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First published online May 13, 2004
Journal of Experimental Biology 207, 2055-2064 (2004)
Published by The Company of Biologists 2004
doi: 10.1242/jeb.00971
Contributions of different NaPi cotransporter isoforms to dietary regulation of P transport in the pyloric caeca and intestine of rainbow trout
New Jersey Medical School, Department of Pharmacology and Physiology, University of Medicine and Dentistry of New Jersey, Newark, NJ 07103, USA
* Author for correspondence (e-mail: Ferraris{at}umdnj.edu)
Accepted 10 March 2004
The anatomical proximity and embryological relationship of the pyloric
caeca (PC) and small intestine of rainbow trout has led to the frequent
assumption, on little evidence, that they have the same enzymes and
transporters. In trout, the PC is an important absorptive organ for dietary
nutrients, but its role in dietary P absorption has not been reported. We
found that apical inorganic phosphate (Pi) transport in PC comprises
carrier-mediated and diffusive components. Carrier-mediated uptake was energy-
and temperature-dependent, competitively inhibited and
Na+-independent, and greater than the Na+-dependent
intestinal uptake. Pi uptake in PC was pH-sensitive in the presence of
Na+. Despite the active Pi transport system in PC, high
postprandial luminal Pi concentrations (
20 mmol l1)
indicate that diffusive uptake represents
92% of total Pi uptake in PC of
fed fish. The nucleotide sequence of a sodium-phosphate cotransporter
(NaPi-II) isoform isolated from PC was
8% different from the intestinal
NaPi cotransporter. PC-NaPi mRNA was abundant in PC but rare in the intestine,
whereas intestinal NaPi mRNA was abundant in the intestine but scarce in PC.
Dietary P restriction reduced serum and bone P concentrations, increased
intestine-type, but not PC-type, NaPi mRNA in PC, and increased Pi uptake in
intestine but not in PC. Intestine-type NaPi expression may be useful for
predicting dietary P deficiency.
Key words: NaPi cotransport, phosphorus, rainbow trout, pyloric caeca, intestine
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