Meeting details menu

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

Acta Physiologica Congress

Back

Acta Physiologica 2006; Volume 187, Supplement 659
The Scandinavian Physiological Society's Annual Meeting
8/11/2006-8/13/2006
Reykjavik, Iceland


NA+/H+ EXCHANGER ISOFORM 3 IN THE RAT INTESTINE
Abstract number: P45

RYBOVA1,2 M, BRYNDOVA1 J, PACHA1 J

1Institute of Physiology, Academy of Sciences of the Czech Republic, Videnska 1083,Prague
22ndMedical School, Charles University, Prague, Czech Republic [email protected]

Ion transporters called Na+/H+ exchangers (NHEs) play a significant role in Na+ absorption and regulation of intracellular pH and cell volume. The isoforms NHE1, NHE2, and NHE3, were identified in the intestinal epithelium. The NHE3 isoform that is localized on provides the electroneutral transcellular Na+ transport. Previous investigations showed differences in regulation of NHE3 expression during ontogenetic development and during diurnal cycle in renal tubules. However, little is known about this regulation in colon. The present study investigated, therefore, (1) the diurnal variations of colonic NHE3 mRNA transcript, (2) it's ontogenetic profile in suckling, weanling and adult rats and (3) the changes of NHE3 transcript during intestinal inflammation (TNBS-colitis) using the quantitative RT-PCR of NHE3 mRNA. We found that NHE3 mRNA level display circadian changes with higher value at the beginning of the night and this rythmicity are shifted by reverse feeding. The level of NHE3 mRNA was very high in sucklings, decreases during weaning period and partially increases again during pubescence. The level of NHE3 mRNA in adulthood was not invariable but could be up-regulated during colonic inflammation. We conclude that NHE3 is temporally regulated transporter that is controlled not only during postnatal ontogenesis but also by circadian oscilator and by the inflammatory state.

Supported by Ministry of Health grant NR 8576-3.

To cite this abstract, please use the following information:
Acta Physiologica 2006; Volume 187, Supplement 659 :P45

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