Activation of carbonic anhydrase in branchial cavity tissues of lobsters (Homarus gammarus) by dilute seawater exposure

Activities of carbonic anhydrase (CA) and its distribution in the branchial cavity tissues were studied in European lobsters (Homarus gammarus) from ambient seawater (SW; salinity=38 ppt, 1126 mosmol/l) and acclimated to dilute seawater (DSW; salinity=20 ppt, 548 mosmol/l). Acetazolamide inhibited dose dependently the activity of CA in homogenates of epipodites, where the inhibition constant (IC₅₀=0.12 μM) did not differ significantly from that of membrane vesicles and cytosolic fraction. In DSW-acclimated lobsters, almost 70% of total CA in tissues of the branchial cavity was found in epipodites (E) and the rest was equally distributed between branchiostegites (B) and gills (G). Upon acclimation to dilute seawater, CA activity in membrane fractions of E and B was increased 6-fold and in homogenates, respectively 5- and 13-fold compared to SW-acclimated lobsters. Exposure to DSW enhanced cytosolic CA in E (8-fold) and B (7-fold) over SW-acclimated animals. Slight activation of CA in homogenates and in partially purified membranes of G was not confirmed as a statistically significant difference between SW and DSW groups. In DSW, cytosol specific activity of CA was increased compare to the SW cytosol. These results indicate the importance of E and B in CA induction when lobsters are acclimated to DSW. In subcellular fractions from DSW-acclimated lobsters, the main proportion of 75.8% (E), 61.0% (B) of total CA activity in each of these tissues remained in cytosol portion. Partially purified membranes contained 6.8% (E) and 16.2% (B) and the remainder of 15% (E) and 27% (B) was found in mitochondrial and nuclear fractions. In gills, 49.2% and 9.0 % of total gill CA activity was found respectively in cytosol and partially purified vesicles and the rest in mitochondrial and nuclear fractions.