Abstract

Lithium salts are used in the treatment and prophylaxis of bipolar or mood disorders. The mechanism of action by which the cation exerts its therapeutic influence is unknown. A knowledge of brain Li concentration, its distribution in the brain, and its properties in the cellular microenvironment may have a strong influence on the understanding of Li function. The differentiation of lithium in the intra and extracellular environments has been achieved in a noninvasive manner in red blood cell (RBC) model. The two distinct transverse relaxation ( T 2) components have been observed in the blood sample drawn from lithium treated rats. These results indicate two different environments for Li with a fast ( T 2f) and a slow ( T 2s) component in the RBC model corresponding fractions that contribute to each relaxation component. The results compare well with the intra- and extracellular RBC lithium measured using shift reagents. Our studies indicate that the T 2 method has utility in estimating the intracellular Li in systems that exhibit similar T 2 behavior. The studies performed at different Li doses in the rat model indicate that the method may have utility in following a wide range of intracellular Li.

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