Oxygen uptake, transport, models

Reeves, P.C., and M.A. Celia. 1996. A functional relationships between capillary pressure, saturation, and interfacial area as revealed by a pore-scale network model. Water Resour. Res. 32 2345-2358. Rice, J.A. 1995. Mathematical statistics and data analysis. 2nd ed. Duxbury Press, Belmont, CA. Skopp, J. 1985. Oxygen uptake and transport in soils Analysis of the air-water interfacial area. Soil Sci. Soc. Am. J. 49 1327-1331. 

It is contended that the renal slice technique measures primarily basolateral uptake of substrates or nephrotoxins, based on histological evidence of collapsed tubular lumens. This results in the inaccessibility of brush-border surfaces for reabsorptive transport (Burg and Orloff, 1969 Cohen and Kamm, 1976). This observation limits the ability of this model to accurately reflect reactions to nephrotoxins that occur as the result of brush-border accumulation of an injurious agent. Ultrastructurally, a number of alterations, particularly in the plasma membrane and mitochondrial compartments, have been shown to occur over a 2-h incubation period (Martel-Pelletier et al., 1977). This deterioration in morphology is very likely a consequence of the insufficient diffusion of oxygen, metabolic substrates, and waste products in the innermost regions of the kidney slice (Cohen and Kamm, 1976). Such factors also limit the use of slices in studying renal metabolism and transport functions. 

Figure 8.7 Simplified model of nicotiniamine (NA) function in plant cells. Iron is transported across the plasma membrane by the Strategy I or Strategy II uptake systems. Once inside the cell, NA is the default chelator of iron to avoid precipitation and catalysis of radical oxygen species. The iron is then donated to proteins, iron-sulfur clusters and haem, while ferritin and iron precipitation are only present during iron excess. (From Hell and Stephan, 2003. With kind permission of Springer Science and Business Media.)...

Most models of gas uptake in the respiratory tract have been concerned with carbon dioxide, carbon monoxide, oxygen, and anesthetic gases like chloroform, ether, nitrous oxide, benzene, and carbon disulfide (e.g., see Lin and Gumming and Papper and Kitz ). Unfortunately, there are only a few preliminary models of pollutant-gas transport and uptake in the respiratory tract. 

If both MT-1 and HO-1 mRNA induction by heme-hemopexin involves a copper-redox enzyme in both heme transport (and consequent induction of HO-1 mRNA) and the signaling pathway for MT-1 expression, a plausible working model can be formulated by analogy with aspects of the yeast iron uptake processes and with redox reactions in transport (Figure 5-6). First, the ferric heme-iron bound to hemopexin can act as an electron acceptor, and reduction is proposed to be required for heme release. The ferrous heme and oxygen are substrates for an oxidase, possibly NADH-dependent, in the system for heme transport. Like ferrous iron, ferrous heme is more water soluble than ferric heme and thus more suitable as a transport intermediate between the heme-binding site on hemopexin and the next protein in the overall uptake process. The hemopexin system would also include a copper-redox protein in which the copper electrons would be available to produce Cu(I), either as the copper oxidase or for Cu(I) transport across the plasma membrane to cytosolic copper carrier proteins for incorporation into copper-requiring proteins [145]. The copper requirement for iron transport in yeast is detectable only under low levels of extracellular copper as occur in the serum-free experimental conditions often used. 

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