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[Mechanisms of oxygen transport across biological membranes].

Using metallic microelectrodes, intracellular measurements were performed of changes in O2 concentration for spherical oocytes of hens by their replacement from normal (PO2=150 torr) to hyperoxic (to 600 torr) conditions, and vice versa. The curves of O2 influx and efflux were recorded in pulse regime of the working electrode polarization. The character of these curves can be expressed by the following equations: m(t)==c==e=y1t+y0 and m (t) =e-y1t+v0+c, where v1 is determined by the coefficient of cell membrane permeability for O2. Valid differences were shown between values of v1 for oxygen influx and efflux which vanish after the action of cyanides. It is suggested that O2 transport into the cell involves a base component which may be physical diffusion, and an additional component which can be depressed by cyanides.

Animals

Biological amine transport in chromaffin ghosts. Coupling to the transmembrane proton and potential gradients.

The effect of the transmembrane proton gradient (delta pH) and potential gradient (delta psi) upon the rate and extent of amine accumulation was investigated in chromaffin ghosts. The chromaffin ghosts were formed by hypo-osmotic lysis of isolated bovine chromaffin granules and extensive dialysis in order to remove intragranular binding components and dissipate the endogenous electrochemical gradients. Upon ATP addition to suspensions of chromaffin ghosts, a transmembrane proton gradient alone, a transmembrane gradient alone, or both, could be established, depending upon the compositions of the media in which the ghosts were formed and resuspended. When chloride was present in the medium, addition of ATP resulted in the generation of a transmembrane proton gradient, acidic inside of 1 pH unit (measured by [14C]methylamine distribution), and no transmembrane potential (measured by [14C]-thiocyanate distribution). When ATP was added to chromaffin ghosts suspended in a medium in which chloride was substituted by isethionate, a transmembrane potential, inside positive, of 45 mV and no transmembrane proton gradient, was measured. In each medium, the addition of agents known to affect proton or potential gradients, respectively, exerted a predictable mechanism of action. Accumulation of [14C]epinephrine or [14C]5-hydroxytryptamine was over 1 order of magnitude greater in the presence of the transmembrane proton gradient or the transmembrane potential than in the absence of any gradient and, moreover, was related to the magnitude of the proton or potential gradient in a dose-dependent manner. When ghosts were added to a medium containing chloride and isethionate, both a delta pH and delta psi could be generated upon addition of ATP. In this preparation, the maximal rate of amine accumulation was observed. The results indicate that amine accumulation into chromaffin ghosts can occur in the presence of either a transmembrane proton gradient, or a transmembrane potential gradient, and that the maximal rate of accumulation may exist when both components of the protonmotive force are present.

Adenosine Triphosphate

Testing transport models with substrates and reversible inhibitors.

The kinetic behavior of five models for biological transport, only one of which is based on the classical carrier mechanism, is investigated. All give hyperbolic substrate saturation curves in accord with experimental observations on many systems. Several simple kinetic tests with substrates and competitive inhibitors serve to exclude or confirm proposed models. The tests involve measuring rates of efflux of radioactive substrate in the presence of (i) a competitive inhibitor outside the cell; (ii) inhibitor inside and outside; and (iii) unlabeled substrate outside. Rules for testing hypothetical mechanisms are presented in tables which may be consulted directly, disregarding the mathematical derivation.

Biological Transport

Lipophilicity and biological acitivity. Drug transport and drug distribution in model systems and in biological systems.

Different equilibrium and non-equilibrium models are used to simulate drug transport and drug distribution. The percentage of absorbed drug, the rate constants of drug absorption and the drug concentrations in the different compartments of the models can be described quantitatively by the bilinear model, e.g., log ci = a log P-b log (betaP + 1) + c. A nearly perfect fit is obtained for the simulated data from this model. Drug absorption and distribution in biological systems can be explained and described by the model-derived equations. Examples from the literature include buccal absorption, gastric and intestinal in situ and in vitro absorption, colonic absorption, renal clearance, and absorption through the skin and the blood-brain barrier; in all those cases the bilinear model gives an excellent fit of the experimental data. Combination of the pH-partition theory with the bilinear model leads to a simple quantitative model for the precise description of the relationships between lipophilicity, degree of ionization, and absorption, distribution and biological activity of drugs.

Absorption

Percutaneous absorption after twenty-five years: or "old wine in new wineskins".

Two developments have greatly added to our knowledge of percutaneous absorption over the past quarter century: (1) proof that the entire stratum corneum is the effective barrier layer of the skin, and (2) the advent of highly sensitive analytical techniques. The first enabled us to measure permeation rates on excised skin and the second greatly extended the kinds of substances that could be studied in vivo and in vitro. The process of percutaneous absorption is beginning to be understood more quantitatively. New light has been shed on the elementary mechanisms of permeation, the site of diffusional resistance at the molecular level, the effect of specific functional groups on solute permeation, the role of skin appendages, and the effects of vehicles.

Biological Transport