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Effects of dietary salt intake on plasma arginine

  • Georgetown School of Medicine
  • Georgetown University Medical Center

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)

Abstract

Because L-arginine is degraded by hepatic arginase to ornithine and urea and is transported by the regulated 2A cationic amino acid y+ transporter (CAT2A), hepatic transport may regulate plasma arginine concentration. Groups of rats (n = 6) were fed a diet of either low salt (LS) or high salt (HS) for 7 days to test the hypothesis that dietary salt intake regulates plasma arginine concentration and renal nitric oxide (NO) generation by measuring plasma arginine and ornithine concentrations, renal NO excretion, and expression of hepatic CAT2A, and arginase. LS rats had lower excretion of NO metabolites and cGMP, lower plasma arginine concentration (LS: 83 ± 7 vs. HS: 165 ± 10 μmol/1, P < 0.001), but higher plasma ornithine concentration (LS: 82 ± 6 vs. HS: 66 ± 4 μmol/1, P < 0.05) and urea excretion. However, neither the in vitro hepatic arginase activity nor the mRNA for hepatic arginase I was different between groups. In contrast, LS rats had twice the abundance of mRNA for hepatic CAT2A (LS: 3.4 ± 0.4 vs. HS: 1.6 ± 0.5, P < 0.05). The reduced plasma arginine concentration with increased plasma ornithine concentration and urea excretion during LS indicates increased arginine metabolism by arginase. This cannot be ascribed to changes in hepatic arginase expression but may be a consequence of increased hepatic arginine uptake via CAT2A.

Original languageEnglish
Pages (from-to)R1069-R1075
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Volume280
Issue number4 49-4
DOIs
Publication statusPublished - 2001
Externally publishedYes

Keywords

  • Cationic amino acid transporter
  • Nitric oxide
  • Ornithine
  • System y transport
  • Urea

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