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At least 307 records · Page 17Linked to original sources

[Characteristics of the formation of human cardiovascular system reactions to acute hypoxia].

"Emergency" adaptation of the cardiovascular system of a healthy person to acute hypoxia produced by inspiration of a gas mixture containing 11% oxygen was accomplished in two ways: (a) with prevalence of the cardiac component, increase in the cardiac and systolic indices and end-diastolic volume in unaltered ejection fraction and diminished general vascular tonus; (b) with prevalence of the vascular component, decrease in the cardiac and systolic indices, end-diastolic volume, and muscular and skin blood flow and increase in peripheral resistance. After 10 days of training for hypoxia in a pressure chamber the reaction of the cardiorespiratory system to the hypoxia test was less pronounced but its trend was maintained.

Acute Disease↗

[Normal and abnormal aging of cardiovascular system].

Studies of normal aging in the cardiovascular system in humans are affected by the study population. Besides intrinsic biological aging, extrinsic factors including overt or latent cardiovascular diseases as well as life style variables such as physical activity, diet, alcohol and smoking may influence the age-related changes of cardiovascular function. We have recruited "normal" elderly subjects from community-dwelling volunteers by extensive health screening procedures including treadmill maximum exercise tests. Some of their cardiovascular functions, such as various cardiovascular regulatory functions, were altered compared to normal young subjects, while others such as resting hemodynamics were not. Interrelationships among various autonomic functions in the elderly were not recognized. Although general effects of life styles on circulatory regulatory functions were not clearly indicated, variables such as sodium intake or body mass index appeared to affect some of the sympathetic nervous functions. Furthermore, hypertension in the elderly had much less impact on cardiovascular functions than is generally expected, based on the results from young or middle-aged subjects. To identify factors which either modify (accelerate) or do not affect the aging of the cardiovascular functions is important not only to achieve a good aging process but also to establish therapeutic goals in elderly subjects.

Aged↗

[The effect of neurotensin on the cardiovascular system].

Neurotensin is a peptide involved in regulation of cardiovascular system. Neurotensin immunoreactivity is found in myocardium, conduction system of the heart, intracardiac ganglion cells, coronary vessels. High content of this peptide is also determined in structures of sympathoadrenal system. This creates the possibility of hormonal neurotensin action on the heart following sympathetic activation. Neurotensin accelerates heart rate, increases myocardial contractility, affects central haemodynamics, regional blood flow and coronary circulation. Neurotensin modulates autonomic influences on the heart and plays role in mechanisms of cardiac arrhythmogenesis, especially in dynamics of vagally induced cardiac rhythm disorders. Cardiovascular effects of this peptide may be associated with direct influence on the heart and vessels, stimulating action on release of histamine and catecholamines and activation of capsaicin-sensitive afferent neurons which contain calcitonin-gene related peptide and substance P. Cardiovascular action of neurotensin is species dependent and it is followed by pronounced tachyphylaxis. Cellular mechanism of neurotensin action is associated with stimulation of phosphoinositide turnover, elevation of intracellular calcium and cyclic nucleotides level.

Animals↗

[An estimation of the prevalence of risk factors for the cardiovascular system among female telephone operators].

The dissemination of the standard risk factors for the cardiovascular system--smoking, family history of hypertension and abnormal weight in telephone operators is evaluated by including one, two or three of these factors (p = 260). A high relative part is taken by persons in the presence of the evaluated factors--75.8%, as the most highly spread is the factor "smoking" (58.8%) and smoking and family predisposition (15.4"). In persons with high blood pressure the dissemination of one or two of the examined risk factors is nearly the same, with heightened presence of "smoking and abnormal weight". In spite of the lack correlation between the studied risk factors and the arterial blood pressure, their dissemination on a large scale as well as the specific character of the telephone operators work certify a heightened risk of diseases of the cardiovascular system and the necessity of special attention to these endangered people.

Adult↗

[Effect of experimental hypokinesia on adrenergic reactivity of the cardiovascular system in rabbits].

In the experiments on rabbits under prolonged hypokinesia the functions of the cardiovascular system and the adrenergic reactivity of blood pressure were studied. The increase of the heart rate at rest, clear tendency to the decrease of the arterial blood pressure and no changes of the venous pressure are shown. The reliable decrease of the maximum size and duration of the blood pressure reactions to adrenaline are demonstrated. These changes prove the decrease of the functional possibilities and adrenergic reactivity of the cardiovascular system under hypokinetic conditions.

Animals↗

Lack of effect of acetaldehyde on the cardiovascular system in rats.

The present study was designed to evaluate the kinetics of acetaldehyde (ACT) and and its action on the cardiovascular system in rats. ACT (3, 6, 12 mg/kg i.p.) causes accumulation of this metabolite in the blood, at a concentration corresponding to that obtained from ethanol metabolism after its administration in doses of 1, 2, 4 g/kg p.o., respectively. After intraperitoneal injection of ACT there were no significant changes in blood pressure and heart rate in comparison to the control group. It appears that, in rats, ACT has no influence on the function of the cardiovascular system after the ingestion of ethanol.

Acetaldehyde↗

Cyclic nucleotide phosphodiesterase-mediated integration of cGMP and cAMP signaling in cells of the cardiovascular system.

Numerous pharmacological and physiological agents acting via either cAMP- or cGMP-mediated impact the activities of cells of the cardiovascular system. While most define cAMP and cGMP signaling systems as separate and independent, recent advances in our understanding of cyclic nucleotide signaling, and more specifically, of the roles which cyclic nucleotide phosphodiesterases (PDEs) play in these events, have altered this view. In this short chapter, I will review the data identifying expression of several PDEs in cells of the cardiovascular system. In addition, I will review the data that identify PDEs as enzymes capable of allowing integration between cAMP and cGMP signaling in cells, and propose that cAMP and cGMP signaling systems can represent parallel and interdependent signaling systems. Moreover, I will propose that cGMP-mediated effects on the activities of variants of the Phosphodiesterase 2 (PDE2), PDE3 and PDE5 families may act to coordinate linkage between cAMP and cGMP signaling in these cells.

3',5'-Cyclic-AMP Phosphodiesterases↗

[The cardiovascular system at long periods after radiotherapy of lymphogranulomatosis].

The cardiovascular system was analysed in 157 patients with Hodgkin's disease in a prolonged remission after radiation therapy including irradiation of the mediastinum. The revealed myocardial changes were equally often noted in different irradiation volumes of the heart within the range of 31 to 45 Gy. The number of changes was growing with time. Functional disorders of the pulmonary, hepatic and capillary vessels were also revealed.

Adult↗

Protective effects of estrogen on the cardiovascular system.

Estrogen has direct and indirect effects on the cardiovascular system that are mediated by the estrogen receptors ER-alpha and ER-beta. The direct effects of estrogen occur through rapid nongenomic and longer-term genomic pathways. The rapid effects of estrogen are mediated by ERs and result in the activation of endothelial nitric oxide synthase, leading to arterial vasodilation. Longer-term effects involve changes in gene and protein expression, modulating the response to injury and atherosclerosis. Estrogen also indirectly influences serum lipoprotein and triglyceride profiles, and the expression of coagulant and fibrinolytic proteins. Advanced atherosclerosis and certain progestins, however, may attenuate some of the protective effects of estrogen.

Animals↗

Molecular biology of calcium channels in the cardiovascular system.

Calcium ions are key intracellular messengers in the cardiovascular system. Calcium homeostasis is regulated by an extracellular cycle, which controls the entry and removal of calcium between the cytosol and extracellular space, and an intracellular cycle, which controls calcium fluxes between the cytosol and intracellular stores in the sarcoplasmic reticulum. Several protein families mediate these calcium fluxes including those that (1) regulate the entry of calcium into the cytosol; (2) recognize calcium within the cytosol; and (3) remove calcium from the cytosol. Intracellular calcium binding proteins (the "E-F hand" proteins) recognize the appearance of calcium in the cytosol; in the heart and vascular smooth muscle, these proteins initiate excitation-contraction coupling. Calcium efflux occurs via adenosine triphosphate (ATP)-dependent calcium pumps and sodium-calcium exchangers, while two families of channels--intracellular release calcium channels and plasma membrane calcium channels--regulate calcium entry into the cytosol. The plasma membrane calcium channels, which include the L- and T-type channels, are of the greatest clinical interest because they are targets for pharmacologic therapy. T-type calcium channels, which activate contraction in vascular smooth muscle but have little or no role in cardiac excitation-contraction coupling, appear to be involved in signal transduction pathways that promote cell growth and proliferation. Calcium channel blockers that selectively block T-type calcium channels, therefore, offer a novel approach to cardiovascular drug therapy.

Calcium↗

[The effect of atenolol on the cardiovascular system (author's transl)].

Effects of atenolol on the cardiovascular system were studied in rats and dogs. Atenolol (10 microgram/kg - 3 mg/kg) did not increase heart rate significantly in rats pretreated with reserpine (5 mg/kg), while a significant increase occurred with practolol (30 microgram/kg - 3 mg/kg). Atenolol (100 microgram/kg) inhibited the response of canine heart (heart rate and myocardial contractile force) to isoproterenol to a similar degree as seen with propranolol (100 microgram/kg) did. The ability of atenolol to inhibit vasodilating action of isoproterenol, however, was about 1/12 of that of propranolol. Atenolol (0.5 mg/kg) did not inhibit hemodynamic responses to ouabain and CaCl2 in dogs, while this drug inhibited these responses to isoproterenol. Atenolol decreased heart rate, myocardial contractile force, left ventricular pressure, and rate of rise of the left ventricular pressure (dp/dt LV max) dose-dependently. Atenolol (1 mg/kg) decreased coronary venous outflow and myocardial oxygen consumption in dogs, but did not alter the myocardium to a more reduced state, as determined by coronary arterial and venous lactate and pyruvate levels. These results confirmed that atenolol is a potent cardioselective beta-blocker devoid of intrinsic sympathomimetic action. The results also suggest that atenolol inhibits cardiac function without disturbing the intracellular redox state of the myocardium.

Adrenergic beta-Antagonists↗

Primitive-streak origin of the cardiovascular system in avian embryos.

The origin of the avian cardiovascular system from the primitive streak has been mapped by the construction of quail/chick transplantation chimeras, the use of QH-1 (an antiquail endothelial/endocardial cell marker), and injections of a vital fluorescent dye (DiI) into the primitive streak. Our studies reveal that the prospective heart, including its endocardial and myocardial layers and the adjacent parietal pericardium, occupies much of the rostral half of the primitive streak at early primitive-streak stages of gastrulation. The heart originates from the primitive streak in roughly rostrocaudal sequence (i.e., the prospective bulbus cordis arises more rostrally in the streak than does the prospective ventricle, which in turn arises more rostrally than does the prospective sinus venosus), and all layers of the heart at each of its rostrocaudal subdivisions originate in concert from the same level of the primitive streak. Moreover, all rostrocaudal levels of the primitive streak at gastrula and neurula stages contain prospective endothelial cells. Again, these cells are rostrocaudally ordered within the streak, such that head blood vessels (both arteries and veins) arise at more rostral streak levels than do trunk blood vessels. Ingression of cardiogenic cells is complete by midprimitive-streak stages, and the position formerly occupied by prospective cardiogenic cells within the streak becomes occupied by ingressing prospective somitic cells. Additional studies on the state of commitment of prospective cardiogenic and endothelial cells during their ingression through the primitive streak are underway.

Animals↗

[Effect of a new bronchodilator, S-1540 (Bitolterol) and S-1541 on the tracheo-bronchial and cardiovascular system].

The actions on the bronchial smooth muscle and cardiovascular system S-1540 (Bitolterol) (Shionogi Pharmaceuticals), a new bronchodilator which is chemically related to isoprenaline, and S-1541 which is the active metabolite of S-1540 were studied in comparison with the action of isoprenaline (isoproterenol) and orciprenaline (metaproterenol). 1) The relaxing effect on isolated guinea-pig tracheal muscle constricted previously with histamine BaCl2 or acetylcholine was highest with S-1541, followed by isoprenaline and orciprenaline, in that order, and lowest with S-1540. The relaxing effect of S-1541 on acetylcholine-induced tracheal constriction was reduced and that of S-1540 was completely abolished by a previous treatment with propranolol. The relaxing actions of those drugs on bronchial spasms induced by histamine in vivo were highest with S-1541, followed by isoprenaline, and lowest with S-1540. 2) All these drugs exhibited the depressor and positive chronotropic actions in guinea-pigs. The potencies of the actions were found to be in the following order; isoprenaline was most potent, followed by S-1541 with a little less intensity, orciprenaline much weaker, and S-1540 still weaker with a positive chronotropic action of about 1/1000 of S-1541 and depressor action about 1/500. In the open chest guinea-pig, positive inotropic and chronotropic actions of S-1541 were about the same or slightly more potent than those of isoprenaline; S-1540 had a very weak action, being only about 1/1000 as active as S-1541. These actions of S-1540 were completely eliminated by propranolol pretreatment. S-1540 induced to remarkable changes in the electrocardiogram wave forms even in high doses. 3) Those drugs elicited the depressor, positive chronotropic and inotropic actions in rabbits and dogs. In rabbits, isoprenaline was most potent; S-1541 was similar to or a little weaker than isoprenaline; and S-1540 was extremely weak. In the dog, isoprenaline showed the highest of the above effect, followed by S-1541, orciprenaline and S-1540 in that order, with S-1540 having an extremely low activity. 4) The actions of S-1541 and isoprenaline appeared very rapidly but were of short duration, the duration of orciprenaline was moderate, and the actions of S-1540 rapidly appeared and were of an extremely long duration. It is suggested that S-1540 itself has pharmacological activities in vivo and the active metabolites such as S-1541 also have the activities. S-1540 can be administered by the oral route, is of long duration, and is thus considered to be a bronchodilator with a relative high specificity.

Acetylcholine↗

[The comparative dynamic characteristics of the autonomic indices of the cardiovascular system in myocardial infarct patients].

A study was made of the vegetative parameters associated with the cardiac rhythm and central hemodynamics in 60 patients with myocardial infarction. In 45 patients the time course of the urinary excretion of catecholamines was examined. Regulation of cardiovascular system in patients with myocardial infarction in different time spells of the disease course was studied in relation to the particular features of the clinical picture and presence of complications.

Adult↗

Hardware-in-the-loop-simulation of the cardiovascular system, with assist device testing application.

This paper presents a technique for evaluating the performance of biomedical devices by combining physical (mechanical) testing with a numerical, computerised model of a biological system. This technique is developed for evaluation of a cardiac assist device prior to in vivo trials. This device will wrap around a failing heart and provide physical beating assistance (dynamic cardiac compression). In vitro, the device to be tested is placed around a simulator comprising a mechanical simulation of the beating ventricles. This hardware model interfaces with a computerised (software) model of the cardiovascular system. In real time the software model calculates the effect of the assistance on the cardiovascular system and controls the beating motion of the hardware heart simulator appropriately. The software model of the cardiovascular system can represent ventricles in various stages of heart failure, and/or hardened or congested blood vessels as required. The software displays physiological traces showing the cardiac output, depending on the natural function of the modelled heart together with the physical assist power provided. This system was used to evaluate the effectiveness of control techniques applied to the assist device. Experimental results are presented showing the efficacy of prototype assist on healthy and weakened hearts, and the effect of asynchronous assist.

Algorithms↗

[Emphasize the role of bioactive small molecules in the homeostasis regulation of cardiovascular system].

Bioactive small molecules play a crucial role in maintaining structural and functional homeostasis of cardiovascular system. However, systemic research pattern is rare because of the multiple forms, diverse effects and complicated interaction of these molecules. Therefore firstly, they can be classified into different single 'families' according to their internal relationships. Secondly, studies may be focused on the network of members within each 'family' as well as network among different 'families', especially the physiological and pathological significance of each member in the cardiovascular diseases. Lastly, efforts should be made to establish a primary and simple regulation network as the strategy of researches on biology of cardiovascular systems, and to promote the transition to a network covering more complicated multiplex 'families', even the whole body.

Biological Products↗

Long-term effect of molsidomine and pentaerythrityl tetranitrate on cardiovascular system of spontaneously hypertensive rats.

We studied the effects of long-term administration of molsidomine and pentaerythrityl tetranitrate (PETN) on the cardiovascular system of spontaneously hypertensive rats (SHR). One control and three experimental groups of 10-week-old animals were used: 1) control Wistar rats, 2) SHR, 3) SHR treated with molsidomine in tap water (100 mg/kg/day, by gavage), and 4) SHR treated with PETN in tap water (200 mg/kg/day, by gavage). After six weeks, the content of cGMP in platelets and NO synthase (NOS) activity in aortas were evaluated in the experimental groups. For morphological evaluation the rats were perfused at 120 mm Hg with a glutaraldehyde fixative and the arteries were processed for electron microscopy. Blood pressure and heart weight/body weight ratio (HW/BW) were increased in all experimental groups with respect to the controls. HW/BW was lower in the molsidomine group in comparison to both SHR and PETN-treated group. The platelet content of cGMP was increased and the activity of NOS in the aortas was decreased in the molsidomine and PETN-treated groups. Wall thickness and cross-sectional area of thoracic aorta, carotid artery and coronary artery were increased similarly in all experimental groups compared to the controls, but there were no differences among the experimental groups. We summarize that long-term administration of exogenous NO donors did not improve pathological changes of the cardiovascular system in SHR.

Animals↗