Manasa K, Vani R
Department of Biotechnology, Center for Post Graduate Studies, Jain University, #18/3, 9th Main, 3rd Block, Jayanagar, Bangalore, 560011 India.
Indian J Hematol Blood Transfus. 2015 Mar;31(1):90-7. doi: 10.1007/s12288-014-0386-0. Epub 2014 Apr 11.
Hydroxyl and peroxyl radicals are biologically active species because of their likelihood to damage cellular constituents. An in vitro study on Wistar rats was conducted to investigate the influence of hydrogen peroxide (H2O2) and 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) on platelets and compare the vulnerability of platelets to oxidative stress (OS) induced by these two free radical initiators. Isolated platelets were divided into controls (without free radical initiators; n = 5) and experimentals (with free radical initiators; n = 5). Different concentrations (0.5, 1.0 and 2.0) of free radical initiators H2O2 and AAPH were used to treat the platelets and incubated for 5, 15 and 30 min. Biomarkers such as platelet aggregation, superoxide generation, lipid peroxidation (thiobarbituric acid reactive substances, conjugate dienes), protein oxidation (protein carbonyls, sulfhydryls) and antioxidant enzymes were assessed. In H2O2 and AAPH treated platelets, though OS was observed at concentrations of 0.5 and 1.0 mM, platelets could tolerate the oxidative insult. Treatment of platelets with 2.0 mM H2O2 demonstrated the onset of irreversible changes in platelets as observed in the results of increased superoxide generation and lipid peroxidation products. In 2.0 mM AAPH platelets, the oxidative damage was evident as indicated through increased aggregation, superoxide generation and conjugate dienes and lower protein sulfhydryls. Platelets were more susceptible to AAPH than H2O2, as AAPH acted on both lipids and proteins whereas H2O2 acted only on lipids. This study gives insight on platelet survival under different OS situations.
羟基和过氧自由基具有生物活性,因为它们有可能损害细胞成分。本研究以Wistar大鼠为对象进行体外实验,以研究过氧化氢(H2O2)和2,2'-偶氮二(2-脒基丙烷)二盐酸盐(AAPH)对血小板的影响,并比较血小板对这两种自由基引发剂诱导的氧化应激(OS)的易感性。将分离出的血小板分为对照组(无自由基引发剂;n = 5)和实验组(有自由基引发剂;n = 5)。使用不同浓度(0.5、1.0和2.0)的自由基引发剂H2O2和AAPH处理血小板,并孵育5、15和30分钟。评估了血小板聚集、超氧化物生成、脂质过氧化(硫代巴比妥酸反应性物质、共轭二烯)、蛋白质氧化(蛋白质羰基、巯基)和抗氧化酶等生物标志物。在H2O2和AAPH处理的血小板中,虽然在0.5和1.0 mM浓度下观察到了氧化应激,但血小板能够耐受氧化损伤。用2.0 mM H2O2处理血小板显示出血小板发生了不可逆变化,这在超氧化物生成增加和脂质过氧化产物的结果中可以观察到。在2.0 mM AAPH处理的血小板中,氧化损伤明显,表现为聚集增加、超氧化物生成增加和共轭二烯增加,以及蛋白质巯基降低。血小板对AAPH比H2O2更敏感,因为AAPH作用于脂质和蛋白质,而H2O2仅作用于脂质。本研究为不同氧化应激情况下血小板的存活提供了见解。