Aminabee Shaik, Rao Atmakuri Lakshmana, Eswaraiah Maram Chinna
V. V. Institute of Pharmaceutical Sciences, Department of Pharmacology, Gudlavalleru, India.
Anurag College of Pharmacy, Department of Pharmacognosy, Kodad, India.
Turk J Pharm Sci. 2020 Apr;17(2):136-140. doi: 10.4274/tjps.galenos.2018.30306. Epub 2020 Apr 24.
To evaluate the antioxidant activity of chloroform extract fractions of (whole plant) against paracetamolinduced toxicity in rats.
For 7 days, rats were treated with different chloroform extract fractions and toxicity was induced with a single dose of paracetamol by intraperitoneal injection. The group of animals pretreated with 100 mg/kg p.o of fraction D of improved significantly in terms of hepatic superoxide dismutase (SOD), catalase and peroxidase activities, and glutathione levels compared to the control group.
The hepatic SOD, catalase, peroxidase activities, and glutathione levels in the animal groups treated with paracetamol were 33.6±0.09 μ/mg protein, 5.5±0.23 μ/mg protein, 0.131±0.15 μ/mL, and 46.1±5.81 μM, respectively. Hepatic SOD, catalase, peroxidase, and glutathione in the fraction D treated group were 61.8±0.07 μ/mg protein, 10.6±0.16 μ/mg protein, 0.913±0.23 μ/mL, and 87.6±1.4 micro molar, respectively. Therefore, the present study revealed that fraction D of has significant antioxidant activity and can be used to protect tissue from oxidative stress.
From the results, fraction D of at a dose of 100 mg/kg, p.o., improved the SOD, catalase and peroxidase activities, and glutathione levels significantly. Based on this study, we can conclude that fraction D of possesses antioxidant activity and can be employed in protecting tissue from oxidative stress.
评估(全株)氯仿提取物各馏分对大鼠扑热息痛诱导毒性的抗氧化活性。
连续7天,给大鼠给予不同的氯仿提取物馏分,并通过腹腔注射单剂量扑热息痛诱导毒性。与对照组相比,经口服100mg/kg的D馏分预处理的动物组在肝脏超氧化物歧化酶(SOD)、过氧化氢酶和过氧化物酶活性以及谷胱甘肽水平方面有显著改善。
用扑热息痛处理的动物组肝脏SOD、过氧化氢酶、过氧化物酶活性以及谷胱甘肽水平分别为33.6±0.09μ/mg蛋白、5.5±0.23μ/mg蛋白、0.131±0.15μ/mL和46.1±5.81μM。D馏分处理组的肝脏SOD、过氧化氢酶、过氧化物酶和谷胱甘肽分别为61.8±0.07μ/mg蛋白、10.6±0.16μ/mg蛋白、0.913±0.23μ/mL和87.6±1.4微摩尔。因此,本研究表明的D馏分具有显著的抗氧化活性,可用于保护组织免受氧化应激。
结果表明,口服剂量为100mg/kg的的D馏分可显著提高SOD、过氧化氢酶和过氧化物酶活性以及谷胱甘肽水平。基于本研究,我们可以得出结论,的D馏分具有抗氧化活性,可用于保护组织免受氧化应激。