首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Interactions of drugs active at opiate receptors and drugs active at alpha 2-receptors on various test systems.
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Interactions of drugs active at opiate receptors and drugs active at alpha 2-receptors on various test systems.

机译:在各种测试系统上对阿片受体具有活性的药物与对α2-受体具有活性的药物之间的相互作用。

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摘要

1 The actions of the opiate receptor drugs, morphine, methionine-enkephalin (Met-enkephalin) and naloxone were compared with the actions of the alpha 2-receptor drugs, clonidine, xylazine and yohimbine on analgesic tests, in vitro bioassay (guinea-pig ileum and mouse vas deferens), and radioligand displacement studies on rat brain membrane preparations. 2. Both opiate and alpha 2-agonist drugs showed analgesic activity but whilst the alpha 2-agonist analgesic activity was antagonized by only alpha 2-antagonists, the analgesic activity of morphine was antagonized by both naloxone and yohimbine. In the in vitro tests, both groups of agonists inhibited electrically evoked activity; however in these experiments only antagonism of opiates by naloxone and alpha 2-agonists by yohimbine could be shown and it is concluded that in these systems the activity of the alpha 2-agonists is mediated via the presynaptic alpha 2-receptors only. 3 In the radioligand studies the drugs acting at alpha 2-receptors were active in the micromolar range at displacing labelled opioid ligands but opiates did not displace labelled alpha 2-ligands. 4 It is concluded that drugs which act on alpha 2-receptors interfere with the in vivo analgesic effects of opiates and weakly displace opioid radioligand binding, but opioids do not affect alpha 2 agonist analgesia and do not appear to displace alpha 2-agonist radioligand binding.
机译:1将阿片受体药物吗啡,蛋氨酸-脑啡肽(Met-脑啡肽)和纳洛酮的作用与α2受体药物,可乐定,甲苯噻嗪和育亨宾在镇痛试验,体外生物测定(豚鼠)中的作用进行了比较回肠和小鼠输精管),以及对大鼠脑膜制剂的放射性配体置换研究。 2.阿片类药物和α2-激动剂均显示出镇痛作用,但仅α2-激动剂可拮抗α2-激动剂的镇痛作用,纳洛酮和育亨宾均拮抗吗啡的镇痛作用。在体外试验中,两组激动剂均抑制了电诱发的活性。然而,在这些实验中,仅能显示纳洛酮对鸦片剂的拮抗作用和育亨宾对α2-激动剂的拮抗作用,并且得出结论,在这些系统中,α2-激动剂的活性仅通过突触前的α2-受体介导。 3在放射性配体研究中,作用于α2受体的药物在微摩尔范围内具有取代标记的阿片样物质配体的活性,但阿片剂却不能替代标记的α2配体。 4结论是,作用于α2受体的药物干扰了鸦片的体内止痛作用,并弱取代了阿片样物质对放射性配体的结合,但阿片类药物并不影响α2激动剂的镇痛作用,并且似乎不替代α2激动剂的配体结合。 。

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