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一种新型驱虫药:噻嘧啶的药理学方面。

Aspects of the pharmacology of a new anthelmintic: pyrantel.

作者信息

Aubry M L, Cowell P, Davey M J, Shevde S

出版信息

Br J Pharmacol. 1970 Feb;38(2):332-44. doi: 10.1111/j.1476-5381.1970.tb08521.x.

Abstract
  1. The pharmacological properties of an anthelmintic, pyrantel, and some of its analogues have been described and compared with piperazine in a variety of vertebrate and helminth preparations.2. Pyrantel and its analogues in common with nicotine and decamethonium cause spastic paralysis in chicks and contracture of the chick semispinalis and toad rectus abdominis muscles.3. In the soleus and anterior tibialis muscles of the cat, pyrantel in large amounts caused a short-lived neuromuscular block that was preceded by initial depolarization.4. In preparations from cat and rat, pyrantel showed properties common to both competitive and depolarizing neuromuscular blocking drugs.5. Pyrantel blocked the contracture evoked by transmural stimulation and caused a marked contracture of the worm. Piperazine caused a gradually developing reduction in the responses to transmural stimulation and no contracture.6. Pyrantel and its analogues caused a slowly developing contracture of strip preparations of Ascaris, being more than 100 times more active than acetylcholine in this respect. Piperazine caused a relaxation of Ascaris strip preparations and in common with (+)-tubocurarine blocked the responses to acetylcholine and pyrantel analogues on this preparation.7. Pyrantel caused depolarization and increased spike discharge frequency in single muscle cells of Ascaris, these changes being accompanied by increase in tension. Piperazine, on the other hand, caused hyperpolarization and reduction in spike discharge frequency and relaxation, and antagonized the effects of pyrantel.
摘要
  1. 已对驱虫药噻嘧啶及其一些类似物的药理特性进行了描述,并在多种脊椎动物和蠕虫制剂中与哌嗪进行了比较。

  2. 噻嘧啶及其类似物与尼古丁和十烃季铵一样,可使雏鸡发生痉挛性麻痹,并使雏鸡的半棘肌和蟾蜍的腹直肌发生挛缩。

  3. 在猫的比目鱼肌和胫前肌中,大量噻嘧啶可引起短暂的神经肌肉阻滞,在此之前先有初始去极化。

  4. 在猫和大鼠的制剂中,噻嘧啶表现出竞争性和去极化神经肌肉阻滞药物的共同特性。

  5. 噻嘧啶可阻断经壁刺激引起的挛缩,并使蠕虫发生明显的挛缩。哌嗪可使经壁刺激的反应逐渐减弱,但不引起挛缩。

  6. 噻嘧啶及其类似物可使蛔虫条带制剂缓慢发生挛缩,在这方面其活性比乙酰胆碱高100倍以上。哌嗪可使蛔虫条带制剂松弛,与(+)-筒箭毒碱一样,可阻断该制剂对乙酰胆碱和噻嘧啶类似物的反应。

  7. 噻嘧啶可使蛔虫单个肌细胞发生去极化并增加动作电位发放频率,这些变化伴有张力增加。另一方面,哌嗪可引起超极化并降低动作电位发放频率以及松弛,并拮抗噻嘧啶的作用。

相似文献

1
Aspects of the pharmacology of a new anthelmintic: pyrantel.一种新型驱虫药:噻嘧啶的药理学方面。
Br J Pharmacol. 1970 Feb;38(2):332-44. doi: 10.1111/j.1476-5381.1970.tb08521.x.
3
Some pharmacological effects of the nematocide, morantel.驱虫药噻嘧啶的一些药理作用。
Br J Pharmacol. 1973 Jan;47(1):117-23. doi: 10.1111/j.1476-5381.1973.tb08164.x.

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