厚青果叶乙醇提取物的抗炎和抗氧化作用:体外和体外实验研究

Emmanuel Chiagozie Aham , Stephen Chukwubuikem Nnemolisa , Olamide Esther Asaluwala , Ogechukwu Colet Okeke , Michael Chinedu Chukwu , Ernest Chinemerem Nkagbu , Casmir Chima Uzoefuna , Innocent Uzochukwu Okagu
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引用次数: 0

摘要

现有抗炎药物的副作用促使人们寻求更安全、更有效的抗炎药物。民间医学中用于治疗炎症相关疾病的药用植物,如厚皮膜藓(Hymenodictyon pachyantha k.k krause),越来越被认为是抗炎候选物质的潜在来源。目的采用体外实验和计算机模拟技术,研究厚青叶乙醇提取物(EEHP)的抗炎和自由基清除活性。方法:采用气相色谱-火焰电离检测器对EEHP的活性成分进行表征,采用2,2′-氮化喹啉(3-乙基苯-噻唑啉-6-磺酸(ABTS))和过氧化氢(H2O2)清除试验对其抗氧化能力进行评价。通过环氧合酶-2 (COX-2)和5-脂氧合酶(5-LOX)活性评价其抗炎活性的抑制作用。利用计算机技术了解了EEHP对cox - 2,5 - lox和磷脂酶A2 (PLA2)的作用机制以及其植物成分的药物样特性。结果seehp对ABTS和h2o2自由基的清除率分别为74.40 %和70.72 %,而参比抗坏血酸对ABTS和h2o2自由基的清除率分别为86.28 %和72.31 %。EEHP抑制COX-2 (IC50 = 0.65 mg/ml)和5-LOX (IC50 = 0.38 mg/ml)活性。在EEHP中鉴定的月红素、山母酚、花青素和黄烷-3-醇通过与Phe518、Arg120、Ala527、Leu352、Tyr385、Trp387、Leu384、Phe381和Leu384相互作用抑制COX-2,通过与Arg246和Val243相互作用抑制5-LOX,通过与Asp49、Gly30、Gly32、Gly53和Leu130相互作用抑制PLA2。结论pachyantha是具有抗炎和抗氧化特性的植物化学物质的储存库,是开发炎症相关疾病新候选物的潜在资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-inflammatory and antioxidant potentials of ethanol extract of Hymenodictyon pachyantha leaves: An in vitro and in silico study

Background

The side effects of existing anti-inflammatory drugs have spurred the quest for safer and more effective anti-inflammatory agents. Medicinal plants used in folk medicine for inflammation-related conditions, such as Hymenodictyon pachyantha K.Krause, are increasingly recognized as potential sources of anti-inflammatory candidates.

Aim

To investigate the anti-inflammatory and radical-scavenging activities of the H. pachyantha leaves ethanol extract (EEHP) using in vitro and in silico techniques.

Methodology

Gas chromatography-flame ionization detector was used to characterize the bioactive components of EEHP, while 2,2′-azinobis(3-ethylbenz-thiazoline-6-sulfonic acid (ABTS) and hydrogen peroxide (H2O2) scavenging assays were used to evaluate the antioxidant potential. The inhibition of the anti-inflammatory activities was evaluated via cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX) activities. In silico techniques were used to understand the mechanism of action against COX-2, 5-LOX, and phospholipase A2 (PLA2) and the drug-like properties of EEHP’s phytoconstituents.

Results

EEHP scavenged 74.40 % and 70.72 % of ABTS and H2O2-radicals, respectively, compared with 86.28 % and 72.31 %, respectively, by reference antioxidant (ascorbic acid). EEHP inhibited COX-2 (IC50 = 0.65 mg/ml) and 5-LOX (IC50 = 0.38 mg/ml) activities. Lunamarine, kaempferol, anthocyanin, and flavan-3-ol identified in EEHP were shown to inhibit COX-2 by interacting with Phe518, Arg120, Ala527, Leu352, Tyr385, Trp387, Leu384, Phe381, and Leu384), 5-LOX by interacting with Arg246 and Val243, and PLA2 by interacting with Asp49, Gly30, Gly32, Gly53, and Leu130 amino acids crucial for activities.

Conclusion

Our data suggest that H. pachyantha is a reservoir of phytochemicals with anti-inflammatory and antioxidant properties and a potential resource in developing new candidates for inflammation-related conditions.
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