Hypertension, ISSN 0194-911X, 04/2006, Volume 47, Issue 4, pp. 699 - 705
We tested the hypothesis that blockade of angiotensin II type 1 receptors reduces oxidative stress markers in parallel with urinary albumin and type IV...
Oxidative stress | Inflammation | Albuminuria | Angiotensin II | LOSARTAN | MELLITUS | BLOOD-PRESSURE | TRIAL | albuminuria | inflammation | angiotensin II | MICROALBUMINURIA | IN-VIVO | PERIPHERAL VASCULAR DISEASE | COMPLICATIONS | CANDESARTAN | BLOCKADE | oxidative stress | Diabetic Nephropathies - urine | Single-Blind Method | Biomarkers - urine | Valsartan | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Valine - analogs & derivatives | Diabetic Nephropathies - drug therapy | Hypertension - drug therapy | Male | Antihypertensive Agents - therapeutic use | Albuminuria - physiopathology | Trichlormethiazide - therapeutic use | Adult | Female | Tetrazoles - therapeutic use | Valine - therapeutic use | Aged | Oxidative Stress - drug effects | Hypertension - urine | Benzimidazoles - therapeutic use
Oxidative stress | Inflammation | Albuminuria | Angiotensin II | LOSARTAN | MELLITUS | BLOOD-PRESSURE | TRIAL | albuminuria | inflammation | angiotensin II | MICROALBUMINURIA | IN-VIVO | PERIPHERAL VASCULAR DISEASE | COMPLICATIONS | CANDESARTAN | BLOCKADE | oxidative stress | Diabetic Nephropathies - urine | Single-Blind Method | Biomarkers - urine | Valsartan | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Valine - analogs & derivatives | Diabetic Nephropathies - drug therapy | Hypertension - drug therapy | Male | Antihypertensive Agents - therapeutic use | Albuminuria - physiopathology | Trichlormethiazide - therapeutic use | Adult | Female | Tetrazoles - therapeutic use | Valine - therapeutic use | Aged | Oxidative Stress - drug effects | Hypertension - urine | Benzimidazoles - therapeutic use
Journal Article
Clinical and Experimental Hypertension, ISSN 1064-1963, 07/2018, Volume 40, Issue 5, pp. 468 - 475
The aim of this study was to assess the effects of irbesartan alone and combined with amlodipine, efonidipine, or trichlormethiazide on blood pressure (BP) and...
Home blood pressure | irbesartan | microalbuminuria | efonidipine | trichlormethiazide | amlodipine | ACE-INHIBITOR | NONDIABETIC INDIVIDUALS | LOW-GRADE ALBUMINURIA | CALCIUM-CHANNEL BLOCKERS | GENERAL-POPULATION | RENAL PROTECTION | CARDIOVASCULAR MORTALITY | DOUBLE-BLIND | PHARMACOLOGY & PHARMACY | PERIPHERAL VASCULAR DISEASE | CHRONIC KIDNEY-DISEASE | CORONARY-HEART-DISEASE | Albuminuria - complications | Antihypertensive Agents - pharmacology | Tetrazoles - pharmacology | Urinalysis | Humans | Middle Aged | Essential Hypertension - complications | Male | Biphenyl Compounds - therapeutic use | Essential Hypertension - drug therapy | Biphenyl Compounds - pharmacology | Nitrophenols - pharmacology | Trichlormethiazide - therapeutic use | Nitrophenols - therapeutic use | Organophosphorus Compounds - pharmacology | Female | Blood Pressure - drug effects | Trichlormethiazide - pharmacology | Albuminuria - urine | Drug Therapy, Combination | Organophosphorus Compounds - therapeutic use | Antihypertensive Agents - therapeutic use | Amlodipine - therapeutic use | Dihydropyridines - therapeutic use | Irbesartan | Albuminuria - drug therapy | Amlodipine - pharmacology | Dihydropyridines - pharmacology | Tetrazoles - therapeutic use | Aged | Blood Pressure Monitoring, Ambulatory
Home blood pressure | irbesartan | microalbuminuria | efonidipine | trichlormethiazide | amlodipine | ACE-INHIBITOR | NONDIABETIC INDIVIDUALS | LOW-GRADE ALBUMINURIA | CALCIUM-CHANNEL BLOCKERS | GENERAL-POPULATION | RENAL PROTECTION | CARDIOVASCULAR MORTALITY | DOUBLE-BLIND | PHARMACOLOGY & PHARMACY | PERIPHERAL VASCULAR DISEASE | CHRONIC KIDNEY-DISEASE | CORONARY-HEART-DISEASE | Albuminuria - complications | Antihypertensive Agents - pharmacology | Tetrazoles - pharmacology | Urinalysis | Humans | Middle Aged | Essential Hypertension - complications | Male | Biphenyl Compounds - therapeutic use | Essential Hypertension - drug therapy | Biphenyl Compounds - pharmacology | Nitrophenols - pharmacology | Trichlormethiazide - therapeutic use | Nitrophenols - therapeutic use | Organophosphorus Compounds - pharmacology | Female | Blood Pressure - drug effects | Trichlormethiazide - pharmacology | Albuminuria - urine | Drug Therapy, Combination | Organophosphorus Compounds - therapeutic use | Antihypertensive Agents - therapeutic use | Amlodipine - therapeutic use | Dihydropyridines - therapeutic use | Irbesartan | Albuminuria - drug therapy | Amlodipine - pharmacology | Dihydropyridines - pharmacology | Tetrazoles - therapeutic use | Aged | Blood Pressure Monitoring, Ambulatory
Journal Article
Hypertension Research, ISSN 0916-9636, 11/2009, Volume 32, Issue 11, pp. 962 - 968
To achieve the target blood pressure recommended by the latest guidelines, multiple antihypertensive drugs are needed in most patients. In this study, the...
C-REACTIVE PROTEIN | angiotensin II receptor antagonist | thiazide diuretic | PULSE-WAVE VELOCITY | AZELNIDIPINE | COMBINATION THERAPY | LOW-DENSITY-LIPOPROTEIN | CHRONIC KIDNEY | BLOOD-PRESSURE | calcium channel blocker | ARTERIAL STIFFNESS | ANKLE VASCULAR INDEX | PERIPHERAL VASCULAR DISEASE | HEART-RATE | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Ankle Brachial Index | Humans | Middle Aged | Calcium Channel Blockers - therapeutic use | Hypertension - drug therapy | Male | Sodium Chloride Symporter Inhibitors - therapeutic use | Azetidinecarboxylic Acid - analogs & derivatives | Azetidinecarboxylic Acid - therapeutic use | C-Reactive Protein - metabolism | Trichlormethiazide - therapeutic use | Adult | Female | Blood Pressure - drug effects | Imidazoles - therapeutic use | Albuminuria - urine | Drug Therapy, Combination | Glomerular Filtration Rate | Hypertension - physiopathology | Cross-Over Studies | Dihydropyridines - therapeutic use | Albuminuria - drug therapy | Diuretics - therapeutic use | Tetrazoles - therapeutic use | Aged | Lipoproteins, LDL - blood
C-REACTIVE PROTEIN | angiotensin II receptor antagonist | thiazide diuretic | PULSE-WAVE VELOCITY | AZELNIDIPINE | COMBINATION THERAPY | LOW-DENSITY-LIPOPROTEIN | CHRONIC KIDNEY | BLOOD-PRESSURE | calcium channel blocker | ARTERIAL STIFFNESS | ANKLE VASCULAR INDEX | PERIPHERAL VASCULAR DISEASE | HEART-RATE | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Ankle Brachial Index | Humans | Middle Aged | Calcium Channel Blockers - therapeutic use | Hypertension - drug therapy | Male | Sodium Chloride Symporter Inhibitors - therapeutic use | Azetidinecarboxylic Acid - analogs & derivatives | Azetidinecarboxylic Acid - therapeutic use | C-Reactive Protein - metabolism | Trichlormethiazide - therapeutic use | Adult | Female | Blood Pressure - drug effects | Imidazoles - therapeutic use | Albuminuria - urine | Drug Therapy, Combination | Glomerular Filtration Rate | Hypertension - physiopathology | Cross-Over Studies | Dihydropyridines - therapeutic use | Albuminuria - drug therapy | Diuretics - therapeutic use | Tetrazoles - therapeutic use | Aged | Lipoproteins, LDL - blood
Journal Article
MEDICINE, ISSN 0025-7974, 04/2019, Volume 98, Issue 15, p. e14994
Objective: The impact of aldosterone blockade using eplerenone on hypertensives with obesity has not been clarified. We compared the efficacy and safety...
MORTALITY | CHRONIC HEART-FAILURE | MANAGEMENT | EFFICACY | SAFETY | eplerenone | FOLLOW-UP | trichlormethiazide | MINERALOCORTICOID RECEPTOR BLOCKADE | MEDICINE, GENERAL & INTERNAL | INSULIN-RESISTANCE | DOUBLE-BLIND | ALDOSTERONE | glucose metabolism | hypertension | obesity | Hypoglycemic Agents - therapeutic use | Overweight - complications | Overweight - drug therapy | Eplerenone - therapeutic use | Humans | Middle Aged | Hypertension - drug therapy | Male | Treatment Outcome | Overweight - physiopathology | Antihypertensive Agents - therapeutic use | Hypertension - physiopathology | Trichlormethiazide - therapeutic use | Glucose - metabolism | Hypertension - complications | Female | Aged | Blood Pressure - drug effects | Hypertension | Overweight persons | Glucose metabolism | Drug therapy | Health aspects | Patient outcomes
MORTALITY | CHRONIC HEART-FAILURE | MANAGEMENT | EFFICACY | SAFETY | eplerenone | FOLLOW-UP | trichlormethiazide | MINERALOCORTICOID RECEPTOR BLOCKADE | MEDICINE, GENERAL & INTERNAL | INSULIN-RESISTANCE | DOUBLE-BLIND | ALDOSTERONE | glucose metabolism | hypertension | obesity | Hypoglycemic Agents - therapeutic use | Overweight - complications | Overweight - drug therapy | Eplerenone - therapeutic use | Humans | Middle Aged | Hypertension - drug therapy | Male | Treatment Outcome | Overweight - physiopathology | Antihypertensive Agents - therapeutic use | Hypertension - physiopathology | Trichlormethiazide - therapeutic use | Glucose - metabolism | Hypertension - complications | Female | Aged | Blood Pressure - drug effects | Hypertension | Overweight persons | Glucose metabolism | Drug therapy | Health aspects | Patient outcomes
Journal Article
Journal of the American Society of Hypertension, ISSN 1933-1711, 2016, Volume 11, Issue 3, pp. 140 - 147
Abstract The aim of the present study was to compare the effects of olmesartan combined with azelnidipine versus olmesartan combined with trichlormethiazide,...
Cardiovascular | telemedicine system | open-label cross-over pilot study | home blood pressure variability | Antihypertensive medication | SELF-MEASUREMENT | MONOTHERAPY | VALIDATION | CALCIUM-CHANNEL BLOCKERS | EUROPEAN-SOCIETY | AMLODIPINE | RECEPTOR BLOCKER | PERIPHERAL VASCULAR DISEASE | ESSENTIAL-HYPERTENSION | PROTOCOL REVISION 2010 | CARDIOVASCULAR RISK | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Calcium Channel Blockers - therapeutic use | Male | Antihypertensive Agents - therapeutic use | Azetidinecarboxylic Acid - analogs & derivatives | Cross-Over Studies | Dihydropyridines - therapeutic use | Drug Therapy, Combination - methods | Pilot Projects | Azetidinecarboxylic Acid - therapeutic use | Trichlormethiazide - therapeutic use | Hypertension - prevention & control | Diuretics - therapeutic use | Female | Tetrazoles - therapeutic use | Aged | Blood Pressure - drug effects | Blood Pressure Monitoring, Ambulatory - methods | Imidazoles - therapeutic use | Diabetes Mellitus, Type 2 - complications
Cardiovascular | telemedicine system | open-label cross-over pilot study | home blood pressure variability | Antihypertensive medication | SELF-MEASUREMENT | MONOTHERAPY | VALIDATION | CALCIUM-CHANNEL BLOCKERS | EUROPEAN-SOCIETY | AMLODIPINE | RECEPTOR BLOCKER | PERIPHERAL VASCULAR DISEASE | ESSENTIAL-HYPERTENSION | PROTOCOL REVISION 2010 | CARDIOVASCULAR RISK | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Calcium Channel Blockers - therapeutic use | Male | Antihypertensive Agents - therapeutic use | Azetidinecarboxylic Acid - analogs & derivatives | Cross-Over Studies | Dihydropyridines - therapeutic use | Drug Therapy, Combination - methods | Pilot Projects | Azetidinecarboxylic Acid - therapeutic use | Trichlormethiazide - therapeutic use | Hypertension - prevention & control | Diuretics - therapeutic use | Female | Tetrazoles - therapeutic use | Aged | Blood Pressure - drug effects | Blood Pressure Monitoring, Ambulatory - methods | Imidazoles - therapeutic use | Diabetes Mellitus, Type 2 - complications
Journal Article
American Journal of Hypertension, ISSN 0895-7061, 5/2014, Volume 27, Issue 5, pp. 695 - 701
BACKGROUND Endothelial progenitor cells (EPCs) induce neovascularization and repair vascular damage. We have demonstrated that EPC function is impaired in...
blood pressure | angiotensin II receptor blocker | essential hypertension | colony formation | endothelial progenitor cell | human | hypertension | CONVERTING ENZYME | OXIDATIVE STRESS | VIVO | RATS | IN-VITRO | PERIPHERAL VASCULAR DISEASE | ANTAGONISTS | EXPRESSION | CULTURES | CARDIOVASCULAR RISK | LIFE | Prospective Studies | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Hypertension - drug therapy | Male | Stem Cells - metabolism | Time Factors | Trichlormethiazide - therapeutic use | Female | Blood Pressure - drug effects | Hypertension - diagnosis | Endothelial Cells - metabolism | Japan | Cells, Cultured | Treatment Outcome | Antihypertensive Agents - therapeutic use | Hypertension - pathology | Hypertension - physiopathology | Hypertension - metabolism | Cross-Over Studies | Losartan - therapeutic use | Stem Cells - drug effects | Stem Cells - pathology | Diuretics - therapeutic use | Cell Proliferation - drug effects | Oxidative Stress - drug effects | Endothelial Cells - pathology | Endothelial Cells - drug effects | Essential hypertension | Somatic cells | Patient outcomes | Angiotensin II receptor blockers | Dosage and administration | Drug therapy | Health aspects | Endothelium | Hypertension | Colonies & territories | Oxidative stress | Rodents
blood pressure | angiotensin II receptor blocker | essential hypertension | colony formation | endothelial progenitor cell | human | hypertension | CONVERTING ENZYME | OXIDATIVE STRESS | VIVO | RATS | IN-VITRO | PERIPHERAL VASCULAR DISEASE | ANTAGONISTS | EXPRESSION | CULTURES | CARDIOVASCULAR RISK | LIFE | Prospective Studies | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Hypertension - drug therapy | Male | Stem Cells - metabolism | Time Factors | Trichlormethiazide - therapeutic use | Female | Blood Pressure - drug effects | Hypertension - diagnosis | Endothelial Cells - metabolism | Japan | Cells, Cultured | Treatment Outcome | Antihypertensive Agents - therapeutic use | Hypertension - pathology | Hypertension - physiopathology | Hypertension - metabolism | Cross-Over Studies | Losartan - therapeutic use | Stem Cells - drug effects | Stem Cells - pathology | Diuretics - therapeutic use | Cell Proliferation - drug effects | Oxidative Stress - drug effects | Endothelial Cells - pathology | Endothelial Cells - drug effects | Essential hypertension | Somatic cells | Patient outcomes | Angiotensin II receptor blockers | Dosage and administration | Drug therapy | Health aspects | Endothelium | Hypertension | Colonies & territories | Oxidative stress | Rodents
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2015, Volume 10, Issue 5, p. e0125519
Objective This study compared the efficacy and safety of azelnidipine with that of trichlormethiazide in Japanese type 2 diabetic patients with hypertension....
AMLODIPINE | COMBINATION | IRBESARTAN | MULTIDISCIPLINARY SCIENCES | Calcium Channel Blockers - adverse effects | Dihydropyridines - administration & dosage | Humans | Middle Aged | Calcium Channel Blockers - therapeutic use | Hypertension - drug therapy | Male | Azetidinecarboxylic Acid - adverse effects | Azetidinecarboxylic Acid - analogs & derivatives | Dihydropyridines - adverse effects | Trichlormethiazide - adverse effects | Azetidinecarboxylic Acid - therapeutic use | Trichlormethiazide - therapeutic use | Female | Blood Pressure - drug effects | Diabetes Mellitus, Type 2 - complications | Diuretics - administration & dosage | Trichlormethiazide - administration & dosage | Japan | Risk Factors | Treatment Outcome | Dihydropyridines - therapeutic use | Calcium Channel Blockers - administration & dosage | Hypertension - complications | Diuretics - therapeutic use | Aged | Diabetes Mellitus, Type 2 - drug therapy | Diuretics - adverse effects | Azetidinecarboxylic Acid - administration & dosage | Hypertension | Type 2 diabetes | Trichlormethiazide | Dosage and administration | Research | Diagnosis | Drug therapy | Comparative analysis | Diabetic retinopathy | Edema | Diabetes mellitus | Clinical trials | Glucose | Metabolism | Patients | Insulin | Blood | Medicine | Hospitals | Older people | Diuretics | Blood pressure | Hypoglycemic agents | Diabetes | Health risk assessment | Drug dosages | Endocrinology
AMLODIPINE | COMBINATION | IRBESARTAN | MULTIDISCIPLINARY SCIENCES | Calcium Channel Blockers - adverse effects | Dihydropyridines - administration & dosage | Humans | Middle Aged | Calcium Channel Blockers - therapeutic use | Hypertension - drug therapy | Male | Azetidinecarboxylic Acid - adverse effects | Azetidinecarboxylic Acid - analogs & derivatives | Dihydropyridines - adverse effects | Trichlormethiazide - adverse effects | Azetidinecarboxylic Acid - therapeutic use | Trichlormethiazide - therapeutic use | Female | Blood Pressure - drug effects | Diabetes Mellitus, Type 2 - complications | Diuretics - administration & dosage | Trichlormethiazide - administration & dosage | Japan | Risk Factors | Treatment Outcome | Dihydropyridines - therapeutic use | Calcium Channel Blockers - administration & dosage | Hypertension - complications | Diuretics - therapeutic use | Aged | Diabetes Mellitus, Type 2 - drug therapy | Diuretics - adverse effects | Azetidinecarboxylic Acid - administration & dosage | Hypertension | Type 2 diabetes | Trichlormethiazide | Dosage and administration | Research | Diagnosis | Drug therapy | Comparative analysis | Diabetic retinopathy | Edema | Diabetes mellitus | Clinical trials | Glucose | Metabolism | Patients | Insulin | Blood | Medicine | Hospitals | Older people | Diuretics | Blood pressure | Hypoglycemic agents | Diabetes | Health risk assessment | Drug dosages | Endocrinology
Journal Article
American Journal of Pathology, The, ISSN 0002-9440, 2014, Volume 184, Issue 2, pp. 442 - 453
Much concern has arisen regarding critical adverse effects of thiazolidinediones (TZDs), including rosiglitazone and pioglitazone, on cardiac tissue. Although...
Pathology | PLACEBO-CONTROLLED CROSSOVER | CARDIOMYOCYTE | ACTIVATED-RECEPTOR-GAMMA | DOUBLE-BLIND | PPAR-GAMMA | DEATH | ROSIGLITAZONE | PATHOLOGY | CONGESTIVE-HEART-FAILURE | INDUCED FLUID RETENTION | WATER | Extracellular Signal-Regulated MAP Kinases - metabolism | PPAR gamma - metabolism | Furosemide - therapeutic use | Spironolactone - pharmacology | Trichlormethiazide - therapeutic use | Ultrasonography | Lipid Metabolism - genetics | Trichlormethiazide - pharmacology | Spironolactone - therapeutic use | Insulin - pharmacology | Diuretics - pharmacology | Mice, Inbred C57BL | Cardiomegaly - diagnostic imaging | Cardiomegaly - drug therapy | Signal Transduction - genetics | Thiazolidinediones - adverse effects | Cardiac Volume - drug effects | Gene Expression Regulation - drug effects | Animals | Cardiomegaly - prevention & control | Signal Transduction - drug effects | Lipid Metabolism - drug effects | Cardiomegaly - chemically induced | Glucose - metabolism | Diuretics - therapeutic use | Mice | Furosemide - pharmacology | Regular
Pathology | PLACEBO-CONTROLLED CROSSOVER | CARDIOMYOCYTE | ACTIVATED-RECEPTOR-GAMMA | DOUBLE-BLIND | PPAR-GAMMA | DEATH | ROSIGLITAZONE | PATHOLOGY | CONGESTIVE-HEART-FAILURE | INDUCED FLUID RETENTION | WATER | Extracellular Signal-Regulated MAP Kinases - metabolism | PPAR gamma - metabolism | Furosemide - therapeutic use | Spironolactone - pharmacology | Trichlormethiazide - therapeutic use | Ultrasonography | Lipid Metabolism - genetics | Trichlormethiazide - pharmacology | Spironolactone - therapeutic use | Insulin - pharmacology | Diuretics - pharmacology | Mice, Inbred C57BL | Cardiomegaly - diagnostic imaging | Cardiomegaly - drug therapy | Signal Transduction - genetics | Thiazolidinediones - adverse effects | Cardiac Volume - drug effects | Gene Expression Regulation - drug effects | Animals | Cardiomegaly - prevention & control | Signal Transduction - drug effects | Lipid Metabolism - drug effects | Cardiomegaly - chemically induced | Glucose - metabolism | Diuretics - therapeutic use | Mice | Furosemide - pharmacology | Regular
Journal Article
American Journal of Hypertension, ISSN 0895-7061, 01/2008, Volume 21, Issue 1, pp. 72 - 77
Background Angiotensin II (Ang II) receptor blocker (ARB) has been reported to have protective effects on the cardiovascular system independent of blood...
MYOCARDIAL-INFARCTION | OXIDASE | RENIN-ANGIOTENSIN SYSTEM | DISEASE | GENE-EXPRESSION | RATS | STEM-CELL | PERIPHERAL VASCULAR DISEASE | NEOVASCULARIZATION | STRESS | NEOINTIMA | Antihypertensive Agents - pharmacology | Tetrazoles - pharmacology | Angiotensin II Type 1 Receptor Blockers - therapeutic use | NADPH Oxidases - metabolism | Hypertension - drug therapy | Male | Vascular Endothelial Growth Factor A - metabolism | Aorta - metabolism | Spin Labels | RNA, Messenger - metabolism | Vascular Endothelial Growth Factor A - genetics | Angiotensin II Type 1 Receptor Blockers - pharmacology | Cyclic N-Oxides - pharmacology | Myocardium - metabolism | NADPH Oxidases - genetics | Trichlormethiazide - pharmacology | Benzimidazoles - therapeutic use | Disease Models, Animal | Endothelial Cells - metabolism | Rats | Antihypertensive Agents - therapeutic use | Hypertension - metabolism | Cell Movement - drug effects | Chemokine CXCL12 - metabolism | Benzimidazoles - pharmacology | Oxidative Stress - drug effects | Endothelial Cells - enzymology | Sodium Chloride, Dietary - administration & dosage | Rats, Inbred WKY | Proto-Oncogene Proteins c-kit - metabolism | Stem Cells - metabolism | Chemokine CXCL12 - genetics | Stem Cells - enzymology | Proto-Oncogene Proteins c-kit - genetics | Blood Pressure - drug effects | Aorta - enzymology | Rats, Inbred SHR | Diuretics - pharmacology | Aorta - drug effects | Cells, Cultured | Renin-Angiotensin System - genetics | Thiobarbituric Acid Reactive Substances - metabolism | Antioxidants - pharmacology | Hypertension - physiopathology | Antioxidants - therapeutic use | Myocardium - enzymology | Animals | Stem Cells - drug effects | Renin-Angiotensin System - drug effects | Tetrazoles - therapeutic use | Cell Proliferation - drug effects | Endothelial Cells - drug effects | Hypertension | Physiological aspects | Oxidation-reduction reaction | Angiotensin II receptor blockers | Endothelium
MYOCARDIAL-INFARCTION | OXIDASE | RENIN-ANGIOTENSIN SYSTEM | DISEASE | GENE-EXPRESSION | RATS | STEM-CELL | PERIPHERAL VASCULAR DISEASE | NEOVASCULARIZATION | STRESS | NEOINTIMA | Antihypertensive Agents - pharmacology | Tetrazoles - pharmacology | Angiotensin II Type 1 Receptor Blockers - therapeutic use | NADPH Oxidases - metabolism | Hypertension - drug therapy | Male | Vascular Endothelial Growth Factor A - metabolism | Aorta - metabolism | Spin Labels | RNA, Messenger - metabolism | Vascular Endothelial Growth Factor A - genetics | Angiotensin II Type 1 Receptor Blockers - pharmacology | Cyclic N-Oxides - pharmacology | Myocardium - metabolism | NADPH Oxidases - genetics | Trichlormethiazide - pharmacology | Benzimidazoles - therapeutic use | Disease Models, Animal | Endothelial Cells - metabolism | Rats | Antihypertensive Agents - therapeutic use | Hypertension - metabolism | Cell Movement - drug effects | Chemokine CXCL12 - metabolism | Benzimidazoles - pharmacology | Oxidative Stress - drug effects | Endothelial Cells - enzymology | Sodium Chloride, Dietary - administration & dosage | Rats, Inbred WKY | Proto-Oncogene Proteins c-kit - metabolism | Stem Cells - metabolism | Chemokine CXCL12 - genetics | Stem Cells - enzymology | Proto-Oncogene Proteins c-kit - genetics | Blood Pressure - drug effects | Aorta - enzymology | Rats, Inbred SHR | Diuretics - pharmacology | Aorta - drug effects | Cells, Cultured | Renin-Angiotensin System - genetics | Thiobarbituric Acid Reactive Substances - metabolism | Antioxidants - pharmacology | Hypertension - physiopathology | Antioxidants - therapeutic use | Myocardium - enzymology | Animals | Stem Cells - drug effects | Renin-Angiotensin System - drug effects | Tetrazoles - therapeutic use | Cell Proliferation - drug effects | Endothelial Cells - drug effects | Hypertension | Physiological aspects | Oxidation-reduction reaction | Angiotensin II receptor blockers | Endothelium
Journal Article
10.
Full Text
A case of nephrogenic diabetes insipidus during transsphenoidal pituitary adenomectomy
Journal of Neurosurgical Anesthesiology, ISSN 0898-4921, 01/2016, Volume 28, Issue 1, pp. 79 - 80
SURGERY | ANESTHESIOLOGY | CLINICAL NEUROLOGY | Pituitary Neoplasms - surgery | Diabetes Insipidus, Nephrogenic - drug therapy | Diabetes Insipidus, Nephrogenic - complications | Trichlormethiazide - therapeutic use | Vasopressins - therapeutic use | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Pituitary Gland - surgery | Humans | Female | Aged | Sodium Chloride Symporter Inhibitors - therapeutic use | Intraoperative Complications - drug therapy
Journal Article
Hypertension, ISSN 0194-911X, 1999, Volume 34, Issue 5, pp. 1129 - 1133
Although diuretics are recommended for the treatment of hypertension, decreased diuretic use and increased calcium antagonist use necessitate a comparison of...
Hypertension | Diuretics | Elderly | Calcium antagonist | Double-Blind Method | Humans | Calcium Channel Blockers - therapeutic use | Pulse | Hypertension - drug therapy | Male | Nicardipine - therapeutic use | Sodium Chloride Symporter Inhibitors - therapeutic use | Hypertension - physiopathology | Trichlormethiazide - adverse effects | Nicardipine - adverse effects | Trichlormethiazide - therapeutic use | Hypertension - complications | Female | Aged | Blood Pressure - drug effects
Hypertension | Diuretics | Elderly | Calcium antagonist | Double-Blind Method | Humans | Calcium Channel Blockers - therapeutic use | Pulse | Hypertension - drug therapy | Male | Nicardipine - therapeutic use | Sodium Chloride Symporter Inhibitors - therapeutic use | Hypertension - physiopathology | Trichlormethiazide - adverse effects | Nicardipine - adverse effects | Trichlormethiazide - therapeutic use | Hypertension - complications | Female | Aged | Blood Pressure - drug effects
Journal Article
The American Journal of the Medical Sciences, ISSN 0002-9629, 05/2010, Volume 339, Issue 5, pp. 433 - 439
The optimal combination treatment for hypertension has not been established. We investigated the effect of a calcium channel blocker or a diuretic added to...
Hypertension | Angiotensin receptor blocker | Combination therapy | Calcium channel blocker | Wave reflection | Calcium channelblocker | CONVERTING ENZYME-INHIBITOR | OXIDATIVE STRESS | ASYMMETRIC DIMETHYLARGININE | WAVE-FORM | ANTIHYPERTENSIVE DRUG | CENTRAL AORTIC PRESSURE | BLOOD-PRESSURE | ACE-INHIBITORS | MEDICINE, GENERAL & INTERNAL | ARTERIAL STIFFNESS | NITRIC-OXIDE | Diuretics - administration & dosage | Trichlormethiazide - administration & dosage | Dihydropyridines - administration & dosage | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Calcium Channel Blockers - therapeutic use | Hypertension - drug therapy | Male | Azetidinecarboxylic Acid - analogs & derivatives | Hypertension - physiopathology | Dihydropyridines - therapeutic use | Azetidinecarboxylic Acid - therapeutic use | Trichlormethiazide - therapeutic use | Calcium Channel Blockers - administration & dosage | Diuretics - therapeutic use | Female | Aged | Blood Pressure - drug effects | Drug Therapy, Combination | Angiotensin II Type 1 Receptor Blockers - administration & dosage | Azetidinecarboxylic Acid - administration & dosage
Hypertension | Angiotensin receptor blocker | Combination therapy | Calcium channel blocker | Wave reflection | Calcium channelblocker | CONVERTING ENZYME-INHIBITOR | OXIDATIVE STRESS | ASYMMETRIC DIMETHYLARGININE | WAVE-FORM | ANTIHYPERTENSIVE DRUG | CENTRAL AORTIC PRESSURE | BLOOD-PRESSURE | ACE-INHIBITORS | MEDICINE, GENERAL & INTERNAL | ARTERIAL STIFFNESS | NITRIC-OXIDE | Diuretics - administration & dosage | Trichlormethiazide - administration & dosage | Dihydropyridines - administration & dosage | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Calcium Channel Blockers - therapeutic use | Hypertension - drug therapy | Male | Azetidinecarboxylic Acid - analogs & derivatives | Hypertension - physiopathology | Dihydropyridines - therapeutic use | Azetidinecarboxylic Acid - therapeutic use | Trichlormethiazide - therapeutic use | Calcium Channel Blockers - administration & dosage | Diuretics - therapeutic use | Female | Aged | Blood Pressure - drug effects | Drug Therapy, Combination | Angiotensin II Type 1 Receptor Blockers - administration & dosage | Azetidinecarboxylic Acid - administration & dosage
Journal Article
Indian Journal of Pharmacology, ISSN 0253-7613, 11/2014, Volume 46, Issue 6, pp. 657 - 659
Hyponatremia is a known adverse effect of duloxetine, and it can lead to potentially life-threatening complications. Administration of thiazide diuretics also...
duloxetine | Drug interaction | syndrome of inappropriate secretion of antidiuretic hormone syndrome | trichlormethiazide | PHARMACOLOGY & PHARMACY | Hyponatremia - chemically induced | Drug Interactions | Thiophenes - adverse effects | Trichlormethiazide - therapeutic use | Humans | Aged, 80 and over | Duloxetine Hydrochloride | Female | Antidepressive Agents - adverse effects | Sodium Chloride Symporter Inhibitors - therapeutic use | Causes of | Diuretics | Aged patients | Dosage and administration | Hyponatremia | Drug therapy | Drug Watch
duloxetine | Drug interaction | syndrome of inappropriate secretion of antidiuretic hormone syndrome | trichlormethiazide | PHARMACOLOGY & PHARMACY | Hyponatremia - chemically induced | Drug Interactions | Thiophenes - adverse effects | Trichlormethiazide - therapeutic use | Humans | Aged, 80 and over | Duloxetine Hydrochloride | Female | Antidepressive Agents - adverse effects | Sodium Chloride Symporter Inhibitors - therapeutic use | Causes of | Diuretics | Aged patients | Dosage and administration | Hyponatremia | Drug therapy | Drug Watch
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 9/2013, Volume 28, Issue 9, pp. 1881 - 1884
Four genes responsible for pseudohypoaldosteronism type II (PHA-II) have been identified, thereby facilitating molecular diagnostic testing.A 1-year-old boy...
Hypertension | Pediatrics | Sodium-chloride co-transporter | Hyperkalemia | Medicine & Public Health | Pseudohypoaldosteronism | Cullin-3 | Metabolic acidosis | ACIDOSIS | UROLOGY & NEPHROLOGY | PEDIATRICS | MUTATIONS | Acid-Base Imbalance - blood | Pseudohypoaldosteronism - therapy | Genetic Testing | Introns - genetics | Acidosis - etiology | Pseudohypoaldosteronism - genetics | Humans | RNA, Messenger - genetics | Exons - genetics | Infant | Male | Acidosis - therapy | Acid-Base Imbalance - genetics | Cullin Proteins - genetics | Trichlormethiazide - therapeutic use | Pseudohypoaldosteronism - diagnosis | Diuretics - therapeutic use | Potassium - blood | Bicarbonates - blood | Blood Pressure - physiology | Chlorides - blood | Real-Time Polymerase Chain Reaction | Case studies | Medical research | Medicine, Experimental | Hypoaldosteronism | Children | Diseases | Acidosis
Hypertension | Pediatrics | Sodium-chloride co-transporter | Hyperkalemia | Medicine & Public Health | Pseudohypoaldosteronism | Cullin-3 | Metabolic acidosis | ACIDOSIS | UROLOGY & NEPHROLOGY | PEDIATRICS | MUTATIONS | Acid-Base Imbalance - blood | Pseudohypoaldosteronism - therapy | Genetic Testing | Introns - genetics | Acidosis - etiology | Pseudohypoaldosteronism - genetics | Humans | RNA, Messenger - genetics | Exons - genetics | Infant | Male | Acidosis - therapy | Acid-Base Imbalance - genetics | Cullin Proteins - genetics | Trichlormethiazide - therapeutic use | Pseudohypoaldosteronism - diagnosis | Diuretics - therapeutic use | Potassium - blood | Bicarbonates - blood | Blood Pressure - physiology | Chlorides - blood | Real-Time Polymerase Chain Reaction | Case studies | Medical research | Medicine, Experimental | Hypoaldosteronism | Children | Diseases | Acidosis
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 2009, Volume 24, Issue 6, pp. 1235 - 1238
The administration of angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin type 1 receptor blockers (ARBs) to pregnant women has been reported to...
Water restriction test | Urine cyclic AMP | Angiotensin receptor blocker fetopathy | Nephrotoxicity | Urinary concentrating ability | Vasopressin V2 receptor | RATS | UROLOGY & NEPHROLOGY | PEDIATRICS | MECHANISMS | ENZYME-INHIBITOR FETOPATHY | ENALAPRIL | Prenatal Exposure Delayed Effects | Angiotensin II Type 1 Receptor Blockers - adverse effects | Diabetes Insipidus, Nephrogenic - physiopathology | Humans | Child, Preschool | Male | Treatment Outcome | Aspartic Acid - therapeutic use | Sodium Chloride Symporter Inhibitors - therapeutic use | Kidney Function Tests | Pregnancy | Glomerular Filtration Rate - drug effects | Renal Insufficiency - therapy | Arginine Vasopressin - metabolism | Trichlormethiazide - therapeutic use | Female | Peritoneal Dialysis - methods | Child | Cyclic AMP - urine | Diabetes Insipidus, Nephrogenic - chemically induced | Causes of | Antihypertensive drugs | Complications and side effects | Usage | Diabetes insipidus | Index Medicus
Water restriction test | Urine cyclic AMP | Angiotensin receptor blocker fetopathy | Nephrotoxicity | Urinary concentrating ability | Vasopressin V2 receptor | RATS | UROLOGY & NEPHROLOGY | PEDIATRICS | MECHANISMS | ENZYME-INHIBITOR FETOPATHY | ENALAPRIL | Prenatal Exposure Delayed Effects | Angiotensin II Type 1 Receptor Blockers - adverse effects | Diabetes Insipidus, Nephrogenic - physiopathology | Humans | Child, Preschool | Male | Treatment Outcome | Aspartic Acid - therapeutic use | Sodium Chloride Symporter Inhibitors - therapeutic use | Kidney Function Tests | Pregnancy | Glomerular Filtration Rate - drug effects | Renal Insufficiency - therapy | Arginine Vasopressin - metabolism | Trichlormethiazide - therapeutic use | Female | Peritoneal Dialysis - methods | Child | Cyclic AMP - urine | Diabetes Insipidus, Nephrogenic - chemically induced | Causes of | Antihypertensive drugs | Complications and side effects | Usage | Diabetes insipidus | Index Medicus
Journal Article
Clinical and Experimental Hypertension, ISSN 1064-1963, 12/2009, Volume 31, Issue 8, pp. 648 - 656
This study was performed to investigate the additional anti-hypertensive effects and safety of low-dose thiazide diuretic, trichlormethiazide (TCTZ), and a...
spironolactone | hypertension | thiazide diuretics | Hypertension | Spironolactone | Thiazide diuretics | PHARMACOLOGY & PHARMACY | PERIPHERAL VASCULAR DISEASE | ALDOSTERONE | BLOOD-PRESSURE | Diuretics - administration & dosage | Trichlormethiazide - administration & dosage | Prospective Studies | Spironolactone - administration & dosage | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Hypertension - drug therapy | Treatment Outcome | Angiotensin-Converting Enzyme Inhibitors - administration & dosage | Hypertension - physiopathology | Dose-Response Relationship, Drug | Outpatients | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Trichlormethiazide - therapeutic use | Diuretics - therapeutic use | Aged | Blood Pressure - drug effects | Drug Therapy, Combination | Spironolactone - therapeutic use | Angiotensin II Type 1 Receptor Blockers - administration & dosage
spironolactone | hypertension | thiazide diuretics | Hypertension | Spironolactone | Thiazide diuretics | PHARMACOLOGY & PHARMACY | PERIPHERAL VASCULAR DISEASE | ALDOSTERONE | BLOOD-PRESSURE | Diuretics - administration & dosage | Trichlormethiazide - administration & dosage | Prospective Studies | Spironolactone - administration & dosage | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Middle Aged | Hypertension - drug therapy | Treatment Outcome | Angiotensin-Converting Enzyme Inhibitors - administration & dosage | Hypertension - physiopathology | Dose-Response Relationship, Drug | Outpatients | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Trichlormethiazide - therapeutic use | Diuretics - therapeutic use | Aged | Blood Pressure - drug effects | Drug Therapy, Combination | Spironolactone - therapeutic use | Angiotensin II Type 1 Receptor Blockers - administration & dosage
Journal Article
Clinical and Experimental Hypertension, ISSN 1064-1963, 2/2015, Volume 37, Issue 1, pp. 33 - 38
Abstract Sympathoexcitation and oxidative stress in the brain have pivotal roles in hypertension with metabolic syndrome (MetS). Here, we examined whether oral...
metabolic syndrome | combination therapy | sympathetic activity | Angiotensin II receptor blocker | diuretics | hypertension | Hypertension | Diuretics | Sympathetic activity | Combination therapy | Metabolic syndrome | SYMPATHOEXCITATION | OXIDATIVE STRESS | RECEPTOR BLOCKADE | NERVE ACTIVITY | TELMISARTAN | OBESITY | CARDIOVASCULAR REGULATION |
metabolic syndrome | combination therapy | sympathetic activity | Angiotensin II receptor blocker | diuretics | hypertension | Hypertension | Diuretics | Sympathetic activity | Combination therapy | Metabolic syndrome | SYMPATHOEXCITATION | OXIDATIVE STRESS | RECEPTOR BLOCKADE | NERVE ACTIVITY | TELMISARTAN | OBESITY | CARDIOVASCULAR REGULATION |