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去甲肾上腺素能和血清素能系统在外周抗伤害作用中的协同作用在小鼠中。

Collaborative action between noradrenergic and serotoninergic systems in peripheral antinociception in mice.

机构信息

Department of Pharmacology, Institute of Biological Sciences, UFMG, Av. Antoˆ nio Carlos, 31.270-100, Belo Horizonte 6627, Brazil.

出版信息

J Biosci. 2024;49.

PMID:38920106
Abstract

Noradrenaline (NA) and serotonin (5-HT) induce nociception and antinociception. This antagonistic effect can be explained by the dose and type of activated receptors. We investigated the existence of synergism between the noradrenergic and serotonergic systems during peripheral antinociception. The paw pressure test was performed in mice that had increased sensitivity by intraplantar injection of prostaglandin E (PGE). Noradrenaline (80 ng) administered intraplantarly induced an antinociceptive effect, that was reversed by the administration of selective antagonists of serotoninergic receptors 5-HT isamoltan, 5-HT BRL15572, 5-HT ketanserin, 5-HT ondansetron, but not by selective receptor antagonist 5-HT SB-269970. The administration of escitalopram, a serotonin reuptake inhibitor, potentiated the antinociceptive effect at a submaximal dose of NA. These results, indicate the existence of synergism between the noradrenergic and serotonergic systems in peripheral antinociception in mice.

摘要

去甲肾上腺素(NA)和血清素(5-HT)可引起痛觉和镇痛。这种拮抗作用可以通过激活受体的剂量和类型来解释。我们研究了在周围镇痛期间去甲肾上腺素能和 5-羟色胺能系统之间是否存在协同作用。在通过足底注射前列腺素 E(PGE)增加敏感性的小鼠中进行了足底压力测试。局部给予去甲肾上腺素(80ng)可引起镇痛作用,该作用可被 5-HT 异莫兰、5-HT BRL15572、5-HT 酮色林、5-HT 昂丹司琼等 5-HT 受体选择性拮抗剂逆转,但不能被 5-HT SB-269970 等选择性受体拮抗剂逆转。选择性 5-羟色胺再摄取抑制剂艾司西酞普兰的给药增强了去甲肾上腺素的亚最大剂量的镇痛作用。这些结果表明,在小鼠的外周镇痛中,去甲肾上腺素能和 5-羟色胺能系统之间存在协同作用。

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