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胡椒科树木油和贝壳杉烯酸的抗伤害活性在小鼠体内的研究。

Antinociceptive activity of Copaifera officinalis Jacq. L oil and kaurenoic acid in mice.

机构信息

Graduated Program in Pharmacology, Federal University of Santa Maria (UFSM), Avenida Roraima, 1000, building 21, room 5207, Santa Maria, RS, 97105-900, Brazil.

Graduated Program in Health Sciences, University of the Extreme South of Santa Catarina (Unesc), Criciúma, SC, 88006-000, Brazil.

出版信息

Inflammopharmacology. 2019 Aug;27(4):829-844. doi: 10.1007/s10787-019-00588-3. Epub 2019 May 16.

Abstract

Copaifera officinalis L. possesses traditional uses as an analgesic, anti-inflammatory, and antiseptic. However, until now the antinociceptive effect and the mechanism of action were not described for Copaifera officinalis L. oil and no compound present in this oil was identified to be responsible for its biological effects. The goal of this study was to identify the presence of kaurenoic acid in Copaifera officinalis oil and investigate its antinociceptive effect, mechanism of action, and possible adverse effects in mice. The quantification of kaurenoic acid in Copaifera officinalis oil was done by HPLC-DAD technique. Male and female albino Swiss mice (25-35 g) were used to test the antinociceptive effect of Copaifera officinalis (10 mg/kg, intragastric) or kaurenoic acid (1 mg/kg) in the tail-flick test, intraplantar injection of capsaicin, allyl isothiocyanate (AITC) or complete Freund's adjuvant (CFA). Copaifera officinalis oil and kaurenoic acid caused the antinociceptive effect in the tail-flick test in a dose-dependent manner, and their effect was reversed by naloxone (an opioid antagonist). Copaifera officinalis oil or kaurenoic acid reduced the nociception caused by capsaicin or AITC and produced an anti-allodynic effect in the CFA model (after acute or repeated administration for 7 days). Possible adverse effects were also observed, and non-detectable adverse effect was observed for the intragastric administration of Copaiba officinalis oil or kaurenoic acid and in the same way, the treatments were neither genotoxic nor mutagenic at the doses tested. Thus, Copaiba officinalis oil, and kaurenoic acid possess antinociceptive action without adverse effects.

摘要

药用巴西苏木油具有镇痛、抗炎和防腐的传统用途。然而,到目前为止,还没有描述药用巴西苏木油的镇痛作用及其作用机制,也没有鉴定出这种油中的任何化合物是其生物效应的原因。本研究的目的是鉴定出药用巴西苏木油中存在贝壳杉烯酸,并研究其在小鼠中的镇痛作用、作用机制和可能的不良反应。采用高效液相色谱-二极管阵列检测技术(HPLC-DAD)对药用巴西苏木油中的贝壳杉烯酸进行定量分析。雄性和雌性白化瑞士小鼠(25-35g)用于测试药用巴西苏木(10mg/kg,灌胃)或贝壳杉烯酸(1mg/kg)对尾部闪烁试验、辣椒素、丙烯基异硫氰酸酯(AITC)或完全弗氏佐剂(CFA)的镇痛作用。药用巴西苏木油和贝壳杉烯酸在尾部闪烁试验中呈剂量依赖性地引起镇痛作用,其作用被纳洛酮(阿片类拮抗剂)逆转。药用巴西苏木油或贝壳杉烯酸减轻了辣椒素或 AITC 引起的疼痛,并在 CFA 模型中产生了抗痛觉过敏作用(急性或重复给药 7 天后)。还观察到了可能的不良反应,灌胃给予药用巴西苏木油或贝壳杉烯酸没有检测到不良反应,同样,在测试剂量下,这些治疗方法既没有遗传毒性也没有致突变性。因此,药用巴西苏木油和贝壳杉烯酸具有镇痛作用而无不良反应。

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