膳食补充葡萄籽提取物通过 5-HT3/7 和 GABA 受体介导对三叉神经伤害感受的抑制。

5-HT3/7 and GABA receptors mediate inhibition of trigeminal nociception by dietary supplementation of grape seed extract.

机构信息

Missouri State University, Springfield, MO, USA.

出版信息

Nutr Neurosci. 2022 Aug;25(8):1565-1576. doi: 10.1080/1028415X.2021.1880211. Epub 2021 Feb 5.

Abstract

Temporomandibular joint disorder is a prevalent orofacial pain condition involving sensitization and activation of trigeminal nociceptive neurons. Dietary supplementation with a proanthocyanin-enriched grape seed extract (GSE) was found to inhibit trigeminal nociception in a chronic TMD model. In this study, the cellular mechanisms by which GSE inhibits sustained trigeminal nociception in male and female Sprague Dawley rats were investigated. Some animals were supplemented with 0.5% GSE dissolved in their water one week prior to neck muscle inflammation induced by injection of complete Freund's adjuvant into the trapezius. To investigate the mechanism of GSE, some animals were injected intracisternally with antagonists of 5-HT3, 5-HT7, GABAA, or GABAB, receptor prior to jaw opening. In males and females, trapezius inflammation prior to jaw opening resulted in sustained mechanical hypersensitivity of trigeminal nociceptors that was significantly inhibited by GSE. Further, GSE beginning 14 days post jaw opening also inhibited trigeminal nociception. Intracisternal injection of antagonists of the 5-HT3/7 and GABAB, but not GABAA receptors reduced the anti-nocifensive effect of GSE in both sexes. Neuronal expression of GABAB protein and mRNA in the spinal cord and trigeminal ganglion were detected. The inhibitory effect of GSE is mediated via activation of 5-HT3/7 receptors and GABAB to enhance central descending inhibitory pain pathways and suppress ongoing trigeminal nociception. Further, our findings support the use of GSE as a dietary supplement in the management of pain associated with TMD and other orofacial pain conditions involving central sensitization and dysfunction of descending pain modulation.

摘要

颞下颌关节紊乱是一种常见的口腔面部疼痛病症,涉及三叉神经伤害感受神经元的敏化和激活。研究发现,富含原花青素的葡萄籽提取物(GSE)的饮食补充可以抑制慢性 TMD 模型中的三叉神经伤害感受。在这项研究中,研究了 GSE 抑制雄性和雌性 Sprague Dawley 大鼠持续三叉神经伤害感受的细胞机制。一些动物在斜方肌注射完全弗氏佐剂引起颈部肌肉炎症前一周,用溶于水的 0.5% GSE 补充饮食。为了研究 GSE 的机制,一些动物在开口前向脑室内注射 5-HT3、5-HT7、GABAA 或 GABAB 受体拮抗剂。在雄性和雌性中,开口前的斜方肌炎症导致三叉神经伤害感受器的持续机械超敏反应,GSE 显著抑制了这种超敏反应。此外,开口后 14 天开始的 GSE 也抑制了三叉神经伤害感受。脑室内注射 5-HT3/7 和 GABAB 受体拮抗剂,但不是 GABAA 受体拮抗剂,降低了两性的 GSE 的抗伤害感受作用。检测了脊髓和三叉神经节中 GABAB 蛋白和 mRNA 的神经元表达。GSE 的抑制作用是通过激活 5-HT3/7 受体和 GABAB 来增强中枢下行抑制性疼痛通路并抑制持续的三叉神经伤害感受来介导的。此外,我们的发现支持将 GSE 用作 TMD 及其他涉及中枢敏化和下行疼痛调节功能障碍的口腔面部疼痛病症的疼痛管理的饮食补充剂。

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