Rapid activation of gill Na+, K+-ATPase the euryhaline teleost Fundulus heteroclitus
The rapid activation of gill Na + ,K + -ATPase was analyzed in the mummichog ( Fundulus heteroclitus ) and Atlantic salmon ( Salmo salar ) transferred from low salinity (0.1 ppt) to high salinity (25–35 ppt). In parr and presmolt, Salmo salar gill Na + ,K + -ATPase activity started to increase 3 days after transfer. Exposure of Fundulus heteroclitus to 35 ppt seawater (SW) induced a rise in gill Na + ,K + -ATPase activity 3 hr after transfer. After 12 hr, the values dropped to initial levels but showed a second significant increase 3 days after transfer. The absence of detergent in the enzyme assay resulted in lower values of gill Na + ,K + -ATPase, and the rapid increase after transfer to SW was not observed. Na + ,K + -ATPase activity of gill filaments in vitro for 3 hr increased proportionally to the osmolality of the culture medium (600 mosm/kg > 500 mosm/kg > 300 mosm/kg). Osmolality of 800 mosm/kg resulted in lower gill Na + ,K + -ATPase activity relative to 600 mosm/kg. Increasing medium osmolality to 600 mosm/kg with mannitol also increased gill Na + ,K + -ATPase. Cycloheximide inhibited the increase in gill Na + ,K + -ATPase activity observed in hyperosmotic medium in a dose-dependent manner (10 –4 M > 10 –5 M > 10 –6 M). Actinomycin D or bumetanide in the culture (doses of 10 –4 M, 10 –5 M, and 10 –6 M) did not affect gill Na + ,K + -ATPase. Injection of fish with actinomycin D prior to gill organ culture, however, prevented the increase in gill Na + ,K + -ATPase activity in hyperosmotic media. The results show a very rapid and transitory increase in gill Na + ,K + -ATPase activity in the first hours after the transfer of Fundulus heteroclitus to SW that is dependent on translational and transcriptional processes.