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Amelioration of the reduced antinociceptive effect of morphine in the unpredictable chronic mild stress model mice by noradrenalin but not serotonin reuptake inhibitors

机译:去甲肾上腺素而不是5-羟色胺再摄取抑制剂可改善吗啡在不可预测的慢性轻度应激模型小鼠中降低的伤害感受作用

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摘要

BackgroundAlthough alterations in not only the pain sensitivity but also the analgesic effects of opioids have been reported under conditions of stress, the influence of unpredictable chronic mild stress (UCMS) on the antinociceptive effects of opioid analgesics remains to be fully investigated. The present study examined the influence of UCMS on the thermal pain sensitivity and antinociceptive effects of two opioid analgesics, morphine (an agonist of opioid receptors) and tramadol (an agonist of μ-opioid receptor and an inhibitor of both noradrenaline and serotonin transporters). We also examined the effects of pretreatment with maprotiline (a noradrenaline reuptake inhibitor) and escitalopram (a serotonin reuptake inhibitor) on the antinociceptive action of morphine in mice under an UCMS condition.
机译:背景技术尽管在压力下阿片类药物的疼痛敏感性和镇痛作用均已改变,但不可预知的慢性轻度应激(UCMS)对阿片类镇痛药抗伤害感受的影响尚待充分研究。本研究检查了UCMS对两种阿片类镇痛药吗啡(阿片受体激动剂)和曲马多(μ阿片受体激动剂以及去甲肾上腺素和5-羟色胺转运蛋白的抑制剂)的热痛敏感性和镇痛作用的影响。我们还检查了在UCMS条件下用马普替林(去甲肾上腺素再摄取抑制剂)和依西酞普兰(5-羟色胺再摄取抑制剂)预处理对吗啡的抗伤害感受作用的作用。

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