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Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 2015, Volume 84, pp. 24 - 35
Abstract Unresolved inflammation is a major contributor to the development of heart failure following myocardial infarction (MI). Pro-resolving lipid... 
Cardiovascular | Myocardial infarction | Splenic remodeling | Resolution of inflammation | Metabololipidomics | Resolvin D1 | Neutrophils | SURVIVAL | CHRONIC HEART-FAILURE | PROTECTIVE ACTIONS | CARDIAC & CARDIOVASCULAR SYSTEMS | RESOLUTION | TISSUE | RECEPTOR | LIPID MEDIATORS | CELL BIOLOGY | THERAPY | PATHWAY | DISEASE | Cell Count | Male | Myocardial Infarction - diagnostic imaging | Spleen - drug effects | Extracellular Matrix - genetics | Inflammation - complications | Pulmonary Edema - physiopathology | Inflammation - drug therapy | Pulmonary Edema - complications | Receptors, Formyl Peptide - metabolism | Ultrasonography | Myocardial Infarction - physiopathology | Cell Polarity - drug effects | Spleen - pathology | Neutrophil Infiltration - drug effects | Ventricular Function - drug effects | Docosahexaenoic Acids - therapeutic use | Arachidonate 5-Lipoxygenase - metabolism | Docosahexaenoic Acids - chemistry | Extracellular Matrix - drug effects | Mice, Inbred C57BL | Cardiomegaly - diagnostic imaging | Cardiomegaly - drug therapy | Cardiomegaly - physiopathology | Pulmonary Edema - drug therapy | Cardiomegaly - complications | Collagen - metabolism | Docosahexaenoic Acids - pharmacology | Myocardial Infarction - complications | Macrophages - metabolism | Animals | Myocardial Infarction - drug therapy | Heart Ventricles - physiopathology | Prostaglandin-Endoperoxide Synthases - metabolism | Macrophages - drug effects | Ventricular Remodeling - drug effects | Heart Ventricles - drug effects | Inflammation | Heart attack | metabololipidomics | liposomes | myocardial infarction | splenic remodeling | neutrophils | resolution of inflammation
Journal Article
Journal Article
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2012, Volume 59, Issue 8, pp. 751 - 763
Objectives This study evaluated the use of an injectable hydrogel derived from ventricular extracellular matrix (ECM) for treating myocardial infarction (MI)... 
Cardiovascular | Internal Medicine | heart failure | biomaterial | scaffold | extracellular matrix | myocardial infarction | STEM-CELLS | CARDIAC & CARDIOVASCULAR SYSTEMS | MYOCARDIAL-INFARCTION | HEART-FAILURE | SKELETAL MYOBLASTS | TISSUE | FIBROBLAST-GROWTH-FACTOR | MARROW-CELL TRANSPLANTATION | DISEASE | AUTOLOGOUS MYOBLAST TRANSPLANTATION | INTRACORONARY INJECTION | Immunohistochemistry | Follow-Up Studies | Recovery of Function - drug effects | Catheterization - methods | Cell Count | Rats | Magnetic Resonance Imaging, Cine | Myocardial Infarction - metabolism | Rats, Sprague-Dawley | Extracellular Matrix - chemistry | Myocytes, Cardiac - pathology | Injections | Animals | Hydrogel, Polyethylene Glycol Dimethacrylate - administration & dosage | Myocardial Infarction - drug therapy | Swine | Myocardial Infarction - pathology | Myocytes, Cardiac - metabolism | Female | Heart Ventricles - metabolism | Heart Ventricles - pathology | Disease Models, Animal | Hydrogel, Polyethylene Glycol Dimethacrylate - metabolism | Ventricular Function - drug effects | Heart failure | Biological products | Surface active agents | Electrocardiogram | Electrocardiography | Liquid chromatography | Sulfates | Mass spectrometry | Chromatography | Heart | Medical colleges | Heart attack | Heart attacks | Nuclear magnetic resonance--NMR | Peptides | Hydrogels | Tissue engineering | Cardiomyocytes | Studies | Biomedical materials | Acids | Rodents | Extracellular matrix | Laboratory animals
Journal Article
Journal Article
Journal Article
British Journal of Pharmacology, ISSN 0007-1188, 10/2017, Volume 174, Issue 19, pp. 3302 - 3314
Background and Purpose In cor pulmonale, the increased afterload imposed on the right ventricle (RV) generates a maladaptive response, impairing the... 
SPRAGUE-DAWLEY RATS | DOSE-ESCALATION | PRESSURE-OVERLOAD | CONCISE GUIDE | HEART-FAILURE | ARTERIAL-HYPERTENSION | ENDOTHELIAL-CELLS | IN-VIVO | PHARMACOLOGY & PHARMACY | INDUCED CARDIAC-HYPERTROPHY | AQUEOUS SOLUBILITY | Liver - pathology | 2-Hydroxypropyl-beta-cyclodextrin - pharmacology | Rats, Wistar | Stilbenes - therapeutic use | Monocrotaline | NADPH Oxidases - metabolism | Hypertension, Pulmonary - physiopathology | Systole - drug effects | Male | Stilbenes - chemistry | Stilbenes - pharmacology | Liver - drug effects | Hypertension, Pulmonary - drug therapy | Superoxide Dismutase - metabolism | Ventricular Function - drug effects | Glutathione Peroxidase - metabolism | Lung - pathology | Echocardiography | Hypertension, Pulmonary - metabolism | Catalase - metabolism | Animals | Cardiomegaly - prevention & control | 2-Hydroxypropyl-beta-cyclodextrin - chemistry | Lung - drug effects | 2-Hydroxypropyl-beta-cyclodextrin - therapeutic use | Heart Ventricles - metabolism | Oxidative Stress - drug effects | Hypertension, Pulmonary - pathology | Heart Ventricles - drug effects | Prevention | Oxidases | Antioxidants | Heart | Oxidative stress | Cor pulmonale | Superoxide | Cyclodextrins | Pulmonary hypertension | Hypertrophy | Hypertension | Contractility | Bioavailability | Muscle contraction | NAD(P)H oxidase | Cyclodextrin | Anions | Rodents | Ventricle | Superoxide anions | Heart diseases | Research Papers | Research Paper
Journal Article
PLoS ONE, ISSN 1932-6203, 2009, Volume 4, Issue 12, p. e8443
Background: Differentiation of human embryonic stem cells into endothelial cells (hESC-ECs) has the potential to provide an unlimited source of cells for novel... 
PROGENITOR CELLS | SURVIVAL | MORPHOGENESIS | MULTIDISCIPLINARY SCIENCES | CORD BLOOD | ISCHEMIA | EXTRACELLULAR-MATRIX | PERIPHERAL-BLOOD | CARDIOMYOCYTES | NEOVASCULARIZATION | TRANSPLANTATION | Embryo, Mammalian - drug effects | Embryonic Stem Cells - metabolism | Neovascularization, Physiologic - drug effects | Transcription, Genetic - drug effects | Embryonic Stem Cells - cytology | Oligonucleotide Array Sequence Analysis | Recovery of Function - drug effects | Humans | Endothelial Cells - transplantation | Myocardial Contraction - drug effects | Gene Expression Profiling | Tissue Survival - drug effects | Embryo, Mammalian - metabolism | Stem Cell Transplantation | Cell Differentiation - genetics | Myocardial Infarction - therapy | Myocardial Infarction - pathology | Polymerase Chain Reaction | Female | Myocardial Infarction - physiopathology | Collagen - pharmacology | Cell Line | Cell Survival - drug effects | Reproducibility of Results | Endothelial Cells - metabolism | Embryo, Mammalian - blood supply | Ventricular Function, Left - drug effects | Mice, SCID | Gene Expression Regulation - drug effects | Animals | Embryonic Stem Cells - drug effects | Cell Differentiation - drug effects | Endothelial Cells - cytology | Mice | Endothelial Cells - drug effects | Stem cells | Genetic aspects | Transplantation | Genetic transcription | Embryonic stem cells | Heart attack | Endothelium | Myocardial infarction | Heart | Cell culture | Therapy | Transcription | Embryo cells | Stem cell transplantation | Cardiovascular disease | Genomes | Angiogenesis | Allografts | Ischemia | Cell fate | Fibroblasts | Bone marrow | Extracellular matrix | Cardiology | Heart diseases | Cytokines | Developmental biology | Blood vessels | Cardiomyocytes | Embryo fibroblasts | Embryos | Coronary artery disease | Endothelial cells | Medicine | DNA microarrays | Collagen | Infarction | In vivo methods and tests | Umbilical cord | Differentiation | Umbilical vein | Apoptosis
Journal Article
Journal Article
Journal Article
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 2015, Volume 309, Issue 9, pp. H1579 - H1590
Vagal nerve stimulation (VNS) has been shown to have antiarrhythmic effects, but many of these benefits were demonstrated in the setting of vagal nerve... 
Electrophysiology | Parasympathetic | Afferent cardiac neurotransmission | Vagotomy | VAGUS NERVE | ARRHYTHMIAS | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | afferent cardiac neurotransmission | BAROREFLEX SENSITIVITY | vagotomy | VENTRICULAR-FIBRILLATION | RECOVERY INTERVALS | REPERFUSION INJURY | parasympathetic | electrophysiology | HEART-RATE-VARIABILITY | ACUTE MYOCARDIAL-INFARCTION | PERIPHERAL VASCULAR DISEASE | MODULATION | RABBIT HEART | Ventricular Function - physiology | Efferent Pathways - physiology | Heart - physiology | Male | Hemodynamics - physiology | Vagus Nerve Stimulation | Heart Rate - drug effects | Swine | Heart Rate - physiology | Female | Parasympathetic Nervous System - physiology | Action Potentials - drug effects | Heart - innervation | Ventricular Function - drug effects | Atropine - pharmacology | Vagus Nerve - surgery | Parasympatholytics - pharmacology | Action Potentials - physiology | Vagus Nerve - physiology | Animals | Afferent Pathways - physiology | Parasympathetic Nervous System - drug effects | Heart - drug effects | Heart Ventricles - innervation | Hemodynamics - drug effects | Sus scrofa | Heart Ventricles - drug effects | Usage | Analysis | Anti-arrhythmia drugs | Influence | Vagus nerve stimulation | Neural transmission | Research | Integrative Cardiovascular Physiology and Pathophysiology
Journal Article