Oyagbemi Ademola Adetokunbo, Bester Dirk, Esterhuyse Johan, Farombi Ebenezer Olatunde
Department of Veterinary Physiology, Biochemistry and Pharmacology, University of Ibadan, Nigeria.
Department of Biomedical Sciences, Faculty of Health and Wellness Sciences, Oxidative Stress Research Centre, Cape Peninsula University of Technology, Bellville, 7535, South Africa.
J Intercult Ethnopharmacol. 2016 Sep 28;6(1):42-49. doi: 10.5455/jice.20160923100223. eCollection 2017 Jan-Mar.
The study was designed to investigate the ameliorative effect of Kolaviron (KV) on ischemic/reperfusion injury in experimental animal models.
Male Wistar rats were randomly divided into two groups: Group 1 received corn oil as a vehicle and rats in Group 2 were administered KV at 200 mg/kg for 4 weeks. The rats were fed with rat standard chow pellet and water administered . After 4 weeks of KV administration, hearts were excised and mounted on the working heart perfusion system. Western blot analysis for protein expression was carried out on frozen heart samples.
There was significant ( < 0.05) reduction in the activity of catalase, superoxide dismutase, and glutathione peroxidase with concomitant reduction in oxygen radical absorbance capacity in ischemic rat heart of control compared to group pre-treated with KV, respectively. Similarly, intracellular reactive oxygen species and malondialdehyde were significantly elevated in control compared to KV pre-treated rats. KV significantly increased total Akt/protein kinase B (PKB), phosphorylated Akt/PKB at serine 473 and also caused a significant reduction in p38 mitogen-activated protein kinase, Caspase 3, and cleaved poly adenosine diphosphate ribose polymerase.
Taken together, KV offered significant cardioprotection via free radical scavenging activity and upregulation of pro-survival pathway.
本研究旨在探讨可乐维隆(KV)对实验动物模型缺血/再灌注损伤的改善作用。
雄性Wistar大鼠随机分为两组:第1组给予玉米油作为赋形剂,第2组大鼠以200mg/kg的剂量给予KV,持续4周。给大鼠喂食大鼠标准饲料颗粒并给予水。给予KV 4周后,取出心脏并安装在工作心脏灌注系统上。对冷冻的心脏样本进行蛋白质表达的蛋白质印迹分析。
与用KV预处理的组相比,对照组缺血大鼠心脏中过氧化氢酶、超氧化物歧化酶和谷胱甘肽过氧化物酶的活性显著降低(<0.05),同时氧自由基吸收能力也降低。同样,与KV预处理的大鼠相比,对照组细胞内活性氧和丙二醛显著升高。KV显著增加总Akt/蛋白激酶B(PKB)、丝氨酸473处的磷酸化Akt/PKB,并且还导致p38丝裂原活化蛋白激酶、半胱天冬酶3和裂解的聚腺苷二磷酸核糖聚合酶显著降低。
综上所述,KV通过自由基清除活性和上调生存促进途径提供了显著的心脏保护作用。