Effects of aminonucleoside, daunomycin, and adriamycin on carbon oxidation by glomeruli
- PMID: 1249918
Effects of aminonucleoside, daunomycin, and adriamycin on carbon oxidation by glomeruli
Abstract
The purpose of these experiments was to determine whether reported changes in substrate metabolism by isolated glomeruli from rats with aminonucleoside nephrosis could be explained by the glomerular changes associated with proteinuria or, alternatively, whether these metabolic changes and proteinuria were synchronous but causally unrelated events. Aminonucleoside of puromycin produced proteinuria within 7 days when injected intraperitoneally or subcutaneously. However, when aminonucleoside of puromycin as well as adenine were given, the onset of proteinuria was delayed until after day 7. A significant reduction in U-14C-glucose oxidation to CO2 was found at day 7 by glomeruli from rats given aminonucleoside of puromycin intraperitoneally but no significant changes were found with aminonucleoside of puromycin given subcutaneously on days 7 and 9 and aminonucleoside of puromycin + adenine given subcutaneously on days 7 and 9. Rats given daunomycin or adriamycin had developed proteinuria by day 14. U-14C-glucose oxidation to CO2 was significantly reduced on day 14 in glomeruli from rats given daunomycin but no significant changes were found on day 21 with daunomycin, or on days 14 and 21 with adriamycin. There was a reduction in pyruvic-acid carbon metabolism but not in glutamine-carbon oxidation 14 days after treatment with daunomycin. These results suggest that the observed changes in glomerular metabolism occur independently of, albeit synchronous with, the development of proteinuria. A causal relationship between these metabolic alterations and proteinuria therefore may be unlikely.
Similar articles
-
Glomerular sclerosis in nephrotic rats. Comparison of the long-term effects of adriamycin and aminonucleoside.Lab Invest. 1984 Sep;51(3):277-85. Lab Invest. 1984. PMID: 6471809
-
Alterations in proteoglycan metabolism in the nephrotic syndrome induced by the aminonucleoside of puromycin.Lab Invest. 1984 May;50(5):543-51. Lab Invest. 1984. PMID: 6232422
-
Incorporation of 35sulfate into the glomerular basement membrane in puromycin aminonucleoside nephrosis.Int J Pediatr Nephrol. 1985 Apr-Jun;6(2):117-20. Int J Pediatr Nephrol. 1985. PMID: 4030221
-
Focal glomerular hyalinosis and sclerosis in aminonucleoside and adriamycin nephrosis: pathogenetic and therapeutic considerations.Contrib Nephrol. 1988;60:73-82. doi: 10.1159/000414792. Contrib Nephrol. 1988. PMID: 3278860 Review. No abstract available.
-
Application of puromycin aminonucleoside and adriamycin to induce chronic renal failure in the rat.Contrib Nephrol. 1988;60:83-93. doi: 10.1159/000414793. Contrib Nephrol. 1988. PMID: 3278861 Review. No abstract available.
Cited by
-
Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice.J Clin Invest. 2010 Nov;120(11):4055-64. doi: 10.1172/JCI43721. Epub 2010 Oct 18. J Clin Invest. 2010. PMID: 20978358 Free PMC article.
-
Focal segmental glomerulosclerosis is induced by microRNA-193a and its downregulation of WT1.Nat Med. 2013 Apr;19(4):481-7. doi: 10.1038/nm.3142. Epub 2013 Mar 17. Nat Med. 2013. PMID: 23502960