the agent. The experimental model used in the present study provides a means for investigation of effects of certain drugs when their metabolism is impaired.

摘要

对硝基苯基磷酸双酯(BNPP)是一种有机磷酸酯类酶抑制剂,已被用于抑制羧酸酯水解酶(EC 3.1.1.1)。酯酶在体内丙泮尼地的快速代谢中起主要作用;事实上,这种静脉麻醉剂作用时间短就是由于其快速水解。在健康杂种犬中,单独使用丙泮尼地时麻醉持续时间为10.1±2.1(标准误)分钟。当犬用BNPP预处理后,丙泮尼地麻醉时间延长至38.2±7.9(标准误)分钟。血清丙泮尼地浓度测量表明,丙泮尼地长时间高水平与麻醉时间延长相关。因此,BNPP可通过抑制负责该药物快速水解的酶系统,显著改变丙泮尼地的麻醉作用。本研究中使用的实验模型为研究某些药物代谢受损时的作用效果提供了一种手段。

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