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Of extracellular

Fig. 3. Cation and anion composition of extracellular and intracellular 1 fluids. Fig. 3. Cation and anion composition of extracellular and intracellular 1 fluids.
The volume of extracellular fluid is direcdy related to the Na" concentration which is closely controlled by the kidneys. Homeostatic control of Na" concentration depends on the hormone aldosterone. The kidney secretes a proteolytic enzyme, rennin, which is essential in the first of a series of reactions leading to aldosterone. In response to a decrease in plasma volume and Na" concentration, the secretion of rennin stimulates the production of aldosterone resulting in increased sodium retention and increased volume of extracellular fluid (51,55). [Pg.380]

Stimulation of the neuron lea ding to electrical activation of the nerve terminal in a physiologically relevant manner should eUcit a calcium-dependent release of the neurotransmitter. Although release is dependent on extracellular calcium, intracellular calcium homeostasis may also modulate the process. Neurotransmitter release that is independent of extracellular calcium is usually artifactual, or in some cases may represent release from a non-neuronal sources such as gha (3). [Pg.517]

Excitation of smooth muscle via alpha-1 receptors (eg, in the utems, vascular smooth muscle) is accompanied by an increase in intraceUular-free calcium, possibly by stimulation of phosphoUpase C which accelerates the breakdown of polyphosphoinositides to form the second messengers inositol triphosphate (IP3) and diacylglycerol (DAG). IP3 releases intracellular calcium, and DAG, by activation of protein kinase C, may also contribute to signal transduction. In addition, it is also thought that alpha-1 adrenergic receptors may be coupled to another second messenger, a pertussis toxin-sensitive G-protein that mediates the translocation of extracellular calcium. [Pg.359]

Coiicin E (from E.coli) [11032-88-5], Purified by salt extraction of extracellular-bound colicin followed by salt fractionation and ion-exchange chromatography on a DEAE-Sephadex column, and then by CM-Sephadex column chromatography [Schwartz and Helinski J Biol Chem 246 6318 1971],... [Pg.523]

The integrity of mammalian kidneys is vital to body homeostasis, because the kidneys play the principal role in the excretion of metabolic wastes and the regulation of extracellular fluid volume, electrolyte balance, and acid-base... [Pg.301]

Loikkanen, J., Naarala, J., and Savolainen, K. M. (1998). Modification of glutamate-induced oxidative stress by lead The role of extracellular calcium. Free Rad. Biol. Med., 24, 377-384,... [Pg.340]

In addition, adenosine is implicated in sleep regulation. During periods of extended wakefulness, extracellular adenosine levels rise as a result of metabolic activity in the brain, and this increase promotes sleepiness. During sleep, adenosine levels fall. Caffeine promotes wakefulness by blocking the interaction of extracellular adenosine with its neuronal receptors. ... [Pg.332]

As already noted, microtubules are also the fundamental building blocks of cilia and flagella. Cilia are short, cylindrical, hairlike projections on the surfaces of the cells of many animals and lower plants. The beating motion of cilia functions either to move cells from place to place or to facilitate the movement of extracellular fluid over the cell surface. Flagella are much longer structures found singly or a few at a time on certain cells (such as sperm cells). They pro-... [Pg.535]

Inhibition of the metabolism of extracellular adenosine or its uptake proteins is being explored for therapeutic purposes. AK inhibitors have been proposed for the treatment of pain and seizures however, the promising clinical development of these efficacious compounds was discontinued due to toxicity. [Pg.20]

Apelin receptors activate several signalling pathways including coupling through inhibitory G-proteins (G ) and Ras-independent activation of extracellular-regulated kinases (ERKs) via protein kinase C (PKC). The apelin receptor is one of number of G-protein-coupled receptors that can act as an alternative coreceptor for entry into cells of HIV and simian immunodeficiency vims (SIV) strains in human U87 cells expressing CD4 in vitro. Apelin peptides blocks entry of HIV but display different potencies, with apelin-36 being more effective than shorter sequences [3]. [Pg.204]

Ca2+ sensing receptor, a member of G-protein coupled receptors, is composed of seven transmembrane spanning domains. The extracellular domain contains clusters of negatively charged amino acids sensing even small fluctuations of extracellular calcium. Mutations in this receptor cause inheritable hypo- and hypercalcemic syndromes. [Pg.291]

The extracellular calcium Ca -sensing receptor plays a central role in maintaining a nearly constant level of extracellular calcium by sensing small changes in Ca and directly and/or indirectly altering the translocation of calcium ions into or out of the extracellular fluid so as to normalize CaQ+. Changes in the level of expression and/or function of the CaR reset the level of CaQ+. Recently developed activators (calcimimetics)... [Pg.300]

Diuretics promote the urinary excretion of sodium and water by inhibiting the absorption of filtered fluid across the renal tubular epithelium. The ensuing reduction in Na reabsorption reduces the Na content of the body, the critical determinant of extracellular and plasma fluid volumes. Thus, the use of diuretics is primarily indicated in the treatment of edematous diseases and of arterial hypertension. [Pg.429]

Integrins constitute a large family of a (3 heterodimeric cell surface, transmembrane proteins that interact with a large number of extracellular matrix components through a metal ion-dependent interaction. The term integrin reflects their function in integrating cell adhesion and migration with the cystoskeleton. [Pg.638]

Occurs when the volume of extracellular fluid is significantly diminished. Examples include hemorrhage, fluid loss caused by burns, diarrhea, vomiting, or excess diuresis Occurs when the heart is unable to deliver an adequate cardiac output to maintain perfusion to the vital organs. Examples include as the result of an acute myocardial infarction, ventricular arrhythmias, congestive heart failure (CHF), or severe cardiomyopathy. [Pg.204]

Systemic and coronary arteries are influenced by movement of calcium across cell membranes of vascular smooth muscle. The contractions of cardiac and vascular smooth muscle depend on movement of extracellular calcium ions into these walls through specific ion channels. Calcium channel blockers, such as amlodipine (Norvasc), diltiazem (Cardizem), nicardipine (Cardene), nifedipine (Procardia), and verapamil (Calan), inhibit die movement of calcium ions across cell membranes. This results in less calcium available for the transmission of nerve impulses (Fig. 41-1). This drug action of the calcium channel blockers (also known as slow channel blockers) has several effects on die heart, including an effect on die smooth muscle of arteries and arterioles. These drug dilate coronary arteries and arterioles, which in turn deliver more oxygen to cardiac muscle. Dilation of peripheral arteries reduces die workload of die heart. The end effect of these drug is the same as that of die nitrates. [Pg.381]

Chitosan freeze-dried fleeces support chondrocyte attachment and synthesis of extracellular matrix [344]. Chitosan was used to assist the spontaneous tissue repair of the meniscus [345]. The repair of the cartilage and the prevention of its degradation in osteoarthritis is, however, possible with the association of glucosamine sulfate salt and chondroitine sulfate, the latter being particularly effective [346]. [Pg.198]


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See also in sourсe #XX -- [ Pg.276 ]




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Adverse effects of changes in extracellular potassium concentration

Assay of Activities in the Extracellular

Chemistry of Extracellular Electron Transfer

Composition and Functioning of the Extracellular Matrix

Extracellular Degradation of PHA

Extracellular and Membrane-Bound Proteases of B. subtilis

Extracellular domain, of chemokine

Extracellular domain, of chemokine receptors

Extracellular levels of adenosine

Extracellular volume of distribution

Influx of Ca2 from the Extracellular Region

Influx of Extracellular Calcium

Killing of intracellular bacteria and large parasites in the extracellular fluid

PH of extracellular fluid

Proteoglycans of the extracellular matrix

Role of the Extracellular Matrix

Structures of the extracellular matrix

The Extracellular Domain of Transmembrane Receptors

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