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在大鼠中,先用单胺氧化酶抑制剂预处理后,拟交感神经药物引发对利血平的高血压反应的作用。

Effect of sympathomimetic drugs in eliciting hypertensive responses to reserpine in the rat, after pretreatment with monoamineoxidase inhibitors.

作者信息

Cashin C H

出版信息

Br J Pharmacol. 1972 Feb;44(2):203-9. doi: 10.1111/j.1476-5381.1972.tb07256.x.

Abstract
  1. The effects of some rapidly metabolized sympathomimetic amines, such as beta-phenylethylamine and p-tyramine, in eliciting hypertensive responses to reserpine in the anaesthetized rat, have been studied.2. Retardation of metabolism, by pretreatment with the monoamineoxidase inhibitors iproniazid or phenelzine, causes beta-phenylethylamine (which in untreated rats has no effect) to induce hypertensive responses to reserpine. Tyramine and other hydroxy substituted phenylethylamines are much less active in this respect, probably because of relatively poor lipid solubility.3. Hypertensive responses to reserpine are due to catecholamine release, which is believed to be from stores made accessible to indirectly acting sympathomimetic amines with high lipid solubility by an action of reserpine on cell membranes.
摘要
  1. 已经研究了一些快速代谢的拟交感胺,如β-苯乙胺和对-酪胺,在麻醉大鼠中引发对利血平的高血压反应的作用。

  2. 通过用单胺氧化酶抑制剂异烟肼或苯乙肼预处理来延缓代谢,会使β-苯乙胺(在未处理的大鼠中无作用)诱导对利血平的高血压反应。酪胺和其他羟基取代的苯乙胺在这方面的活性要低得多,可能是因为脂溶性相对较差。

  3. 对利血平的高血压反应是由于儿茶酚胺释放,据信这是利血平作用于细胞膜,使具有高脂溶性的间接作用拟交感胺能够接触到储存部位所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d8d/1666082/fd27f686c1f3/brjpharm00486-0049-a.jpg

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