Nutraceutical Rumex nervosus as a Natural Drug Candidate; its Metabolite Profiling and Pharmacological Estimation for Health Applications.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Sidra Islam, Arusa Aftab, Zainab Maqbool, Zubaida Yousaf, Zill-E-Huma Aftab
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引用次数: 0

Abstract

Background: Rumex nervosus Vahl is a phenomenal plant from Arabian Peninsula and East African areas. It potentially contains massive therapeutic phytochemicals, including Omeprazole, sitosterols, fatty acids, flavonoids and carotenes. Omepazole (a commercial drug) is used to treat stomach ulcers, gastroesophageal reflux and cardiac disorders. Beta-sitosterol (commercial drug) reduces cholesterol levels and body swelling. It is also known to manage rheumatoid arthritis.

Methodology: The present study evaluated the pharmacological potential and metabolite profiling of Rumex nervosus through various extracts. The extraction was performed using different solvents (Petroleum ether, Chloroform, n-Hexane, Butanol, Methanol, and distilled water) through soxhlet extraction method. Serial dilutions of (100-3.125 mg/mL) were prepared. The biological activities, antimicrobial, anti-diabetic, Hemolytic, anti-inflammatory, and antioxidant (DPPH radical Scavenging, Total anti-oxidant and total phenolic content assays) were performed. Statistical analysis of experimental data was carried out by using SPSS Version 20 and Origin 6.0. Data was represented as mean ± standard deviation (n=3). Differences among mean values were determined using Two-way ANOVA and Tukey's test. The level of statistical significance was set at p ≤ 0.05. The potential extracts were further analyzed for phytochemicals through GC-MS and Network pharmacology (In silico approach).

Results: The plant exhibited the best antioxidant activity (86.7% ± 1.92) at 100 mg/mL with distilled water extract. The highest anti-inflammatory activity (90.64 ± 2.34) (88.31 ± 2.37) was given by n-butanol and distilled water extracts at 100 mg/mL. The optimum anti-diabetic activity (92.78 ± 1.89) was observed at 100 mg/mL with n-butanol.

Discussion: The maximum zone of inhibition was measured with n-butanol extract against Pseudomonas aeruginosa (36.67 ± 0.32) at 100mg/mL, and in the case of Xanthomonas oryzae again n-butanol extract showed maximum zone of inhibition (30.47 ± 0.32) at 100 mg/mL. The maximum fungal zone of inhibition (22.33 ± 0.40) was noticed with n-butanol extract against Fusarium oxysporom at 100 mg/mL, and in the case of Aspergillus niger maximum fungal zone of inhibition was measured with n-butanol extract (16.20 ± 0.25) at 100 mg/mL. Hemolysis activity was highest (4.12 ± 0.01) with the methanol extract at 3.125 mg/mL. R. nervosus displayed the best activities with n-butanol and distilled water extract. GCMS and network pharmacology combined approach identified seven phytochemicals associated with oxidative stress and infectious diseases (1-Tetradecanol, Stigmast-5-ene, Phthalic acid 2-ethylhexyl isohexyl ester, A-Norcholestan-3-one, 5-ethenyl-, (5.beta.), 16-Heptadecenal, gamma-Sitosterol, Omeprazole). Degree score method selected 10 top hub genes, including AKT1, TNF, and EGFR, as potential targets for the identified phytochemicals. Omeprazole and 1- Tetradecanol are currently being used as medicines for treating gastric problems and inflammation.

Conclusion: R. nervosus has been confirmed as a potential source of these compounds through a multifaceted approach, hence it could thus be considered a safe, significant therapeutic source.

作为天然候选药物的神经酸乳鼠其代谢物分析和健康应用的药理学评估。
背景:鲁麦斯(Rumex nervosus Vahl)是阿拉伯半岛和东非地区的一种现象性植物。它可能含有大量的治疗植物化学物质,包括奥美拉唑、谷甾醇、脂肪酸、类黄酮和胡萝卜素。奥美唑(一种商业药物)用于治疗胃溃疡、胃食管反流和心脏疾病。谷甾醇(商业药物)降低胆固醇水平和身体肿胀。它也被认为可以治疗类风湿关节炎。方法:本研究通过对不同提取物的研究,评价了其药理潜力和代谢物谱。采用索氏萃取法对不同溶剂(石油醚、氯仿、正己烷、丁醇、甲醇、蒸馏水)进行提取。连续稀释(100-3.125 mg/mL)。生物活性、抗菌、抗糖尿病、溶血、抗炎和抗氧化(DPPH自由基清除、总抗氧化和总酚含量测定)。采用SPSS Version 20和Origin 6.0对实验数据进行统计分析。数据用均数±标准差表示(n=3)。采用双因素方差分析和Tukey检验确定平均值之间的差异。p≤0.05为差异有统计学意义。通过GC-MS和网络药理学(In silico approach)进一步分析潜在提取物的植物化学成分。结果:100 mg/mL蒸馏水提取物的抗氧化活性最高,为86.7%±1.92。100 mg/mL正丁醇和蒸馏水提取物的抗炎活性最高,分别为90.64±2.34(88.31±2.37)。正丁醇浓度为100 mg/mL时,抗糖尿病活性最高(92.78±1.89)。讨论:100mg/mL正丁醇提取物对铜绿假单胞菌的最大抑制区为36.67±0.32,100mg/mL对米黄单胞菌的最大抑制区为30.47±0.32。100 mg/mL正丁醇提取物对尖孢镰刀菌的最大抑菌区为22.33±0.40,100 mg/mL正丁醇提取物对黑曲霉的最大抑菌区为16.20±0.25。甲醇提取物浓度为3.125 mg/mL时溶血活性最高(4.12±0.01);正丁醇和蒸馏水提取物对神经松茸的活性最好。GCMS和网络药理学相结合的方法鉴定了7种与氧化应激和传染病相关的植物化学物质(1-十四醇、5-烯、邻苯二甲酸2-乙基己基异己基酯、a-去胆甾醇-3- 1,5 -乙烯基-、(5 - β)、16-庚二烯、-谷甾醇、奥美拉唑)。度评分法选择了10个顶级枢纽基因,包括AKT1、TNF和EGFR,作为鉴定的植物化学物质的潜在靶点。奥美拉唑和1-十四醇目前被用作治疗胃病和炎症的药物。结论:神经鼠已被证实为这些化合物的潜在来源,因此它可以被认为是一个安全的、重要的治疗来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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