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睡莲科植物莲甲醇叶提取物的抗伤害感受、抗炎作用及抗伤害感受作用的可能机制

Anti-nociceptive, anti-inflammatory and possible mechanism of anti-nociceptive action of methanol leaf extract of Linn (Nymphaeceae).

作者信息

Rege Musa G, Ayanwuyi Lydia O, Zezi Abdulkadir U, Odoma Saidi

机构信息

Department of Pharmacy Technician Training, Kebbi State School of Health Technology, Jega, Nigeria.

Department of Pharmacology and Therapeutics, Faculty of Pharmaceutical Sciences, Ahmadu Bello University, Zaria, Nigeria.

出版信息

J Tradit Complement Med. 2020 Feb 28;11(2):123-129. doi: 10.1016/j.jtcme.2020.02.010. eCollection 2021 Mar.

Abstract

The leaf of has been used traditionally for the management of pain and inflammatory diseases. The methanol leaf extract of (NLE) was evaluated for possible anti-nociceptive and anti-inflammatory activities in rats and mice (at the doses of 250, 500 and 1,000 mg/kg) to investigate the existence of scientific basis for the folkloric use of the plant. The standard drugs used were piroxicam (10 mg/kg) and morphine (10 mg/kg). The possible pharmacological mechanism involved in the anti-nociceptive activity was also investigated. The acute toxicity was determined in mice and rats using method of Lorke. The anti-nociceptive activity was evaluated using acetic acid-induced writhing and hot plate tests in mice, while the anti-inflammatory activity was evaluated using carrageenan-induced hind paw edema model in rats. The oral median lethal dose of NLE was found to be greater than 5,000 mg/kg in rats and mice. NLE demonstrated significant and dose-dependent protection against acetic acid induced writhes and increased the reaction time of mice in hot plate test. Pretreatment of the animals with naloxone (2 mg/kg) significantly ( < 0.05) attenuated the anti-nociception elicited by both NLE and morphine. NLE at the doses of 250 and 1,000 mg/kg significantly ( < 0.05) decreased rat paw edema at the 2 hour in the carrageenan-induced paw edema test. The result of the study revealed that possesses anti-nociceptive activities which may be mediated via the opioidergic system as well as mild anti-inflammatory activities thus providing scientific basis for the use of the plant in the management of pain and inflammatory diseases.

摘要

[植物名称]的叶子在传统上被用于治疗疼痛和炎症性疾病。对[植物名称]的甲醇叶提取物(NLE)在大鼠和小鼠中(剂量为250、500和1000毫克/千克)进行了可能的抗伤害感受和抗炎活性评估,以研究该植物民间用途的科学依据。所使用的标准药物为吡罗昔康(10毫克/千克)和吗啡(10毫克/千克)。还研究了抗伤害感受活性可能涉及的药理机制。使用洛克方法在小鼠和大鼠中测定急性毒性。在小鼠中使用醋酸诱导扭体和热板试验评估抗伤害感受活性,而在大鼠中使用角叉菜胶诱导的后爪水肿模型评估抗炎活性。发现NLE在大鼠和小鼠中的口服半数致死剂量大于5000毫克/千克。NLE对醋酸诱导的扭体表现出显著且剂量依赖性的保护作用,并增加了小鼠在热板试验中的反应时间。用纳洛酮(2毫克/千克)预处理动物可显著(P<0.05)减弱NLE和吗啡引起的抗伤害感受作用。在角叉菜胶诱导的爪水肿试验中,250和1000毫克/千克剂量的NLE在2小时时显著(P<0.05)减轻了大鼠爪水肿。研究结果表明,[植物名称]具有抗伤害感受活性,可能通过阿片样物质系统介导,还具有轻度抗炎活性,从而为该植物用于治疗疼痛和炎症性疾病提供了科学依据。

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