Department of Pharmacology, Toxicology and Pharmacotherapy, Faculty of Pharmacy, Medical University "Prof. Dr. Paraskev Stoyanov", Varna 9000, Bulgaria.
Department of Biology, Faculty of Pharmacy, Medical University "Prof. Dr. Paraskev Stoyanov", Varna 9000, Bulgaria.
Biomed Res Int. 2020 Aug 11;2020:4018412. doi: 10.1155/2020/4018412. eCollection 2020.
is an anthracycline antibiotic that is used for the treatment of various types of cancer. However, its clinical usage is limited due to its potential life-threatening adverse effects, such as cardio- and nephrotoxicities. Nonetheless, simultaneous administration of and antioxidants, such as those found in leaves, could reduce cardiac and renal tissue damage caused by oxidative stress. The methylxanthine fraction isolated from leaves were tested for its antioxidant activity and for its organoprotective properties against -induced cardio- and nephrotoxicities in a rat model. The study was conducted on male Wistar rats divided into 6 groups. Methylxanthines were administered at high (5 mg/kg body weight) and low (1 mg/kg body weight) doses, while doxorubicin was administered at a cumulative dose of 20 mg/kg body weight. Serum creatinine, uric acid, and urea concentrations, as well as serum enzyme levels (creatinine kinase (CK), creatinine kinase MB fraction (CK-MB), aspartate aminotransferase (AST), and lactate dehydrogenase (LDH)) and electrolytes (Na, K, and Cl), were analysed. In addition, histological analysis was performed to assess cardiac and renal tissue damage. The concomitant administration of methylxanthines and showed a dose-dependent reduction in the serum biochemical parameters, indicating a decrease in the cardiac and renal tissue damage caused by the antibiotic. Histological analysis showed that pretreatment with methylxanthines at the dose of 5 mg/kg resulted in an almost normal myocardial structure and a significant decrease in the morphological kidney changes caused by exposure compared with the group that received alone. The putative mechanism is most likely related to a reduction in the oxidative stress caused by doxorubicin.
是一种蒽环类抗生素,用于治疗各种类型的癌症。然而,由于其潜在的危及生命的不良反应,如心脏毒性和肾毒性,其临床应用受到限制。尽管如此,同时给予 和抗氧化剂,如 叶中的抗氧化剂,可减少氧化应激引起的心脏和肾脏组织损伤。从 叶中分离出的甲基黄嘌呤部分被测试其抗氧化活性和对 -诱导的心脏和肾脏毒性的器官保护特性在大鼠模型中。该研究在雄性 Wistar 大鼠上进行,分为 6 组。给予甲基黄嘌呤高(5mg/kg 体重)和低(1mg/kg 体重)剂量,而阿霉素累积剂量为 20mg/kg 体重。分析血清肌酐、尿酸和尿素浓度以及血清酶水平(肌酸激酶(CK)、肌酸激酶 MB 部分(CK-MB)、天冬氨酸氨基转移酶(AST)和乳酸脱氢酶(LDH))和电解质(Na、K 和 Cl)。此外,进行组织学分析以评估心脏和肾脏组织损伤。同时给予 甲基黄嘌呤和 表现出剂量依赖性降低血清生化参数,表明抗生素引起的心脏和肾脏组织损伤减少。组织学分析表明,与单独接受 组相比,5mg/kg 剂量的甲基黄嘌呤预处理导致心肌结构几乎正常,并且暴露于 引起的形态学肾脏变化显著减少。其可能的机制很可能与减少阿霉素引起的氧化应激有关。