Sheikh Yunus, Maibam Beebina Chanu, Talukdar Narayan Chandra, Deka Dibakar Chandra, Borah Jagat Chandra
Laboratory of Natural Medicinal Chemistry, Natural Product Chemistry & Pharmacology Programme, Institute of Bioresources & Sustainable Development, Takyelpat, Imphal 795001, Manipur, India.
Department of Chemistry, Gauhati University, Guwahati 781014, Assam, India.
J Ethnopharmacol. 2016 Sep 15;191:21-28. doi: 10.1016/j.jep.2016.06.015. Epub 2016 Jun 6.
Parkia roxburghii G. Don. is a traditional medicinal plant and its pods are extensively used as food and medicine. It is believed by the traditional healers to have medicinal properties to treat diabetes, hypertension and urinary tract infections (Jamaluddin et al., 1994).
The methanolic extract of pods of P roxburghii and fractions were screened for their α-glucosidase and α-amylase inhibitory activity. Anti-hyperglycemic effects were studied on streptozotocin (45mg/kg b.w.) induced diabetes in albino rats (seven groups, n=7 n=6), using different doses for 14 days. Plasma glucose concentration (HbA1c) was analysed using whole blood, while SGOT, SGPT, TG, TC and uric acid were analysed using serum, employing commercial kits. Quantitative analysis of the major active constituent was carried out by HPLC-PDA.
Bioactivity guided chemical investigation of the edible pods of P roxburghii identified sub-fraction EA-Fr 5 which significantly inhibited α-glucosidase (IC50 0.39±0.06 µgmL(-1)), reduced the blood glucose level to normal, and lowered the elevated levels of liver function enzymes SGOT and SGPT in STZ-induced diabetic rats. EA-Fr 5 was found to contain epigallocatechin gallate (1) and hyperin (2) which exhibited significantly higher α-glucosidase inhibitory potency with IC50 0.51±0.09 and 0.71±0.03µM respectively. EA-Fr 5 contained 379.82±2.90mg/g of EGCG, the major active constituent which manifests a broad spectrum of biological activities.
The present investigation for the first time reports the occurrence of EGCG and hyperin in P roxburghii and substantiates the traditional use of pods of P roxburghii as dietary supplement for management of diabetes with significantly promising α-glucosidase inhibitory potency and anti-hyperglycemic as well as hepatoprotective effects.
罗氏球花豆(Parkia roxburghii G. Don.)是一种传统药用植物,其豆荚被广泛用作食物和药物。传统治疗师认为它具有治疗糖尿病、高血压和尿路感染的药用特性(Jamaluddin等人,1994年)。
对罗氏球花豆豆荚的甲醇提取物及其馏分进行α-葡萄糖苷酶和α-淀粉酶抑制活性筛选。使用不同剂量对链脲佐菌素(45mg/kg体重)诱导的白化病大鼠糖尿病(七组,n = 7,n = 6)进行抗高血糖作用研究,持续14天。使用全血分析血浆葡萄糖浓度(糖化血红蛋白),而使用商业试剂盒通过血清分析谷草转氨酶、谷丙转氨酶、甘油三酯、总胆固醇和尿酸。通过高效液相色谱-光电二极管阵列检测器对主要活性成分进行定量分析。
对罗氏球花豆可食用豆荚进行生物活性导向的化学研究,鉴定出亚馏分EA-Fr 5,其显著抑制α-葡萄糖苷酶(IC50为0.39±0.06µg/mL(-1)),将血糖水平降至正常,并降低链脲佐菌素诱导的糖尿病大鼠中升高的肝功能酶谷草转氨酶和谷丙转氨酶水平。发现EA-Fr 5含有表没食子儿茶素没食子酸酯(1)和金丝桃苷(2),它们分别表现出显著更高的α-葡萄糖苷酶抑制效力,IC50分别为0.51±0.09和0.71±0.03µM。EA-Fr 5含有379.82±2.90mg/g的表没食子儿茶素没食子酸酯,这是表现出广泛生物活性的主要活性成分。
本研究首次报道了罗氏球花豆中表没食子儿茶素没食子酸酯和金丝桃苷的存在,并证实了罗氏球花豆荚作为膳食补充剂用于管理糖尿病的传统用途,其具有显著的α-葡萄糖苷酶抑制效力以及抗高血糖和肝保护作用。