BRANCHIAL CALCIUM-UPTAKE - POSSIBLE MECHANISMS OF CONTROL BY STANNIOCALCIN

Citation
Pm. Verbost et al., BRANCHIAL CALCIUM-UPTAKE - POSSIBLE MECHANISMS OF CONTROL BY STANNIOCALCIN, Fish physiology and biochemistry, 11(1-6), 1993, pp. 205-215
Citations number
31
Categorie Soggetti
Biology,Fisheries
ISSN journal
09201742
Volume
11
Issue
1-6
Year of publication
1993
Pages
205 - 215
Database
ISI
SICI code
0920-1742(1993)11:1-6<205:BC-PMO>2.0.ZU;2-W
Abstract
The branchial Ca2+ uptake by teleost fish is under inhibitory control by the hormone stanniocalcine (STC) which is generated by the corpuscl es of Stannius (CS). Removal of the CS in North American eel, Anguilla rostrata LeSueur, induced a rapid rise in blood calcium levels. Branc hial Ca2+ influx following the extirpation of the CS (stanniectomy, ST X) increased during the first four days and stayed elevated thereafter (in agreement with previous studies). The transepithelial potential ( TEP) across the gills did not change after STX and this means that the electrochemical gradient for Ca2+ is less favourable for passive infl ux of Ca2+ in STX eel. Therefore, the Call influx in STX eels is a tra nscellular flux, with Ca2+ crossing the apical and basolateral membran e barrier. The kinetics of ATP-driven Ca2+-transport across basolatera l plasma membranes from eel gills did not change after STX. Thus, the increased Ca2+-influx after STX is not correlated with changes in ATP- dependent Ca2+-extrusion across the basolateral membrane, suggesting a regulation at the apical membrane. Moreover, STC did not affect ATP-d riven Ca2+-transport in isolated basolateral membranes (in vitro). STC (0.1 nM) reduced cAMP levels in dispersed eel gill cells. It had no s ignificant effect on the IP3 levels in these cells. We postulate that STC controls the permeability to Ca2+ of the apical membranes of the C a2 + transporting cells of fish gills by controlling second messenger operated Ca2+ channels in the apical membrane.