A new terpenoid from Olea europaea L. leaves and potential aptitude of different leaf extracts as anti-inflammatory agents

IF 0.7 Q4 PHARMACOLOGY & PHARMACY Egyptian Pharmaceutical Journal Pub Date : 2023-01-01 DOI:10.4103/epj.epj_131_22
M. Ghanem, W. Tawfik, El-sayed Mahdy, M. Abdelgawad, T. Mohamed, A. Hamed, Shingi Ohta, Mohamed Hegazy, N. Abdel-Azim, A. Shahat, Moustafa El-Missiry
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Abstract

Background The olive tree (Olea europaea L.) has played a significant role in medical history, being used to relieve a wide range of illnesses in traditional medicine. The value of olive leaves came from their medicinal and nutritional properties. In recent times, it has been proven that there is a potential role of leaves in cancer prevention and inflammatory illnesses. Objective The purpose of this study was to look at the chemical makeup of methylene chloride fraction and also to evaluate the chemopreventive properties and the anti-inflammatory activity of different olive leave fractions using hepa1c1c7 cells and RAW264.7 macrophages activated by lipopolysaccharides, respectively. Materials and methods Air-dried powdered olive leaves were defatted with hexane, and the marc was then soaked in 80% methanol and successively extracted with CH2Cl2, EtOAc, and n-BuOH. Phytochemical investigation of CH2Cl2 fraction was done. The chemopreventive effect was determined in vitro using a hepa1c1c7 human carcinoma cell line, and the anti-inflammatory was carried out using RAW264.7 macrophages. Results and conclusion One novel compound, identified and given the name oleuropeinone (1), was obtained together with two known compounds, blumenol A (2) and megaritolactonol (3). Spectroscopic data such as 1H and 13C NMR were used to identify their chemical structures. The CH2Cl2 fraction is the most effective fraction to inhibit inflammatory markers inducible nitric oxide synthase and COX-2 protein expression in RAW264.7 macrophages. Moreover, it has a potent effect in inducing the chemopreventive marker NQO1 protein expression.
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油橄榄叶中一个新的萜类化合物及其不同叶提取物作为抗炎剂的潜在潜力
橄榄树(Olea europaea L.)在医学史上发挥了重要作用,在传统医学中被用来缓解各种疾病。橄榄叶的价值来自于它们的药用和营养特性。近年来,已经证明叶子在预防癌症和炎症性疾病方面具有潜在的作用。目的利用脂多糖激活的hepa1c1c7细胞和RAW264.7巨噬细胞,研究橄榄叶不同部位二氯甲烷的化学组成,评价不同部位的化学预防性能和抗炎活性。材料与方法风干的橄榄叶粉状物用己烷脱脂,用80%的甲醇浸泡,分别用CH2Cl2、乙酸乙酯和正丁醇提取。对CH2Cl2馏分进行了植物化学研究。体外化学预防作用采用hepa1c1c7人癌细胞系,抗炎作用采用RAW264.7巨噬细胞。结果与结论与已知化合物blumenol A(2)和megaritolactonol(3)一起得到了一个新化合物oleuropeinone(1),并用1H和13C NMR等光谱数据对其化学结构进行了鉴定。CH2Cl2部位是抑制RAW264.7巨噬细胞炎症标志物诱导的一氧化氮合酶和COX-2蛋白表达最有效的部位。此外,它还能诱导化学预防标志物NQO1蛋白的表达。
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来源期刊
Egyptian Pharmaceutical Journal
Egyptian Pharmaceutical Journal PHARMACOLOGY & PHARMACY-
CiteScore
1.10
自引率
0.00%
发文量
37
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