Menezes-Rodrigues Francisco Sandro, Errante Paolo Ruggero, Ferreira Regiane Miranda, Tavares José Gustavo Padrão, Paula Luciana de, Araújo Erisvaldo Amarante, Govato Tânia Carmem Peñaranda, Tikazawa Eduardo Hiroshi, Reis Maria do Carmo Maia, Luna-Filho Bráulio, Ferraz Renato Ribeiro Nogueira, Oliveira-Júnior Itamar de Souza, Taha Murched Omar, Caricati-Neto Afonso
Fellow PhD degree, Postgraduate Program in Pharmacology, Universidade Federal de São Paulo (UNIFESP), Brazil. Conception and design of the study, analysis and interpretation of data, manuscript writing.
Fellow PhD degree, Postgraduate Program in Pharmacology, UNIFESP, Sao Paulo-SP, Brazil. Pharmacological assays, analysis and interpretation of data.
Acta Cir Bras. 2018 Jun;33(6):524-532. doi: 10.1590/s0102-865020180060000007.
To evaluate in vivo animal model of cardiac ischemia/reperfusion the cardioprotective activity of pancreatic lipase inhibitor of the orlistat.
Adult male Wistar rats were anesthetized, placed on mechanical ventilation and underwent surgery to induce cardiac I/R by obstructing left descending coronary artery followed by reperfusion to evaluation of ventricular arrhythmias (VA), atrioventricular block (AVB) and lethality (LET) with pancreatic lipase inhibitor orlistat (ORL). At the end of reperfusion, blood samples were collected for determination of triglycerides (TG), very low-density lipoprotein (VLDL), low-density lipoprotein (LDL), high-density lipoprotein (HDL), lactate dehydrogenase (LDH), creatine kinase (CK), and creatine kinase-MB (CK-MB).
Treatment with ORL has been able to decrease the incidence of VA, AVB and LET. Besides that, treatment with ORL reduced serum concentrations of CK and LDL, but did not alter the levels of serum concentration of TG, VLDL and HDL.
The reduction of ventricular arrhythmias, atrioventricular block, and lethality and serum levels of creatine kinase produced by treatment with orlistat in animal model of cardiac isquemia/reperfusion injury suggest that ORL could be used as an efficient cardioprotective therapeutic strategy to attenuate myocardial damage related to acute myocardial infarction.
在心脏缺血/再灌注的体内动物模型中评估奥利司他这种胰脂肪酶抑制剂的心脏保护活性。
成年雄性Wistar大鼠麻醉后,进行机械通气,并通过阻塞左冠状动脉随后再灌注来诱导心脏缺血/再灌注,以评估胰脂肪酶抑制剂奥利司他(ORL)对室性心律失常(VA)、房室传导阻滞(AVB)和致死率(LET)的影响。再灌注结束时,采集血样以测定甘油三酯(TG)、极低密度脂蛋白(VLDL)、低密度脂蛋白(LDL)、高密度脂蛋白(HDL)、乳酸脱氢酶(LDH)、肌酸激酶(CK)和肌酸激酶同工酶MB(CK-MB)。
ORL治疗能够降低VA、AVB的发生率和LET。除此之外,ORL治疗降低了CK和LDL的血清浓度,但未改变TG、VLDL和HDL的血清浓度水平。
在心脏缺血/再灌注损伤动物模型中,奥利司他治疗可降低室性心律失常、房室传导阻滞和致死率以及肌酸激酶的血清水平,这表明ORL可作为一种有效的心脏保护治疗策略,以减轻与急性心肌梗死相关的心肌损伤。