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Query: UMLS:C0020538 (hypertension)
170,190 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In a presentation of the treatment of high blood pressure with saluretics, the course of action especially and the therapeutic aspects of medical prohibition of salt in this indication are discussed in addition to referring to the pathogenetic importance of sodium for hypertension. Two phases of action can be differentiated in the lowering of blood pressure after saluretics. The antihypertensive action in the first (renal) phase is based on the reduction in volume of the extracellular fluid which accompanies the elimination of sodium and water, in the second (extrarenal) phase a lowering of vessel tone and peripheral resistance is responsible.
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PMID:[Saluretics in the treatment of hypertension (author's transl)]. 80 19

The following experiments demonstrate that the severity of toxemia is proportional to the degree of reduction in blood flow to the pregnant uterus. Blood pressure and blood flow variations were studied in 21 nonpregnant and pregnant dogs following the placement of a progressive stricture on the abdominal aorta below the renal arteries. The immediate effect of the stricture was a mild hypertension in half of the pregnant dogs; in addition, in all the dogs, the blood flow progressively dropped in the arteries below the stricture (femoral and uterine) while it remained constant in the arteries above (ovarian and renal). In 3 of 5 pregnant dogs the delayed effect of the aortic stricture was hypertension associated with all the other signs of experimental toxemia. Removal of the aortic stricture after 10 days immediately improved the blood flow below the stricture. No noticeable preferential distribution of blood toward the pregnant uterus was noted during the constriction.
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PMID:Hemodynamic studies in experimental toxemia of the dog. 89 98

The incidence of hypertension (HT) in renal parenchymal disease of the young is very high, varying from 38 to 78%. This points to the central role of the kidneys in normal blood pressure control. HT in chronic renal failure (CRF) and end-stage renal disease (ESRD) depends on the nature of the underlying disease. The degree of renal failure has a highly variable effect. The clinical signs and symptoms of this form of HT are often superimposed on those of the basic (renal) disorder. The pathogenesis of HT in CRF is dominated by volume- and renin-mediated mechanisms. In addition, a wide variety of humoral and neural factors play a role. The HT seen in patients on renal replacement therapy (RRT) and after renal transplantation (Tx) poses special problems. In this paper these various aspects of HT in CRF are discussed and the principles of treatment are reviewed. It has been shown beyond any doubt that control of HT in young patients with CRF and ESRD, treated conservatively or on RRT and after renal Tx is of utmost importance for their long-term outcome. This is an important challenge for all pediatricians looking after young patients with CRF and ESRD.
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PMID:Hypertension in children and adolescents with chronic renal failure and end-stage renal disease. 177 94

Functional studies in humans and animals with essential hypertension have shown a hyperventilation under resting conditions and striking respiratory and circulatory reactions to hypoxic and hyperoxic tests. There is some evidence that these reactions are due to enhanced activity of the peripheral arterial chemoreceptors. In contrast, in secondary (renal) hypertension such findings could not be observed. Many morphological, morphometrical and biochemical studies have been performed on the carotid bodies of a variety of hypertensive patients and animal models. Whilst their structure and catecholamine content are changed in hypertension, there are many differences in different types of hypertension and, furthermore, a convincing link between the morphological and biochemical findings from the carotid body studies and their functional overactivity has not been shown. Some of these alterations are caused by the elevated blood pressure (e.g. vascular pathology); others are the expression of general disturbances in the hypertensive disease state (e.g. differences in catecholamine content) whilst others are probably of genetic origin but independent of elevated blood pressure (carotid body volume in different rat models of hypertension). This paper reviews the findings on carotid body structure and function in a variety of animal models of hypertension and in primary and secondary human hypertension.
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PMID:Peripheral arterial chemoreceptors and hypertension. 194 13

Previous studies strongly suggest that adenosine receptors on juxtaglomerular cells function to restrain the secretion of renin induced by a variety of stimuli. The clinical significance of this is that caffeine, a widely consumed adenosine receptor antagonist, could augment renin release responses to diseases such as renovascular hypertension, liver cirrhosis and heart failure and to therapeutic maneuvers such as salt restriction, diuretics and vasodilators. Caffeine may be particularly troublesome in this regard because this methylxanthine has central nervous system effects and intracellular actions that also might contribute to the overall ability of caffeine to potentiate renin secretion. The purpose of this study was to document the effects of caffeine on renin release responses to a vasodilator and to investigate what mechanisms were responsible for any augmentation of vasodilator-induced renin secretion. Accordingly, we compared the effects of caffeine vs. 1,3-dipropyl-8-p-sulfophenylxanthine (DPSPX; a xanthine that we documented in this study not to significantly enter the brain or penetrate cell membranes) on base-line and hydralazine-induced renin release in both normal and beta adrenoceptor-blocked (propranolol, 15 mg/kg) rats. Both xanthines (at a dose of 10 mg/kg plus 150 micrograms/min) attenuated adenosine-mediated hypotension and bradycardia, and DPSPX was at least as effective as caffeine in antagonizing peripheral adenosine receptors. Caffeine and DPSPX increased base-line plasma renin activity to a similar extent regardless of whether the animals were pretreated with propranolol. In rats with an intact beta adrenergic system, caffeine, but not DPSPX, increased the renin release response to low-dose hydralazine (1 mg/kg). Although both xanthines augmented the renin release response to high-dose hydralazine (10 mg/kg), caffeine was more efficacious in this regard. In beta adrenoceptor-blocked rats, neither caffeine nor DPSPX augmented the renin release response to low-dose hydralazine, whereas both xanthines equally potentiated the renin release response to high-dose hydralazine. These data demonstrate that caffeine increases base-line renin release primarily by blocking peripheral (most likely renal), cell-surface adenosine receptors; however, caffeine potentiates vasodilator-induced renin secretion in part by blocking peripheral (most likely renal), cell-surface adenosine receptors and in part by additional central nervous system and/or intracellular mechanism(s) that involve the beta adrenergic system.
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PMID:Caffeine potentiates vasodilator-induced renin release. 200 84

The incidence of district (cardiac, cerebral, renal) and systemic vascular complications was studied in a population of 3992 hypertensive in-patients during the period from 1984 to 1988. The total number of male hypertensive patients was always higher (2355) than that of female hypertensive patients (1637). From the analysis of results it appears that 11.01% of male hypertensive patients and 15.85% of female hypertensive patients were diagnosed as being affected by uncomplicated essential arterial hypertension, whereas 88.97% of male and 84.12% of female hypertensive patients suffered from arterial hypertension with varying percentages of cardiac, cerebral, renal or systemic-type atheroarteriosclerotic complications. The prevalence of the male sex was particularly evident in the case of cardiac complications. Given the peak incidence of the various types of complications when analysed by decade of age, an earlier incidence of cardiac and renal complications was found in male hypertensive patients which anticipates the complications found in female hypertensive patients by approximately one decade. Lastly, the paper underlines the social importance of essential arterial hypertension and the need to develop efficacious primary and secondary prevention in order to reduce the incidence of complications which today represent the most severe aspect of hypertension.
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PMID:[Incidence of the most frequent complications in hypertensive patients]. 209 50

We have developed a new method of total intravenous anesthesia with droperidol, fentanyl and ketamine and have administered it to more than 400 surgical patients, ranging in ages from 4 to 80 years. Cardiac and neurosurgical patients were excluded. After establishing a routine monitoring, droperidol 0.06-0.1 ml.kg-1 was slowly given. After 5 minutes, fentanyl 1-2 micrograms.kg-1 and ketamine 1.0-1.5 mg.kg-1 were slowly administered intravenously. Trachea was intubated following intravenous succinylcholine. A total dose of 5-15 micrograms.kg-1 of fentanyl was given intravenously with a continuous infusion of ketamine 2 mg.kg-1.hr-1 during surgical procedure. Air and O2 (FIO2 0.30-0.35) were given and muscle relaxation was achieved with necessary dose of intravenous pancuronium or vecuronium and no inhaled anesthetic was given. Total intravenous anesthesia has many advantages such as no air pollution in the operating theatre, empty bowels, no organ (hepato-renal) toxicity, good peripheral perfusion and low cost, while this method has several disadvantages to overcome such as hypertension. There are many anesthetic agents for total intravenous anesthesia. However, sufentanil, alfentanil and propofol are not available. Droperidol, fentanyl and ketamine are the best combination for this purpose in Japan so far.
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PMID:[Clinical study on total intravenous anesthesia with droperidol, fentanyl and ketamine--1. Introduction]. 224 9

In healthy adolescents, patients with essential hypertension (EH) or symptomatic (renal) hypertension (SRH), erythrocyte electrolyte composition and membrane permeability were studied for Na+ and K+ (as an example Na+ and K+ current rates being studied by the Garay and Meyer method, 1979). Study into the erythrocyte Na+ and K+ concentrations in adolescents demonstrated that those having EH exhibited higher Na+ concentrations than in healthy ones. The adolescents with EH showed abnormal erythrocyte membrane permeability that appeared as changed Na+ and K+ current rates. Such changes were not detected in the erythrocytes of adolescents with SRH. The results of the study into erythrocyte membrane permeability in healthy adolescents and patients with EH or SRH confirm the fact that this index may be used as an additional test for differential diagnosis of EH and SRH.
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PMID:[Erythrocyte membrane permeability to monovalent ions of sodium and potassium in adolescents with essential arterial hypertension and renal hypertension]. 238 Nov 22

The data on erythrocyte membrane permeability for Na and K ions, obtained in the studies of Na+-K+ cotransport in erythrocytes of 38 patients with essential hypertension, stage I and II, 9 patients with borderline hypertension and 12 patients with symptomatic (renal) hypertension are reviewed. The data demonstrate that Na+-K+ cotransport in Na+ loaded and K+-depleted erythrocytes under the effect of P-chlormercuribenzoate was considerably reduced in patients with essential hypertension and borderline hypertension than in the control group. No deviations from the normal Na+-K+ cotransport were observed in renal hypertension. Disturbances of erythrocyte membrane permeability have been also revealed in practically healthy subjects (15 cases) with family history of hypertension.
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PMID:[Characteristics of the Na+-K+-cotransport system in the erythrocyte membrane of patients with hypertension and symptomatic (renal) hypertension]. 243 Jun 41

The form and surface architectonic of erythrocytes studied in 18 teenagers and men with hypertensive disease of I stage (HD) and in 7 men with symptomatic (renal) hypertension (SH). Simultaneously permeability of erythrocyte membranes for Na+ and K+ was studies. The change in the form and surface architectonics was found in the erythrocytes of the patients with hypertensive disease, I stage. The same was true for the patients with renal hypertension but the difference was not so prominent. Rapid shift of correlation of erythrocyte morphological varieties has been revealed during the study of Na+ and K+ ions' transport rate after the treatment by p-chloromercuribenzoate acid. Increase of irreversible transformation of erythrocytes was discovered in patients with HD. Besides in some cases there was decrease in the size of echinocytes. The transformation of erythrocytes into echinocytes is more prominent in healthy subjects and in patients with SH. Our data suggest that the change in erythrocyte form is related to the change of erythrocyte membrane permeability to Na+ and K+ ions and the alteration of membrane structure is the basis for these disturbances.
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PMID:[Erythrocyte membrane permeability for univalent cations (Na+, K+) and their transformation in patients with hypertension and symptomatic (renal) hypertension]. 273 86


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