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A Medici

Publications and source records attributed to A Medici.

41 records · Page 3Linked to original sources

The influence of external caesium ions on potassium efflux in frog skeletal muscle.

1. At a concentration of 2.5 mM in the external solution, Cs ions reduced K efflux in muscles incubated in Na media. This effect was demonstrated in the presence or absence of 2.5 mM-K and in the presence or absence of 10(-4)M ouabain.2. In Ringer solution in which NaCl was replaced by an osmotic equivalent of MgCl(2), external Cs ions increased K efflux if the solution was K-free and decreased K efflux if the solution contained 2.5 mM-K.3. External Cs ions reduced the inward rate of leakage of Na ions into muscle cells by about 25% when the medium was K-free and contained 10(-5)M ouabain.4. The effects of 2.5 mM-K ions and 2.5 mM-Cs ions on the muscle fibre membrane potential were about the same. The influence of Cs ions on K efflux cannot be explained by changes in the resting membrane potential.5. The results suggest that a large part of the K efflux from muscle cells is mediated by a K:K exchange mechanism that is inhibited by external Cs ions.6. The results also suggest that a smaller part of the K efflux is due to K:Na exchange that is also inhibited by external Cs ions.7. In the absence of either external K or Na ions for internal K to exchange with, Cs ions promote a small amount of K exchange, perhaps via both mechanisms.

Animals↗

Biotransformations on steroid nucleus of bile acids.

The bile acids in mammals are all derivatives of 5 beta-cholan-26-oic acid. They represent the major quantitative pathway by which cholesterol is metabolized in the body. This article covers the microbial and enzymatic transformations of free, saturated bile acids, that kept unaltered the C-24 cyclopentane-perhydrophenantrene nucleus. The bile acids that have been considered include the primary cholic and chenodeoxycholic acids, the secondary deoxycholic and lithocholic acids as well as the relevant dehydrocholic, ursocholic and ursodeoxycholic acids. Among the bile acid biotransformations, attention is paid to reactions that lead to pharmaceutically significant compounds. This is the case of 7 alpha-hydroxy epimerization of chenodeoxycholic acid to ursodeoxycholic acid, currently used for cholesterol galistone dissolution therapy and in the treatment of cholestatic liver diseases. Emphasis has placed on reporting reactions that may be of general interest and on the practical aspects of work in the field of biotransformations.

Animals↗