Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1981;74(4):374-8.
doi: 10.1007/BF00432751.

Studies on the disposition of Li+ in the guinea-pig and rat

Studies on the disposition of Li+ in the guinea-pig and rat

N Murray et al. Psychopharmacology (Berl). 1981.

Abstract

Rats and guinea-pigs were given LiCl acutely (2 mmol/kg IP or intragastrically) or chronically (daily doses 0.6-4 mmol/kg) and plasma, erythrocytes, kidney, liver and brain were analysed for Li+. Generally, after acute LiCl, tissue Li+ levels followed changes in plasma Li+ levels. However, brain Li+ concentrations changed more slowly and in the rat, but not in the guinea-pig, paralleled erythrocyte Li+ concentrations. Li+ was absorbed more slowly from the gastrointestinal tract of the rat. After chronic LiCl, the erythrocyte:plasma Li+ ratio was about 0.1 in the guinea-pig and about 2 in the rat. Relative Li+ tissue concentrations were as follows: guinea-pig, plasma greater than kidney greater than liver greater than brain greater than erythrocyte;rat much greater than erythrocyte = brain greater than liver = plasma. A Na+-dependent Li+ efflux was demonstrated in the erythrocytes of the guinea-pig and human, but not the rat. This process was inhibited by phloretin (0.2 mM), but not frusemide (2.0 mM). The marked differences in the activity of the erythrocyte Na+-dependent Li+ countertransport process in the guinea-pig and rat could extend to other tissues and explain the observed interspecies differences in tissue Li+ distribution.

PubMed Disclaimer

Similar articles

References

    1. Nature. 1975 Dec 4;258(5534):425-7 - PubMed
    1. Psychopharmacol Commun. 1976;2(2):91-103 - PubMed
    1. Med J Aust. 1949 Sep 3;2(10):349-52 - PubMed
    1. J Gen Physiol. 1978 Aug;72(2):249-65 - PubMed
    1. Br J Pharmacol. 1976 Apr;56(4):399-402 - PubMed

LinkOut - more resources