桑科榕茎皮提取物生物活性分馏法的抗伤害和抗炎作用。

Q2 Medicine
Oluwaseyi K Wakeel, Abraham I Abe, Oluropo B Awosan, Mokaila K Olapade, Temitope J Olatoyan-Layonu, Olugbenga A Olowe, Oluwaseyi A Adeyeba
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引用次数: 0

摘要

目的:采用生物引导分馏法研究红ficus capensis (AEFC)水提物的抗炎和抗炎活性。方法:分别采用醋酸扭体法、热板法、甩尾法、福尔马林法和角叉胶法观察AEFC(250、500、1000 mg/kg, i.p)对小鼠的抗伤害和抗炎作用。根据极性差异将AEFC分馏为丁醇、乙酸乙酯和正己烷馏分。所得馏分(500 mg/kg)采用上述相同的实验程序。发挥最大生产活性的EAF进一步进行分馏,得到6个馏分(标记为CF1-CF6)。测定了这些组分(200 mg/kg)潜在的抗炎和抗炎活性。利用伤性通路的主要拮抗剂(纳洛酮和阿托品)来评价羊草抗伤性作用的机制。结果与讨论:AEFC、BF、EAF和CF4均引起显著的(p)差异。结论:本研究结果支持了capensis在治疗各种疼痛和炎症相关疾病中的传统应用。柱段CF4表现出毒蕈碱受体介导的抗伤害性活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Nociceptive and Anti-Inflammatory Effects of Stem Bark Extract of Ficus Capensis Thunb (Moraceae) by Bioactivity Fractionation.

Objective: This study investigated the antinociceptive and anti-inflammatory activities of the aqueous extract of Ficus capensis (AEFC) by bio-guided fractionation.

Methods: The anti-nociceptive and anti-inflammatory effects of AEFC (250, 500, 1000 mg/kg, i.p) were assessed using acetic acid-induced writhing, hot plate, tail-flick, formalin tests, and carrageenan- induced paw edema, respectively. The AEFC was fractionated base on polarity difference into butanol, ethyl acetate, and n-hexane fractions. The fractions (500 mg/kg) obtained were subjected to the same experimental procedures mentioned above. The EAF, which exerted the most productive activities, was further subjected to fractionation procedures that yielded six fractions (labeled CF1-CF6). These fractions (200 mg/kg) were tested for potential antinociceptive and anti-inflammatory activities. Notable antagonists (Naloxone and atropine) of the nociceptive pathway were used to evaluate the mechanism of the antinociceptive action of F. capensis.

Results and discussion: The AEFC, BF, EAF, and CF4 caused a significant (p<0.05) reduction in the number of abdominal writhes, an increase in reaction time against the hot plate, tail-flick tests, and a significant (p<0.05) inhibition in both phases of formalin test. The AEFC, BF, EAF, CF4, and CF6 caused a significant (p<0.05) inhibition of paw edema development due to carrageenan. Atropine significantly reversed the antinociceptive effect of CF4 in both phases of the formalin test. The results obtained revealed that CF4 produced central and peripheral antinociceptive effects, while CF6 is peripherally mediated.

Conclusion: The results support the traditional uses of F. capensis in the treatment of various diseases associated with pain and inflammation. The column fraction CF4 exhibited muscarinic receptor- mediated antinociceptive activity.

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来源期刊
Anti-Inflammatory and Anti-Allergy Agents in Medicinal Chemistry
Anti-Inflammatory and Anti-Allergy Agents in Medicinal Chemistry Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
3.30
自引率
0.00%
发文量
11
期刊介绍: Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry aims to cover all the latest and outstanding developments in medicinal chemistry and rational drug design for the discovery of new anti-inflammatory & anti-allergy agents. Publishing a series of timely in-depth reviews written by leaders in the field covering a range of current topics, Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments in the field.
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