Cardiovascular system blood

Angiotensin II is an octapeptide hormone that plays an important role in the regulation of the cardiovascular system (blood pressure and sustained hyperten-... 

Elevated blood pressure was a concern for many AAS users. This was mostly due to an elevation in water and electrolyte retention caused by some AAS. This puts a strain on the cardiovascular system. Blood pressure should be monitored, and values higher than 140/90 should be treated by a doctor. This side effect usually normalized a few weeks after AAS are discontinued. 

Cardiovascular system Blood pressure, heart rate, and electrophysiology, including electrocardiographic studies. Electrophysiological studies are conducted to examine the potential for QT interval prolongation. 

Individual susceptibility Individuals undergoing very stressful situations such as athletes/football players who practice in very hot temperatures, extensive workout for muscle building or people who fast to achieve weight loss are particularly susceptible. Ephedra puts an undue stress in these individuals by increasing the blood pressure and causing additional stress on the cardiovascular system, blood supply in the brain, which may result in heart attack or stroke. 

The arterial blood pressure within the mammalian organism, whether normal or abnormal, is ultimately determined by cardiac output and peripheral resistance to flow. Of the several physical and chemical variables of the cardiovascular system, blood pressure is ordinarily the most constant. This is especially remarkable if one considers the large variations encountered in cardiac output and in heart rate. This feat is accomplished by a negative feedback system. The chief mechanism involves the baroreceptor reflex. 

CHRONIC HEALTH RISKS no information found targets eyes, respiratory system, central nervous system, cardiovascular system, blood cholinesterase. 

BIOLOGICAL ACTIONS Gastrointestinal smooth muscle Reproductive smooth muscle Respiratory smooth muscle Cardiovascular system Blood platelet aggregation Metabolic effects... 

Lead is toxic to the kidney, cardiovascular system, developiag red blood cells, and the nervous system. The toxicity of lead to the kidney is manifested by chronic nephropathy and appears to result from long-term, relatively high dose exposure to lead. It appears that the toxicity of lead to the kidney results from effects on the cells lining the proximal tubules. Lead inhibits the metaboHc activation of vitamin D in these cells, and induces the formation of dense lead—protein complexes, causing a progressive destmction of the proximal tubules (13). Lead has been impHcated in causing hypertension as a result of a direct action on vascular smooth muscle as well as the toxic effects on the kidneys (12,13). 

The heart, a four-chambered muscular pump has as its primary purpose the propelling of blood throughout the cardiovascular system. The left ventricle is the principal pumping chamber and is therefore the largest of the four chambers in terms of muscle mass. The efficiency of the heart as a pump can be assessed by measuring cardiac output, left ventricular pressure, and the amount of work requHed to accomplish any requHed amount of pumping. 

Methyldopa, through its metaboHte, CX-methyInorepinephrine formed in the brain, acts on the postsynaptic tt2-adrenoceptor in the central nervous system. It reduces the adrenergic outflow to the cardiovascular system, thereby decreasing arterial blood pressure. If the conversion of methyldopa to CX-methyl norepinephrine in the brain is prevented by a dopamine -hydroxylase inhibitor capable of penetrating into the brain, it loses its antihypertensive effects. 

Mean arterial pressure and cardiac output, an expression of the amount of blood that the heart pumps each minute, are the key Indicators of the normal functioning of the cardiovascular system. Mean arterial pressure is strictly controlled, but by changing the cardiac output, a person can adapt, e.g., to increased oxygen requirement due to increased workload. Blood flow in vital organs may vary for many reasons, but is usually due to decreased cardiac output. However, there can be very dramatic changes in blood pressure, e.g., blood pressure plummets during an anaphylactic allergic reaction. Also cytotoxic chemicals, such as heavy metals, may decrease the blood pressure. 

Angiotensin converting enzyme (ACE) plays a central role in cardiovascular hemostasis. Its major function is the generation of angiotensin (ANG) II from ANGI and the degradation of bradykinin. Both peptides have profound impact on the cardiovascular system and beyond. ACE inhibitors are used to decrease blood pressure in hypertensive patients, to improve cardiac function, and to reduce work load of the heart in patients with cardiac failure. 

Ca2+ is an important intracellular second messenger that controls cellular functions including muscle contraction in smooth and cardiac muscle. Ca2+ channel blockers inhibit depolarization-induced Ca2+ entry into muscle cells in the cardiovascular system causing a decrease in blood pressure, decreased cardiac contractility, and antiarrhythmic effects. Therefore, these drugs are used clinically to treat hypertension, myocardial ischemia, and cardiac arrhythmias. 

Alimentary tract and metabolism Blood and blood-forming organs Cardiovascular system Dermatologicals... 

Heart and cardiovascular system Atherosclerosis Red blood cells... 

Atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), and C-type natriuretic peptide (CNP) are members of a family of so-called natriuretic peptides, synthesized predominantly in the cardiac atrium, ventricle, and vascular endothelial cells, respectively (G13, Y2). ANP is a 28-amino-acid polypeptide hormone released into the circulation in response to atrial stretch (L3). ANP acts (Fig. 8) on the kidney to increase sodium excretion and glomerular filtration rate (GFR), to antagonize renal vasoconstriction, and to inhibit renin secretion (Ml). In the cardiovascular system, ANP antagonizes vasoconstriction and shifts fluid from the intravascular to the interstitial compartment (G14). In the adrenal cortex, ANP is a powerful inhibitor of aldosterone synthesis (E6, N3). At the hypothalamic level, ANP inhibits vasopressin secretion (S3). It has been shown that some of the effects of ANP are mediated via a newly discovered hormone, called adreno-medullin, controlling fluid and electrolyte homeostasis (S8). The diuretic and blood pressure-lowering effect of ANP may be partially due to adrenomedullin (V5). 

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