山奈酚抗伤感受作用可能涉及血清素能机制

S. Jabbari, M. Bananej, M. Zarei, A. Komaki, R. Hajikhani
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引用次数: 1

摘要

背景和目的:类黄酮山奈酚(KM)具有抗炎作用,据报道能够预防代谢性疾病。尽管如此,对山奈酚的镇痛作用进行的研究数量有限。目的:本研究旨在通过甩尾试验研究雄性Wistar大鼠KM的镇痛样活性与5-羟色胺受体的关系。材料和方法:将化合物(即KM、吗啡和双氯芬酸)侧脑室注射给大鼠,用甩尾试验检查其对热痛的中枢作用。为了评估5-羟色胺受体在山奈酚可能的镇痛作用中的作用,使用了几种拮抗剂(即托烷司琼、克坦色林、GR113808、WAY 100635和彭布托醇)。此外,通过转棒试验研究KM治疗后的运动活性和运动反应。结果:侧脑室微量注射KM后,甩尾试验显示有明显的镇痛作用。1和10mg的托烷司琼作为5-HT3受体拮抗剂预处理完全逆转了KM相关的镇痛感受。此外,在10mg时,酮坦色林(5-HT2A受体拮抗剂)和GR113808(5-HT4受体拮抗剂;5-HT1A受体拮抗剂WAY 100635和5-HT1B拮抗剂朋布托醇均未降低KM相关的镇痛感受。未观察到所有KM剂量对运动活动或运动反应有显著影响。结论:本研究结果表明,5-羟色胺能受体(即5-HT2A、5-HT3和5-HT4)对雄性大鼠的KM镇痛活性有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Possible Involvement of Serotonergic Mechanism(s) in the Antinociceptive Effects of kaempferol
Background and Objectives: A flavonoid kaempferol (KM) exerts an anti-inflammatory effect and is reportedly capable of preventing metabolic diseases. Nonetheless, a limited number of studies have been carried out on the antinociceptive effects of kaempferol. Objectives: The present study aimed to investigate the involvement of serotonin receptors in the antinociceptive-like activity of KM in male Wistar rats using the tail-flick test. Materials and Methods: The compounds (i.e., KM, morphine, and diclofenac) were intracerebroventricularly administered to rats for the examination of central effects on the thermal pain using the tail-flick test. For the evaluation of the involvement of serotonin receptors in the possible antinociceptive effects of kaempferol, several antagonists (i.e., tropisetron, ketanserin, GR113808, WAY 100635, and penbutolol) were used. Additionally, locomotor activity and motor responses were investigated by the rotarod test after KM treatment. Results: The intracerebroventricular microinjections of KM showed antinociceptive effects using the tail-flick test. The pretreatment with tropisetron as a 5-HT3 receptor antagonist at 1 and 10 mg completely reversed the KM-related antinociception. Furthermore, ketanserin (5-HT2A receptor antagonist) and GR113808 (5-HT4 receptor antagonist) both at 10 mg reduced KM-related antinociception; however, 5-HT1A receptor antagonist WAY 100635 and 5-HT1B antagonist penbutolol did not decrease KM-related antinociception. All KM doses were not observed with a significant effect on locomotor activity or motor reactions. Conclusion: The results of the current study suggested that serotonergic receptors (i.e., 5-HT2A, 5-HT3, and 5-HT4) are effective in the KM antinociceptive activity in male rats.
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