首页> 美国卫生研究院文献>African Journal of Traditional Complementary and Alternative Medicines >Ethanolic Extract of Aconiti Brachypodi Radix Attenuates Nociceptive Pain Probably Via Inhibition of Voltage-Dependent NA+ Channel
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Ethanolic Extract of Aconiti Brachypodi Radix Attenuates Nociceptive Pain Probably Via Inhibition of Voltage-Dependent NA+ Channel

机译:乌头乌头的乙醇提取物可能通过抑制电压依赖性NA +通道来减轻伤害性疼痛。

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摘要

Aconiti Brachypodi Radix, belonging to the genus of Aconitum (Family Ranunculaceae), are used clinically as anti-rheumatic, anti-inflammatory and anti-nociceptive in traditional medicine of China. However, its mechanism and influence on nociceptive threshold are unknown and need further investigation. The analgesic effects of ethanolic extract of Aconiti Brachypodi Radix (EABR) were thus studied in vivo and in vitro. Three pain models in mice were used to assess the effect of EABR on nociceptive threshold. In vitro study was conducted to clarify the modulation of the extract on the tetrodotoxin-sensitive (TTX-S) sodium currents in rat's dorsal root ganglion (DRG) neurons using whole-cell patch clamp technique. The results showed that EABR (5–20 mg/kg, i.g.) could produce dose-dependent analgesic effect on hot-plate tests as well as writhing response induced by acetic acid. In addition, administration of 2.5–10 mg/kg EABR (i.g.) caused significant decrease in pain responses in the first and second phases of formalin test without altering the PGE2 production in the hind paw of the mice. Moreover, EABR (10 µg/ml −1 mg/ml) could suppress TTX-S voltage-gated sodium currents in a dose-dependent way, indicating the underlying electrophysiological mechanism of the analgesic effect of the folk plant medicine. Collectively, our results indicated that EABR has analgesic property in three pain models and useful influence on TTX-S sodium currents in DRG neurons, suggesting that the interference with pain messages caused by the modulation of EABR on TTX-S sodium currents in DRG neurones may explain some of its analgesic effect.
机译:乌头属(乌头科)的乌头(Aconiti Brachypodi Radix)在中国传统医学中被临床用作抗风湿,消炎和镇痛药。但是,其机理和对伤害阈值的影响尚不清楚,需要进一步研究。因此在体内和体外研究了乌头乌头乙醇提取物(EABR)的镇痛作用。使用小鼠中的三种疼痛模型评估EABR对伤害性阈值的影响。使用全细胞膜片钳技术进行了体外研究,以阐明提取物对大鼠背根神经节(DRG)神经元中河豚毒素敏感(TTX-S)钠电流的调节。结果表明,EABR(5–20 mg / kg,例如)可以在热板试验中产生剂量依赖性的镇痛作用,也可以产生乙酸引起的扭体反应。此外,在福尔马林试验的第一和第二阶段,给予2.5–10 mg / kg EABR(例如)可使疼痛反应显着降低,而不会改变小鼠后爪中PGE2的产生。此外,EABR(10 µg / ml -1 mg / ml)可以剂量依赖的方式抑制TTX-S电压门控钠电流,这表明了民间植物药镇痛作用的潜在电生理机制。总体而言,我们的结果表明,EABR在三种疼痛模型中均具有镇痛作用,并且对DRG神经元中的TTX-S钠电流具有有益的影响,这表明EABR调节DRG神经元中的TTX-S钠电流对疼痛信息的干扰可能解释其止痛作用。

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