Zahoor Muhammad, Bari Wasim Ul, Zeb Alam, Khan Irfan
Biochemistry Department, University of Malakand, Chakdara, Dir Lower, 18800 KPK, Pakistan.
Department of Chemistry, University of Malakand, Chakdara, Dir Lower, KPK, Pakistan.
J Basic Clin Physiol Pharmacol. 2020 Jan 11;31(2):/j/jbcpp.2020.31.issue-2/jbcpp-2019-0220/jbcpp-2019-0220.xml. doi: 10.1515/jbcpp-2019-0220.
Background In this study, Grewia optiva Drummond ex Burret root extracts were assessed for use as a remedy for oxidative stress, diabetes mellitus and neurological disorders. Methods The antioxidative potentials of the extracts were determined using DPPH and ABTS assays, whereas their enzyme inhibitory potentials were determined against acetylcholinesterase (AChE), butyrylcholinesterase (BChE), α-glucosidase and α-amylase. In the in vivo experiments, methanol extract was orally administered to mice (n = 5) at four doses of 200, 300, 400 and 500 mg kg-1 for 30 days and its effect on glucose, triglycerides, total cholesterol, etc. were investigated. Results The highest free radical scavenging activities against DPPH and ABTS radicals were recorded for the methanol and ethyl acetate extracts, and their respective IC50 values were 75 and 88 μg/mL. In addition, these two fractions were highly active in inhibiting AChE and BChE, with IC50 values of 120 and 185 μg/mL, respectively. Moderate inhibition (μg/mL) was recorded against α-glucosidase (69.02 ± 1.02 and 64.29 ± 2.41) and α-amylase (65.12 ± 2.02 and 63.29 ± 1.41) and these were comparable to the inhibitory activities exhibited by the standard, acarbose. All the extracts showed high phenolic and flavonoid contents, which correlated with their antioxidant, anticholinesterase, α-glucosidase and α-amylase activities. The phenolic compounds in the crude extract and fractions were determined using the standard HPLC method and bioactive compounds, namely, morin, ellagic acid, kaempferol-3-(p-coumaroyl-diglucoside)-7-glucoside, apigenin-7-O-rutinoside, quercetin-3-(caffeoyl-diglucoside)-7-glucoside, etc., which were detected at various retention times. Significant decrease in cholesterol, triglyceride and blood glucose levels were observed. Conclusion G. optiva is a good source of antioxidants and other phytochemicals, some of which possess anticholinesterase, anti-glucosidase, and anti-amylase activities, and can be used to treat different health conditions such as oxidative stress, neurological disorders, and diabetes mellitus.
背景 在本研究中,对小花扁担杆(Grewia optiva Drummond ex Burret)根提取物作为氧化应激、糖尿病和神经紊乱的治疗药物进行了评估。方法 使用DPPH和ABTS法测定提取物的抗氧化潜力,同时测定其对乙酰胆碱酯酶(AChE)、丁酰胆碱酯酶(BChE)、α-葡萄糖苷酶和α-淀粉酶的酶抑制潜力。在体内实验中,将甲醇提取物以200、300、400和500 mg kg-1的四种剂量口服给予小鼠(n = 5),持续30天,并研究其对葡萄糖、甘油三酯、总胆固醇等的影响。结果 甲醇提取物和乙酸乙酯提取物对DPPH和ABTS自由基的自由基清除活性最高,其各自的IC50值分别为75和88 μg/mL。此外,这两个馏分对AChE和BChE具有高度活性抑制作用,IC50值分别为120和185 μg/mL。对α-葡萄糖苷酶(69.02 ± 1.02和64.29 ± 2.41)和α-淀粉酶(65.12 ± 2.02和63.29 ± 1.41)有中度抑制作用(μg/mL),且与标准品阿卡波糖的抑制活性相当。所有提取物均显示出高酚类和黄酮类含量,这与其抗氧化、抗胆碱酯酶、α-葡萄糖苷酶和α-淀粉酶活性相关。使用标准HPLC法测定粗提取物和馏分中的酚类化合物,并在不同保留时间检测到生物活性化合物,即桑色素、鞣花酸、山柰酚-3-(对香豆酰二葡萄糖苷)-7-葡萄糖苷、芹菜素-7-O-芸香糖苷、槲皮素-3-(咖啡酰二葡萄糖苷)-7-葡萄糖苷等。观察到胆固醇、甘油三酯和血糖水平显著降低。结论 小花扁担杆是抗氧化剂和其他植物化学物质的良好来源,其中一些具有抗胆碱酯酶、抗葡萄糖苷酶和抗淀粉酶活性,可用于治疗不同的健康状况,如氧化应激、神经紊乱和糖尿病。