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芝麻素的抗伤害感受作用评估:5-羟色胺能受体的作用

Evaluation of the Antinociceptive Effect of Sesamin: Role of 5HT Serotonergic Receptors.

作者信息

Camacho-Cruz Roberto, Alcalá-Hernández David Francisco, Huerta-Cruz Juan Carlos, Arrieta-Valencia Jesús, Sánchez-Mendoza María Elena, Flores-Murrieta Francisco Javier, Navarrete Andrés, Reyes-García Juan Gerardo, Rocha-González Héctor Isaac

机构信息

Escuela Superior de Medicina, Instituto Politécnico Nacional, Mexico City 11340, Mexico.

División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana Unidad Iztapalapa, Mexico City 09340, Mexico.

出版信息

Pharmaceutics. 2025 Mar 3;17(3):330. doi: 10.3390/pharmaceutics17030330.

DOI:10.3390/pharmaceutics17030330
PMID:40142993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11944384/
Abstract

Sesame ( L.) is used in folk medicine to treat painful disorders. Sesamin is the main lignan found in this plant; however, its antinociceptive potential has scarcely been studied. The aim was to investigate the antinociceptive effect of sesamin on inflammatory and neuropathic pain models, as well as the possible mechanism of action through which sesamin mediates its own antinociceptive effect. Formalin and carrageenan animal models were used to assess inflammatory pain, whereas an L5/L6-spinal-nerve-ligated rat model was employed to evaluate neuropathic pain. Oral sesamin significantly reduced carrageenan-induced hyperalgesia and inflammation, formalin-induced nociception, and L5/L6-spinal-nerve-ligation-induced allodynia. Sesamin was more effective than diclofenac in the inflammatory pain models, but it was less effective than pregabalin in the neuropathic pain model. The antinociceptive effect of sesamin, in the formalin test, was prevented by the intraperitoneal administration of methiothepin (5-HT antagonist), but not by naltrexone (an opioid antagonist) or L-NAME (an NOS inhibitor). In addition, WAY-100635 (5-HT antagonist), but not SB-224289 (5-HT antagonist), BRL-15542 (5-HT antagonist), and SB-699551 (5-HT antagonist), impeded sesamin-induced antinociception. This study's results support the use of sesamin to treat inflammatory pain disorders and suggest that 5-HT receptors influence the antinociceptive effect of this drug.

摘要

芝麻(Sesamum indicum L.)在民间医学中用于治疗疼痛性疾病。芝麻素是该植物中发现的主要木脂素;然而,其抗伤害感受的潜力几乎未被研究。本研究旨在探讨芝麻素对炎症性和神经性疼痛模型的抗伤害感受作用,以及芝麻素介导其自身抗伤害感受作用的可能作用机制。使用福尔马林和角叉菜胶动物模型评估炎症性疼痛,而采用L5/L6脊髓神经结扎大鼠模型评估神经性疼痛。口服芝麻素可显著减轻角叉菜胶诱导的痛觉过敏和炎症、福尔马林诱导的伤害感受以及L5/L6脊髓神经结扎诱导的异常性疼痛。在炎症性疼痛模型中,芝麻素比双氯芬酸更有效,但在神经性疼痛模型中,其效果不如普瑞巴林。在福尔马林试验中,腹腔注射甲硫噻平(5-羟色胺拮抗剂)可阻断芝麻素的抗伤害感受作用,但纳曲酮(阿片类拮抗剂)或L- NAME(一氧化氮合酶抑制剂)则不能。此外,WAY - 100635(5-羟色胺拮抗剂)可阻断芝麻素诱导的抗伤害感受作用,但SB - 224289(5-羟色胺拮抗剂)、BRL - 15542(5-羟色胺拮抗剂)和SB - 699551(5-羟色胺拮抗剂)则不能。本研究结果支持使用芝麻素治疗炎症性疼痛疾病,并表明5-羟色胺受体影响该药物的抗伤害感受作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/f4e3492efbab/pharmaceutics-17-00330-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/e7d4d30da322/pharmaceutics-17-00330-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/f2bde34fe33f/pharmaceutics-17-00330-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/e526bdb9684b/pharmaceutics-17-00330-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/3d0b1c82c6e3/pharmaceutics-17-00330-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/f4e3492efbab/pharmaceutics-17-00330-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/e7d4d30da322/pharmaceutics-17-00330-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/f2bde34fe33f/pharmaceutics-17-00330-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/e526bdb9684b/pharmaceutics-17-00330-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/3d0b1c82c6e3/pharmaceutics-17-00330-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35b/11944384/f4e3492efbab/pharmaceutics-17-00330-g005.jpg

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本文引用的文献

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