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Calcium cell membrane transport

Cystinuria is the prototype of a number of inborn errors of metabolism believed to result from the deficiency of carrier proteins involved in transporting molecules through the cell membrane. Transport defects in kidney, intestine, or both have also been described for other amino acids— glycine, cystine, tryptophan, methionine—for glucose and galactose, and even for electrolytes such as calcium, chloride, and sodium [173]. Some of these inborn errors are described in other chapters. [Pg.230]

Catoptromers —. see Enantiomers Cell division calcium, 6.595 Cell membranes alkali metal transport, 3, 54 Cells labelled... [Pg.99]

JR Williamson, SK Joseph, KE Coll, AP Thomas, A Verhoeven, M Prentki. (1986). Hormone-induced inositol lipid breakdown and calcium-mediated cellular responses in liver. In G Poste, ST Crooke, eds. New Insights into Cell and Membrane Transport Processes. New York Plenum Press, pp 217-247. [Pg.390]

The sodium and calcium pumps can be isolated to near purity and still exhibit most of the biochemical properties of the native pump. Some kinetic properties of these pumps in native membranes are altered or disappear as membrane preparations are purified. For example, when measured in intact membranes, the time-dependencies of phosphorylation and dephosphorylation of the pump catalytic sites exhibit biphasic fast to slow rate transition this characteristic progressively disappears as the membranes are treated with mild detergents. One suggested explanation is that, as the pumps begin to cycle, the catalytic subunits associate into higher oligomers that may permit more efficient transfer of the energy from ATP into the ion transport process [29, 30], Some structural evidence indicates that Na,K pumps exist in cell membranes as multimers of (a 3)2 [31]. [Pg.82]

ATP is used not only to power muscle contraction, but also to re-establish the resting state of the cell. At the end of the contraction cycle, calcium must be transported back into the sarcoplasmic reticulum, a process which is ATP driven by an active pump mechanism. Additionally, an active sodium-potassium ATPase pump is required to reset the membrane potential by extruding sodium from the sarcoplasm after each wave of depolarization. When cytoplasmic Ca2- falls, tropomyosin takes up its original position on the actin and prevents myosin binding and the muscle relaxes. Once back in the sarcoplasmic reticulum, calcium binds with a protein called calsequestrin, where it remains until the muscle is again stimulated by a neural impulse leading to calcium release into the cytosol and the cycle repeats. [Pg.236]

There is reason to beheve that cardiac glycosides, like other inotropic substances, act on the contractibility of the heart by affecting the process of calcium ion transfer through the membrane of myocardiocytes. The effect of cellular membranes in electric conductivity is mediated by transport of sodium, calcium, and potassium ions, which is a result of indirect inhibitor action on the (Na+-K+) ATPase of cell membranes. [Pg.238]

Mecfianism of Action An antiarrhythmic that decreases sodium influx during depolarization, potassium efflux during repolarization, and reduces calcium transport across the myocardial cell membrane.Decreases myocardial excitability, conduction velocity, and contractility Therapeutic Effect Suppresses arrhythmias. Pharmacokinetics Almost completely absorbed after PO administration. Protein binding 80%-90%. Metabolized in liver. Excreted in urine. Removed by hemodialysis. Half-life 6-8 hr. [Pg.1068]

Digitalis acts by interfering with the sodium and potassium transport across the cell membrane and by increasing the amount of coupling calcium i.e. making more calcium available for excitation-contraction coupling. [Pg.171]

Complexes of alkali metals and alkaline-earth metals with carbohydrates have been reviewed in this Series,134 and the interaction of alkaline-earth metals with maltose has been described.135 Standard procedures for the preparation of adducts of D-glucose and maltose with the hydroxides of barium, calcium, and strontium have been established. The medium most suitable for the preparation of the adduct was found to be 80% methanol. It is of interest that the composition of the adducts, from D-glucose, maltose, sucrose, and a,a-trehalose was the same, namely, 1 1, in all cases. The value of such complex-forming reactions in the recovery of metals from industrial wastes has been recognized. Metal hydroxide-sugar complexes may also play an important biological role in the transport of metal hydroxides across cell membranes. [Pg.245]

There are instances in which toxicants have chemical or structural similarities to endogenous chemicals that rely on these special transport mechanisms for normal physiological uptake and can thus utilize the same system for membrane transport. Useful examples of drugs known to be transported by this mechanism include levodopa, which is used in treating Parkinson s disease, and fluorouracil, a cytotoxic drug. Levodopa is taken up by the carrier that normally transports phenylalanine, and fluorouracil is transported by the system that carries the natural pyrimidines, thymine, and uracil. Iron is absorbed by a specific carrier in the mucosal cells of the jejunum, and calcium by a vitamin D-dependent carrier system. Lead may be more quickly moved by a transport system that is normally involved in the uptake of calcium. [Pg.84]

The SR membrane contains a very efficient calcium uptake transporter, which maintains free cytoplasmic calcium at very low levels during diastole by pumping calcium into the SR. The amount of calcium sequestered in the SR is thus determined, in part, by the amount accessible to this transporter. This in turn is dependent on the balance of calcium influx (primarily through the voltage-gated membrane calcium channels) and calcium efflux, the amount removed from the cell (primarily via the sodium-calcium exchanger, a transporter in the cell membrane). [Pg.290]

Sodium, potassium and chloride are the primary dietary ions that influence the electrolytic balance and acid-base status, and the proper dietary balance of sodium, potassium and chloride is necessary for growth, bone development, eggshell quality and AA utilization. Potassium is the third most abundant mineral in the body after calcium and phosphorus, and is the most abundant mineral in muscle tissue. It is involved in electrolyte balance and neuromuscular function. The content of potassium in poultry diets is usually adequate. Chloride is present in gastric juice and chlorine is part of the HC1 molecule which assists in the breakdown of feed in the proventriculus. Sodium is essential for nerve membrane stimulation and ionic transport across cell membranes. Signs of sodium, potassium or chloride deficiency include reduced appetite, poor growth, dehydration and increased mortality. [Pg.38]

Limited data are available on in vitro effects of barium on the endocrine system. Studies done with isolated pancreatic islet cells from mice show barium is transported across the cell membrane and incorporated into organelles, especially the mitochondria and secretory granules (Berggren et al. 1983). Barium was found to increase cytoplasmic calcium consequently, the insulin- releasing action of barium may be mediated by calcium. Barium has also been found capable of stimulating the calcitonin secretion system of the thyroid in pigs (Pento 1979). [Pg.46]

Defect in sodium or calcium transport across cell membranes Multiple interactive effects... [Pg.247]


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See also in sourсe #XX -- [ Pg.539 ]




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