José Gustavo Padrão Tavares
Federal University of São Paulo
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Featured researches published by José Gustavo Padrão Tavares.
Archive | 2015
Regina Célia Coelho; Salety Ferreira Baracho; Vinicius Veloso de Melo; José Gustavo Padrão Tavares; Carlos Marcelo Gurjão de Godoy
Heart attack preceded by ischemia is responsible for many deaths worldwide. Thus, the detection of ischemic cardiac areas is very important not only to help the prevention of that mortal disease but also for teaching/learning purposes. This work presents the results of a new approach for ischemic region detection in rat heart photo. Such an approach is based on segmentation using “Distance Regularized Level Set Evolution” method (DRLSE). The DRLSE method is an improvement on “Level Set method”. Evolving Interfaces in geometry, fluid mechanics, computer vision and materials sciences, 1999). The advantage of DRLSE is that the restart of level set function is not necessary. It was verified that the best identification of the ischemic region was obtained by using the yellow channel image in the processing, instead of the other color channels. Results show that the present approach is able to fairly segment ischemic regions in heart photos, being suitable for teaching/learning purposes.
Acta Cirurgica Brasileira | 2018
Francisco Sandro Menezes-Rodrigues; Paolo Ruggero Errante; Regiane Miranda Ferreira; José Gustavo Padrão Tavares; Luciana de Paula; Erisvaldo Amarante de Araújo; Tânia Carmem Peñaranda Govato; Eduardo Hiroshi Tikazawa; Maria do Carmo Maia Reis; Bráulio Luna-Filho; Renato Ribeiro Nogueira FerrazI; Itamar de Souza Oliveira-Júnior; Murched Omar Taha; Afonso Caricati-Neto
PURPOSE To evaluate in vivo animal model of cardiac ischemia/reperfusion the cardioprotective activity of pancreatic lipase inhibitor of the orlistat. METHODS 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). RESULTS 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. CONCLUSION 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.
Frontiers in Cardiovascular Medicine | 2018
Carlos Marcelo Gurjão de Godoy; Ênio R. Vasques; Afonso Caricati-Neto; José Gustavo Padrão Tavares; Beatriz J. Alves; Juliana Duarte; Regiane Miranda-Ferreira; Marcelo A. Lima; Helena B. Nader; Ivarne L.S. Tersariol
Background: Blockage of the Na+/Ca2+ exchanger (NCX) is used to determine the role of NCX in arrhythmogenesis. Trisulfated heparin disaccharide (TD) and Low Molecular Weight Heparins (LMWHs) can directly interact with the NCX and accelerate its activity. Objective: In this work, we investigated the antiarrhythmic effect of heparin oligosaccharides related to the NCX activity. Methods: The effects of heparin oligosaccharides were tested on the NCX current (patch clamping) and intracellular calcium transient in rat cardiomyocytes. The effects of heparin oligosaccharides were further investigated in arrhythmia induced in isolated rat atria and rats in vivo. Results: The intracellular Ca2+ concentration decreases upon treatment with either enoxaparin or ardeparin. These drugs abolished arrhythmia induction in isolated atria. The NCX antagonist KB-R7943 abolished the enoxaparin or ardeparin antiarrhythmic effects in isolated atria. In the in vivo measurements, injection of TD 15 min both before coronary occlusion or immediately after reperfusion, significantly prevented the occurrence of reperfusion-induced arrhythmias (ventricular arrhythmia and total AV block) and reduced the lethality rate. The patch clamping experiments showed that, mechanistically, TD increases the forward mode NCX current. Conclusion: Together, the data shows that heparin oligosaccharides may constitute a new class of antiarrhythmic drug that acts by accelerating the forward mode NCX under calcium overload.
Acta Cirurgica Brasileira | 2018
José Gustavo Padrão Tavares; Paolo Ruggero Errante; Tânia Carmem Peñaranda Govato; Ênio R. Vasques; Renato Ribeiro Nogueira Ferraz; Murched Omar Taha; Francisco Sandro Menezes-Rodrigues; Afonso Caricati-Neto
PURPOSE To investigate the cardioprotective effects of ischemic preconditioning (preIC) and postconditioning (postIC) in animal model of cardiac ischemia/reperfusion. METHODS Adult rats were submitted to protocol of cardiac ischemia/reperfusion (I/R) and randomized into three experimental groups: cardiac I/R (n=33), preCI + cardiac I/R (n=7) and postCI + cardiac I/R (n=8). After this I/R protocol, the incidence of ventricular arrhythmia (VA), atrioventricular block (AVB) and lethality (LET) was evaluated using the electrocardiogram (ECG) analysis. RESULTS After reestablishment of coronary blood flow, we observed variations of the ECG trace with increased incidence of ventricular arrhythmia (VA) (85%), atrioventricular block (AVB) (79%), and increase of lethality (70%) in cardiac I/R group. The comparison between I/R + preIC group with I/R group demonstrated significant reduction in VA incidence to 28%, AVB to 0% and lethality to 14%. The comparison of I/R + postIC group with I/R group was observed significance reduction in AVB incidence to 25% and lethality to 25%. CONCLUSION The preconditioning strategies produce cardioprotection more efficient that postconditioning against myocardial dysfunctions and lethality by cardiac ischemia and reperfusion.
Journal of Molecular Imaging | 2017
José Gustavo Padrão Tavares; Francisco S; ro Menezes-Rodrigues; Ênio R. Vasques; Maria do Carmo Maia Reis; Luciana de Paula; Bráulio Luna-Filho; Paolo Ruggero Errante; Afonso Caricati-Neto; Le; ro Bueno Bergantin
To study cardioprotective drugs, we developed a simple and efficient methodology to evaluate effects of drugs on cardiac electrical activity using electrocardiogram (ECG) in rats submitted to cardiac ischemia-reperfusion (I/R). Using adult male Wistar rats (14 - 16-week-old) anesthetized (urethane 1.25 g/kg, i.p.) and kept under mechanical ventilation, we used surgical procedures to induce cardiac I/R by means mechanical occlusion of left anterior descendent coronary artery for 10 min (ischemia) with silk suture (tourniquet) followed by its removal to allow coronary recirculation (reperfusion). To evaluate the effects of surgical process, a group of rats (SHAM-operated) was submitted to surgical procedures previously described, but without coronary occlusion. To evaluate cardiac electrical activity in rats submitted to cardiac I/R and SHAM-operated, the ECG system was coupled to animal body to determine the incidence of ventricular arrhythmia (VA), atrio-ventricular blockade (AVB) and lethality (LET). To evaluate injury biomarkers production in rats submitted to cardiac I/R and SHAM-operated, serum concentrations of creatine kinase fraction (MB/CK-MB) and troponin I were determined by biochemical techniques. Using the methodology proposed in this work, we observed that VA, AVB and LET incidence was significantly higher in cardiac I/R group (85%, 79% and 70%, respectively) than in SHAM-operated group (0%, 0% and 0%, respectively). Serum levels of CK-MB and troponin I were also significantly higher in cardiac I/R (1,850 ± 222 U/L and 0.031 ± 0.009 ng/mL, respectively) compared to SHAM-operated group (808 ± 72 U/L and 0.200 ± 0.027 ng/mL). To evaluate efficiency of methodology proposed in this work to study the effect of cardioprotective drugs, the effects of the L-type Ca2+ channel blocker (CCB) nifedipine (30 mg/kg, intravenously - IV) in rats submitted to cardiac I/R were studied. The treatment with nifedipine (before ischemia) significantly reduced the incidence of VA (from 85% to 28%), AVB (from 79% to 14%), and LET (from 70% to 14%). These results indicate that the methodology described in the present work is simple, and efficient, to evaluate cardiac functional and biochemical alterations induced by cardiac I/R, and also the study of cardioprotective drugs in rats. This methodology could contribute to the development of new pharmacological cardioprotective strategies for to treatment of ischemic cardiac diseases in humans, such as myocardial infarction.
Archive | 2013
José Gustavo Padrão Tavares; Afonso Caricati-Neto; S. Cukierman; Carlos Marcelo Gurjão de Godoy
It has been showed, in Langendorff preparation of rat hearts, that the depression of cardiac parameters were importantly mediated by substances released by the own heart in the perfusate (low volume- 100 ml; closed circulation). In this study we tested if electric stimulation (ES) would reverse such a cardiac depression. Three physiological parameters of rat isolated hearts were quantified: cardiac frequency, left ventricular pressure and cardiac perfusion flow. The results showed that it is possible to partially reverse cardiac depressing functionality by renewing perfusate while using 10 min of cardiac arrest by ES. However, ES alone is not enough to prevent the decay on cardiac parameters.
Journal of Thrombosis and Circulation: Open Access | 2017
Francisco S; ro Menezes-Rodrigues; José Gustavo Padrão Tavares; Erisvaldo Amarante de Araújo; Luciana de Paula; Paolo Ruggero Errante; Afonso Caricati-Neto; Le; ro Bueno Bergantin
Journal of Thrombosis and Circulation: Open Access | 2017
Francisco Sandro Menezes-Rodrigues; José Gustavo Padrão Tavares; Paolo Ruggero Errante; Ênio R. Vasques; Maria do Carmo Maia Reis; Bráulio Luna-Filho; Fulvio A. Scorza; Afonso Caricati-Neto; Leandro Bueno Bergantin
Revista de Pesquisa e Inovação Farmacêutica | 2015
Paolo Ruggero Errante; Francisco Sandro Menezes-Rodrigues; José Gustavo Padrão Tavares; Maria do Carmo Maia Reis; Marcelo Y. Icimoto; Renato Ribeiro Nogueira Ferraz; Afonso Caricati-Neto
Revista de Pesquisa e Inovação Farmacêutica | 2015
Francisco Sandro Menezes Rodrigues; Marcelo Akira Yasuda; Luciana de Paula; Diego Castro Musial; Guilherme Henrique Souza Bomfim; José Gustavo Padrão Tavares; Edney Posteral Silva Lima; Regiane Miranda-Ferreira; Paolo Ruggero Errante; Afonso Caricati-Neto