American Journal of Physiology - Renal Physiology, ISSN 0363-6127, 05/2014, Volume 306, Issue 9, pp. F931 - F940
The arginine vasopressin (AVP) type 2 receptor (V2R) is unique among AVP receptor subtypes in signaling through cAMP. Its key function is in the kidneys,...
Arginine vasopressin | Desmopressin | PHYSIOLOGY | COLLECTING DUCT CELLS | arginine vasopressin V-2 receptor | POLYCYSTIC KIDNEY-DISEASE | BREAST-CANCER CELLS | arginine vasopressin | ARGININE-VASOPRESSIN | extrarenal vasopressin V-2 receptor | UROLOGY & NEPHROLOGY | X-CHROMOSOME INACTIVATION | vasopressin V-2 receptor | PERIPHERAL-BLOOD LYMPHOCYTES | ORALLY DISINTEGRATING TABLET | PLACEBO-CONTROLLED TRIAL | NEPHROGENIC DIABETES-INSIPIDUS | desmopressin | THICK ASCENDING LIMB | Kidney - drug effects | Humans | Gene Expression Regulation | Receptors, Vasopressin - metabolism | Genotype | Male | Vasopressins - metabolism | Hormone Antagonists - pharmacology | Kidney - metabolism | Phenotype | Animals | Signal Transduction - drug effects | Receptors, Vasopressin - genetics | Female | Water-Electrolyte Balance | Antidiuretic Hormone Receptor Antagonists | Cyclic AMP - metabolism | Kidney - physiopathology | Physiology, Pathological | Medical research | Arginine | Physiological aspects | Medicine, Experimental | Research | Vasopressin
Arginine vasopressin | Desmopressin | PHYSIOLOGY | COLLECTING DUCT CELLS | arginine vasopressin V-2 receptor | POLYCYSTIC KIDNEY-DISEASE | BREAST-CANCER CELLS | arginine vasopressin | ARGININE-VASOPRESSIN | extrarenal vasopressin V-2 receptor | UROLOGY & NEPHROLOGY | X-CHROMOSOME INACTIVATION | vasopressin V-2 receptor | PERIPHERAL-BLOOD LYMPHOCYTES | ORALLY DISINTEGRATING TABLET | PLACEBO-CONTROLLED TRIAL | NEPHROGENIC DIABETES-INSIPIDUS | desmopressin | THICK ASCENDING LIMB | Kidney - drug effects | Humans | Gene Expression Regulation | Receptors, Vasopressin - metabolism | Genotype | Male | Vasopressins - metabolism | Hormone Antagonists - pharmacology | Kidney - metabolism | Phenotype | Animals | Signal Transduction - drug effects | Receptors, Vasopressin - genetics | Female | Water-Electrolyte Balance | Antidiuretic Hormone Receptor Antagonists | Cyclic AMP - metabolism | Kidney - physiopathology | Physiology, Pathological | Medical research | Arginine | Physiological aspects | Medicine, Experimental | Research | Vasopressin
Journal Article
Journal of Molecular Endocrinology, ISSN 0952-5041, 08/2002, Volume 29, Issue 1, pp. 1 - 9
Hyponatremia, whether due to the syndrome of inappropriate antidiuretic hormone secretion (SIADH) or disorders of water retention such as congestive heart...
Animals | Humans | Receptors, Vasopressin - classification | Antidiuretic Hormone Receptor Antagonists | Arginine Vasopressin - blood | Arginine Vasopressin - secretion | Inappropriate ADH Syndrome - drug therapy
Animals | Humans | Receptors, Vasopressin - classification | Antidiuretic Hormone Receptor Antagonists | Arginine Vasopressin - blood | Arginine Vasopressin - secretion | Inappropriate ADH Syndrome - drug therapy
Journal Article
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Vasopressin V2 receptors, ENaC, and sodium reabsorption: A risk factor for hypertension?
American Journal of Physiology - Renal Physiology, ISSN 0363-6127, 11/2010, Volume 299, Issue 5, pp. F917 - F928
Bankir L, Bichet DG, Bouby N. Vasopressin V2 receptors, ENaC, and sodium reabsorption: a risk factor for hypertension? Am J Physiol Renal Physiol 299:...
Water conservation | Sodium excretion | Collecting duct | Antidiuresis | URINE CONCENTRATION | HEALTHY HUMANS | PHYSIOLOGY | RAT-KIDNEY | EPITHELIAL NA+ CHANNEL | NONCOORDINATE REGULATION | water conservation | DOCA-SALT HYPERTENSION | antidiuresis | ARGININE-VASOPRESSIN | collecting duct | CORTICAL COLLECTING DUCT | UROLOGY & NEPHROLOGY | sodium excretion | BLOOD-PRESSURE VARIATION | SUSTAINED HYPERTENSION | Antihypertensive Agents - pharmacology | Humans | Risk Factors | Water - metabolism | Rats | Sodium - metabolism | Hypertension - physiopathology | Receptors, Vasopressin - drug effects | Hypertension - metabolism | Kidney - metabolism | Animals | Epithelial Sodium Channels - genetics | Epithelial Sodium Channels - drug effects | Sodium - urine | Receptors, Vasopressin - genetics | Blood Pressure - physiology | Hypertension - epidemiology | Vasopressins - physiology
Water conservation | Sodium excretion | Collecting duct | Antidiuresis | URINE CONCENTRATION | HEALTHY HUMANS | PHYSIOLOGY | RAT-KIDNEY | EPITHELIAL NA+ CHANNEL | NONCOORDINATE REGULATION | water conservation | DOCA-SALT HYPERTENSION | antidiuresis | ARGININE-VASOPRESSIN | collecting duct | CORTICAL COLLECTING DUCT | UROLOGY & NEPHROLOGY | sodium excretion | BLOOD-PRESSURE VARIATION | SUSTAINED HYPERTENSION | Antihypertensive Agents - pharmacology | Humans | Risk Factors | Water - metabolism | Rats | Sodium - metabolism | Hypertension - physiopathology | Receptors, Vasopressin - drug effects | Hypertension - metabolism | Kidney - metabolism | Animals | Epithelial Sodium Channels - genetics | Epithelial Sodium Channels - drug effects | Sodium - urine | Receptors, Vasopressin - genetics | Blood Pressure - physiology | Hypertension - epidemiology | Vasopressins - physiology
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 0363-6127, 02/2016, Volume 310, Issue 4, pp. F284 - F293
Renin is synthesized in the principal cells of the collecting duct (CD), and its production is increased via cAMP in angiotensin (ANG) II-dependent...
Intrarenal renin-angiotensin system | Collecting duct | Water deprivation | Distal tubular renin | PKA/CREB | Prorenin | PROTEIN-KINASE-C | ANGIOTENSIN-II LEVELS | PHYSIOLOGY | AT RECEPTOR | distal tubular renin | JUXTAGLOMERULAR CELLS | HEART-FAILURE | CAMP ACCUMULATION | CYCLASE TYPE-6 ACTIVATION | water deprivation | intrarenal renin-angiotensin system | collecting duct | MESSENGER-RNA | INFUSED RATS | UROLOGY & NEPHROLOGY | prorenin | HYPERTENSIVE-RATS | Cyclic AMP-Dependent Protein Kinases - metabolism | Kidney Tubules, Collecting - drug effects | Cell Line | RNA, Small Interfering - genetics | Phosphorylation | Renin - biosynthesis | Kidney Medulla - drug effects | Sulfonamides - pharmacology | Angiotensin II Type 1 Receptor Blockers - pharmacology | Gene Knockdown Techniques | Kidney Tubules, Collecting - metabolism | Animals | Isoquinolines - pharmacology | RNA, Small Interfering - biosynthesis | Receptor, Angiotensin, Type 1 - metabolism | Cyclic AMP Response Element-Binding Protein - metabolism | Kidney Medulla - metabolism | Renin-Angiotensin System - drug effects | Angiotensin-Converting Enzyme Inhibitors - pharmacology | Mice | Protein Kinase Inhibitors - pharmacology | Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors | Deamino Arginine Vasopressin - pharmacology | Receptors, Vasopressin - agonists | Renin | Kidneys | Health aspects | Vasopressin | RNA | Aquaporins | Angiotensin | Protein binding | CREB | PKA
Intrarenal renin-angiotensin system | Collecting duct | Water deprivation | Distal tubular renin | PKA/CREB | Prorenin | PROTEIN-KINASE-C | ANGIOTENSIN-II LEVELS | PHYSIOLOGY | AT RECEPTOR | distal tubular renin | JUXTAGLOMERULAR CELLS | HEART-FAILURE | CAMP ACCUMULATION | CYCLASE TYPE-6 ACTIVATION | water deprivation | intrarenal renin-angiotensin system | collecting duct | MESSENGER-RNA | INFUSED RATS | UROLOGY & NEPHROLOGY | prorenin | HYPERTENSIVE-RATS | Cyclic AMP-Dependent Protein Kinases - metabolism | Kidney Tubules, Collecting - drug effects | Cell Line | RNA, Small Interfering - genetics | Phosphorylation | Renin - biosynthesis | Kidney Medulla - drug effects | Sulfonamides - pharmacology | Angiotensin II Type 1 Receptor Blockers - pharmacology | Gene Knockdown Techniques | Kidney Tubules, Collecting - metabolism | Animals | Isoquinolines - pharmacology | RNA, Small Interfering - biosynthesis | Receptor, Angiotensin, Type 1 - metabolism | Cyclic AMP Response Element-Binding Protein - metabolism | Kidney Medulla - metabolism | Renin-Angiotensin System - drug effects | Angiotensin-Converting Enzyme Inhibitors - pharmacology | Mice | Protein Kinase Inhibitors - pharmacology | Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors | Deamino Arginine Vasopressin - pharmacology | Receptors, Vasopressin - agonists | Renin | Kidneys | Health aspects | Vasopressin | RNA | Aquaporins | Angiotensin | Protein binding | CREB | PKA
Journal Article
Molecular Endocrinology, ISSN 0888-8809, 04/2003, Volume 17, Issue 4, pp. 677 - 691
G protein-coupled receptor (GPCR) oligomerization is a growing concept that has emerged from several studies suggesting that GPCRs can form both homo- and...
HETEROMERIC COMPLEXES | RAT-KIDNEY | REVERSE TRANSCRIPTION | ENDOCRINOLOGY & METABOLISM | RESONANCE ENERGY-TRANSFER | PROTEIN-COUPLED RECEPTORS | POLYMERASE CHAIN-REACTION | ENDOPLASMIC-RETICULUM | DELTA-OPIOID RECEPTOR | GABA(B) RECEPTOR | LIVING CELLS | Kidney - embryology | Receptors, Oxytocin - genetics | Humans | Receptors, Vasopressin - metabolism | Luminescent Measurements | Recombinant Fusion Proteins - metabolism | Receptors, Oxytocin - biosynthesis | Dimerization | Receptors, Vasopressin - agonists | Kidney - drug effects | Signal Transduction | Cells, Cultured | Morpholines - pharmacology | Receptors, Vasopressin - biosynthesis | Kidney - cytology | Precipitin Tests | Receptors, Oxytocin - metabolism | Receptors, Vasopressin - genetics | Recombinant Fusion Proteins - genetics | Ligands | Luminescent Proteins - genetics | Antidiuretic Hormone Receptor Antagonists | Biophysics - methods | Subcellular Fractions | Spiro Compounds - pharmacology | Luminescent Proteins - metabolism
HETEROMERIC COMPLEXES | RAT-KIDNEY | REVERSE TRANSCRIPTION | ENDOCRINOLOGY & METABOLISM | RESONANCE ENERGY-TRANSFER | PROTEIN-COUPLED RECEPTORS | POLYMERASE CHAIN-REACTION | ENDOPLASMIC-RETICULUM | DELTA-OPIOID RECEPTOR | GABA(B) RECEPTOR | LIVING CELLS | Kidney - embryology | Receptors, Oxytocin - genetics | Humans | Receptors, Vasopressin - metabolism | Luminescent Measurements | Recombinant Fusion Proteins - metabolism | Receptors, Oxytocin - biosynthesis | Dimerization | Receptors, Vasopressin - agonists | Kidney - drug effects | Signal Transduction | Cells, Cultured | Morpholines - pharmacology | Receptors, Vasopressin - biosynthesis | Kidney - cytology | Precipitin Tests | Receptors, Oxytocin - metabolism | Receptors, Vasopressin - genetics | Recombinant Fusion Proteins - genetics | Ligands | Luminescent Proteins - genetics | Antidiuretic Hormone Receptor Antagonists | Biophysics - methods | Subcellular Fractions | Spiro Compounds - pharmacology | Luminescent Proteins - metabolism
Journal Article
世界胃肠病学杂志:英文版, ISSN 1007-9327, 2015, Volume 21, Issue 41, pp. 11584 - 11596
Hyponatremia is a frequent complication of advanced cirrhosis with ascites associated with increased morbidity and mortality. It is caused by an impairment in...
Liver | cirrhosis;Ascites;Hyponatremia;Pathophysiolo | Hyponatremia | V2 receptor antagonist | Pathophysiology | Ascites | Liver cirrhosis | RENAL WATER-EXCRETION | PLASMA ARGININE VASOPRESSIN | HEPATORENAL-SYNDROME | LIVER-CIRRHOSIS PATIENTS | AQUAPORIN-2 URINARY-EXCRETION | EARLY HEPATIC CIRRHOSIS | DOUBLE-BLIND | NITRIC-OXIDE | PLACEBO-CONTROLLED TRIAL | GASTROENTEROLOGY & HEPATOLOGY | INCREASES SERUM SODIUM | Ascites - etiology | Liver Cirrhosis - diagnosis | Protein Precursors - blood | Liver Cirrhosis - complications | Humans | Risk Factors | Receptors, Vasopressin - metabolism | Treatment Outcome | Water-Electrolyte Balance - drug effects | Biomarkers - blood | Receptors, Vasopressin - drug effects | Vasopressins - blood | Antidiuretic Hormone Receptor Antagonists - therapeutic use | Ascites - diagnosis | Ascites - drug therapy | Patient Selection | Antidiuretic Hormone Receptor Antagonists - adverse effects | Aquaporin 2 - metabolism | Animals | Ascites - metabolism | Neurophysins - blood | Topic Highlight
Liver | cirrhosis;Ascites;Hyponatremia;Pathophysiolo | Hyponatremia | V2 receptor antagonist | Pathophysiology | Ascites | Liver cirrhosis | RENAL WATER-EXCRETION | PLASMA ARGININE VASOPRESSIN | HEPATORENAL-SYNDROME | LIVER-CIRRHOSIS PATIENTS | AQUAPORIN-2 URINARY-EXCRETION | EARLY HEPATIC CIRRHOSIS | DOUBLE-BLIND | NITRIC-OXIDE | PLACEBO-CONTROLLED TRIAL | GASTROENTEROLOGY & HEPATOLOGY | INCREASES SERUM SODIUM | Ascites - etiology | Liver Cirrhosis - diagnosis | Protein Precursors - blood | Liver Cirrhosis - complications | Humans | Risk Factors | Receptors, Vasopressin - metabolism | Treatment Outcome | Water-Electrolyte Balance - drug effects | Biomarkers - blood | Receptors, Vasopressin - drug effects | Vasopressins - blood | Antidiuretic Hormone Receptor Antagonists - therapeutic use | Ascites - diagnosis | Ascites - drug therapy | Patient Selection | Antidiuretic Hormone Receptor Antagonists - adverse effects | Aquaporin 2 - metabolism | Animals | Ascites - metabolism | Neurophysins - blood | Topic Highlight
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2008, Volume 52, Issue 19, pp. 1540 - 1545
Objectives: This study sought to assess the acute hemodynamic effect of vasopressin V receptor antagonism. Background: In decompensated heart failure (HF),...
heart failure | vasopressin antagonists | hemodynamics | Multivariate Analysis | Prospective Studies | Follow-Up Studies | Benzazepines - adverse effects | Humans | Middle Aged | Male | Reference Values | Hemodynamics - physiology | Dose-Response Relationship, Drug | Female | Heart Function Tests | Severity of Illness Index | Double-Blind Method | Drug Administration Schedule | Heart Failure, Systolic - drug therapy | Receptors, Vasopressin - administration & dosage | Risk Assessment | Administration, Oral | Heart Failure, Systolic - mortality | Probability | Survival Rate | Treatment Outcome | International Cooperation | Heart Failure, Systolic - diagnosis | Aged | Benzazepines - administration & dosage | Hemodynamics - drug effects | Antidiuretic Hormone Receptor Antagonists | Heart failure | Enzymes | Heart attacks | Statistical analysis | Angioplasty | Pulmonary arteries | Drug therapy | Drug dosages | Veins & arteries | Index Medicus | Abridged Index Medicus
heart failure | vasopressin antagonists | hemodynamics | Multivariate Analysis | Prospective Studies | Follow-Up Studies | Benzazepines - adverse effects | Humans | Middle Aged | Male | Reference Values | Hemodynamics - physiology | Dose-Response Relationship, Drug | Female | Heart Function Tests | Severity of Illness Index | Double-Blind Method | Drug Administration Schedule | Heart Failure, Systolic - drug therapy | Receptors, Vasopressin - administration & dosage | Risk Assessment | Administration, Oral | Heart Failure, Systolic - mortality | Probability | Survival Rate | Treatment Outcome | International Cooperation | Heart Failure, Systolic - diagnosis | Aged | Benzazepines - administration & dosage | Hemodynamics - drug effects | Antidiuretic Hormone Receptor Antagonists | Heart failure | Enzymes | Heart attacks | Statistical analysis | Angioplasty | Pulmonary arteries | Drug therapy | Drug dosages | Veins & arteries | Index Medicus | Abridged Index Medicus
Journal Article
American Journal of Kidney Diseases, ISSN 0272-6386, 03/2019, Volume 73, Issue 3, pp. 354 - 362
The vasopressin V2 receptor antagonist (V2RA) tolvaptan is the first drug that has been shown to slow the rate of kidney function decline in patients with...
tolvaptan | side effect | osmolar load | polyuria | salt | kidney function | aquaresis | urine volume | vasopressin (AVP) | osmoles | sodium | Autosomal dominant polycystic kidney disease (ADPKD) | glomerular filtration rate (GFR) | vasopressin V2 receptor antagonist (V2RA) | total kidney volume (TKV) | GLOMERULAR-FILTRATION-RATE | DIAGNOSIS | SODIUM | PHARMACOKINETICS | POLYCYSTIC KIDNEY-DISEASE | UROLOGY & NEPHROLOGY | WATER-INTAKE | PHARMACODYNAMICS
tolvaptan | side effect | osmolar load | polyuria | salt | kidney function | aquaresis | urine volume | vasopressin (AVP) | osmoles | sodium | Autosomal dominant polycystic kidney disease (ADPKD) | glomerular filtration rate (GFR) | vasopressin V2 receptor antagonist (V2RA) | total kidney volume (TKV) | GLOMERULAR-FILTRATION-RATE | DIAGNOSIS | SODIUM | PHARMACOKINETICS | POLYCYSTIC KIDNEY-DISEASE | UROLOGY & NEPHROLOGY | WATER-INTAKE | PHARMACODYNAMICS
Journal Article
International Journal of Molecular Sciences, ISSN 1422-0067, 11/2019, Volume 20, Issue 22, p. 5764
Chronic vasopressin secretion induced by recurrent mild heat stress exposure is significantly enhanced by limited rehydration with a fructose-containing...
aldose reductase | cortisol | fructokinase | angiotensin ii | vasopressin | sgk1
aldose reductase | cortisol | fructokinase | angiotensin ii | vasopressin | sgk1
Journal Article
Nature Medicine, ISSN 1078-8956, 10/2003, Volume 9, Issue 10, pp. 1323 - 1326
The polycystic kidney diseases (PKDs) are a group of genetic disorders causing significant renal failure and death in children and adults. There are no...
MEDICINE, RESEARCH & EXPERIMENTAL | PROTEIN | MEDULLARY COLLECTING DUCTS | M-1 CELLS | POLYCYSTIC KIDNEY-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | NEPHRONOPHTHISIS | PROLIFERATION | CELL BIOLOGY | IN-VITRO | CA2 | EXPRESSION | CAMP | Polycystic Kidney Diseases - metabolism | Aquaporin 6 | Kidney - pathology | Humans | Receptors, Vasopressin - metabolism | Rats | Aquaporins - metabolism | Polycystic Kidney Diseases - drug therapy | Rats, Sprague-Dawley | Aquaporins - genetics | Disease Progression | Proteins - genetics | Kidney - metabolism | Animals | Polycystic Kidney Diseases - physiopathology | Proteins - metabolism | Benzazepines - therapeutic use | TRPP Cation Channels | Mice | Benzazepines - metabolism | Antidiuretic Hormone Receptor Antagonists | Cyclic AMP - metabolism | Aquaporin 2 | Disease Models, Animal
MEDICINE, RESEARCH & EXPERIMENTAL | PROTEIN | MEDULLARY COLLECTING DUCTS | M-1 CELLS | POLYCYSTIC KIDNEY-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | NEPHRONOPHTHISIS | PROLIFERATION | CELL BIOLOGY | IN-VITRO | CA2 | EXPRESSION | CAMP | Polycystic Kidney Diseases - metabolism | Aquaporin 6 | Kidney - pathology | Humans | Receptors, Vasopressin - metabolism | Rats | Aquaporins - metabolism | Polycystic Kidney Diseases - drug therapy | Rats, Sprague-Dawley | Aquaporins - genetics | Disease Progression | Proteins - genetics | Kidney - metabolism | Animals | Polycystic Kidney Diseases - physiopathology | Proteins - metabolism | Benzazepines - therapeutic use | TRPP Cation Channels | Mice | Benzazepines - metabolism | Antidiuretic Hormone Receptor Antagonists | Cyclic AMP - metabolism | Aquaporin 2 | Disease Models, Animal
Journal Article
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, ISSN 1931-857X, 10/2019, Volume 317, Issue 4, pp. F789 - F804
Vasopressin controls water balance largely through PKA-dependent effects to regulate the collecting duct water channel aquaporin-2 (AQP2). Although...
PROTEIN-KINASE-A | PHYSIOLOGY | aquaporin-2 | PHOSPHATASE | TRAFFICKING | WATER CHANNELS | AQP2 | protein kinase | protein phosphatase | UROLOGY & NEPHROLOGY | AQUAPORIN-2 PHOSPHORYLATION | NA+/H+ EXCHANGER | APICAL MEMBRANE | EXPRESSION | CAMP
PROTEIN-KINASE-A | PHYSIOLOGY | aquaporin-2 | PHOSPHATASE | TRAFFICKING | WATER CHANNELS | AQP2 | protein kinase | protein phosphatase | UROLOGY & NEPHROLOGY | AQUAPORIN-2 PHOSPHORYLATION | NA+/H+ EXCHANGER | APICAL MEMBRANE | EXPRESSION | CAMP
Journal Article
Cardiovascular Research, ISSN 0008-6363, 08/2001, Volume 51, Issue 3, pp. 391 - 402
Hyponatremia due to the syndrome of inappropriate antidiuretic hormone secretion (SIADH) and disorders of water retention such as congestive heart failure and...
Heart failure | Receptors | Renal function | Hormones | Vasoactive agents | heart failure | CARDIAC & CARDIOVASCULAR SYSTEMS | receptors | hormones | NONPEPTIDE V-2 ANTAGONIST | vasoactive agents | INAPPROPRIATE SECRETION | HYPONATREMIC ENCEPHALOPATHY | ARGININE-VASOPRESSIN | THERAPEUTIC-EFFICACY | IN-VIVO | renal function | V-2-RECEPTOR ANTAGONIST | PHARMACOLOGICAL PROFILE | CONGESTIVE-HEART-FAILURE | LONG-TERM TREATMENT | Animals | Inappropriate ADH Syndrome - physiopathology | Humans | Water-Electrolyte Imbalance - physiopathology | Water-Electrolyte Imbalance - drug therapy | Clinical Trials as Topic | Antidiuretic Hormone Receptor Antagonists | Inappropriate ADH Syndrome - drug therapy
Heart failure | Receptors | Renal function | Hormones | Vasoactive agents | heart failure | CARDIAC & CARDIOVASCULAR SYSTEMS | receptors | hormones | NONPEPTIDE V-2 ANTAGONIST | vasoactive agents | INAPPROPRIATE SECRETION | HYPONATREMIC ENCEPHALOPATHY | ARGININE-VASOPRESSIN | THERAPEUTIC-EFFICACY | IN-VIVO | renal function | V-2-RECEPTOR ANTAGONIST | PHARMACOLOGICAL PROFILE | CONGESTIVE-HEART-FAILURE | LONG-TERM TREATMENT | Animals | Inappropriate ADH Syndrome - physiopathology | Humans | Water-Electrolyte Imbalance - physiopathology | Water-Electrolyte Imbalance - drug therapy | Clinical Trials as Topic | Antidiuretic Hormone Receptor Antagonists | Inappropriate ADH Syndrome - drug therapy
Journal Article
Molecular and Cellular Proteomics, ISSN 1535-9476, 02/2012, Volume 11, Issue 2, p. M111.014613
G protein-coupled receptors (GPCRs) regulate diverse physiological processes, and many human diseases are due to defects in GPCR signaling. To identify the...
RENAL PRINCIPAL CELLS | LC-MS/MS | MEDULLARY COLLECTING DUCT | ACTIVATION | KINASE-A | PHOSPHORYLATION | IN-VIVO | BIOCHEMICAL RESEARCH METHODS | AQUAPORIN-2 TRAFFICKING | BETA-CATENIN | IDENTIFICATION | Phosphorylation | Receptors, G-Protein-Coupled - metabolism | Signal Transduction | Humans | Receptors, Vasopressin - metabolism | Rats | Proteome - analysis | Kidney Tubules, Collecting - cytology | Phosphoproteins - metabolism | Kidney Tubules, Collecting - metabolism | Animals | Proteomics | Chromatography, Liquid | Phosphopeptides - metabolism | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Cyclic AMP - metabolism | Research
RENAL PRINCIPAL CELLS | LC-MS/MS | MEDULLARY COLLECTING DUCT | ACTIVATION | KINASE-A | PHOSPHORYLATION | IN-VIVO | BIOCHEMICAL RESEARCH METHODS | AQUAPORIN-2 TRAFFICKING | BETA-CATENIN | IDENTIFICATION | Phosphorylation | Receptors, G-Protein-Coupled - metabolism | Signal Transduction | Humans | Receptors, Vasopressin - metabolism | Rats | Proteome - analysis | Kidney Tubules, Collecting - cytology | Phosphoproteins - metabolism | Kidney Tubules, Collecting - metabolism | Animals | Proteomics | Chromatography, Liquid | Phosphopeptides - metabolism | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Cyclic AMP - metabolism | Research
Journal Article
American Journal of Nephrology, ISSN 0250-8095, 06/2019, Volume 49, Issue 6, pp. 487 - 493
Background: Vasopressin V2 receptor inhibition is a clinically validated mechanism of action in the treatment of autosomal dominant polycystic kidney disease...
Patient-Oriented, Translational Research: Research Article | Vasopressin V2 receptor antagonist | TOLVAPTAN | UROLOGY & NEPHROLOGY | PCK rat model | Lixivaptan | NONPEPTIDE | Polycystic kidney disease
Patient-Oriented, Translational Research: Research Article | Vasopressin V2 receptor antagonist | TOLVAPTAN | UROLOGY & NEPHROLOGY | PCK rat model | Lixivaptan | NONPEPTIDE | Polycystic kidney disease
Journal Article
British Journal of Pharmacology, ISSN 0007-1188, 05/2019, Volume 176, Issue 9, pp. 1315 - 1327
Background and Purpose We investigated the inhibitory effect and associated molecular mechanisms of tolvaptan on angiotensin II (AngII)‐induced aldosterone...
Corticosteroids | RNA | Angiotensin | Cytochrome P-450 | Aldosterone | Vasopressin | Steroids | Diuresis | Phosphorylation | Argipressin | Secretion | Aldosterone synthase | Gene expression | Kinases | Proteins | Molecular modelling | Protein folding | Inhibition | Angiotensin II
Corticosteroids | RNA | Angiotensin | Cytochrome P-450 | Aldosterone | Vasopressin | Steroids | Diuresis | Phosphorylation | Argipressin | Secretion | Aldosterone synthase | Gene expression | Kinases | Proteins | Molecular modelling | Protein folding | Inhibition | Angiotensin II
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 2005, Volume 16, Issue 7, pp. 1920 - 1928
In addition to its effect on water permeability, vasopressin, through its V2 receptors (AVPR2), stimulates Na reabsorption in the collecting duct by increasing...
UROLOGY & NEPHROLOGY | Diabetes Insipidus - physiopathology | Humans | Male | Renal Agents - pharmacology | Sodium Channels - drug effects | Sodium Channels - physiology | Aquaporins - genetics | Receptors, Vasopressin - drug effects | Diabetes Insipidus - genetics | Adolescent | Receptors, Vasopressin - genetics | Receptors, Vasopressin - physiology | Adult | Female | Child | Sodium - physiology | Aquaporin 2 | Deamino Arginine Vasopressin - pharmacology | Diabetes Insipidus - metabolism
UROLOGY & NEPHROLOGY | Diabetes Insipidus - physiopathology | Humans | Male | Renal Agents - pharmacology | Sodium Channels - drug effects | Sodium Channels - physiology | Aquaporins - genetics | Receptors, Vasopressin - drug effects | Diabetes Insipidus - genetics | Adolescent | Receptors, Vasopressin - genetics | Receptors, Vasopressin - physiology | Adult | Female | Child | Sodium - physiology | Aquaporin 2 | Deamino Arginine Vasopressin - pharmacology | Diabetes Insipidus - metabolism
Journal Article
The American Journal of the Medical Sciences, ISSN 0002-9629, 02/2019, Volume 357, Issue 2, pp. 151 - 159
Myocardial fibrosis is a major pathophysiologic substrate of heart failure with preserved ejection fraction. Vasopressin is an important therapeutic target in...
Heart failure with preserved ejection fraction | Animal model | Diastolic dysfunction | Myocardial fibrosis | Vasopressin | HOMOCYSTEINE | HEART-FAILURE | PRESERVED EJECTION FRACTION | FOLIC-ACID | CARDIAC FIBROBLASTS | HYPERTROPHY | MEDICINE, GENERAL & INTERNAL | ARGININE-VASOPRESSIN | HYPERHOMOCYSTEINEMIA LEADS | THERAPIES | DYSFUNCTION
Heart failure with preserved ejection fraction | Animal model | Diastolic dysfunction | Myocardial fibrosis | Vasopressin | HOMOCYSTEINE | HEART-FAILURE | PRESERVED EJECTION FRACTION | FOLIC-ACID | CARDIAC FIBROBLASTS | HYPERTROPHY | MEDICINE, GENERAL & INTERNAL | ARGININE-VASOPRESSIN | HYPERHOMOCYSTEINEMIA LEADS | THERAPIES | DYSFUNCTION
Journal Article