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青藤碱在大鼠术后疼痛模型中的镇痛作用。

Antinociceptive effects of sinomenine in a rat model of postoperative pain.

作者信息

Zhu Qing, Sun Yuehua, Mao Lina, Liu Chengpeng, Jiang Bo, Zhang Wei, Li Jun-Xu

机构信息

School of Pharmacy, Nantong University, Nantong, Jiangsu Province, China.

出版信息

Br J Pharmacol. 2016 May;173(10):1693-702. doi: 10.1111/bph.13470. Epub 2016 Mar 31.

Abstract

BACKGROUND AND PURPOSE

This study examined the antinociceptive effects of sinomenine in a rat model of postoperative pain.

EXPERIMENTAL APPROACH

Male and female rats were subjected to a surgical incision in the right hind paw, and the von Frey filament test was used to measure mechanical hypersensitivity after drug or vehicle treatment (p.o. or i.p.). Rats were treated daily with sinomenine before or after the surgery and the AUCs of the antinociceptive effects measured during a 4 h period were calculated to determine the ED50 values of sinomenine. The anti-hyperalgesic effects of different doses of a combination of sinomenine and acetaminophen (paracetamol) were assessed in another group of rats. Dose combinations were determined by using a fixed ratio dose-addition analysis method.

KEY RESULTS

Sinomenine (5-80 mg·kg(-1) ) produced dose-dependent antinociceptive effects in rats that had been subjected to surgery and this effect lasted for 4 h. The potency of sinomenine, given i.p. or p.o., did not differ between male and female rats. However, sinomenine was fourfold more potent when given i.p. than p.o. The GABAA receptor antagonist bicuculline blocked the antinociceptive effects of sinomenine. The antinociceptive effect of a daily treatment with sinomenine remained stable throughout the course of postoperative pain. Pretreatment with sinomenine did not alter the mechanical hypersensitivity post-surgery. The combination of sinomenine with acetaminophen produced an infra-additive interaction.

CONCLUSIONS AND IMPLICATIONS

Sinomenine demonstrated significant antinociceptive activity against postoperative pain and may be a useful novel pharmacotherapy for the management of postoperative pain.

摘要

背景与目的

本研究在大鼠术后疼痛模型中考察了青藤碱的抗伤害感受作用。

实验方法

对雄性和雌性大鼠右后爪进行手术切口,在给予药物或赋形剂(口服或腹腔注射)后,采用von Frey细丝试验测量机械性超敏反应。在手术前或手术后每日用青藤碱对大鼠进行治疗,并计算4小时内抗伤害感受作用的曲线下面积(AUC)以确定青藤碱的半数有效剂量(ED50)值。在另一组大鼠中评估不同剂量青藤碱与对乙酰氨基酚(扑热息痛)联合使用的抗痛觉过敏作用。通过固定比例剂量相加分析法确定剂量组合。

主要结果

青藤碱(5 - 80mg·kg⁻¹)在接受手术的大鼠中产生剂量依赖性抗伤害感受作用,且该作用持续4小时。腹腔注射或口服给予青藤碱时,雄性和雌性大鼠的效能无差异。然而,腹腔注射时青藤碱的效能是口服时的四倍。GABAA受体拮抗剂荷包牡丹碱可阻断青藤碱的抗伤害感受作用。在术后疼痛过程中,每日用青藤碱治疗的抗伤害感受作用保持稳定。青藤碱预处理未改变术后的机械性超敏反应。青藤碱与对乙酰氨基酚联合使用产生低于相加的相互作用。

结论与意义

青藤碱对术后疼痛表现出显著的抗伤害感受活性,可能是一种用于管理术后疼痛的有用的新型药物疗法。

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