HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Downregulation of organic anion transporters OAT1 and OAT3 correlates with impaired secretion of para-aminohippurate after ischemic acute renal failure in rats.

Abstract
Ischemic acute renal failure (iARF) was described to reduce renal extraction of the organic anion para-aminohippurate (PAH) in humans. The rate-limiting step of renal organic anion secretion is its basolateral uptake into proximal tubular cells. This process is mediated by the organic anion transporters OAT1 and OAT3, which both have a broad spectrum of substrates including a variety of pharmaceutics and toxins. Using a rat model of iARF, we investigated whether impairing the secretion of the organic anion PAH might be associated with downregulation of OAT1 or OAT3. Inulin and PAH clearance was determined starting from 6 up to 336 h after ischemia-reperfusion (I/R) injury. Net secretion of PAH was calculated and OAT1 as well as OAT3 expression was analyzed by RT-PCR and Western blotting. Inulin and PAH clearance along with PAH net secretion were initially diminished after I/R injury with a gradual recovery during follow-up. This initial impairment after iARF was accompanied by decreased mRNA and protein levels of OAT1 and OAT3 in clamped animals compared with sham-operated controls. In correlation to the improvement of kidney function, both mRNA and protein levels of OAT1 and OAT3 were upregulated during the follow-up. Thus decreased expression of OAT1 and OAT3 is sufficient to explain the decline of PAH secretion after iARF. As a result, this may have substantial impact on excretion kinetics and half-life of organic anions. As a consequence, the biological effects of a variety of organic anions may be affected after iARF.
AuthorsR Schneider, C Sauvant, B Betz, M Otremba, D Fischer, H Holzinger, C Wanner, J Galle, M Gekle
JournalAmerican journal of physiology. Renal physiology (Am J Physiol Renal Physiol) Vol. 292 Issue 5 Pg. F1599-605 (May 2007) ISSN: 1931-857X [Print] United States
PMID17244891 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Organic Anion Transport Protein 1
  • Organic Anion Transporters, Sodium-Independent
  • RNA, Messenger
  • Slc22a6 protein, rat
  • organic anion transport protein 3
  • Inulin
  • p-Aminohippuric Acid
Topics
  • Animals
  • Blotting, Western
  • Down-Regulation
  • Female
  • Inulin (metabolism)
  • Ischemia (complications)
  • Kidney (blood supply)
  • Organic Anion Transport Protein 1 (genetics, metabolism)
  • Organic Anion Transporters, Sodium-Independent (genetics, metabolism)
  • RNA, Messenger (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Renal Insufficiency (etiology, metabolism)
  • Reperfusion Injury (metabolism)
  • Reverse Transcriptase Polymerase Chain Reaction
  • p-Aminohippuric Acid (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: