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首页> 外文期刊>Pain. >Co-administration of delta- and mu-opioid receptor agonists promotes peripheral opioid receptor function.
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Co-administration of delta- and mu-opioid receptor agonists promotes peripheral opioid receptor function.

机译:共同使用δ-阿片受体激动剂和μ-阿片受体激动剂可促进外周阿片受体功能。

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摘要

Enhancement of peripheral opioid analgesia following tissue injury or inflammation in animal models is well-documented, but clinical results of peripheral opioid therapy remain inconsistent. Previous studies in the central nervous system have shown that co-administration of mu- and delta-opioid receptor agonists can enhance analgesic outcomes; however, less is known about the functional consequences of opioid receptor interactions in the periphery. The present study examines the effects of intraplantar injection of the mu- and delta-opioid receptor agonists, morphine and deltorphin, alone and in combination on behavioral tests of nociception in naive rats and on potassium-evoked release of CGRP from sciatic nerves of naive rats. Neither drug alone affected nociceptive behaviors or CGRP release. Two separate measures of mechanical nociceptive sensitivity remained unchanged after co-administration of the two drugs. In contrast, when deltorphin was co-injected with morphine, dose-dependent and peripherally restricted increases in paw withdrawal latencies to radiant heat were observed. Similarly, concentration-dependent inhibition of CGRP release was observed when deltorphin and morphine were administered in sequence prior to potassium stimulation. However, no inhibition was observed when morphine was administered prior to deltorphin. All combined opioid effects were blocked by co-application of antagonists. Deltorphin exposure also enhanced the in vivo and in vitro effects of another mu-opioid receptor agonist, DAMGO. Together, these results suggest that under normal conditions, delta-opioid receptor agonists enhance the effect of mu-opioid receptor agonists in the periphery, and local co-administration of delta- and mu-opioid receptor agonists may improve results of peripheral opioid therapy for the treatment of pain.
机译:在动物模型中组织损伤或炎症后增强外周阿片类药物镇痛作用已有充分文献记载,但外周阿片类药物治疗的临床结果仍不一致。先前在中枢神经系统中的研究表明,同时使用mu和delta类阿片受体激动剂可以增强镇痛效果;然而,人们对周围的阿片受体相互作用的功能后果知之甚少。本研究探讨了单独和联合使用mu-和δ-阿片样物质受体激动剂吗啡和deltorphin足底内注射对幼稚大鼠的伤害感受行为测试以及对幼稚大鼠坐骨神经钾诱发的CGRP释放的影响。 。两种药物均不影响伤害感受行为或CGRP释放。两种药物合用后,两种机械伤害感受敏感性的单独测量保持不变。相反,当将deltorphin与吗啡共注射时,观察到剂量依赖性和外围受限的爪子退缩对辐射热的潜伏性增加。类似地,在钾刺激之前依序给予deltorphin和吗啡时,观察到了CGRP释放的浓度依赖性抑制作用。然而,在吗啡之前给予吗啡没有观察到抑制作用。联合应用拮抗剂可阻断所有联合的阿片类药物作用。 Deltorphin暴露还增强了另一种阿片类阿片受体激动剂DAMGO的体内和体外作用。总之,这些结果表明,在正常情况下,δ-阿片受体激动剂可增强外周阿片类阿片受体激动剂的作用,而δ-和μ-阿片类受体激动剂的局部共同给药可改善阿片类药物对阿片类药物的治疗效果。疼痛的治疗。

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