In-silico and biochemical analysis of ethyl acetate fraction of Olax subscorpioidea leaf on DMBA-induced cell proliferation in female rats

Q3 Pharmacology, Toxicology and Pharmaceutics
A. A. Adelegan, T. Johnson, T. Dokunmu, E. Iweala
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引用次数: 0

Abstract

Introduction: Olax subscorpioidea is a medicinal plant that Africans use to treat numerous ailments, including cancer. This research examines the antioxidant, anticancer, and in-silico properties of ethyl acetate fraction of Olax subscorpioidea’s (OSEA) on 7,12-Dimethylbenz(α) anthracene (DMBA)-induced cell proliferation in female rats. Methods: Forty female Sprague Dawley rats averaging 110 ± 20 g were induced proliferation with DMBA (80 mg/kg) and treated with ethyl acetate fraction (250 mg/kg BW) of O. subscorpioidea or tamoxifen (6.6 mg/kg BW) before and after induction. The trial lasted 22 weeks. In-vivo antioxidant parameters such as superoxide dismutase (SOD), malondialdehyde (MDA), and reduced glutathione (GSH) were examined. Likewise, carcinoma antigen marker (CA153), and DNA methyltransferase 3-like (DNMT3L) activity were measured. Gas chromatography-mass spectrometry (GC-MS) detected the bioactive compounds, and molecular docking studies predicted the mechanism of action of OSEA against DNA methyltransferase. Results: Treatment with OSEA significantly increased the SOD activity, enhanced GSH levels, and lowered the levels of MDA, CA-153, and DNMT3L in DMBA-exposed rats. The GC-MS analysis of OSEA revealed the presence of 40 bioactive compounds. The molecular docking revealed that 4-cyclopentene-1,3-dione (-6.407 kcal/mol), 2-(2-hydroxyethylthio) (-4.926 kcal/mol) and 3,4,5,6-tetrahydrophthalic anhydride (-6.16 kcal/mol) had the lowest binding energies against DNMT1, DNMT3A, and DNMT3B, respectively. 2-(2-hydroxyethylthio) was the least toxic. The molecular dynamic simulation revealed that the interaction between DNMT3A and 2-(2-hydroxyethylthio) propionic was stable to an extent. : The in-silico and biochemical analysis of the ethyl acetate fraction of O. subscorpioidea showed that it can protect against lipid peroxidation and oxidative stress and may be a potent source of drug that serves as an effective therapeutic in the future.
Olax subscorpioidea 叶乙酸乙酯馏分对 DMBA 诱导的雌性大鼠细胞增殖的分子内和生物化学分析
简介Olax subscorpioidea 是一种药用植物,非洲人用它来治疗包括癌症在内的多种疾病。本研究探讨了Olax subscorpioidea的乙酸乙酯馏分(OSEA)对7,12-二甲基苯(α)蒽(DMBA)诱导的雌性大鼠细胞增殖的抗氧化、抗癌和微观特性。研究方法用 DMBA(80 毫克/千克)诱导 40 只体重为 110 ± 20 克的雌性 Sprague Dawley 大鼠细胞增殖,并在诱导前后使用 O. subscorpioidea 的乙酸乙酯馏分(250 毫克/千克体重)或他莫昔芬(6.6 毫克/千克体重)进行治疗。试验持续了 22 周。对超氧化物歧化酶(SOD)、丙二醛(MDA)和还原型谷胱甘肽(GSH)等体内抗氧化参数进行了检测。同样,还测定了癌抗原标记物(CA153)和 DNA 甲基转移酶 3-like (DNMT3L) 的活性。气相色谱-质谱(GC-MS)检测了生物活性化合物,分子对接研究预测了 OSEA 对 DNA 甲基转移酶的作用机制。结果显示OSEA能明显提高DMBA暴露大鼠的SOD活性,提高GSH水平,降低MDA、CA-153和DNMT3L水平。对 OSEA 的气相色谱-质谱(GC-MS)分析表明,其中含有 40 种生物活性化合物。分子对接显示,4-环戊烯-1,3-二酮(-6.407 kcal/mol)、2-(2-羟乙基硫基)(-4.926 kcal/mol)和 3,4,5,6- 四氢邻苯二甲酸酐(-6.16 kcal/mol)分别与 DNMT1、DNMT3A 和 DNMT3B 的结合能最低。2-(2-hydroxyethylthio) 的毒性最小。分子动力学模拟显示,DNMT3A 和 2-(2-羟乙基硫代)丙酸之间的相互作用在一定程度上是稳定的。 对 O. subscorpioidea 的乙酸乙酯馏分进行的分子内和生化分析表明,它可以防止脂质过氧化和氧化应激,可能是一种有效的药物来源,未来可作为一种有效的治疗手段。
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来源期刊
Journal of HerbMed Pharmacology
Journal of HerbMed Pharmacology Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
2.50
自引率
0.00%
发文量
49
审稿时长
12 weeks
期刊介绍: Journal of Herbmed Pharmacology (J Herbmed Pharmacol) is the intersection between medicinal plants and pharmacology. This international journal publishes manuscripts in the fields of medicinal plants, pharmacology and therapeutic. This journal aims to reach all relevant national and international medical institutions and persons in electronic version free of charge. J Herbmed Pharmacol has pursued this aim through publishing editorials, original research articles, reviews, mini-reviews, commentaries, letters to the editor, hypothesis, case reports, epidemiology and prevention, news and views. In this journal, particular emphasis is given to research, both experimental and clinical, aimed at protection/prevention of diseases. A further aim of this journal is to emphasize and strengthen the link between herbalists and pharmacologists. In addition, J Herbmed Pharmacol welcomes basic biomedical as well as pharmaceutical scientific research applied to clinical pharmacology. Contributions in any of these formats are invited for editorial consideration following peer review by at least two experts in the field.
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