Synergistic interaction between Bambusa arundinacea and Euphorbia hirta leaf extract on antioxidant, antiglycation and DNA protective properties.

Macwan Dipeksha, Hiteshkumar V. Patel
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Abstract

Oxidative stress and enhanced non-enzymatic protein glycation result in the pathogenesis of various disorders in humans, including diabetes mellitus. This study examined the synergistic action of Bambusa arundinacea with Euphorbia hirta leaf extract for anti-oxidant potential, antiglycation effect on fructose-mediated proteins, and DNA-protective properties. The methanolic extract shows significantly (P<0.01) higher total phenolic and flavonoid content when compared with ethyl acetate and hexane extract in both plants. The combined methanolic extract (CME) of both plants exhibits higher antioxidant potential, as indicated by the lower IC50 values obtained for DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging activity (4.82 μg/ml) and NO (nitric oxide) scavenging activity (3.94 μg/ml) with stronger Trolox equivalent antioxidant capacity when compared to B. arundinacea and E. hirta individually. The antiglycation analysis revealed that CME is more potent to inhibit fructose-mediated glycation of human serum albumin (HSA) at the early and middle stages. In addition to this, CME more effectively inhibits protein glycation in the late phase, which was confirmed by declining fluorescence intensity. Furthermore, a high degree of positive correlation was obtained between antioxidant and antiglycation capacities through Pearson’s correlation coefficient. The results also demonstrated that CME displays a synergistic effect in protecting DNA from oxidative damage and preventing the formation of glycation of DNA.
黄竹与大戟叶提取物抗氧化、抗糖化及DNA保护作用的协同作用
氧化应激和增强的非酶蛋白糖基化导致人类各种疾病的发病机制,包括糖尿病。本研究考察了黄竹与大戟叶提取物的协同抗氧化作用、对果糖介导蛋白的抗糖基化作用以及dna保护作用。与乙酸乙酯和己烷提取物相比,两种植物的甲醇提取物总酚和类黄酮含量均显著(P<0.01)高于乙酸乙酯和己烷提取物。两种植物的联合甲醇提取物(CME)对DPPH(2,2-二苯基-1-吡啶肼基)自由基的清除活性(4.82 μg/ml)和NO(一氧化氮)的清除活性(3.94 μg/ml)的IC50值较低,具有较强的Trolox当量抗氧化能力,显示出较高的抗氧化潜力。抗糖化分析显示,CME在早期和中期更有效地抑制果糖介导的人血清白蛋白(HSA)糖化。除此之外,CME在后期更有效地抑制蛋白糖基化,荧光强度下降证实了这一点。此外,通过Pearson相关系数,抗氧化能力和抗糖化能力之间存在高度正相关。结果还表明,CME在保护DNA免受氧化损伤和防止DNA糖基化形成方面具有协同作用。
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