首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Cytoprotective effects of DL-alpha-lipoic acid or squalene on cyclophosphamide-induced oxidative injury: An experimental study on rat myocardium, testicles and urinary bladder
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Cytoprotective effects of DL-alpha-lipoic acid or squalene on cyclophosphamide-induced oxidative injury: An experimental study on rat myocardium, testicles and urinary bladder

机译:DL-α-硫辛酸或角鲨烯对环磷酰胺引起的氧化损伤的细胞保护作用:对大鼠心肌,睾丸和膀胱的实验研究

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摘要

The present study aimed to evaluate the role of DL-alpha-lipoic acid (LA) and squalene (SQ) on oxidative cardiac, testicular and urotoxic damage induced by cyclophosphamide (CP). Male Wistar rats were divided into four groups; three groups received a single intraperitoneal injection of CP (200 mg/kg BW) to induce toxicity, and two of these groups received either LA (35 mg/kg BW) or SQ. (0.4 ml/rat) orally 7 days before and 7 days after CP injection. A vehicle-treated control group was also included. Oxidative damage was observed by decreased serum total antioxidant capacity (TAC) level and abnormal alterations in glutathione peroxidase (GPx) and glutathione reductase (GR) activities, levels of glutathi-one (GSH), malondialdehyde (MDA), nitric oxide (NO) and calcium (Ca+2) in the heart, testes and urinary bladder of CP-administered rats. Cardiac marker enzyme activities; creatine phosphokinase (CPK), lactate dehydrogenase (LDH), and aspartate transaminase (AST) showed severe declines whereas testicular markers; sorbitol dehydrogenase (SDH), Y-glutamyl transferase (y-GT), acid and alkaline phosphatases (ACP and ALP), serum testosterone (T) level and haemoglobin (Hb) absorbance were abnormal. Histopa-thological observations were also altered. These CP-induced pathological alterations were attenuated by treatment with LA or SQ, These findings highlight the efficacy of LA and SQ as cytoprotectants in CP-induced toxicity.
机译:本研究旨在评估DL-α-硫辛酸(LA)和角鲨烯(SQ)在环磷酰胺(CP)引起的氧化性心脏,睾丸和尿毒症损害中的作用。将雄性Wistar大鼠分为四组:三组接受一次腹膜内注射CP(200 mg / kg BW)诱导毒性,其中两组接受LA(35 mg / kg BW)或SQ。注射前7天和注射后7天口服(0.4 ml /大鼠)。车辆治疗对照组也包括在内。血清总抗氧化剂能力(TAC)降低,谷胱甘肽过氧化物酶(GPx)和谷胱甘肽还原酶(GR)活性,谷胱甘肽一酮(GSH),丙二醛(MDA),一氧化氮(NO)含量异常改变,从而观察到氧化损伤。 CP给药的大鼠心脏,睾丸和膀胱中的钙(Ca + 2)。心脏标记酶活性;肌酸磷酸激酶(CPK),乳酸脱氢酶(LDH)和天冬氨酸转氨酶(AST)显示出严重的下降,而睾丸标志物;山梨糖醇脱氢酶(SDH),Y-谷氨酰转移酶(y-GT),酸性和碱性磷酸酶(ACP和ALP),血清睾丸激素(T)水平和血红蛋白(Hb)吸收异常。组织形态学观察也改变了。这些CP诱导的病理改变通过LA或SQ的治疗得以减弱。这些发现强调了LA和SQ作为细胞保护剂在CP诱导的毒性中的功效。

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