Razali Nurhanani, Mat Junit Sarni, Ariffin Azhar, Ramli Nur Siti Fatimah, Abdul Aziz Azlina
Department of Molecular Medicine, Faculty of Medicine, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Department of Chemistry, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.
BMC Complement Altern Med. 2015 Dec 18;15:438. doi: 10.1186/s12906-015-0963-2.
Tamarindus indica L. (T. indica) or locally known as "asam jawa" belongs to the family Leguminosae. T. indica seeds as by-products from the fruits were previously reported to contain high polyphenolic content. However, identification of their bioactive polyphenols using recent technologies is less well researched but nonetheless important. Hence, it was the aim of this study to provide further information on the polyphenolic content and antioxidant activities as well as to identify and quantify its bioactive polyphenols.
T. indica seeds were extracted with methanol and were then fractionated with different compositions of hexane, ethyl acetate and methanol. Polyphenolic contents were measured using Folin-Ciocalteu assay while antioxidant activities were measured using DPPH radical scavenging and ferric reducing (FRAP) activities. The cytotoxic activities of the crude extract and the active fraction were evaluated in HepG2 cells using MTT assay. The cells were then pre-treated with the IC20 concentrations and induced with H2O2 before measuring their cellular antioxidant activities including FRAP, DPPH, lipid peroxidation, ROS generation and antioxidant enzymes, SOD, GPx and CAT. Analyses of polyphenols in the crude extract and its active fraction were done using UHPLC and NMR.
Amongst the 7 isolated fractions, fraction F3 showed the highest polyphenolic content and antioxidant activities. When HepG2 cells were treated with fraction F3 or the crude extract, the former demonstrated higher antioxidant activities. F3 also showed stronger inhibition of lipid peroxidation and ROS generation, and enhanced activities of SOD, GPx and CAT of HepG2 cells following H2O2-induced oxidative damage. UHPLC analyses revealed the presence of catechin, procyanidin B2, caffeic acid, ferulic acid, chloramphenicol, myricetin, morin, quercetin, apigenin and kaempferol, in the crude seed extract of T. indica. UHPLC and NMR analyses identified the presence of caffeic acid in fraction F3. Our studies were the first to report caffeic acid as the active polyphenol isolated from T. indica seeds which likely contributed to the potent antioxidant defense system of HepG2 cells.
Results from this study indicate that caffeic acid together with other polyphenols in T. indica seeds can enhance the antioxidant activities of treated HepG2 cells which can provide protection against oxidative damage.
罗望子(Tamarindus indica L.),当地称为“酸角”,属于豆科。此前有报道称,罗望子果实的副产品种子含有高含量的多酚。然而,利用最新技术对其生物活性多酚进行鉴定的研究较少,但仍然很重要。因此,本研究的目的是提供有关多酚含量和抗氧化活性的更多信息,并鉴定和定量其生物活性多酚。
用甲醇提取罗望子种子,然后用不同组成的己烷、乙酸乙酯和甲醇进行分级分离。使用福林-酚试剂法测定多酚含量,使用DPPH自由基清除法和铁还原抗氧化能力(FRAP)测定抗氧化活性。使用MTT法在HepG2细胞中评估粗提物和活性组分的细胞毒性活性。然后在测量细胞抗氧化活性(包括FRAP、DPPH、脂质过氧化、活性氧生成和抗氧化酶超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT))之前,用IC20浓度预处理细胞并用H2O2诱导。使用超高效液相色谱(UHPLC)和核磁共振(NMR)对粗提物及其活性组分中的多酚进行分析。
在7个分离组分中,F3组分显示出最高的多酚含量和抗氧化活性。当用F3组分或粗提物处理HepG2细胞时,前者表现出更高的抗氧化活性。F3还显示出对脂质过氧化和活性氧生成的更强抑制作用,并增强了H2O2诱导的氧化损伤后HepG2细胞的SOD、GPx和CAT活性。UHPLC分析显示,罗望子种子粗提物中存在儿茶素、原花青素B2、咖啡酸、阿魏酸、氯霉素、杨梅素、桑色素、槲皮素、芹菜素和山奈酚。UHPLC和NMR分析确定F3组分中存在咖啡酸。我们的研究首次报道咖啡酸是从罗望子种子中分离出的活性多酚,它可能有助于HepG2细胞强大的抗氧化防御系统。
本研究结果表明,罗望子种子中的咖啡酸与其他多酚一起可以增强处理过HepG2细胞的抗氧化活性,从而提供对氧化损伤的保护。