Comparative Impact of Solvent Extracts of Spondias mombin Leaves on In-vitro Antioxidant and Acetylcholinesterase Inhibitory Activities

U. Evuen, E. D. Kpomah
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引用次数: 1

Abstract

The underlying cause of a number of neurological disorders is oxidative stress. Given the dearth of medications now available to treat such disorders and their accompanying detrimental impacts, an urgent need exists for the global identification of brand-new antioxidants and acetylcholinesterase (AChE) inhibitors. This study evaluated the comparative impacts of the antioxidant and acetylcholinesterase activities of n-hexane, ethyl acetate, and methanol extracts of S. mombin leaves. The dried leaf samples of the plant were triturated. Following maceration of the powdered plant materials in each of the three extraction solvents (methanol, n-hexane, and ethyl acetate), the resulting solutions were separately subjected to lyophilization. The in-vitro antioxidant analysis was determined by employing the 2,2-diphenyl-1-picrylhydrazyl (DPPH) and lipid peroxidation (LPO) assays. Acetylcholinesterase (AChE) inhibitory abilities of the various extracts were also evaluated using a standard protocol. The methanol extract showed the greatest DPPH scavenging (75.91%) and AChE inhibitory (40.17%) properties in the DPPH and AChE inhibitory assays, respectively. The DPPH and lipid peroxidation assays also demonstrated that all extracts had dose-dependent antioxidant properties. In addition, evaluations of each extract's ability to inhibit lipid peroxidation revealed that, at initial concentrations of 0.05 mg/L and 0.1 mg/L, the methanol extract displayed stronger LPO inhibitory effects (5.90%, 6.15%) than the n-hexane (4.00%, 5.4%) and ethyl acetate (3.26%, 3.99%) extracts. Nonetheless, the n-hexane extract showed a greater LPO inhibitory effect (10.00%, 10.34%) at higher dosages of 0.2 mg/L and 0.5 mg/L respectively. The results of this study have shown that methanol is the best solvent for exploiting the pharmacological benefits of S. mombin leaves thereby reasserting the numerous applications of the plant in traditional medicine. It has also paved the way for the development of novel therapeutic alternatives for a range of neurodegenerative disorders and other health concerns.
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海棘叶溶剂提取物对体外抗氧化和抑制乙酰胆碱酯酶活性的影响
许多神经系统疾病的潜在原因是氧化应激。鉴于目前可用于治疗此类疾病及其伴随的有害影响的药物的缺乏,迫切需要在全球范围内识别新的抗氧化剂和乙酰胆碱酯酶(AChE)抑制剂。本研究比较了山楂叶正己烷、乙酸乙酯和甲醇提取物对抗氧化活性和乙酰胆碱酯酶活性的影响。这种植物的干叶样品经过了发酵。在三种提取溶剂(甲醇,正己烷和乙酸乙酯)中浸泡粉末状植物材料后,将所得溶液分别进行冻干。体外抗氧化分析采用2,2-二苯基-1-苦味酰肼(DPPH)和脂质过氧化(LPO)测定。各种提取物的乙酰胆碱酯酶(AChE)抑制能力也使用标准方案进行了评估。在DPPH和AChE抑制实验中,甲醇提取物对DPPH和AChE的清除率分别为75.91%和40.17%。DPPH和脂质过氧化实验也表明,所有提取物都具有剂量依赖性的抗氧化特性。此外,对各提取物抑制脂质过氧化的能力进行了评价,结果表明,在初始浓度为0.05 mg/L和0.1 mg/L时,甲醇提取物的LPO抑制作用(5.90%、6.15%)强于正己烷提取物(4.00%、5.4%)和乙酸乙酯提取物(3.26%、3.99%)。而正己烷提取物在0.2 mg/L和0.5 mg/L的剂量下对LPO的抑制作用为10.00%,10.34%。本研究结果表明,甲醇是开发山楂叶药理作用的最佳溶剂,从而重申了该植物在传统医学中的众多应用。它还为一系列神经退行性疾病和其他健康问题的新型治疗方案的发展铺平了道路。
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