Journal
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
Volume 293, Issue 1, Pages F382-F390Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajprenal.00441.2006
Keywords
rat; kidney; D-serine toxicity; glutathione
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Funding
- NIDDK NIH HHS [DK-16294] Funding Source: Medline
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Serine selectively causes necrosis of S-3 segments of proximal tubules in rats. This leads to aminoaciduria and glucosuria. Coinjection of the nonmetabolizable amino acid alpha-aminoisobutyric acid (AIB) prevents the tubulopathy. D-serine is selectively reabsorbed in S-3, thereby gaining access to peroxisomal D-amino acid oxidase (D-AAO). D-AAO-mediated metabolism produces reactive oxygen species. We determined the fractional excretion of amino acids and glucose in rats after intraperitoneal injection of D-serine alone or together with reduced glutathione (GSH) or AIB. Both compounds prevented the hyperaminoaciduria. We measured GSH concentrations in renal tissue before (control) and after D-serine injection and found that GSH levels decreased to similar to 30% of control. This decrease was prevented when equimolar GSH was coinjected with D-serine. To find out why AIB protected the tubule from D-serine toxicity, we microinfused D-[C-14] serine or [C-14] AIB (0.36 mmol/l) together with [H-3] inulin in late proximal tubules in vivo and measured the radioactivity in the final urine. Fractional reabsorption of D-[C-14] serine and [C-14] AIB amounted to 55 and 70%, respectively, and 80 mmol/l of AIB or D-serine mutually prevented reabsorption to a great extent. D-AAO activity measured in vitro (using D- serine as substrate) was not influenced by a 10-fold higher AIB concentration. We conclude from these results that 1) D-AAO-mediated D-serine metabolism lowers renal GSH concentrations and thereby provokes tubular damage because reduction of reactive oxygen species by GSH is diminished and 2) AIB prevents D- serine-induced tubulopathy by inhibition of D-serine uptake in S3 segments rather than by interfering with intracellular D-AAO-mediated D-serine metabolism.
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