Chemical constituents, free radical scavenging and enzyme inhibitory potential of selected Nigerian bee (Apis mellifera) propolis

O. S. Balogun, Z. Liu
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Abstract

Extracts of propolis from southwest Nigeria (Ondo and Ife) were analysed using GC-MS and were evaluated in vitro for free radical scavenging potentials and inhibitory activities on alpha-glucosidase and porcine lipase enzyme. Crude methanolic extracts of both propolis were separately defatted with n-hexane to give n-hexane fractions and defatted fractions. Each fraction was analysed using GC-MS. Diphenyl-2-picrylhydrazyl radical scavenging potentials of the crude and defatted extracts were evaluated while in vitro antihyperglycemic and antihyperlipidemic were also determined using spectrophotometric method. The GC-MS analysis indicated 18 (88.38 %) and 20 (99.99%) compounds for n-hexane fraction of propolis from Ife (BPIH) and Ondo (BPOH) respectively. For the defatted extracts propolis from Ife (BPID) and Ondo (BPOD), 21 compounds each were identified, accounting for 100% composition in each extracts. The IC DPPH radical scavenging activities of all 50 the propolis samples were moderate compared to the standard (32.61 ± 2.60 μg/mL) however, BPOD demonstrated highest radical scavenging activity (141.49±0.29 μg/mL) among the propolis fraction tested. All the extracts demonstrated better inhibition than the standard acarbose, however, BPOD inhibited the enzyme the most with IC value of 25.35±0.48 μg/mL. The anti-lipase activities of the propolis were fairly moderate but 50 much lower compared to the standard orlistat (0.88 ± 0.12 μg/mL). The excellent inhibitory performance of the propolis extracts on alpha-glucosidase enyzme gives credence to its traditional use in treatment of diabetic patients, also the moderate free radical scavenging and antipase activities make bee propolis an important bioresource for discovery of lead drugs.
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尼日利亚蜜蜂(Apis mellifera)蜂胶的化学成分、自由基清除能力和酶抑制潜力
采用气相色谱-质谱法对尼日利亚西南部(Ondo和Ife)的蜂胶提取物进行了分析,并对其体外自由基清除能力和α -葡萄糖苷酶和猪脂肪酶的抑制活性进行了评价。分别用正己烷对两种蜂胶粗甲醇提取物进行脱脂,得到正己烷馏分和脱脂馏分。各组分采用气相色谱-质谱分析。采用分光光度法测定了粗提取物和脱脂提取物对二苯基-2-苦味酰肼自由基的清除能力,并测定了其体外抗高血糖和抗高脂血症的作用。GC-MS分析表明,Ife (BPIH)和Ondo (BPOH)蜂胶正己烷组分中分别含有18个(88.38%)和20个(99.99%)化合物。从Ife (BPID)和Ondo (BPOD)的脱脂蜂胶提取物中分别鉴定出21个化合物,占各提取物成分的100%。50个蜂胶样品对IC DPPH自由基的清除能力(32.61±2.60 μg/mL)均为中等水平,其中BPOD对IC DPPH自由基的清除能力最高(141.49±0.29 μg/mL)。各提取物均优于标准阿卡波糖,其中BPOD对酶的抑制作用最大,IC值为25.35±0.48 μg/mL。蜂胶的抗脂肪酶活性较标准奥利司他(0.88±0.12 μg/mL)低50%。蜂胶提取物对α -葡萄糖苷酶具有良好的抑制作用,这为其在糖尿病患者治疗中的传统应用提供了依据;蜂胶提取物具有中等的自由基清除和抗酶活性,也使其成为先导药物开发的重要生物资源。
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