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首页> 外文期刊>European journal of oral sciences >Effect of resveratrol on c-fos expression of rat trigeminal spinal nucleus caudalis and C1 dorsal horn neurons following mustard oil-induced acute inflammation
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Effect of resveratrol on c-fos expression of rat trigeminal spinal nucleus caudalis and C1 dorsal horn neurons following mustard oil-induced acute inflammation

机译:白藜芦醇对大鼠三叉脊髓核C-FOS表达的影响芥菜急性炎症后CAUDALIN脊髓核核心腺炎和C1背角神经元的影响

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摘要

The dietary constituent, resveratrol, was recently identified as a transient receptor potential ankyrin 1 (TRPA1) antagonist, voltage-dependent sodium ion (Na+) channel, and cyclooxygenase-2 (COX-2) inhibitor. The aim of the present study was to investigate whether pretreatment with resveratrol attenuates acute inflammation-induced sensitization of nociceptive processing in rat spinal trigeminal nucleus caudalis (SpVc) and upper cervical (C1) dorsal horn neurons, via c-fos immunoreactivity. Mustard oil (MO), a TRPA1 channel agonist, was injected into the whisker pads of rats to induce inflammation. Pretreatment with resveratrol significantly decreased the mean thickness of inflammation-induced edema in whisker pads compared with those of untreated, inflamed rats. Ipsilateral of both the superficial and deep laminae of SpVc and C1 dorsal horn, there were significantly more c-fos-immunoreactive SpVc/C1 neurons in inflamed rats compared with naive rats, and resveratrol pretreatment significantly decreased that number relative to untreated, inflamed rats. These results suggest that systemic administration of resveratrol attenuates acute inflammation-induced augmented nociceptive processing of trigeminal SpVc and C1 neurons. These findings support resveratrol as a potential therapeutic agent for use in alternative, complementary medicine to attenuate, or even prevent, acute trigeminal inflammatory pain.
机译:最近将膳食成分,白藜芦醇鉴定为瞬时受体潜在的肛门蛋白1(TRPA1)拮抗剂,电压依赖性钠离子(Na +)通道和环氧氧酶-2(COX-2)抑制剂。本研究的目的是研究与白藜芦醇的预处理是否衰减急性炎症诱导的急性炎症诱导的伤害性加工致敏性,通过C-FOS免疫反应性。芥菜油(Mo)是TRPA1通道激动剂,注入大鼠的晶须以诱导炎症。与未处理发炎的大鼠相比,与白藜芦醇的预处理显着降低了晶须垫中炎症诱导的水肿的平均厚度。与幼稚大鼠相比,SPVC和C1背角的浅表和深层椎板的浅表和深层椎板,在发炎大鼠中有明显更多的C-FOS-免疫反应性SPVC / C1神经元,并且白藜芦醇预处理显着降低了相对于未经处理的发炎大鼠的数量。这些结果表明,白藜芦醇的全身施用衰减急性炎症诱导的三叉脂SPVC和C1神经元的增强伤害加工。这些发现支持白藜芦醇作为用于替代,互补药物的潜在治疗剂以衰减,甚至预防急性三叉炎症疼痛。

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