Shamsi Tooba Naz, Parveen Romana, Afreen Sumbul, Azam Mudasser, Sen Priyankar, Sharma Yamini, Haque Qazi Mohd Rizwanul, Fatma Tasneem, Manzoor Nikhat, Fatima Sadaf
a Department of Biotechnology , Jamia Millia Islamia , New Delhi , India.
b Department of Biosciences , Jamia Millia Islamia , New Delhi , India.
J Diet Suppl. 2018 Nov 2;15(6):939-950. doi: 10.1080/19390211.2017.1407383. Epub 2018 Jan 18.
Protease inhibitors are one of the most promising and investigated subjects for their role in pharmacognostic and pharmacological studies. This study aimed to investigate antioxidant, anti-inflammatory, and antimicrobial activities of trypsin inhibitors (TIs) from two plant sources (Cajanus cajan and Phaseolus limensis). TI was purified from C. cajan (PUSA-992) by ammonium sulfate precipitation followed by ion exchange chromatography. TI from Phaseolus limensis (lima bean trypsin inhibitor; LBTI) was procured from Sigma-Aldrich, St. Louis, Missouri, United States. The antioxidant activity was analyzed by ferric ion reducing antioxidant power (FRAP) and 2,2-diphenyl-1-picrylhydrazyl (DPPH). The anti-inflammatory property of TIs was determined by inhibition of albumin denaturation assay. Ascorbic acid and aspirin were used as standards for antioxidant and anti-inflammatory assays, respectively. These TIs were tested against various bacterial and fungal strains. The TIs showed DPPH radical-scavenging activity in a concentration-dependent manner with IC values comparable to ascorbic acid. The FRAP values were also observed comparable to ascorbic acid and followed the trend of dose-dependent manner. The half maximal inhibitory concentration (IC) values of CCTI and LBTI in anti-inflammatory test showed that LBTI is more potent than CCTI. The TIs showed potent antibacterial activity, but apparently no action against fungi. This study has reported the biological properties of CCTI and LBTI for the first time. The results show that TIs possess the ability to inhibit diseases caused by oxidative stress, inflammation, and bacterial infestation.
蛋白酶抑制剂因其在生药学和药理学研究中的作用,是最具前景且研究最多的课题之一。本研究旨在探究来自两种植物来源(木豆和利马豆)的胰蛋白酶抑制剂(TIs)的抗氧化、抗炎和抗菌活性。通过硫酸铵沉淀,随后进行离子交换色谱法,从木豆(PUSA - 992)中纯化出TI。来自利马豆的TI(利马豆胰蛋白酶抑制剂;LBTI)购自美国密苏里州圣路易斯的西格玛奥德里奇公司。通过铁离子还原抗氧化能力(FRAP)和2,2 - 二苯基 - 1 - 苦基肼(DPPH)分析抗氧化活性。通过抑制白蛋白变性试验测定TIs的抗炎特性。分别使用抗坏血酸和阿司匹林作为抗氧化和抗炎试验的标准品。对这些TIs针对各种细菌和真菌菌株进行了测试。TIs以浓度依赖性方式表现出DPPH自由基清除活性,其IC值与抗坏血酸相当。还观察到FRAP值与抗坏血酸相当,并呈剂量依赖性趋势。在抗炎试验中,CCTI和LBTI的半数最大抑制浓度(IC)值表明,LBTI比CCTI更有效。TIs表现出强大的抗菌活性,但对真菌显然无作用。本研究首次报道了CCTI和LBTI的生物学特性。结果表明,TIs具有抑制由氧化应激、炎症和细菌感染引起的疾病的能力。