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Gastrointestinal tract blood flow

Toxicity. The toxicity of barium compounds depends on solubility (47—49). The free ion is readily absorbed from the lung and gastrointestinal tract. The mammalian intestinal mucosa is highly permeable to Ba " ions and is involved in the rapid flow of soluble barium salts into the blood. Barium is also deposited in the muscles where it remains for the first 30 h and then is slowly removed from the site (50). Very Httle is retained by the fiver, kidneys, or spleen and practically none by the brain, heart, and hair. [Pg.483]

Prostaglandins play critical roles in a number of physiological processes. These molecules regulate blood flow to organs, stimulate secretion of protective mucosal linings in the gastrointestinal tract, participate in the initiation of platelet aggrega-... [Pg.169]

These functions are carried out most effectively and efficiently when the involved tissues receive an abundant blood flow. Under normal resting conditions, the kidneys, which account for only 1% of the body s weight, receive 20% of the cardiac output (CO) the gastrointestinal tract receives approximately 27% of the CO and the skin receives 6 to 15% of the blood pumped by the heart per minute. Because these tissues receive more blood than they need to support metabolic activity, they can easily tolerate a... [Pg.194]

The physiological changes and other aspects in the elderly makes this even more complicated. Example of this is decreased stomach acidity decreased motility decreased blood-flow to liver and gastrointestinal tract changed pharmacokinetics and -dynamics polypharmacy swallowing problems bad nutritional status and lack of documentation. [Pg.108]

Cimetidine is used for treating ulcer problems of the stomach and duodenum and for other conditions accompanied by an elevation of acidity and excess secretion of gastric juice. It is used for preventing injuries and the blood flow of the upper regions of the gastrointestinal tract. Synonyms of this drug are tagamet, cinamet, and belomet. [Pg.232]

The model assumes that the drug enters compartment 1, representing mainly the gastrointestinal tract. The drug is then absorbed into the blood flow, represented by compartment 2. The absorption rate is kaq, where is the... [Pg.91]

Blood flow the lungs have a better blood flow than the gastrointestinal tract and the skin has a poor blood flow. [Pg.424]

The gastrointestinal tract is a major site site of absorption primarily because of its very large surface area and extensive blood flow (Table 11.2). Most of the absorptive surface area of the gastrointestinal tract is in the small intestine and thus most absorption from the gastrointestinal tract occurs there. [Pg.292]

The primary purpose of the skin is to serve as a covering that protects the body from the external environment. Compared with the lung and gastrointestinal tract, the skin has much lower surface area and blood flow, as well as a considerably thicker absorption barrier (Table 11.1). Nonetheless, the skin can represent a significant pathway for exposure and absorption. [Pg.295]

Actions Meperidine causes a depression of respiration similar to that of morphine, but there is no significant cardiovascular action when the drug is given orally. On intravenous (IV) administration, meperidine produces a decrease in peripheral resistance and an increase in peripheral blood flow, and may cause an increase in cardiac rate. As with morphine, meperidine dilates cerebral vessels, increases cerebrospinal fluid pressure, and contracts smooth muscle (the latter to a lesser extent than does morphine). In the gastrointestinal tract, meperidine impedes motility, and chronic use results in constipation. Meperidine does not cause pinpoint pupils, but rather causes the pupils to dilate because of an atropine-like activity. [Pg.149]

Both urea and creatinine will be elevated with renal injury, and the elevations in both are usually proportional. Calculation of the ureaxreatinine ratio may implicate extrarenal causes for the analyte elevations (see Limitations of the Method , below). Extremely high ureaxreatinine when both are elevated (where urea is elevated markedly out of proportion to creatinine) indicates decreased renal blood flow, urinary tract obstruction or extravasation of urine into the peritoneal cavity. Elevation in the ureaxreatinine ratio as a consequence of pure urea elevation implicates gastrointestinal hemorrhage, high protein diet, increased protein catabolism, or loss of muscle mass. A decreased ratio indicates primary liver dysfunction (due... [Pg.115]

For almost one century, acetylcholine has been recognized as a neurotransmitter both in the central nervous system and the peripheral nervous system. In the peripheral nervous system, acetylcholine has been identified as the neurotransmitter of autonomic ganglia and the neuromuscular junction. Acetylcholine is involved in different peripheral functions such as heart rate, blood flow, gastrointestinal tract motility, and sweat production and smooth muscle activity. In the CNS, cholinergic neurotransmission plays a crucial role in a variety of CNS functions including sensory perception, motor function, cognitive processing, memory, arousal, attention, sleep, nociception, motivation, reward, mood, and psychosis. [Pg.18]

Paradoxically, the structures and functions of the liver predispose it to chemical toxicity. Hepatocytes are exposed to orally administered xenobiotics without systemic modification or dilution because they flow directly to the liver by the portal venous blood that delivers absorbed nutrients from the gastrointestinal tract. Xenobiotics may be extensively metabolized by the liver so that little of the parent xenobiotic enters the systemic circulation, a phenomenon known as the first pass effect. The movement of xenobiotics into the liver coupled with an opposing move-... [Pg.671]

Cerium-141 141Ce 32.5 days Gastrointestinal tract diagnosis, measuring regional myocardial blood flow... [Pg.186]


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See also in sourсe #XX -- [ Pg.4 ]




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