首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >Neonatal pain modulates in adolescent rats the antinociceptive effects of fluoxetine and buspirone administrated to their depressive dams during gestation
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Neonatal pain modulates in adolescent rats the antinociceptive effects of fluoxetine and buspirone administrated to their depressive dams during gestation

机译:新生儿疼痛调节青少年大鼠在妊娠期间氟西汀和母猪血酮在抑郁坝上给予抑郁坝的抗血质作用

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摘要

Previously, we have shown that the administration of a selective serotonin reuptake inhibitor fluoxetine or a 5-HT1A receptor agonist buspirone to stressed rats during gestation causes in the offspring alleviation of formalin-induced pain, strengthened by prenatal stress. We have also found that neonatal inflammatory pain strengthens formalin-induced pain in prenatally unstressed rats in later life. In the present study, we investigated the effect of neonatal inflammatory pain on the time-course of the biphasic pain response in the formalin test in prenatally stressed adolescent rats of both sexes to evaluate whether neonatal pain affects the antinociceptive properties of these drugs administered to their depressed mothers during gestation. Our findings demonstrate that neonatal pain modulates in prenatally stressed rats the antinociceptive effect of fluoxetine and buspirone depending on the level of organization of pain response in the central nervous system, the phase of the time-course of the formalin-induced pain, and sex of the rat.
机译:在此之前,我们已经证明,在妊娠期对应激大鼠施用选择性5-羟色胺再摄取抑制剂氟西汀或5-HT1A受体激动剂丁螺环酮可减轻福尔马林诱导的疼痛,并通过产前应激得到加强。我们还发现,新生儿炎症性疼痛会增强出生前无应激大鼠在晚年福尔马林诱导的疼痛。在本研究中,我们通过福尔马林试验在产前应激的青春期雄性大鼠中研究了新生儿炎症性疼痛对双相疼痛反应时程的影响,以评估新生儿疼痛是否影响怀孕期间给抑郁母亲服用的这些药物的抗伤害性。我们的研究结果表明,新生儿疼痛在产前应激大鼠中调节氟西汀和丁螺环酮的抗伤害作用,这取决于中枢神经系统疼痛反应的组织水平、福尔马林诱导疼痛的时间过程阶段以及大鼠的性别。

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