The Journal of Physiology, ISSN 0022-3751, 05/2013, Volume 591, Issue 9, pp. 2287 - 2306
Key points • Acid extrusion from ventricular myocytes typically occurs via Na+/H+ exchange (NHE1) and Na+–HCO3− co‐transporters (NBC). This maintains...
PROTON MOBILITY | CELLS | PHYSIOLOGY | CA2 | CARDIAC MYOCYTES | HEART-FAILURE | ACIDOSIS | H+-ION MOBILITY | GUINEA-PIG | SARCOPLASMIC-RETICULUM | NA+-HCO3-COTRANSPORTER | NEUROSCIENCES | Guinea Pigs | Sarcolemma - physiology | Rats | Male | Rats, Sprague-Dawley | Sodium-Bicarbonate Symporters - metabolism | Sodium-Hydrogen Exchangers - metabolism | Heart Ventricles | Animals | Calcium - physiology | Myocytes, Cardiac - physiology | Electric Capacitance | Female | Hydrogen-Ion Concentration | Acids | Localization | Rodents | Cardiovascular
PROTON MOBILITY | CELLS | PHYSIOLOGY | CA2 | CARDIAC MYOCYTES | HEART-FAILURE | ACIDOSIS | H+-ION MOBILITY | GUINEA-PIG | SARCOPLASMIC-RETICULUM | NA+-HCO3-COTRANSPORTER | NEUROSCIENCES | Guinea Pigs | Sarcolemma - physiology | Rats | Male | Rats, Sprague-Dawley | Sodium-Bicarbonate Symporters - metabolism | Sodium-Hydrogen Exchangers - metabolism | Heart Ventricles | Animals | Calcium - physiology | Myocytes, Cardiac - physiology | Electric Capacitance | Female | Hydrogen-Ion Concentration | Acids | Localization | Rodents | Cardiovascular
Journal Article
Scientific Reports, ISSN 2045-2322, 10/2016, Volume 6, Issue 1, p. 35475
Puerarin, a known isoflavone, is commonly found as a Chinese herb medicine. It is widely used in China to treat cardiac diseases such as angina, cardiac...
CELLS | MYOCARDIAL-INFARCTION | MULTIDISCIPLINARY SCIENCES | BAICALIN | IMPROVES CARDIAC-FUNCTION | GUINEA-PIG | MESENTERIC-ARTERY | UNSTABLE ANGINA-PECTORIS | I-KS | POTASSIUM CHANNEL | KCNQ1 MUTATION | Cyclic AMP-Dependent Protein Kinases - metabolism | Heart Ventricles - cytology | Vasodilator Agents - pharmacology | Isoflavones - pharmacology | Rats | Dose-Response Relationship, Drug | Animals | Signal Transduction - drug effects | Adenosine Diphosphate - metabolism | Potassium Channels, Inwardly Rectifying - metabolism | Action Potentials - drug effects | Heart Ventricles - drug effects | Ventricular Function - drug effects | Protein kinase A | Arrhythmia | Potassium channels (inwardly-rectifying) | Cardiac muscle | Action potential | Angina | Myocytes | Velocity | Coronary artery disease | Depolarization | Rodents | Potassium channels (voltage-gated) | Infarction | Membrane potential | Ventricle | Cardiovascular diseases | Heart diseases | Isoflavones
CELLS | MYOCARDIAL-INFARCTION | MULTIDISCIPLINARY SCIENCES | BAICALIN | IMPROVES CARDIAC-FUNCTION | GUINEA-PIG | MESENTERIC-ARTERY | UNSTABLE ANGINA-PECTORIS | I-KS | POTASSIUM CHANNEL | KCNQ1 MUTATION | Cyclic AMP-Dependent Protein Kinases - metabolism | Heart Ventricles - cytology | Vasodilator Agents - pharmacology | Isoflavones - pharmacology | Rats | Dose-Response Relationship, Drug | Animals | Signal Transduction - drug effects | Adenosine Diphosphate - metabolism | Potassium Channels, Inwardly Rectifying - metabolism | Action Potentials - drug effects | Heart Ventricles - drug effects | Ventricular Function - drug effects | Protein kinase A | Arrhythmia | Potassium channels (inwardly-rectifying) | Cardiac muscle | Action potential | Angina | Myocytes | Velocity | Coronary artery disease | Depolarization | Rodents | Potassium channels (voltage-gated) | Infarction | Membrane potential | Ventricle | Cardiovascular diseases | Heart diseases | Isoflavones
Journal Article
Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 2014, Volume 76, pp. 265 - 274
Abstract Mechanical stretch of cardiac muscle modulates action potential propagation velocity, causing potentially arrhythmogenic conduction slowing. The...
Cardiovascular | Cardiac mechanoelectric feedback | Caveolae | Capacitance | CARDIAC & CARDIOVASCULAR SYSTEMS | PRIMARY CULTURE | MEMBRANE | CARDIAC MYOCYTES | TISSUE | GUINEA-PIG | CARDIOMYOCYTES | CELL-CULTURES | CELL BIOLOGY | MUSCLE FIBERS | IN-VITRO MODEL | SURFACE | Heart Ventricles - cytology | Caveolin 3 - genetics | Heart Conduction System | Mice, Inbred C57BL | Cells, Cultured | Ventricular Function | Caveolae - physiology | Mice, Knockout | Action Potentials | Mechanotransduction, Cellular | Patch-Clamp Techniques | Animals | Myocytes, Cardiac - physiology | Ventricular Pressure | Caveolin 3 - metabolism | Myocytes, Cardiac - ultrastructure | Sarcolemma - metabolism | Cyclodextrins | cardiac mechanoelectric feedback | caveolae | capacitance
Cardiovascular | Cardiac mechanoelectric feedback | Caveolae | Capacitance | CARDIAC & CARDIOVASCULAR SYSTEMS | PRIMARY CULTURE | MEMBRANE | CARDIAC MYOCYTES | TISSUE | GUINEA-PIG | CARDIOMYOCYTES | CELL-CULTURES | CELL BIOLOGY | MUSCLE FIBERS | IN-VITRO MODEL | SURFACE | Heart Ventricles - cytology | Caveolin 3 - genetics | Heart Conduction System | Mice, Inbred C57BL | Cells, Cultured | Ventricular Function | Caveolae - physiology | Mice, Knockout | Action Potentials | Mechanotransduction, Cellular | Patch-Clamp Techniques | Animals | Myocytes, Cardiac - physiology | Ventricular Pressure | Caveolin 3 - metabolism | Myocytes, Cardiac - ultrastructure | Sarcolemma - metabolism | Cyclodextrins | cardiac mechanoelectric feedback | caveolae | capacitance
Journal Article
Cardiovascular Research, ISSN 0008-6363, 2/2010, Volume 85, Issue 3, pp. 454 - 463
Aims Calmodulin (CaM) regulates Na+ channel gating through binding to an IQ-like motif in the C-terminus. Ca2+/CaM-dependent protein kinase II (CaMKII)...
MOLECULAR-MECHANISM | BETA-ADRENERGIC STIMULATION | CARDIAC & CARDIOVASCULAR SYSTEMS | Calcium | ALPHA-SUBUNIT | Na-channel | CAMKII | CARDIAC SODIUM-CHANNEL | EXCITABILITY | CA2 | Calmodulin | MODULATION | Ca2+/CaM-dependent protein kinase II | Action Potentials | Calmodulin - physiology | Cyclic AMP-Dependent Protein Kinases - physiology | Ion Channel Gating - physiology | Phosphorylation | Animals | Calcium - physiology | Guinea Pigs | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - physiology | Sodium Channels - physiology | CaM-dependent protein kinase II | Ca2 | Original
MOLECULAR-MECHANISM | BETA-ADRENERGIC STIMULATION | CARDIAC & CARDIOVASCULAR SYSTEMS | Calcium | ALPHA-SUBUNIT | Na-channel | CAMKII | CARDIAC SODIUM-CHANNEL | EXCITABILITY | CA2 | Calmodulin | MODULATION | Ca2+/CaM-dependent protein kinase II | Action Potentials | Calmodulin - physiology | Cyclic AMP-Dependent Protein Kinases - physiology | Ion Channel Gating - physiology | Phosphorylation | Animals | Calcium - physiology | Guinea Pigs | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - physiology | Sodium Channels - physiology | CaM-dependent protein kinase II | Ca2 | Original
Journal Article
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 07/2010, Volume 299, Issue 1, pp. H36 - H45
Farrell SR, Ross JL, Howlett SE. Sex differences in mechanisms of cardiac excitation-contraction coupling in rat ventricular myocytes. Am J Physiol Heart Circ...
Calcium transients | Gender | Calcium release | Calcium sparks | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | gender | SUPINE EXERCISE | GUINEA-PIG | GENDER-RELATED DIFFERENCES | calcium transients | REPOLARIZATION | INTRACELLULAR CA2 | HEART | FEMALE RATS | calcium release | PERIPHERAL VASCULAR DISEASE | calcium sparks | PROTEIN-KINASE-II | AGE | Myocardial Contraction | Excitation Contraction Coupling | Rats, Inbred F344 | Rats | Male | Action Potentials | Microscopy, Confocal | Animals | Sex Factors | Myocytes, Cardiac - metabolism | Female | Heart Ventricles - metabolism | Sarcoplasmic Reticulum - metabolism | Kinetics | In Vitro Techniques | Calcium Signaling | Heart | Excitation (Physiology) | Demographic aspects | Comparative analysis | Contraction
Calcium transients | Gender | Calcium release | Calcium sparks | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | gender | SUPINE EXERCISE | GUINEA-PIG | GENDER-RELATED DIFFERENCES | calcium transients | REPOLARIZATION | INTRACELLULAR CA2 | HEART | FEMALE RATS | calcium release | PERIPHERAL VASCULAR DISEASE | calcium sparks | PROTEIN-KINASE-II | AGE | Myocardial Contraction | Excitation Contraction Coupling | Rats, Inbred F344 | Rats | Male | Action Potentials | Microscopy, Confocal | Animals | Sex Factors | Myocytes, Cardiac - metabolism | Female | Heart Ventricles - metabolism | Sarcoplasmic Reticulum - metabolism | Kinetics | In Vitro Techniques | Calcium Signaling | Heart | Excitation (Physiology) | Demographic aspects | Comparative analysis | Contraction
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 11/2013, Volume 288, Issue 44, pp. 31984 - 31992
The cardiac Na+/Ca2+ exchanger (NCX) is the major Ca2+ efflux pathway on the sarcolemma, counterbalancing Ca2+ influx via L-type Ca2+ current during...
CELLS | ISCHEMIA/REPERFUSION INJURY | SELECTIVE INHIBITOR | DEPENDENT REGULATION | SODIUM-CALCIUM EXCHANGER | INDUCED HEART-FAILURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC SARCOLEMMAL VESICLES | NA+-CA2+ EXCHANGER | RAT-HEART | EXPRESSION | Guinea Pigs | Oxidation-Reduction | Calcium - metabolism | NADPH Oxidases - antagonists & inhibitors | Cells, Cultured | Enzyme Inhibitors - pharmacology | NADPH Oxidases - metabolism | Onium Compounds - pharmacology | Glycoproteins - pharmacology | Hydrogen Peroxide - metabolism | Catalase - metabolism | Myocardial Reperfusion Injury - metabolism | Myocytes, Cardiac - pathology | Myocardial Reperfusion Injury - pathology | Animals | Sodium-Calcium Exchanger - metabolism | Myocytes, Cardiac - metabolism | Heart Ventricles - metabolism | Homeostasis - drug effects | Heart Ventricles - pathology | NAD - metabolism | Sodium Calcium Exchange | NADH | Reactive Oxygen Species (ROS) | Ischemia | Membrane Biology | Excitation-Contraction Coupling | Metabolism
CELLS | ISCHEMIA/REPERFUSION INJURY | SELECTIVE INHIBITOR | DEPENDENT REGULATION | SODIUM-CALCIUM EXCHANGER | INDUCED HEART-FAILURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC SARCOLEMMAL VESICLES | NA+-CA2+ EXCHANGER | RAT-HEART | EXPRESSION | Guinea Pigs | Oxidation-Reduction | Calcium - metabolism | NADPH Oxidases - antagonists & inhibitors | Cells, Cultured | Enzyme Inhibitors - pharmacology | NADPH Oxidases - metabolism | Onium Compounds - pharmacology | Glycoproteins - pharmacology | Hydrogen Peroxide - metabolism | Catalase - metabolism | Myocardial Reperfusion Injury - metabolism | Myocytes, Cardiac - pathology | Myocardial Reperfusion Injury - pathology | Animals | Sodium-Calcium Exchanger - metabolism | Myocytes, Cardiac - metabolism | Heart Ventricles - metabolism | Homeostasis - drug effects | Heart Ventricles - pathology | NAD - metabolism | Sodium Calcium Exchange | NADH | Reactive Oxygen Species (ROS) | Ischemia | Membrane Biology | Excitation-Contraction Coupling | Metabolism
Journal Article
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 03/2012, Volume 302, Issue 5, pp. H1023 - H1030
O'Hara T, Rudy Y. Quantitative comparison of cardiac ventricular myocyte electrophysiology and response to drugs in human and nonhuman species. Am J Physiol...
Cardiac action potential | Drug effects | Delayed rectifier current | Human cardiac model | RATE-DEPENDENCE | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | HEART-FAILURE | drug effects | human cardiac model | QT INTERVAL | GUINEA-PIG | MODEL | I-KS | REPOLARIZATION | ACTION-POTENTIAL DURATION | delayed rectifier current | PERIPHERAL VASCULAR DISEASE | cardiac action potential | ION CHANNELS | CANINE | Guinea Pigs | Sodium-Potassium-Exchanging ATPase - physiology | Ventricular Function - physiology | Models, Cardiovascular | Humans | Adrenergic beta-Agonists - pharmacology | Sodium - metabolism | Action Potentials - physiology | Animals | Myocytes, Cardiac - drug effects | Delayed Rectifier Potassium Channels - physiology | Myocytes, Cardiac - physiology | Computer Simulation | Isoproterenol - pharmacology | Dogs | Cardiac Electrophysiology | Sodium - physiology | Action Potentials - drug effects | Ventricular Function - drug effects | Drugs | Heart ventricles | Physiological aspects | Electrophysiology | Muscle cells | Comparative analysis | Health aspects
Cardiac action potential | Drug effects | Delayed rectifier current | Human cardiac model | RATE-DEPENDENCE | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | HEART-FAILURE | drug effects | human cardiac model | QT INTERVAL | GUINEA-PIG | MODEL | I-KS | REPOLARIZATION | ACTION-POTENTIAL DURATION | delayed rectifier current | PERIPHERAL VASCULAR DISEASE | cardiac action potential | ION CHANNELS | CANINE | Guinea Pigs | Sodium-Potassium-Exchanging ATPase - physiology | Ventricular Function - physiology | Models, Cardiovascular | Humans | Adrenergic beta-Agonists - pharmacology | Sodium - metabolism | Action Potentials - physiology | Animals | Myocytes, Cardiac - drug effects | Delayed Rectifier Potassium Channels - physiology | Myocytes, Cardiac - physiology | Computer Simulation | Isoproterenol - pharmacology | Dogs | Cardiac Electrophysiology | Sodium - physiology | Action Potentials - drug effects | Ventricular Function - drug effects | Drugs | Heart ventricles | Physiological aspects | Electrophysiology | Muscle cells | Comparative analysis | Health aspects
Journal Article
JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, ISSN 0867-5910, 08/2014, Volume 65, Issue 4, pp. 497 - 509
Alcohol consumption may result in electrocardiographic changes and arrhythmias. Important role of modifications of the inward rectifier potassium current I-K1...
ACTIVATION | PHYSIOLOGY | KIR2.1 | inward rectifier | RECTIFYING K+ CHANNEL | GUINEA-PIG | ALCOHOL-CONSUMPTION | CARDIOMYOCYTES | ethanol | rat ventricular myocytes | ATRIAL-FIBRILLATION | HEART | INHIBITION | dual effect | MEMBRANE-POTENTIALS | arrhythmia | rat ventricular action potential model
ACTIVATION | PHYSIOLOGY | KIR2.1 | inward rectifier | RECTIFYING K+ CHANNEL | GUINEA-PIG | ALCOHOL-CONSUMPTION | CARDIOMYOCYTES | ethanol | rat ventricular myocytes | ATRIAL-FIBRILLATION | HEART | INHIBITION | dual effect | MEMBRANE-POTENTIALS | arrhythmia | rat ventricular action potential model
Journal Article
Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 10/2014, Volume 75, pp. 162 - 173
Previous studies have shown that ventricular myocytes from female rats have smaller contractions and Ca transients than males. As cardiac contraction is...
Calcium transient | Calcium spark | Gender | Excitation–contraction coupling | Gain | Phosphodiesterase | Excitation-contraction coupling | PROTEIN-KINASE-A | BETA-ADRENERGIC STIMULATION | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIAC MYOCYTES | GUINEA-PIG | GENDER-RELATED DIFFERENCES | CELL BIOLOGY | INTRACELLULAR CA2 | NUCLEOTIDE PHOSPHODIESTERASE ACTIVITY | FEMALE RATS | CALCIUM-RELEASE | RYANODINE-RECEPTOR
Calcium transient | Calcium spark | Gender | Excitation–contraction coupling | Gain | Phosphodiesterase | Excitation-contraction coupling | PROTEIN-KINASE-A | BETA-ADRENERGIC STIMULATION | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIAC MYOCYTES | GUINEA-PIG | GENDER-RELATED DIFFERENCES | CELL BIOLOGY | INTRACELLULAR CA2 | NUCLEOTIDE PHOSPHODIESTERASE ACTIVITY | FEMALE RATS | CALCIUM-RELEASE | RYANODINE-RECEPTOR
Journal Article
Journal of Electrocardiology, ISSN 0022-0736, 2017, Volume 50, Issue 4, pp. 437 - 443
Abstract Ischemia/reperfusion (I/R) induce prolongation of QT interval and action potential duration (APD), which is a major cardiac electrical disorder in...
Cardiovascular | QT interval | Arrhythmia | IKr current | Vitamin E | Ischemia/reperfusion | current | DE-POINTES | CARDIAC & CARDIOVASCULAR SYSTEMS | VITRO MODEL | PROTEIN-KINASE | PROLONGS CARDIAC REPOLARIZATION | GUINEA-PIG | SIMULATED-ISCHEMIA | I-Kr current | K+ CHANNEL FUNCTION | ISCHEMIA-REPERFUSION INJURY | HEART | Guinea Pigs | Myocytes, Cardiac - cytology | Cells, Cultured | Male | ERG1 Potassium Channel - metabolism | Sulfates | Long QT Syndrome - physiopathology | Myocardial Reperfusion Injury - metabolism | Animals | Myocytes, Cardiac - drug effects | Electrocardiography | Myocytes, Cardiac - metabolism | ERG1 Potassium Channel - antagonists & inhibitors | Long QT Syndrome - drug therapy | Action Potentials - drug effects | Myocardial Reperfusion Injury - prevention & control | Disease Models, Animal | Vitamin E - pharmacology | Cardiac patients
Cardiovascular | QT interval | Arrhythmia | IKr current | Vitamin E | Ischemia/reperfusion | current | DE-POINTES | CARDIAC & CARDIOVASCULAR SYSTEMS | VITRO MODEL | PROTEIN-KINASE | PROLONGS CARDIAC REPOLARIZATION | GUINEA-PIG | SIMULATED-ISCHEMIA | I-Kr current | K+ CHANNEL FUNCTION | ISCHEMIA-REPERFUSION INJURY | HEART | Guinea Pigs | Myocytes, Cardiac - cytology | Cells, Cultured | Male | ERG1 Potassium Channel - metabolism | Sulfates | Long QT Syndrome - physiopathology | Myocardial Reperfusion Injury - metabolism | Animals | Myocytes, Cardiac - drug effects | Electrocardiography | Myocytes, Cardiac - metabolism | ERG1 Potassium Channel - antagonists & inhibitors | Long QT Syndrome - drug therapy | Action Potentials - drug effects | Myocardial Reperfusion Injury - prevention & control | Disease Models, Animal | Vitamin E - pharmacology | Cardiac patients
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 10/2018, Volume 72, Issue 16, p. C78
Journal Article
Endocrinology, ISSN 0013-7227, 02/2012, Volume 153, Issue 2, pp. 712 - 720
Previously we showed that 17β-estradiol (E2) and/or the xenoestrogen bisphenol A (BPA) alter ventricular myocyte Ca2+ handing, resulting in increased cardiac...
HEART | SMALL EXPOSURES | RAT | CONTRACTION | ENDOCRINOLOGY & METABOLISM | GUINEA-PIG | CEREBELLAR NEURONS | GENDER-DIFFERENCES | ISOLATED CARDIAC MYOCYTES | ER-ALPHA | BETA | Receptors, Estrogen - metabolism | Receptors, Estrogen - genetics | Benzhydryl Compounds | Calcium - metabolism | Calcium Signaling - physiology | Cells, Cultured | Estradiol - administration & dosage | Myocardial Contraction - drug effects | Rats | Male | Sex Characteristics | Rats, Sprague-Dawley | Mice, Knockout | Dose-Response Relationship, Drug | Animals | Endocrine Disruptors - pharmacology | Myocytes, Cardiac - drug effects | Myocytes, Cardiac - physiology | Female | Phenols - administration & dosage | Mice | Estradiol - pharmacology | Phenols - pharmacology | General Endocrinology
HEART | SMALL EXPOSURES | RAT | CONTRACTION | ENDOCRINOLOGY & METABOLISM | GUINEA-PIG | CEREBELLAR NEURONS | GENDER-DIFFERENCES | ISOLATED CARDIAC MYOCYTES | ER-ALPHA | BETA | Receptors, Estrogen - metabolism | Receptors, Estrogen - genetics | Benzhydryl Compounds | Calcium - metabolism | Calcium Signaling - physiology | Cells, Cultured | Estradiol - administration & dosage | Myocardial Contraction - drug effects | Rats | Male | Sex Characteristics | Rats, Sprague-Dawley | Mice, Knockout | Dose-Response Relationship, Drug | Animals | Endocrine Disruptors - pharmacology | Myocytes, Cardiac - drug effects | Myocytes, Cardiac - physiology | Female | Phenols - administration & dosage | Mice | Estradiol - pharmacology | Phenols - pharmacology | General Endocrinology
Journal Article
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, ISSN 0028-1298, 08/2019, Volume 392, Issue 8, pp. 949 - 959
Pinacidil, a nonselective ATP-sensitive K+ (KATP) channel opener, has cardioprotective effects for hypertension, ischemia/reperfusion injury, and arrhythmia....
Pinacidil | SENSITIVE POTASSIUM CHANNELS | CELLS | Nonselective KATP channel opener | ACTIVATION | SUPEROXIDE | Na+/Ca2+ exchange current (I-NCX) | K-ATP CHANNELS | PROTEIN-KINASE-G | Patch-clamp technique | Cardiac myocytes | FREE-RADICALS | SMOOTH-MUSCLE | CA2 | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | Heart | Reactive oxygen species | Arrhythmia | Guanosine | Myocytes | Glycine | Kinases | Guanylate cyclase | Calcium influx | Proteins | Signal transduction | Mitochondria | Na+/Ca2+-exchanging ATPase | Reperfusion | Ischemia | Cyclic GMP | Fura-2 | Glibenclamide | Phosphodiesterase | Hypertension | Automation | Calcium (intracellular) | Cardiac muscle | NG-Nitroarginine methyl ester | Signaling | Inhibitors | Sodium | Protein kinase | Guinea pigs | Nitric oxide | Sildenafil | Ventricle | NCX1 protein | Potassium | Calcium ions
Pinacidil | SENSITIVE POTASSIUM CHANNELS | CELLS | Nonselective KATP channel opener | ACTIVATION | SUPEROXIDE | Na+/Ca2+ exchange current (I-NCX) | K-ATP CHANNELS | PROTEIN-KINASE-G | Patch-clamp technique | Cardiac myocytes | FREE-RADICALS | SMOOTH-MUSCLE | CA2 | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | Heart | Reactive oxygen species | Arrhythmia | Guanosine | Myocytes | Glycine | Kinases | Guanylate cyclase | Calcium influx | Proteins | Signal transduction | Mitochondria | Na+/Ca2+-exchanging ATPase | Reperfusion | Ischemia | Cyclic GMP | Fura-2 | Glibenclamide | Phosphodiesterase | Hypertension | Automation | Calcium (intracellular) | Cardiac muscle | NG-Nitroarginine methyl ester | Signaling | Inhibitors | Sodium | Protein kinase | Guinea pigs | Nitric oxide | Sildenafil | Ventricle | NCX1 protein | Potassium | Calcium ions
Journal Article
14.
Full Text
Nucleotides maintain the activity of Cav1.2 channels in guinea-pig ventricular myocytes
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 05/2015, Volume 460, Issue 3, pp. 813 - 818
The activity of Cav1.2 Ca channels is maintained in the presence of calmodulin and ATP, even in cell-free patches, and thus a channel ATP-binding site has been...
Nucleotide | Binding site | Cav1.2 | ATP | Ca2+ channel | channel | POTASSIUM CHANNELS | PHOSPHORYLATION | TRANSPORTERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC MYOCYTES | CA2+ CHANNELS | HEART | BIOPHYSICS | CALCIUM-CHANNELS | CALMODULIN KINASE-II | MODULATION | Heart Ventricles - cytology | Animals | Guinea Pigs | Calcium Channels - metabolism | Muscle, Smooth, Vascular - metabolism | Heart Ventricles - metabolism | Nucleotides - physiology | Muscle, Smooth, Vascular - cytology | Calmodulin | Nucleotides | Index Medicus
Nucleotide | Binding site | Cav1.2 | ATP | Ca2+ channel | channel | POTASSIUM CHANNELS | PHOSPHORYLATION | TRANSPORTERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC MYOCYTES | CA2+ CHANNELS | HEART | BIOPHYSICS | CALCIUM-CHANNELS | CALMODULIN KINASE-II | MODULATION | Heart Ventricles - cytology | Animals | Guinea Pigs | Calcium Channels - metabolism | Muscle, Smooth, Vascular - metabolism | Heart Ventricles - metabolism | Nucleotides - physiology | Muscle, Smooth, Vascular - cytology | Calmodulin | Nucleotides | Index Medicus
Journal Article
Biological and Pharmaceutical Bulletin, ISSN 0918-6158, 2013, Volume 36, Issue 4, pp. 515 - 521
Astragaloside IV (AS-IV) is one of the main active constituents of Astragalus membranaceus, which has various actions on the cardiovascular system. However,...
patch clamp | ion channel | action potential | cardiac myocyte | astragaloside IV | Patch clamp | Action potential | Cardiac myocyte | Astragaloside IV | Ion channel | HOMOCYSTEINE | APOPTOSIS | CARDIAC-ARRHYTHMIA | ISCHEMIA | SARCOPLASMIC-RETICULUM | IN-VITRO | PHASE ENDOTHELIAL DYSFUNCTION | A549 CELLS | PHARMACOLOGY & PHARMACY | CHANNEL ACTIVITY | MEMBRANACEUS | Calcium Channels - physiology | Drugs, Chinese Herbal | Heart Ventricles - cytology | Animals | Guinea Pigs | Myocytes, Cardiac - drug effects | Triterpenes - pharmacology | Myocytes, Cardiac - physiology | Potassium Channels - physiology | In Vitro Techniques | Action Potentials - drug effects | Saponins - pharmacology
patch clamp | ion channel | action potential | cardiac myocyte | astragaloside IV | Patch clamp | Action potential | Cardiac myocyte | Astragaloside IV | Ion channel | HOMOCYSTEINE | APOPTOSIS | CARDIAC-ARRHYTHMIA | ISCHEMIA | SARCOPLASMIC-RETICULUM | IN-VITRO | PHASE ENDOTHELIAL DYSFUNCTION | A549 CELLS | PHARMACOLOGY & PHARMACY | CHANNEL ACTIVITY | MEMBRANACEUS | Calcium Channels - physiology | Drugs, Chinese Herbal | Heart Ventricles - cytology | Animals | Guinea Pigs | Myocytes, Cardiac - drug effects | Triterpenes - pharmacology | Myocytes, Cardiac - physiology | Potassium Channels - physiology | In Vitro Techniques | Action Potentials - drug effects | Saponins - pharmacology
Journal Article
Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences, ISSN 1364-503X, 05/2006, Volume 364, Issue 1842, pp. 1171 - 1186
transients during acidosis. These interactions are incorporated into a dynamical model of pH regulation in the myocyte to simulate respiratory acidosis in the...
Protons | Action potentials | Orchards | Myocardium | Cell membranes | Physiological regulation | Respiratory acidosis | Acidosis | Modeling | Cardiac ventricular myocyte | Intracellular calcium handling | Mathematical model | pH regulation | cardiac ventricular myocyte | MULTIDISCIPLINARY SCIENCES | INTRACELLULAR PH | SARCOPLASMIC-RETICULUM | GUINEA-PIG | intracellular calcium handling | MATHEMATICAL-MODEL | PANCREATIC DUCTAL EPITHELIUM | SYSTOLIC CA2 | CONTRACTION | acidosis
Protons | Action potentials | Orchards | Myocardium | Cell membranes | Physiological regulation | Respiratory acidosis | Acidosis | Modeling | Cardiac ventricular myocyte | Intracellular calcium handling | Mathematical model | pH regulation | cardiac ventricular myocyte | MULTIDISCIPLINARY SCIENCES | INTRACELLULAR PH | SARCOPLASMIC-RETICULUM | GUINEA-PIG | intracellular calcium handling | MATHEMATICAL-MODEL | PANCREATIC DUCTAL EPITHELIUM | SYSTOLIC CA2 | CONTRACTION | acidosis