A role for the organic anion transporter OAT3 in renal creatinine secretion in mice

Volker Vallon, Satish A. Eraly, Satish Ramachandra Rao, Maria Gerasimova, Michael Rose, Megha Nagle, Naohiko Anzai, Travis Smith, Kumar Sharma, Sanjay K. Nigam, Timo Rieg

Research output: Contribution to journalArticle

61 Citations (Scopus)

Abstract

Tubular secretion of the organic cation, creatinine, limits its value as a marker of glomerular filtration rate (GFR) but the molecular determinants of this pathway are unclear. The organic anion transporters, OAT1 and OAT3, are expressed on the basolateral membrane of the proximal tubule and transport organic anions but also neutral compounds and cations. Here, we demonstrate specific uptake of creatinine into mouse mOat1-and mOat3-microinjected Xenopus laevis oocytes at a concentration of 10 μM (i.e., similar to physiological plasma levels), which was inhibited by both probenecid and cimetidine, prototypical competitive inhibitors of organic anion and cation transporters, respectively. Renal creatinine clearance was consistently greater than inulin clearance (as a measure of GFR) in wild-type (WT) mice but not in mice lacking OAT1 (Oat1-/-) and OAT3 (Oat3-/-). WT mice presented renal creatinine net secretion (0.23 ± 0.03 μg/min) which represented 45 ± 6% of total renal creatinine excretion. Mean values for renal creatinine net secretion and renal creatinine secretion fraction were not different from zero in Oat1-/- (-0.03 ± 0.10 μg/min; -3 ± 18%) and Oat3-/- (0.01 ± 0.06 μg/min; -6 ± 19%), with greater variability in Oat1-/-. Expression of OAT3 protein in the renal membranes of Oat1-/- mice was reduced to ~6% of WT levels, and that of OAT1 in Oat3-/- mice to ~60%, possibly as a consequence of the genes for Oat1 and Oat3 having adjacent chromosomal locations. Plasma creatinine concentrations of Oat3-/- were elevated in clearance studies under anesthesia but not following brief isoflurane anesthesia, indicating that the former condition enhanced the quantitative contribution of OAT3 for renal creatinine secretion. The results are consistent with a contribution of OAT3 and possibly OAT1 to renal creatinine secretion in mice.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Renal Physiology
Volume302
Issue number10
DOIs
StatePublished - May 15 2012
Externally publishedYes

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Organic Anion Transporters
Creatinine
Kidney
Cations
Glomerular Filtration Rate
Anesthesia
Probenecid
Membranes
Inulin
Isoflurane
Cimetidine
Xenopus laevis
Oocytes
Anions

Keywords

  • Cimetidine
  • Creatinine clearance
  • OAT1
  • Probenecid
  • Proximal tubule

ASJC Scopus subject areas

  • Physiology
  • Urology

Cite this

A role for the organic anion transporter OAT3 in renal creatinine secretion in mice. / Vallon, Volker; Eraly, Satish A.; Rao, Satish Ramachandra; Gerasimova, Maria; Rose, Michael; Nagle, Megha; Anzai, Naohiko; Smith, Travis; Sharma, Kumar; Nigam, Sanjay K.; Rieg, Timo.

In: American Journal of Physiology - Renal Physiology, Vol. 302, No. 10, 15.05.2012.

Research output: Contribution to journalArticle

Vallon, V, Eraly, SA, Rao, SR, Gerasimova, M, Rose, M, Nagle, M, Anzai, N, Smith, T, Sharma, K, Nigam, SK & Rieg, T 2012, 'A role for the organic anion transporter OAT3 in renal creatinine secretion in mice', American Journal of Physiology - Renal Physiology, vol. 302, no. 10. https://doi.org/10.1152/ajprenal.00013.2012
Vallon, Volker ; Eraly, Satish A. ; Rao, Satish Ramachandra ; Gerasimova, Maria ; Rose, Michael ; Nagle, Megha ; Anzai, Naohiko ; Smith, Travis ; Sharma, Kumar ; Nigam, Sanjay K. ; Rieg, Timo. / A role for the organic anion transporter OAT3 in renal creatinine secretion in mice. In: American Journal of Physiology - Renal Physiology. 2012 ; Vol. 302, No. 10.
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