Department of Pharmacology, Institute of Biological Sciences, UFMG, Av. Antônio Carlos, 6627, 31.270-100, Belo Horizonte, Brazil.
Department of Pharmacology, Institute of Biological Sciences, UFMG, Av. Antônio Carlos, 6627, 31.270-100, Belo Horizonte, Brazil.
Biomed Pharmacother. 2018 Jan;97:1434-1437. doi: 10.1016/j.biopha.2017.11.048. Epub 2017 Dec 14.
Studies conducted since 1969 have shown that the release of serotonin (5-HT) in the dorsal horn of the spinal cord contributes to opioid analgesia. In the present study, the participation of the opioidergic system in antinociceptive effect serotonin at the peripheral level was examined.
The paw pressure test was used with mice (Swiss, males from 35 g) which had increased pain sensitivity by intraplantar injection of PGE (2 μg). Serotonin (250 ng), administered locally to the right paw of animals, produces antinociception in this model.
The selective antagonists for mu, delta and kappa opioid receptors, clocinnamox clocinnamox (40 μg), naltrindole (60 μg) and nor-binaltorfimina (200 μg), respectively, inhibited the antinociceptive effect induced by serotonin. Additionally, bestatin (400 μg), an inhibitor of enkephalinases that degrade peptides opioids, enhanced the antinociceptive effect induced by serotonin (low dose of 62.5 ng).
These results suggest that serotonin possibly induce peripheral antinociception through the release of endogenous opioid peptides, possible from immune cells or keratinocytes.
自 1969 年以来进行的研究表明,脊髓背角中 5-羟色胺(5-HT)的释放有助于阿片类药物的镇痛作用。在本研究中,研究了在外周水平上 5-羟色胺的镇痛作用中阿片能系统的参与。
使用对 PGE(2μg)进行足底注射而增加疼痛敏感性的小鼠(瑞士,雄性,体重 35g)进行足底压力测试。局部给予右爪 250ng 的 5-羟色胺可在该模型中产生镇痛作用。
分别为 mu、delta 和 kappa 阿片受体的选择性拮抗剂氯肉桂诺酮(40μg)、纳曲吲哚(60μg)和 nor-binaltorfimina(200μg)抑制了 5-羟色胺诱导的镇痛作用。此外,内啡肽酶抑制剂贝司他汀(400μg)增强了 5-羟色胺(低剂量 62.5ng)诱导的镇痛作用。
这些结果表明,5-羟色胺可能通过释放内源性阿片肽来诱导外周镇痛,这些阿片肽可能来自免疫细胞或角质形成细胞。