气相色谱-质谱分析:羊草挥发物和溶剂提取物的抗氧化活性和酶抑制活性

O. S. Balogun, O. Ajayi, A. Emekako, I. Ogunlowo, Liu Zhiqiang
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摘要

羊角蕨是一种蕨类植物,在西非通常用于治疗由代谢紊乱和氧化应激引起的疾病。本研究采用加氢蒸馏法提取烟果挥发油,采用甲醇水溶液提取醇提物。然后用含有1%三甲基氯硅烷的N, o -二-(三甲基硅基)三氟乙酰胺对酒精提取物进行硅基化。采用气相色谱-质谱法对精油(PTEO)和硅烷化提取物(PTSE)进行了分析,并利用DPPH、α -葡萄糖苷酶和猪胰脂肪酶对其抗氧化和酶抑制活性进行了研究。PTEO鉴定出的主要化合物类别为单萜类(12.30%)、倍半萜类(24.14%)和二萜类(21.26%),PTSE显示糖和脂肪酸占优势,主要成分为果糖呋喃糖(20.31%)、甘露糖(24.14%)和棕榈酸(6.32%)。PTEO和PTSE对DPPH自由基的IC50清除率分别为435.81±1.25µg/mL和280.09±1.14µg/mL,两者的清除率均低于标准抗坏血酸(32.61±2.60µg/mL)。此外,PTEO(308.26±3.67µg/mL)和PTSE(363.45±2.55µg/mL)的降糖活性与阿卡波糖(279±4.21µg/mL)相当。PTSE对猪胰脂肪酶无抑制作用,PTEO的IC50为111.71±2.12µg/mL,而奥利司他的IC50为0.88±0.12µg/mL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GC-MS ANALYSIS, ANTIOXIDANT AND ENZYME INHIBITORY ACTIVITIES OF VOLATILE AND SOLVENT EXTRACT OF Pteris togoensis
Pteris togoensis is a fern commonly used in west Africa for management of medical conditions resulting from metabolic disorder and oxidative stress. In this study, the essential oil of P. togoensis was obtained using hydrodistillation method while the alcoholic extract was obtained using aqueous methanol. The alcoholic extract was thereafter silylated using N, O-bis-(trimethylsilyl) trifluoroacetamide containing 1% trimethylchlorosilane. Both the essential oil (PTEO) and silylated extract (PTSE) were analysed on GC-MS and investigated for antioxidant and enzyme inhibitory activities using DPPH, alpha-glucosidase and porcine pancreatic lipase enzyme. Principal classes of compound identified in PTEO were monoterpenoids (12.30%), sesquiterpenoids (24.14%) and diterpenoids (21.26%) while the PTSE indicated preponderance of sugar and fatty acids, with fructofuranose (20.31%), mannose (24.14%) and palmitic acid (6.32%) as major constituents. The IC50 of DPPH radical scavenging potentials of PTEO (435.81±1.25 µg/mL) and PTSE (280.09±1.14 µg/mL) indicated that both extracts exhibited mild activities which were lower than the standard ascorbic acid (32.61 ± 2.60 µg/mL). Also, hypoglycemic activities of PTEO (308.26±3.67 µg/mL) and PTSE (363.45±2.55 µg/mL) were fairly comparable to the acarbose (279 ± 4.21 µg/mL). PTSE showed no inhibition on porcine pancreatic lipase while PTEO had IC50 of 111.71±2.12 µg/mL compared to 0.88 ± 0.12 µg/mL orlistat.  
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