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Vol. 302, Issue 2, 510-515, August 2002
Graduate School of Pharmaceutical Sciences, University of Tokyo,
Tokyo, Japan (D.-S.W., Y.K., H.K., Y.S.); Core Research for Evolutional
Science and Technology, Japan Science and Technology Corporation,
Tokyo, Japan (Y.K., H.K., Y.S.); and Division of Experimental Therapy,
The Netherlands Cancer Institute, Amsterdam, The Netherlands (J.W.J.,
A.H.S.)
Metformin, a biguanide, is widely used as an oral hypoglycemic agent
for the treatment of type 2 diabetes mellitus. The purpose of
the present study was to investigate the role of organic cation transporter 1 (Oct1) in the disposition of metformin. Transfection of
rat Oct1 cDNA results in the time-dependent and saturable uptake of
metformin by the Chinese hamster ovary cell line with
Km and Vmax
values of 377 µM and 1386 pmol/min/mg of protein, respectively. Buformin and phenformin, two other biguanides, were also transported by
rOct1 with a higher affinity than metformin: their
Km values were 49 and 16 µM, respectively.
To investigate the role of Oct1 in the disposition of metformin, the
tissue distribution of metformin was determined in Oct1 gene-knockout
mice after i.v. administration. Distribution of metformin to the liver
in Oct1(
/
) mice was more than 30 times lower than that in Oct1(+/+)
mice, and can be accounted for by the extracellular space. Distribution
to the small intestine was also decreased in Oct1(
/
) mice, whereas
that to the kidney as well as the urinary excretion profile showed only
minimal differences. In conclusion, the present findings suggest that
Oct1 is responsible for the hepatic uptake as well as playing a role in
the intestinal uptake of metformin, whereas the renal distribution and
excretion are mainly governed by other transport mechanism(s).
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