Meeting details menu

Meeting Authors
Meeting Abstracts
Keynote lectures
Oral communications
Poster presentations
Special symposia
Other

Acta Physiologica Congress

Back

Acta Physiologica 2009; Volume 195, Supplement 669
The 88th Annual Meeting of The German Physiological Society
3/22/2009-3/25/2009
Giessen, Germany


DIFFERENTIAL REGULATION OF THREE RENAL PHOSPHATE TRANSPORTERS BY PARATHYROID HORMONE (PTH)
Abstract number: O215

Capuano1 P., Picard2 N., Stange1 G., Murer1 H., Biber1 J., Wagner1 C.

1Institute of Physiology, Zrich, Switzerland
2Institute of Anatomy, Zrich, Switzerland

Phosphate homeostasis has been considered until now a process mainly controlled by the SLC34 family of sodium dependent contransporters (NaPis) expressed in the intestine and in the kidney. Recently it has been shown that yet another family of transporters, the SLC20 family members Pit-1 and -2, may be involved in the regulation of phosphate homeostasis.

Since PTH is one of the main hormonal regulators of renal phosphate handling, we aimed to study the effect of a short-term application of PTH on the regulation of NaPi-IIc and Pit-2 in rat kidney. Rats were divided in four groups (control 30 minutes, PTH treated 30 minutes, control 60 minutes, PTH treated 60 minutes) and we measured Na-dependent phosphate uptake in the absence and presence of the type II specific transport inhibitor PFA, localization, and mRNA and protein expression of NaPi-IIa, NaPi-IIc, and Pit-2. Immunohistochemistry data show no apparent change in the localization of the NaPi-IIc and Pit2 transporter at both time points. PTH reduced total Na-dependent phosphate transport activity but had only little effect on the PFA-resistant activity. Real time PCR results show that 1h PTH did not alter the amount of NaPi-IIc and Pit-2 mRNA. Western blotting on renal brush border membranes showed similar results.

In conclusion, PTH reduces renal phosphate reabsorption by inducing internalization of NaPi-IIa but has no effects on NaPi-IIc and Pit-2.

To cite this abstract, please use the following information:
Acta Physiologica 2009; Volume 195, Supplement 669 :O215

Our site uses cookies to improve your experience.You can find out more about our use of cookies in our standard cookie policy, including instructions on how to reject and delete cookies if you wish to do so.

By continuing to browse this site you agree to us using cookies as described in our standard cookie policy .

CLOSE