Department of Studies and Research in Biochemistry, Tumkur University, Tumakuru.
Department of Biochemistry Jnansahydri, KuvempuUniversity, Shankarghatta, Shivamogga, Karnataka, India.
Blood Coagul Fibrinolysis. 2020 Jul;31(5):293-302. doi: 10.1097/MBC.0000000000000913.
: To understand the RBC protecting efficiency and antiplatelet activity of methanolic extract of Caesalpinia crista coat (MECCC). RBC-protecting activity of MECCC was evaluated using assays, such as DPPH, level of lipid peroxidation, protein carbonyl content, superoxide dismutase and catalase as a marker of oxidative stress whereas, platelet aggregation inhibition was performed using human platelet-rich plasma (PRP). MECCC showed about 76% of DPPH-scavenging activity, with an IC50 value of 71.89 μg/ml. The MECCC reduced the level of lipid peroxidation and protein carboxylation in RBC caused by NaNO2 in a dose-dependent manner. In addition, MECCC normalized the levels of superoxide dismutase (SOD) and catalase (CAT) in oxidative stress-induced RBC in a dose-dependent manner. This suggested the protective effect of MECCC on RBC against oxidative stress. Furthermore, MECCC also exhibited mild antiplatelet activity by inhibiting both ADP and epinephrine agonists that induced platelet aggregation. The noticed inhibition percentage was found to be 28 and 23%, respectively at the concentration of 150 μg. Interestingly, MECCC did not hydrolyse the RBC suggesting its nontoxic properties. MECCC possesses protective effect of RBC against NaNO2 (10 mmol/l) induce oxidative stress and inhibits platelet aggregation.
为了了解巴西苏木甲素(MECCC)的红细胞保护效率和抗血小板活性。采用 DPPH 法、脂质过氧化水平、蛋白质羰基含量、超氧化物歧化酶和过氧化氢酶等方法评价 MECCC 的红细胞保护活性,作为氧化应激的标志物;而血小板聚集抑制作用则采用人富血小板血浆(PRP)进行。MECCC 对 DPPH 的清除活性约为 76%,IC50 值为 71.89μg/ml。MECCC 可降低 NaNO2 诱导的红细胞脂质过氧化和蛋白质羰基化水平,呈剂量依赖性。此外,MECCC 还可使氧化应激诱导的红细胞中超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的水平恢复正常,呈剂量依赖性。这表明 MECCC 对红细胞具有抗氧化应激的保护作用。此外,MECCC 还通过抑制 ADP 和肾上腺素激动剂诱导的血小板聚集,表现出轻微的抗血小板活性。在 150μg 的浓度下,发现对 ADP 和肾上腺素的抑制率分别为 28%和 23%。有趣的是,MECCC 不会水解 RBC,表明其具有非毒性。MECCC 具有保护 RBC 免受 NaNO2(10mmol/l)诱导的氧化应激和抑制血小板聚集的作用。