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Journal of Lipid Research, Vol 22, 916-920, Copyright © 1981 by Lipid Research, Inc.


ARTICLES

Urinary clearance and metabolism of mevalonate by the isolataed perfused rat kidney

H Brunengraber, SB Weinstock, DL Story and RR Kopito

The urinary excretion and the incorporation into lipids of R[3- 14C]mevalonate was investigated in isolated rat kidneys perfused with physiological concentration sof the substrate (80-500 pmol/ml). The clearance of R[3-14C]mevalonate and of the unnatural enantiomer S[5- 14C]mevalonate were compared to the glomerular filtration ratea measured by the clearance of inulin. Evidence is presented that half of R-mevalonate filtered in the glomerulus is reabsorbed in the tubule whereas S-mevalonate is not reabsorbed. The kidney tubule appears to discriminate between the R and S forms of the mevalonate salt. Urinary excretion and incorporation into lipids accounted for 22% and 46%, respectively, of the uptake of R[3-14C]mevalonate from the perfusate. The label of R[3-14C]mevalonate recovered in lipids was distributed among saponifiable (15%), digitonin-precipitable sterols (18%) and squalene + prenols (67%). Sterol synthesis in the kidney appears to be controlled, at least in part, by the level of circulatinga R-mevalonate.
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I. R. Bederman, A. E. Reszko, T. Kasumov, F. David, D. H. Wasserman, J. K. Kelleher, and H. Brunengraber
Zonation of Labeling of Lipogenic Acetyl-CoA across the Liver: IMPLICATIONS FOR STUDIES OF LIPOGENESIS BY MASS ISOTOPOMER ANALYSIS
J. Biol. Chem., October 8, 2004; 279(41): 43207 - 43216.
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