20 results on '"Viviane Caceres"'
Search Results
2. Stress-Induced Down-Regulation of Nitric Oxide Synthase in the Rat Heart
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Viviane, Caceres, primary, Ana Elisa Teófilo S de, Carvalho, additional, Daniela, Ortolani, additional, Luana Silva, Rodrigues, additional, Lila Missae, Oyama, additional, and Regina, CeliaSpadari, additional
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- 2022
- Full Text
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3. Angina due to coronary artery spasm (variant angina): diagnosis and intervention strategies
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John D. Horowitz, Viviane Caceres, Gao-Jing Ong, Yuliy Y. Chirkov, Thanh H Nguyen, Olivia Girolamo, and Armin Muminovic
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Angina Pectoris, Variant ,medicine.medical_specialty ,Spasm ,Coronary Vasospasm ,Kounis syndrome ,Coronary Angiography ,Angina Pectoris ,Pathogenesis ,Angina ,Intervention (counseling) ,Internal medicine ,Internal Medicine ,medicine ,Humans ,biology ,business.industry ,General Medicine ,medicine.disease ,Troponin ,Coronary Vessels ,Coronary arteries ,medicine.anatomical_structure ,Migraine ,biology.protein ,Cardiology ,Female ,Cardiology and Cardiovascular Medicine ,business ,Artery - Abstract
Introduction Since Prinzmetal first described a "variant" form of angina pectoris, with predominantly resting episodes of pain and cyclic severity variations, it has gradually become apparent that this clinical presentation is caused by episodes of coronary artery spasm (CAS) involving focal or diffuse changes in large and/or small coronary arteries in the presence or absence of "fixed" coronary artery stenoses. However, most clinicians have only limited understanding of this group of disorders. Areas covered We examine the clinical presentation of CAS, associated pathologies outside the coronary vasculature, impediments to making the diagnosis, provocative diagnostic tests, available and emerging treatments, and the current understanding of pathogenesis. Expert opinion CAS remains a poorly understood, often debilitating and substantially under-diagnosed condition, which occurs more frequently in women than in men, and is poorly correlated with all conventional coronary risk factors except smoking. Many patients presenting with CAS crises have non-diagnostic ECGs and normal serum troponin concentrations, but CAS can be suspected on the basis of history and association with migraine, Raynaud's phenomenon and Kounis syndrome. Definitive diagnosis requires provocative testing at coronary angiography. Treatment still centres around the use of calcium antagonists, but with greater understanding of pathogenesis, new management options are emerging.
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- 2021
4. Metabolic remodelling of glucose, fatty acid and redox pathways in the heart of type 2 diabetic mice
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Viviane Caceres, Miguel A. Aon, Sonia Cortassa, Nazareno Paolocci, Carlo G. Tocchetti, Steven J. Sollott, Michel Bernier, Rafael de Cabo, Cortassa, Sonia, Caceres, Viviane, Tocchetti, Carlo G, Bernier, Michel, de Cabo, Rafael, Paolocci, Nazareno, Sollott, Steven J, and Aon, Miguel A
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0301 basic medicine ,medicine.medical_specialty ,Physiology ,Cardiomyopathy ,Oxidative phosphorylation ,Pentose phosphate pathway ,fluxomics ,Diabetes Mellitus, Experimental ,Contractility ,Mice ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Diabetic cardiomyopathy ,medicine ,diabetic cardiomyopathy ,Animals ,Humans ,Catabolism ,Chemistry ,Myocardium ,Fatty Acids ,metabolomics ,Heart ,medicine.disease ,Citric acid cycle ,Glucose ,030104 developmental biology ,Endocrinology ,Diabetes Mellitus, Type 2 ,Heart failure ,Oxidation-Reduction ,030217 neurology & neurosurgery - Abstract
Key points Hearts from type 2 diabetic animals display perturbations in excitation-contraction coupling, impairing myocyte contractility and delaying relaxation, along with altered substrate consumption patterns. Under high glucose and β-adrenergic stimulation conditions, palmitate can, at least in part, offset left ventricle (LV) dysfunction in hearts from diabetic mice, improving contractility and relaxation while restoring coronary perfusion pressure. Fluxome calculations of central catabolism in diabetic hearts show that, in the presence of palmitate, there is a metabolic remodelling involving tricarboxylic acid cycle, polyol and pentose phosphate pathways, leading to improved redox balance in cytoplasmic and mitochondrial compartments. Under high glucose and increased energy demand, the metabolic/fluxomic redirection leading to restored redox balance imparted by palmitate helps explain maintained LV function and may contribute to designing novel therapeutic approaches to prevent cardiac dysfunction in diabetic patients. Abstract Type-2 diabetes (T2DM) leads to reduced myocardial performance, and eventually heart failure. Excessive accumulation of lipids and glucose is central to T2DM cardiomyopathy. Previous data showed that palmitate (Palm) or glutathione preserved heart mitochondrial energy/redox balance under excess glucose, rescuing β-adrenergic-stimulated cardiac excitation-contraction coupling. However, the mechanisms underlying the accompanying improved contractile performance have been largely ignored. Herein we explore in intact heart under substrate excess the metabolic remodelling associated with cardiac function in diabetic db/db mice subjected to stress given by β-adrenergic stimulation with isoproterenol and high glucose compared to their non-diabetic controls (+/+, WT) under euglycaemic conditions. When perfused with Palm, T2DM hearts exhibited improved contractility/relaxation compared to WT, accompanied by extensive metabolic remodelling as demonstrated by metabolomics-fluxomics combined with bioinformatics and computational modelling. The T2DM heart metabolome showed significant differences in the abundance of metabolites in pathways related to glucose, lipids and redox metabolism. Using a validated computational model of heart's central catabolism, comprising glucose and fatty acid (FA) oxidation in cytoplasmic and mitochondrial compartments, we estimated that fluxes through glucose degradation pathways are ∼2-fold lower in heart from T2DM vs. WT under all conditions studied. Palm addition elicits improvement of the redox status via enhanced β-oxidation and decreased glucose uptake, leading to flux-redirection away from redox-consuming pathways (e.g. polyol) while maintaining the flux through redox-generating pathways together with glucose-FA 'shared fuelling' of oxidative phosphorylation. Thus, available FAs such as Palm may help improve function via enhanced redox balance in T2DM hearts during peaks of hyperglycaemia and increased workload.
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- 2019
5. Physical activity moderates the deleterious relationship between cardiovascular disease, or its risk factors, and quality of life: Findings from two population-based cohort studies in Southern Brazil and South Australia
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Viviane Caceres, Robert J. Adams, Marco Aurélio Peres, Dandara Haag, Nigel Stocks, Karen Glazer Peres, and David Alejandro González-Chica
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Male ,Physiology ,Cross-sectional study ,lcsh:Medicine ,Blood Pressure ,Disease ,Cardiovascular Medicine ,030204 cardiovascular system & hematology ,Vascular Medicine ,Geographical locations ,Cohort Studies ,Endocrinology ,0302 clinical medicine ,Quality of life ,Risk Factors ,Medicine and Health Sciences ,030212 general & internal medicine ,lcsh:Science ,education.field_of_study ,Multidisciplinary ,Middle Aged ,humanities ,3. Good health ,Physiological Parameters ,Cardiovascular Diseases ,Research Design ,Hypertension ,Female ,Brazil ,Research Article ,Cohort study ,Adult ,medicine.medical_specialty ,Endocrine Disorders ,Oceania ,Population ,Research and Analysis Methods ,03 medical and health sciences ,Diabetes mellitus ,Diabetes Mellitus ,medicine ,Humans ,Obesity ,education ,Exercise ,Public health ,Body Weight ,lcsh:R ,Australia ,Biology and Life Sciences ,South America ,medicine.disease ,Health Care ,Cross-Sectional Studies ,Metabolic Disorders ,Quality of Life ,lcsh:Q ,People and places ,Demography - Abstract
Background Few studies have investigated the relationship between physical activity (PA) of low intensity and duration with quality of life (QoL) among individuals at risk or with cardiovascular disease (CVD). Objectives To investigate whether PA of different intensity and duration moderates the relationship between CVD and its risk factors (obesity, hypertension, diabetes, dyslipidaemia) and QoL in adults. Methods Population-based cross-sectional studies using data from the EpiFloripa Cohort Study (Southern Brazil; n = 1,220, 38.8±12.0 years, 48.2% males) and the North West Adelaide Health Study (NWAHS, South Australia; n = 1,661, 43.7±11.1 years, 49.7% males). The physical and psychological domains of QoL were assessed using the WHOQOL-Bref (EpiFloripa) or the SF-36 (NWAHS) questionnaires. The diagnosis of CVD and its risk factors were self-reported. PA was self-reported and quantified by its intensity [“walking” or moderate/vigorous (MVPA)] and duration (none, 1–150, ≥150 min/week). Both studies were analysed separately, and results were adjusted for sociodemographic variables. Results Participants at risk or with CVD from both studies showed a lower QoL than ‘healthy’ individuals with a stronger relationship for the physical domain. PA duration showed a direct-trend relationship with QoL, but the associations were stronger for MVPA in both studies. However, when stratified by health status, the magnitude of the association between “walking” duration and a higher physical QoL was greater among those at risk or with CVD compared to ‘healthy’ individuals. Conversely, among Australians with CVD, MVPA was associated with a better physical QoL only when its duration was ≥150 min/week. All associations were stronger in the NWAHS than in the Brazilian study. Conclusions “Walking” was more prevalent than MVPA and was consistently associated with a better physical QoL among those at risk or with CVD. These findings should be considered in the design of public health interventions designed to increase PA and improve QoL.
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- 2018
6. From Metabolomics to Fluxomics: A Computational Procedure to Translate Metabolite Profiles into Metabolic Fluxes
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Lauren N. Bell, Viviane Caceres, Nazareno Paolocci, Miguel A. Aon, Brian O'Rourke, and Sonia Cortassa
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Polymers ,Metabolite ,Glycogenolysis ,Biophysics ,Mice, Transgenic ,Pentose phosphate pathway ,Biology ,Inbred C57BL ,Models, Biological ,Transgenic ,Pentose Phosphate Pathway ,Tissue Culture Techniques ,Mice ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Metabolomics ,Models ,Adenosine Triphosphatases ,Animals ,Glucose ,Glycolysis ,Kinetics ,Linear Models ,Metabolome ,Mice, Inbred C57BL ,Myocardium ,NAD ,NADP ,Computer Simulation ,Fluxomics ,030304 developmental biology ,Systems Biophysics ,0303 health sciences ,Biological ,Biochemistry ,chemistry ,Metabolic control analysis ,030217 neurology & neurosurgery ,Phosphofructokinase - Abstract
We describe a believed-novel procedure for translating metabolite profiles (metabolome) into the set of metabolic fluxes (fluxome) from which they originated. Methodologically, computational modeling is integrated with an analytical platform comprising linear optimization, continuation and dynamic analyses, and metabolic control. The procedure was tested with metabolite profiles obtained from ex vivo mice Langendorff-heart preparations perfused with glucose. The metabolic profiles were analyzed using a detailed kinetic model of the glucose catabolic pathways including glycolysis, pentose phosphate (PP), glycogenolysis, and polyols to translate the glucose metabolome of the heart into the fluxome. After optimization, the ability of the model to simulate the initial metabolite profile was confirmed, and metabolic fluxes as well as the structure of control and regulation of the glucose catabolic network could be calculated. We show that the step catalyzed by phosphofructokinase together with ATP demand and glycogenolysis exert the highest control on the glycolytic flux. The negative flux control exerted by phosphofructokinase on the PP and polyol pathways revealed that the extent of glycolytic flux directly affects flux redirection through these pathways, i.e., the higher the glycolytic flux the lower the PP and polyols. This believed-novel methodological approach represents a step forward that may help in designing therapeutic strategies targeted to diagnose, prevent, and treat metabolic diseases.
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- 2015
7. Cardioprotective mechanism of S-nitroso-N-acetylcysteine via S-nitrosated betadrenoceptor-2 in the LDLr−/− mice
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Viviane Caceres, Ana Iochabel Soares Moretti, Alexandre Bruni-Cardoso, Heraldo Possolo de Souza, Regina C. Spadari, Amarylis C. B. A. Wanschel, Marta Helena Krieger, Francisco R.M. Laurindo, and Hernandes F. Carvalho
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Male ,medicine.medical_specialty ,Cancer Research ,Nitric Oxide Synthase Type III ,Ventricular hypertrophy ,Nitrogen ,Physiology ,Clinical Biochemistry ,Apoptosis ,S-nitrosated ,medicine.disease_cause ,Left ventricular hypertrophy ,Endoplasmic Reticulum ,Biochemistry ,Antioxidants ,chemistry.chemical_compound ,Mice ,Enos ,Superoxides ,Internal medicine ,Betadrenoceptor-2 ,medicine ,Animals ,Myocytes, Cardiac ,S-nitroso-N-acetylscysteine ,Dyslipidemias ,Mice, Knockout ,TUNEL assay ,biology ,Chemistry ,Superoxide ,medicine.disease ,biology.organism_classification ,Hydrogen peroxide ,Acetylcysteine ,Mice, Inbred C57BL ,Oxidative Stress ,Endocrinology ,Atheroma ,Gene Expression Regulation ,Receptors, LDL ,Hypertrophy, Left Ventricular ,Receptors, Adrenergic, beta-2 ,Reactive Oxygen Species ,Oxidative stress - Abstract
Previous studies from our group have demonstrated the protective effect of S-nitroso-N-acetylcysteine (SNAC) on the cardiovascular system in dyslipidemic LDLr−/− mice that develop atheroma and left ventricular hypertrophy after 15days on a high fat diet. We have shown that SNAC treatment attenuates plaque development via the suppression of vascular oxidative stress and protects the heart from structural and functional myocardial alterations, such as heart arrhythmia, by reducing cardiomyocyte sensitivity to catecholamines. Here we investigate the ability of SNAC to modulate oxidative stress and cell survival in cardiomyocytes during remodeling and correlation with β2-AR signaling in mediating this protection. Ventricular superoxide (O2-) and hydrogen peroxide (H2O2) generation was measured by HPLC methods to allow quantification of dihydroethidium (DHE) products. Ventricular histological sections were stained using terminal dUTP nick-end labeling (TUNEL) to identify nuclei with DNA degradation (apoptosis) and this was confirmed by Western blot for cleaved caspase-3 and caspase-7 protein expression. The findings show that O2- and H2O2 production and also cell apoptosis were increased during left ventricular hypertrophy (LVH). SNAC treatment reduced oxidative stress during on cardiac remodeling, measured by decreased H2O2 and O2- production (65% and 52%, respectively), and a decrease in the ratio of p-Ser1177 eNOS/total eNOS. Left ventricle (LV) from SNAC-treated mice revealed a 4-fold increase in β2-AR expression associated with coupling change to Gi; β2-ARs-S-nitrosation (β2-AR-SNO) increased 61%, while apoptosis decreased by 70%. These results suggest that the cardio-protective effect of SNAC treatment is primarily through its anti-oxidant role and is associated with β2-ARs overexpression and β2-AR-SNO via an anti-apoptotic pathway.
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- 2014
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8. Synthesis and Chemical and Biological Comparison of Nitroxyl- and Nitric Oxide-Releasing Diazeniumdiolate-Based Aspirin Derivatives
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Nazareno Paolocci, Julie L. Heinecke, Katrina M. Miranda, Carlos A. Velázquez-Martínez, Ryan J. Holland, Gaurav Bharadwaj, Viviane Caceres, Lisa A. Ridnour, Sa Shi, Regina Celia Spadari-Bratfisch, Robert Y.S. Cheng, David A. Wink, Debashree Basudhar, and Sarthak Jain
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Male ,Lung Neoplasms ,Cell ,Anti-Inflammatory Agents ,Pharmacology ,Inbred C57BL ,Mice ,chemistry.chemical_compound ,Models ,Carcinoma, Non-Small-Cell Lung ,Glyceraldehyde ,Drug Discovery ,Myocytes, Cardiac ,Prodrugs ,Enzyme Inhibitors ,Non-Small-Cell Lung ,Cells, Cultured ,Aspirin ,Animals ,Anti-Inflammatory Agents, Non-Steroidal ,Azo Compounds ,Cell Line, Tumor ,Cell Survival ,Cyclooxygenase 2 ,Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) ,Humans ,Mice, Inbred C57BL ,Models, Chemical ,Molecular Structure ,Nitric Oxide ,Nitrogen Oxides ,Sarcomeres ,Tumor ,Cultured ,Prodrug ,medicine.anatomical_structure ,Biochemistry ,Molecular Medicine ,Non-Steroidal ,Cardiac ,medicine.drug ,Side effect ,Cells ,Chemical ,Article ,Cell Line ,Nitric oxide ,Contractility ,medicine ,Myocytes ,Carcinoma ,Nitroxyl ,chemistry - Abstract
Structural modifications of nonsteroidal anti-inflammatory drugs (NSAIDs) have successfully reduced the side effect of gastrointestinal ulceration without affecting anti-inflammatory activity, but they may increase the risk of myocardial infarction with chronic use. The fact that nitroxyl (HNO) reduces platelet aggregation, preconditions against myocardial infarction, and enhances contractility led us to synthesize a diazeniumdiolate-based HNO-releasing aspirin and to compare it to an NO-releasing analogue. Here, the decomposition mechanisms are described for these compounds. In addition to protection against stomach ulceration, these prodrugs exhibited significantly enhanced cytotoxcity compared to either aspirin or the parent diazeniumdiolate toward nonsmall cell lung carcinoma cells (A549), but they were not appreciably toxic toward endothelial cells (HUVECs). The HNO-NSAID prodrug inhibited cylcooxgenase-2 and glyceraldehyde 3-phosphate dehydrogenase activity and triggered significant sarcomere shortening on murine ventricular myocytes compared to control. Together, these anti-inflammatory, antineoplasic, and contractile properties suggest the potential of HNO-NSAIDs in the treatment of inflammation, cancer, or heart failure.
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- 2013
9. Creatine kinase–mediated improvement of function in failing mouse hearts provides causal evidence the failing heart is energy starved
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Jason Su, Viviane Caceres, Vadappuram P. Chacko, Ashwin Akki, Michelle K. Leppo, Gary Gerstenblith, Robert G. Weiss, D. Brian Foster, Yibin Wang, Ashish Gupta, Sa Shi, Nazareno Paolocci, Jonathan A. Kirk, Charles Steenbergen, and Shenghan Lai
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medicine.medical_specialty ,Gene Expression ,Mice, Transgenic ,Adenosine Triphosphate ,Animals ,Creatine Kinase, MM Form ,Disease Models, Animal ,Dobutamine ,Energy Metabolism ,Heart Failure ,In Vitro Techniques ,Mice ,Mice, Inbred C57BL ,Myocardial Contraction ,Perfusion ,Recombinant Proteins ,Inbred C57BL ,Transgenic ,chemistry.chemical_compound ,In vivo ,Internal medicine ,medicine ,Creatine Kinase ,MM Form ,biology ,Animal ,General Medicine ,medicine.disease ,Endocrinology ,chemistry ,Heart failure ,Disease Models ,biology.protein ,Creatine kinase ,Myofibril ,Adenosine triphosphate ,Ex vivo ,Research Article ,medicine.drug - Abstract
ATP is required for normal cardiac contractile function, and it has long been hypothesized that reduced energy delivery contributes to the contractile dysfunction of heart failure (HF). Despite experimental and clinical HF data showing reduced metabolism through cardiac creatine kinase (CK), the major myocardial energy reserve and temporal ATP buffer, a causal relationship between reduced ATP-CK metabolism and contractile dysfunction in HF has never been demonstrated. Here, we generated mice conditionally overexpressing the myofibrillar isoform of CK (CK-M) to test the hypothesis that augmenting impaired CK-related energy metabolism improves contractile function in HF. CK-M overexpression significantly increased ATP flux through CK ex vivo and in vivo but did not alter contractile function in normal mice. It also led to significantly increased contractile function at baseline and during adrenergic stimulation and increased survival after thoracic aortic constriction (TAC) surgery-induced HF. Withdrawal of CK-M overexpression after TAC resulted in a significant decline in contractile function as compared with animals in which CK-M overexpression was maintained. These observations provide direct evidence that the failing heart is "energy starved" as it relates to CK. In addition, these data identify CK as a promising therapeutic target for preventing and treating HF and possibly diseases involving energy-dependent dysfunction in other organs with temporally varying energy demands.
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- 2012
10. Apoptosis status from rat heart submitted to foot shock stress
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Viviane Caceres, Daniel Araki Ribeiro, Daniela Ortolani, Viviane Carlin, and Regina Celia Spadari-Bratfisch
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medicine.medical_specialty ,Myocardial tissue ,General Medicine ,Rat heart ,Stress protocol ,Biology ,Foot shock ,Pathology and Forensic Medicine ,Stress (mechanics) ,Physical stress ,Endocrinology ,Apoptosis ,Internal medicine ,Immunology ,medicine ,Immunohistochemistry - Abstract
Background and aim: The goal of this study was to investigate whether physical stress is able to modulate apoptotic response in rat myocardial tissue. The effects of foot shock stress on the histopatological changes and immunohistochemistry for p53, bcl-2 and bax were evaluated. Methods: Male Wistar rats (n= 10) were distributed into two groups: group 1, control and group 2, stress. The stress protocol consisted of one daily foot-shock session applied on three consecutive days. Results: The results pointed out no remarkable changes of myocardial tissue between groups. Also, the foot shock stress was not able to modulate p53, bcl-2 or bax expression, as depicted by no significant statistically differences (P > 0.05) between groups for all immunomarkers evaluated. Conclusions: Taken together, our results suggest that foot shock stress did not induce histopathological changes in rat myocardial tissue. It seems that physical stress is not able to modulate apoptotic response in rats. Certainly, this finding offers new insights into the mechanisms underlying the relation between apoptosis and cardiac injury after stress.
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- 2010
11. Removal of abnormal myofilament O-GlcNAcylation restores Ca2+ sensitivity in diabetic cardiac muscle
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Junfeng Ma, Lauren R. DeVine, Luigi Marchionni, Mingguo Xu, Quira Zeidan, Genaro A. Ramirez-Correa, Nazareno Paolocci, Gerald W. Hart, Wei Dong Gao, Xiaoxu Shen, Chad Slawson, Nahyr S. Lugo-Fagundo, Anne M. Murphy, Viviane Caceres, Khalid Chakir, and Robert N. Cole
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Cardiac function curve ,Enzymologic ,Male ,Sarcomeres ,medicine.medical_specialty ,Myofilament ,Complications ,Myosin light-chain kinase ,Diabetic Cardiomyopathies ,Endocrinology, Diabetes and Metabolism ,Sarcomere ,Acetylglucosamine ,Animals ,Calcium ,Diabetes Mellitus, Experimental ,Gene Expression Regulation, Enzymologic ,Humans ,Myocardium ,Myofibrils ,Rats ,Rats, Sprague-Dawley ,beta-N-Acetylhexosaminidases ,Experimental ,Diabetic cardiomyopathy ,Internal medicine ,Internal Medicine ,medicine ,Diabetes Mellitus ,Chemistry ,Cardiac muscle ,medicine.disease ,Tropomyosin ,Endocrinology ,medicine.anatomical_structure ,Biochemistry ,Gene Expression Regulation ,Sprague-Dawley ,Myofibril - Abstract
Contractile dysfunction and increased deposition of O-linked β-N-acetyl-d-glucosamine (O-GlcNAc) in cardiac proteins are a hallmark of the diabetic heart. However, whether and how this posttranslational alteration contributes to lower cardiac function remains unclear. Using a refined β-elimination/Michael addition with tandem mass tags (TMT)–labeling proteomic technique, we show that CpOGA, a bacterial analog of O-GlcNAcase (OGA) that cleaves O-GlcNAc in vivo, removes site-specific O-GlcNAcylation from myofilaments, restoring Ca2+ sensitivity in streptozotocin (STZ) diabetic cardiac muscles. We report that in control rat hearts, O-GlcNAc and O-GlcNAc transferase (OGT) are mainly localized at the Z-line, whereas OGA is at the A-band. Conversely, in diabetic hearts O-GlcNAc levels are increased and OGT and OGA delocalized. Consistent changes were found in human diabetic hearts. STZ diabetic hearts display increased physical interactions of OGA with α-actin, tropomyosin, and myosin light chain 1, along with reduced OGT and increased OGA activities. Our study is the first to reveal that specific removal of O-GlcNAcylation restores myofilament response to Ca2+ in diabetic hearts and that altered O-GlcNAcylation is due to the subcellular redistribution of OGT and OGA rather than to changes in their overall activities. Thus, preventing sarcomeric OGT and OGA displacement represents a new possible strategy for treating diabetic cardiomyopathy.
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- 2015
12. Palmitate Re-Directs Glucose Utilization in Type 2 Diabetic Hearts, Improving Function: A Metabolomic-Fluxomic Study
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Brian O'Rourke, Viviane Caceres, Carlo G. Tocchetti, Sonia Cortassa, Nazareno Paolocci, and Miguel A. Aon
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chemistry.chemical_classification ,medicine.medical_specialty ,Glycogenolysis ,endocrine system diseases ,Glucose uptake ,Biophysics ,nutritional and metabolic diseases ,Fatty acid ,Pentose phosphate pathway ,Biology ,medicine.disease ,Randle cycle ,Endocrinology ,chemistry ,Internal medicine ,Diabetes mellitus ,medicine ,Glycolysis ,Phosphofructokinase - Abstract
Hyperglycemia and hyperlipidemia are two main traits of type-2 diabetes (T2DM). T2DM patients may develop a cardiomyopathy, and the excess in nutrients greatly contributes to systolic and diastolic dysfunction. The Randle cycle postulates that fatty acid (FA) utilization further impairs glucose utilization, impeding its oxidation. Yet recent evidence suggests that, when acutely infused, FAs such as palmitate (Palm) actually help in maintaining function in T2DM hearts stressed with high glucose and catecholamines. Thus, under conditions of sustained stress, lipids may be necessary to maintain function in stressed T2DM hearts. Using a novel procedure for translating metabolomics into metabolic fluxes, here we tested whether Palm is able to redirect the glucose fluxome in T2DM hearts, contributing to a better utilization/oxidation of glucose. We found that Palm, without inhibiting glycolysis, led to a 50% increase in glucose oxidation via the pentose phosphate [PP] pathway. Palm presence shifted the control of the glycolytic flux from phosphofructokinase to glucose uptake, glucose 6-phosphate dehydrogenase and glycogenolysis. Palm-induced remodeling of the glucose fluxome decreased the intracellular levels of glucose by 17-fold, owing to reduced uptake at maintained utilization. Moreover, it augmented the content of reduced GSH, via higher NADPH generation through the PP pathway. Our study provides a mechanistic explanation to the in vitro observation that FAs such as Palm are necessary for the T2DM hearts to maintain function when in presence of hyperglycemia and/or increased workload, by remodeling glucose utilization leading to a higher supply of reducing equivalents to the heart. Present findings suggest that in T2DM subjects the Randle cycle may apply to some but not all pathophysiological contexts.
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- 2015
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13. Evidence for two atypical conformations of beta-adrenoceptors and their interaction with Gi proteins
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Iraides Nunes dos Santos, Marilia F Moreira, Viviane Caceres, Marie Sumitame, Marta Helena Krieger, and Regina Celia Spadari-Bratfisch
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Male ,medicine.medical_specialty ,Protein Conformation ,Hydrochloride ,Adrenergic beta-Antagonists ,Propranolol ,GTP-Binding Protein alpha Subunits, Gi-Go ,In Vitro Techniques ,Pertussis toxin ,Propanolamines ,Norepinephrine (medication) ,Norepinephrine ,chemistry.chemical_compound ,Internal medicine ,Isoprenaline ,Receptors, Adrenergic, beta ,medicine ,Animals ,Sinoaortic denervation ,Heart Atria ,Rats, Wistar ,Binding site ,Pharmacology ,Denervation ,Dose-Response Relationship, Drug ,Imidazoles ,Isoproterenol ,Heart ,Adrenergic beta-Agonists ,Myocardial Contraction ,Rats ,Endocrinology ,Pertussis Toxin ,chemistry ,Receptors, Adrenergic, beta-1 ,Adrenergic alpha-Agonists ,Protein Binding ,medicine.drug - Abstract
In this study, we investigated whether the responses of right atria from sinoaortic denervated rats to CGP12177 (4(3-t-butylamino-2-hydroxypropoxy benzidimidazole-2 one, hydrochloride)), isoprenaline and norepinephrine desensitized in parallel and whether CGP12177 interacted with distinct conformations of beta-adrenoceptors. Right atria from rats 48 h after sinoaortic denervation were subsensitive to isoprenaline, norepinephrine and CGP12177. One week after sinoaortic denervation, the sensitivity to CGP12177 had recovered whereas the responses to isoprenaline and norepinephrine were still subsensitive, suggesting that the binding sites for these molecules showed independent behavior. In atria from 48 h sinoaortic-denervated rats, propranolol or 3 microM CGP20712A (2-hydroxy-5(2-((2-hydroxy-3-(4-((methyl-4-trifluormethyl)1H imidazole-2-yl)-phenoxypropyl) amino) ethoxy)-benzamide monomethane sulphonate)) blocked the responses to 10 nM-1 microM CGP12177 and steepened the curves. The concentration-response curves to CGP12177 in the presence of ICI118,551 (erythro-DL-1(-methylindan-4-yloxy)-3-isopropylamino-butan-2-ol) were biphasic, suggesting that CGP12177 interacted with at least two conformations of beta-adrenoceptors that showed negative cooperativism, one acting through beta(2)-adrenoceptor-Gi and the other via beta(1)-adrenoceptor-Gs. This hypothesis was confirmed in right atria from sinoaortic-denervated rats treated with pertussis toxin.
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- 2005
14. Early postnatal rat ventricle resection leads to long-term preserved cardiac function despite tissue hypoperfusion
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Viviane Caceres, José Cláudio Meneghetti, Juliana Sanajotti Nakamuta, Camila Zogbi, Silvana Prando, Carlos E. Rochitte, Maria Clementina Pinto Giorgi, José Eduardo Krieger, and Ana Elisa Teófilo Saturi de Carvalho
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Cardiac function curve ,Pathology ,medicine.medical_specialty ,medicine.diagnostic_test ,Physiology ,business.industry ,Connexin ,Magnetic resonance imaging ,tissue perfusion ,Stroke volume ,Lesion ,rats ,Apex resection ,medicine.anatomical_structure ,Ventricle ,cardiomyocytes neoformation ,Physiology (medical) ,Troponin I ,medicine ,hemodynamic overload ,medicine.symptom ,business ,Perfusion ,Original Research - Abstract
One‐day‐old mice display a brief capacity for heart regeneration after apex resection. We sought to examine this response in a different model and to determine the impact of this early process on long‐term tissue perfusion and overall cardiac function in response to stress. Apical resection of postnatal rats at day 1 (P1) and 7 (P7) rendered 18 ± 1.0% and 16 ± 1.3% loss of cardiac area estimated by magnetic resonance imaging (MRI), respectively (P > 0.05). P1 was associated with evidence of cardiac neoformation as indicated by Troponin I and Connexin 43 expression at 21 days postresection, while in the P7 group mainly scar tissue replacement ensued. Interestingly, there was an apparent lack of uniform alignment of newly formed cells in P1, and we detected cardiac tissue hypoperfusion for both groups at 21 and 60 days postresection using SPECT scanning. Direct basal cardiac function at 60 days, when the early lesion is undetectable, was preserved in all groups, whereas under hemodynamic stress the degree of change on LVDEP, Stroke Volume and Stroke Work indicated diminished overall cardiac function in P7 (P < 0.05). Furthermore, the End‐Diastolic Pressure–Volume relationship and increased interstitial collagen deposition in P7 is consistent with increased chamber stiffness. Taken together, we provide evidence that early cardiac repair response to apex resection in rats also leads to cardiomyocyte neoformation and is associated to long‐term preservation of cardiac function despite tissue hypoperfusion., We provide evidence that 1‐day‐old rats display early repair capacity after apex resection and this response is lost in 1‐week‐old animals similarly described for mice. The repair response is associated with long‐term preservation of overall cardiac function, despite the fact that repair is incomplete and there is tissue hypoperfusion at 21 and 60 day post injury.
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- 2014
15. HNO enhances SERCA2a activity and cardiomyocyte function by promoting redox-dependent phospholamban oligomerization
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David A. Kass, Vidhya Sivakumaran, Lufang Zhou, Sabine Huke, Brian O'Rourke, Dong I. Lee, Brian A. Stanley, Carlo G. Tocchetti, James E. Mahaney, John P. Toscano, Peter P. Rainer, Evangelia G. Kranias, Gizem Keceli, Viviane Caceres, Jeff D. Ballin, Mark T. Ziolo, Nazareno Paolocci, Gerald M. Wilson, Sivakumaran, V, Stanley, Ba, Tocchetti, CARLO GABRIELE, Ballin, Jd, Caceres, V, Zhou, L, Keceli, G, Rainer, Pp, Lee, Di, Huke, S, Ziolo, Mt, Kranias, Eg, Toscano, Jp, Wilson, Gm, O'Rourke, B, Kass, Da, Mahaney, Je, and Paolocci, N.
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Lusitropy ,Adenosine Triphosphate ,Animals ,Antioxidants ,Calcium ,Calcium Signaling ,Calcium-Binding Proteins ,Cardiotonic Agents ,Cyclic AMP-Dependent Protein Kinases ,Disulfides ,Heart Ventricles ,In Vitro Techniques ,Mice ,Mice, Knockout ,Microsomes ,Myocytes, Cardiac ,Nitrogen Oxides ,Oxidation-Reduction ,Phosphorylation ,Protein Binding ,Protein Conformation ,Protein Interaction Domains and Motifs ,Protein Multimerization ,Protein Stability ,Sarcoplasmic Reticulum ,Sarcoplasmic Reticulum Calcium-Transporting ATPases ,Physiology ,Clinical Biochemistry ,Sarcoplasm ,Biochemistry ,Sarcomere ,Myocyte ,General Environmental Science ,Phospholamban ,Cardiac ,medicine.medical_specialty ,endocrine system ,Knockout ,chemistry.chemical_element ,Contractility ,Internal medicine ,medicine ,Molecular Biology ,Myocytes ,Endoplasmic reticulum ,Cell Biology ,Forum Original Research CommunicationsNitric Oxide Effects (P. Eaton and J. Burgoyne, Eds.) ,Endocrinology ,chemistry ,Biophysics ,General Earth and Planetary Sciences - Abstract
Aims: Nitroxyl (HNO) interacts with thiols to act as a redox-sensitive modulator of protein function. It enhances sarcoplasmic reticular Ca2+ uptake and myofilament Ca2+ sensitivity, improving cardiac contractility. This activity has led to clinical testing of HNO donors for heart failure. Here we tested whether HNO alters the inhibitory interaction between phospholamban (PLN) and the sarcoplasmic reticulum Ca2+-ATPase (SERCA2a) in a redox-dependent manner, improving Ca2+ handling in isolated myocytes/hearts. Results: Ventriculocytes, sarcoplasmic reticulum (SR) vesicles, and whole hearts were isolated from control (wildtype [WT]) or PLN knockout (pln−/−) mice. Compared to WT, pln−/− myocytes displayed enhanced resting sarcomere shortening, peak Ca2+ transient, and blunted β-adrenergic responsiveness. HNO stimulated shortening, relaxation, and Ca2+ transient in WT cardiomyocytes, and evoked positive inotropy/lusitropy in intact hearts. These changes were markedly blunted in pln−/− cells/hearts. HNO enhanced SR Ca2+ uptake in WT but not pln−/− SR-vesicles. Spectroscopic studies in insect cell microsomes expressing SERCA2a±PLN showed that HNO increased Ca2+-dependent SERCA2a conformational flexibility but only when PLN was present. In cardiomyocytes, HNO achieved this effect by stabilizing PLN in an oligomeric disulfide bond-dependent configuration, decreasing the amount of free inhibitory monomeric PLN available. Innovation: HNO-dependent redox changes in myocyte PLN oligomerization relieve PLN inhibition of SERCA2a. Conclusions: PLN plays a central role in HNO-induced enhancement of SERCA2a activity, leading to increased inotropy/lusitropy in intact myocytes and hearts. PLN remains physically associated with SERCA2a; however, less monomeric PLN is available resulting in decreased inhibition of the enzyme. These findings offer new avenues to improve Ca2+ handling in failing hearts. Antioxid. Redox Signal. 19, 1185–1197.
- Published
- 2013
16. GSH or Palmitate Preserves Mitochondrial Energetic/Redox Balance, Preventing Mechanical Dysfunction in Metabolically Challenged Myocytes/Hearts From Type 2 Diabetic Mice
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Brian A. Stanley, Viviane Caceres, Walter H. Watson, Miguel A. Aon, Sonia Cortassa, Carlo G. Tocchetti, Sa Shi, Fadi G. Akar, Chaoqin Xie, Regina Celia Spadari-Bratfisch, Brian O'Rourke, Nazareno Paolocci, Tocchetti, CARLO GABRIELE, Caceres, V, Stanley, Ba, Xie, C, Shi, S, Watson, Wh, O'Rourke, B, Spadari Bratfisch, Rc, Cortassa, S, Akar, Fg, Paolocci, N, and Aon, M. A.
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Mitochondrial ROS ,medicine.medical_specialty ,Endocrinology, Diabetes and Metabolism ,Palmitates ,Type 2 diabetes ,030204 cardiovascular system & hematology ,Mitochondrion ,Biology ,Redox ,Models, Biological ,03 medical and health sciences ,chemistry.chemical_compound ,Mice ,0302 clinical medicine ,Models ,Internal medicine ,Organelle ,Diabetes Mellitus ,Internal Medicine ,medicine ,Myocyte ,Animals ,030304 developmental biology ,chemistry.chemical_classification ,0303 health sciences ,Reactive oxygen species ,Muscle Cells ,Isoproterenol ,Glutathione ,Biological ,medicine.disease ,Mitochondria ,Endocrinology ,Metabolism ,Glucose ,Diabetes Mellitus, Type 2 ,Oxidation-Reduction ,Reactive Oxygen Species ,chemistry ,Type 2 - Abstract
In type 2 diabetes, hyperglycemia and increased sympathetic drive may alter mitochondria energetic/redox properties, decreasing the organelle’s functionality. These perturbations may prompt or sustain basal low-cardiac performance and limited exercise capacity. Yet the precise steps involved in this mitochondrial failure remain elusive. Here, we have identified dysfunctional mitochondrial respiration with substrates of complex I, II, and IV and lowered thioredoxin-2/glutathione (GSH) pools as the main processes accounting for impaired state 4→3 energetic transition shown by mitochondria from hearts of type 2 diabetic db/db mice upon challenge with high glucose (HG) and the β-agonist isoproterenol (ISO). By mimicking clinically relevant conditions in type 2 diabetic patients, this regimen triggers a major overflow of reactive oxygen species (ROS) from mitochondria that directly perturbs cardiac electro-contraction coupling, ultimately leading to heart dysfunction. Exogenous GSH or, even more so, the fatty acid palmitate rescues basal and β-stimulated function in db/db myocyte/heart preparations exposed to HG/ISO. This occurs because both interventions provide the reducing equivalents necessary to counter mitochondrial ROS outburst and energetic failure. Thus, in the presence of poor glycemic control, the diabetic patient’s inability to cope with increased cardiac work demand largely stems from mitochondrial redox/energetic disarrangements that mutually influence each other, leading to myocyte or whole-heart mechanical dysfunction.
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- 2012
17. Aldose Reductase Inhibition or Activation of Transketolase Offset Adverse Metabolic Remodeling Improving Function in Type 2 Diabetes Myocytes Exposed to Hyperglycemia
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Carlo G. Tocchetti, Viviane Caceres, Miguel A. Aon, Nazareno Paolocci, and Sonia Cortassa
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Aldose reductase ,medicine.medical_specialty ,Chemistry ,Biophysics ,Oxidative phosphorylation ,Transketolase ,Pentose phosphate pathway ,Mitochondrion ,Aldose reductase inhibitor ,Endocrinology ,Benfotiamine ,Internal medicine ,cardiovascular system ,medicine ,Glycolysis ,medicine.drug - Abstract
In type 2 diabetes (T2DM), hyperglycemia (HG) and increased sympathetic drive may alter mitochondria energetic/redox properties, decreasing the organelle's functionality. These perturbations sustain basal low-cardiac performance and limited exercise capacity. We have recently reported that improving the redox/energetic balance of T2DM (db/db) murine cardiomyocytes/hearts with GSH or palmitate (Palm) preserves contractile performance under high-energy demand imposed by combined HG and β-adrenergic stimulation. To further understanding the metabolic basis of Palm salutary action, we first applied metabolomics to Langendorff-perfused T2DM murine hearts subjected to energy/redox stress conditions. In the absence of Palm, HG activates polyol pathways (sorbitol, glycerol, xylitol) triggering flux limitations in glycolytic and pentose phosphate (PP) pathways. The metabolite profile under Palm reveals that this fatty acid (FA) reverses the detrimental action of HG by decreasing polyol accumulation and increasing flux through PP, glycolytic, and beta-oxidation pathways, with a concomitant improvement in cardiomyocyte contraction. To confirm this observation, next we inhibited the polyol or activated the PP pathways. Preincubating HG+ISO-treated myocytes with the aldose reductase inhibitor Zopolrestat (1μM) improved the adrenergic inotropic response, in parallel with the re-activation of glycolysis and oxidative phosphorylation. These same effects were observed pre-incubating HG+ISO challenged myocytes with the activator of transketolase benfotiamine (50μM). Present data indicate that in T2DM hearts HG/ISO regimen unveils a status of mitochondrial dysfunction that favors adverse intracellular redox/energetic conditions and a metabolic remodeling that implies a glucose shunt to polyol pathways and an apparent blockade of glycolysis. These changes appear to be relieved by the exogenous administration of the FA Palm.
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- 2013
18. P120. S-Nitroso-N-acetylcysteine (SNAC) effects on the cardiovascular dysfunctions in the LDLr−/− mice
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Viviane Caceres, Amarylis C. B. A. Wanschel, Silvia Mika Shishido, Marta Helena Krieger, Leandro Azevedo Santos, Regina C. Spadri-Bratfisch, and José Antonio Dias Garcia
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Cancer Research ,Physiology ,Chemistry ,Clinical Biochemistry ,LDL receptor ,Pharmacology ,Biochemistry ,S-nitroso-N-acetylcysteine - Published
- 2006
19. Tu-P7:56 Atherogenesis in female LDLR-/- mice: S-nitroso-N-acetylcysteine (SNAC) effects
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Viviane Caceres, L. Dos Santos, José Antonio Dias Garcia, Silvia Mika Shishido, Marta Helena Krieger, and Amarylis C. B. A. Wanschel
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Chemistry ,LDL receptor ,Internal Medicine ,General Medicine ,Pharmacology ,Cardiology and Cardiovascular Medicine ,S-nitroso-N-acetylcysteine - Published
- 2006
20. Palmitate Improves Basal and β-Stimulated Left Ventricle Function in Diabetic Mouse Hearts
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Gabriele C. Tocchetti, Viviane Caceres, Nazareno Paolocci, Regina C. Spadari, and Miguel A. Aon
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chemistry.chemical_classification ,medicine.medical_specialty ,Chemistry ,Wild type ,Biophysics ,Fatty acid ,Stimulation ,medicine.disease_cause ,medicine.disease ,Basal (phylogenetics) ,Endocrinology ,medicine.anatomical_structure ,Ventricle ,Internal medicine ,Diabetes mellitus ,Coronary perfusion pressure ,medicine ,Oxidative stress - Abstract
The heart from a diabetic animal exhibits dysfunction when exposed to challenging energetic and tissue redox conditions. We showed that when cardiomyocytes from type-2 diabetes (db/db) mice are exposed to high glucose (HG) and β-adrenergic stimulation (via isoproterenol, ISO), these cells show blunted β-contractile reserve and increased oxidative stress. Treating these cells with the fatty acid (FA) palmitate (Palm) offsets those changes, an effect likely due to its ability of generating more reducing equivalents. Yet whether Palm infusion may benefit contractile performance and vascular tone of db/db hearts subjected to metabolic/redox stress is unclear. Using a Langendorff approach, we perfused wild type (WT) and db/db mice with HG (30mM glucose) + ISO (10nM), in absence or presence of Palm. WT hearts were infused with 0.2mM Palm and db/db ones with 0.4mM Palm to mimic higher circulating FA content in diabetic animals. Under HG, coronary perfusion pressure (CPP) was higher in db/db hearts (92±8 vs. 63±7 mmHg, p
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