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Movement through membranes

Even though various antileukotriene drugs have been synthesized, none has reached clinical acceptability. Inhibition of histamine release by an apparent mast cell stabilizing mechanism (in lung tissue, but probably not elsewhere) is achieved with the carboxy-chromone derivative cromolyn sodium. The mechanism is believed to involve inhibition of histamine release from pulmonary mast cells by blocking Ca2+ movement through membrane channels. [Pg.629]

The relationship between membrane structure, membrane function, and cell physiology is an area of active, ongoing study. Our interest here is practical what are the basic mechanisms of drug movement through membranes and how can one best predict the rate of permeation of an agent through a membrane barrier To answer that question, this section presents rates of permeation measured in some common experimental systems and models of membrane permeation that can be used for prediction. [Pg.113]

Biology is an additional field in which electrochemistry plays an important role in the development processes. A significant number of phenomena in the living world involve oxidation-reduction reactions or controlled ionic movements through membranes. In addition to its list of increasing widespread uses in the field of biosensors , bio-electrochemistry is likely to grow in other sectors, such as in the development of new processes. [Pg.7]

In general, movement is an intrinsic property of living creatures. It occurs at different structural levels, including ion transfer through membranes, separation of replicated chromosomes, beating of cilia and flagella or, the most common, contraction of muscles. These contractions enable... [Pg.354]

Fig. 9 Schematic representation depicting the movement of molecules from the absorbing (mucosal or apical) surface of the GIT to the basolateral membrane and from there to blood. (A) transcellular movement through the epithelial cell. (B) Paracellular transport via movement between epithelial cells. (Q Specialized carrier-mediated transport into the epithelial cell. (D) Carrier-mediated efflux transport of drug out of the epithelial cell. (Copyright 2000 Saguaro Technical Press, Inc., used with permission.)... Fig. 9 Schematic representation depicting the movement of molecules from the absorbing (mucosal or apical) surface of the GIT to the basolateral membrane and from there to blood. (A) transcellular movement through the epithelial cell. (B) Paracellular transport via movement between epithelial cells. (Q Specialized carrier-mediated transport into the epithelial cell. (D) Carrier-mediated efflux transport of drug out of the epithelial cell. (Copyright 2000 Saguaro Technical Press, Inc., used with permission.)...
The liquid-membrane electrode is another important type of ion-selective electrode. The internal filling solution contains a source of the ion under investigation, i.e. one for which the ion exchanger is specific, while also containing a halide ion to allow the reference electrode to function. The physico-chemical behaviour of the ISE is very similar to that of the fluoride electrode, except that ise and the selectivity are dictated by the porosity of a membrane rather than by movement through a solid-state crystal. [Pg.67]

Brandt, U. (1997) Proton-translocation by membrane-bound NADH ubiquinone-oxidoreductase (complex I) through redoxgated ligand conduction. Biochim Biophys. Acta 1318, 79-91. Advanced discussion of models for electron movement through Complex I. [Pg.746]

The mechanism of action of anticonvulsants remains poorly characterized, both in terms of their anticonvulsant effects or their antimanic/mood stabilizing effects. They may even have multiple mechanisms of action. At the cell membrane, anticonvulsants appear to act on ion channels, including sodium, potassium, and calcium channels. By interfering with sodium movements through voltage-operated sodium... [Pg.267]

Special carrier molecules exist for certain substances that are important for cell function and too large or too insoluble in lipid to diffuse passively through membranes, eg, peptides, amino acids, glucose. These carriers bring about movement by active transport or facilitated diffusion and, unlike passive diffusion, are saturable and inhibitable. Because many drugs are or resemble such naturally occurring peptides, amino acids, or sugars, they can use these carriers to cross membranes. [Pg.8]

Accumulation of potassium within the cell by a cooperative process is a transmembrane event. However, there is also good evidence that movement of potassium ions through membrane channels is modulated by the binding of calcium ions at channel sites - the "plug in the bath" model (7). Membrane surface glycoproteins with polyanionic terminal strands offer a broad and powerful substrate for these cationic interactions. Competition between hydrogen and calcium ions at these sites has been modeled as the initial transductive step in excitation (8). [Pg.275]

The second proton transfer mechanism involves protonation of carboxyl or histidyl groups associated with electron carriers in the membrane and release of protons from these sites through proposed channels when the electron carrier is oxidized. This is essentially a proton channel system with movement through the channel gated by the oxidation-reduction state of the prosthetic group on the electron transport protein. The classical example of this is seen in cytochrome c oxidase (Figure 3). [Pg.172]

Pertinent to the understanding of the operation of an RO system is the fundamental knowledge of various theoretical models describing movement of solutes and water through an RO membrane. By understanding how solutes and water are transported through membranes, appropriate modifications can be made to the membrane polymers to improve performance (flux and rejection). See the book by Richard Baker, Membrane Technology and Applications, 2nd edition (John Wiley Sons, 2004) for more detail about the history and development of membrane and transport models. [Pg.41]

Finkelstein, A. (1987). In Water Movement through Lipid Bilayers, Pores and Plasma Membranes, Theory and Reality. Wiley, New York. [Pg.314]


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See also in sourсe #XX -- [ Pg.87 ]




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