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Membrane transport conductance

Adenosine is produced by many tissues, mainly as a byproduct of ATP breakdown. It is released from neurons, glia and other cells, possibly through the operation of the membrane transport system. Its rate of production varies with the functional state of the tissue and it may play a role as an autocrine or paracrine mediator (e.g. controlling blood flow). The uptake of adenosine is blocked by dipyridamole, which has vasodilatory effects. The effects of adenosine are mediated by a group of G protein-coupled receptors (the Gi/o-coupled Ai- and A3 receptors, and the Gs-coupled A2a-/A2B receptors). Ai receptors can mediate vasoconstriction, block of cardiac atrioventricular conduction and reduction of force of contraction, bronchoconstriction, and inhibition of neurotransmitter release. A2 receptors mediate vasodilatation and are involved in the stimulation of nociceptive afferent neurons. A3 receptors mediate the release of mediators from mast cells. Methylxanthines (e.g. caffeine) function as antagonists of Ai and A2 receptors. Adenosine itself is used to terminate supraventricular tachycardia by intravenous bolus injection. [Pg.19]

Although blood pressure control follows Ohm s law and seems to be simple, it underlies a complex circuit of interrelated systems. Hence, numerous physiologic systems that have pleiotropic effects and interact in complex fashion have been found to modulate blood pressure. Because of their number and complexity it is beyond the scope of the current account to cover all mechanisms and feedback circuits involved in blood pressure control. Rather, an overview of the clinically most relevant ones is presented. These systems include the heart, the blood vessels, the extracellular volume, the kidneys, the nervous system, a variety of humoral factors, and molecular events at the cellular level. They are intertwined to maintain adequate tissue perfusion and nutrition. Normal blood pressure control can be related to cardiac output and the total peripheral resistance. The stroke volume and the heart rate determine cardiac output. Each cycle of cardiac contraction propels a bolus of about 70 ml blood into the systemic arterial system. As one example of the interaction of these multiple systems, the stroke volume is dependent in part on intravascular volume regulated by the kidneys as well as on myocardial contractility. The latter is, in turn, a complex function involving sympathetic and parasympathetic control of heart rate intrinsic activity of the cardiac conduction system complex membrane transport and cellular events requiring influx of calcium, which lead to myocardial fibre shortening and relaxation and affects the humoral substances (e.g., catecholamines) in stimulation heart rate and myocardial fibre tension. [Pg.273]

The flux vector accounts for mass transport by both convection (i.e., blood flow, interstitial fluid flow) and conduction (i.e., molecular diffusion), whereas S describes membrane transport between adjacent compartments and irreversible elimination processes. For the three-subcompartment organ model presented in Figure 2, with concentration both space- and time-dependent, the conservation equations are... [Pg.89]

A fuel cell that has desirable features for transportation and portable power is the polymer electrolyte membrane (PEM) system. The core of this technology is a polymer membrane that conducts... [Pg.4]

Earlier, Gavach et al. studied the superselectivity of Nafion 125 sulfonate membranes in contact with aqueous NaCl solutions using the methods of zero-current membrane potential, electrolyte desorption kinetics into pure water, co-ion and counterion selfdiffusion fluxes, co-ion fluxes under a constant current, and membrane electrical conductance. Superselectivity refers to a condition where anion transport is very small relative to cation transport. The exclusion of the anions in these systems is much greater than that as predicted by simple Donnan equilibrium theory that involves the equality of chemical potentials of cations and anions across the membrane—electrolyte interface as well as the principle of electroneutrality. The results showed the importance of membrane swelling there is a loss of superselectivity, in that there is a decrease in the counterion/co-ion mobility, with greater swelling. [Pg.329]

Polar Cell Systems for Membrane Transport Studies Direct current electrical measurement in epithelia steady-state and transient analysis, 171, 607 impedance analysis in tight epithelia, 171, 628 electrical impedance analysis of leaky epithelia theory, techniques, and leak artifact problems, 171, 642 patch-clamp experiments in epithelia activation by hormones or neurotransmitters, 171, 663 ionic permeation mechanisms in epithelia biionic potentials, dilution potentials, conductances, and streaming potentials, 171, 678 use of ionophores in epithelia characterizing membrane properties, 171, 715 cultures as epithelial models porous-bottom culture dishes for studying transport and differentiation, 171, 736 volume regulation in epithelia experimental approaches, 171, 744 scanning electrode localization of transport pathways in epithelial tissues, 171, 792. [Pg.450]

Epithelial Membrane Transport An introduction, 191, 1 determination of paracellular shunt conductance in epithelia, 191, 4. [Pg.451]

The bicyclic guanidinium tetramer 43 was first reported as a possible binder for helical oligonucleotides. Initial studies with 43 and sulfate anions showed that the tetramer formed double-helical dimers around sulfate counterions [69]. Despite the initial proposal of using this receptor for membrane transport of oligonucleotides, all subsequent work on 43 has been conducted on helical peptides. For example, the binding of 43 with several synthetic peptides caused an increase in the helicity and helical stability of the peptides in 10% water/methanol [70]. The peptide containing four Asp derivatives showed the... [Pg.221]

Proton exchange membranes (PEM) fuel cells (or polymer electrolyte fuel cells - PEFCs), with H -conducting polymeric membranes, transports hydrogen (fuel) cations, generated at the anode, to an ambient air exposed cathode, where they are electro-oxidised to water at low temperatures. [Pg.52]

In a H2/air fuel cell, the protons produced at the anode side need to be transferred to the cathode side to react with 02. This requires a proton transport electrolyte. Nafion membranes, composed of a perfluorosulfonated polymer, are the most commonly used polymer electrolyte membranes to conduct protons. The structure of the Nafion membrane is shown in Figure 1.5. Nafion can take on a... [Pg.7]

The percolation model suggests that it may not be necessary to have a rigid geometry and definite pathway for conduction, as implied by the proton-wire model of membrane transport (Nagle and Mille, 1981). For proton pumps the fluctuating random percolation networks would serve for diffusion of the ion across the water-poor protein surface, to where the active site would apply a vectorial kick. In this view the special nonrandom structure of the active site would be limited in size to a dimension commensurate with that found for active sites of proteins such as enzymes. Control is possible conduction could be switched on or off by the addition or subtraction of a few elements, shifting the fractional occupancy up or down across the percolation threshold. Statistical assemblies of conducting elements need only partially fill a surface or volume to obtain conduction. For a surface the percolation threshold is at half-saturation of the sites. For a three-dimensional pore only one-sixth of the sites need be filled. [Pg.150]

More rigorous treatment of comparison of homogeneous and heterogeneous membranes involving conductivity measurements at different electrolyte strengths can help in characterizing the transport properties of these membranes. [Pg.978]

The sequences suggest that most of the isoenzymes are integral membrane proteins, each with 11 transmembrane helices organized as two sets of six with a large 40-kDa cytoplasmic domain between the sets. This is similar to the organizahon of the cyshc fibrosis transmembrane conductance regulator (Box 26-A) and some other membrane transporters. However, there is no firm evidence that adenylate cyclases contain ion channels. These enzymes are also discussed in Chapter 12, Section D,9. [Pg.556]

The K/DOQI clinical practice guidelines suggest that the adequacy of PD be assessed by using measured Kt/V and CEj three times in the first 6 months of dialysis (i.e., at months 1, 4, and 6). The reasoning behind this frequency is to accurately establish a baseline creatinine and urea excretion rate. Thereafter the KtA and Clcr should be measured every 4 months, at months 10, 14, and so on. The rationale for this is that it is imperative to detect subtle decreases in residual renal function and noncompliance and to make the necessary alterations to the prescribed PD dose to compensate for them. It is recommended that the first PET be conducted within the first month of treatment. Because solute clearance is dependent on peritoneal membrane transport properties, the guidelines also recommend that a PET be conducted within the first month of treatment. Future PET assessment is only recommended for patients with suspected changes in peritoneal membrane transport function, particularly when usual efforts to increase the PD dose are not successful. [Pg.862]

Membrane transport properties in both dilute and concentrated solution environments are presented in Section III. The membrane transport properties under industrial electrolysis conditions will be dealt with in Section IV. For practical cell applications, the conductivity and permeability of the membrane are of great importance. These properties can significantly affect cell performance. These subjects are treated in Section V. [Pg.441]

Essentially, a membrane transport cell is used with oxidant on one side and monomer solution on the other. Where polymerization occurs depends on the relative mobility of the oxidant and the monomer.56 In fact, this can be used to localize conducting polymer formation within the membranes. For example, with a nation membrane and the use of S2082- as oxidant, polymerization is restricted to the oxidant side of the membrane owing to anion exclusion (nation is negatively charged). When Fe3+ is used as oxidant, polymerization occurs throughout the membrane. The use of different solvents can also affect the transport processes for oxidant and monomer. This... [Pg.238]

Phenomena that arise in these materials include conduction processes, mass transport by convection, potential field effects, electron or ion disorder, ion exchange, adsorption, interfacial and colloidal activity, sintering, dendrite growth, wetting, membrane transport, passivity, electrocatalysis, electrokinetic forces, bubble evolution, gaseous discharge (plasma) effects, and many others. [Pg.25]

Figure 2 A diagram summarizing the known and expected effects of INS37217 on RPE ion and fluid transport. Binding of P2Y2 receptor (P2Y2-R) by INS37217 at the apical membrane activates heterotrimeric G proteins and generates intracellular inositol 1,4,5 trisphosphate (IP3), which releases Ca2+ from intracellular endoplasmic reticulum (ER) stores. Elevation of cytosolic Ca2+ in turn leads to an increase in basolateral membrane Cl- conductance, a decrease in apical membrane K+ conductance, and stimulation of net apical-to-basolateral fluid absorption. Figure 2 A diagram summarizing the known and expected effects of INS37217 on RPE ion and fluid transport. Binding of P2Y2 receptor (P2Y2-R) by INS37217 at the apical membrane activates heterotrimeric G proteins and generates intracellular inositol 1,4,5 trisphosphate (IP3), which releases Ca2+ from intracellular endoplasmic reticulum (ER) stores. Elevation of cytosolic Ca2+ in turn leads to an increase in basolateral membrane Cl- conductance, a decrease in apical membrane K+ conductance, and stimulation of net apical-to-basolateral fluid absorption.

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See also in sourсe #XX -- [ Pg.248 , Pg.252 , Pg.253 , Pg.254 , Pg.255 , Pg.256 , Pg.331 ]




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