Zakusov V V, Iasnetsov V V
Farmakol Toksikol. 1983 Jan-Feb;46(1):5-8.
Interaction of tropane derivatives (motropin, atropine, cocaine) with opiates (morphine) and opioids (an enkephalin amide analog) was studied according to varying tests: pain sensitivity, impulse summation in the central nervous system, respiration. It appeared that motropin is a morphine antagonist and enkephalin amide analog from the standpoint of effect on analgetic action and impulse summation, but is not their antagonist as regards the effect on respiration. Atropine is a weak morphine antagonist in terms of the effect on analgesia, impulse summation and respiration as well. Cocaine is a morphine synergist as regards all the tests indicated. Therefore, the effect of tropane derivatives on pain sensitivity, impulse summation and respiration is mediated via different opiate receptors, which does not exclude the involvement of other neurochemical mechanisms in their action.
根据不同测试(疼痛敏感性、中枢神经系统冲动总和、呼吸)研究了托烷衍生物(莫托品、阿托品、可卡因)与阿片类药物(吗啡)和阿片样物质(脑啡肽酰胺类似物)的相互作用。结果显示,从对镇痛作用和冲动总和的影响来看,莫托品是吗啡拮抗剂和脑啡肽酰胺类似物,但就对呼吸的影响而言并非它们的拮抗剂。阿托品在对镇痛、冲动总和及呼吸的影响方面也是一种弱吗啡拮抗剂。就所有所示测试而言,可卡因是吗啡增效剂。因此,托烷衍生物对疼痛敏感性、冲动总和及呼吸的影响是通过不同的阿片受体介导的,这并不排除其他神经化学机制参与其作用。