Plasma protein changes in Atlantic salmon (Salmo salar) during parr-smolt transformation

1. 1. Changes in plasma proteins of Atlantic salmon (Salmon salar) during parr-smolt transformation were analyzed by two-dimensional polyacrylamide gel electrophoresis. 2. 2. An increase in the number of low molecular weight proteins (\u3c29 kilodaltons) was associated with smoltification. 3. 3. Alterations in the quantities and relative proportions of several proteins (molecular weights 57-63 kilodaltons) were observed. 4. 4. These changes may indicate a role for specific plasma proteins in transition and adaptation to the marine environment. © 1989

Investigation of hepatic cytosolic proteins during parr-smolt transformation of Atlantic salmon (Salmo salar)

The diverse metabolic functions of the teleost liver and previous studies of hepatic mitochondria implicate this organ in smolting. To investigate hepatic involvement further, cytosolic proteins were examined in Atlantic salmon during parr-smolt transformation. Two separate studies were conducted in which juvenile salmon were reared with 6-month advanced (6MA), 8-month advanced (8MA) and simulated natural (SNP) photoperiod regimens. The two phase-shifted photoperiods were utilized in an attempt to produce non-smolting controls for discrimination between proteins related to ontogeny and proteins specific to parr-smolt transformation. Branchial Na+ K+-ATPase activities, condition factors and salinity tolerances indicated that SNP fish underwent smolting during a normal time period. Numerous changes in cytosolic proteins were observed in SNP, 6MA and 8MA fish. Seven polypeptides exhibited qualitative or quantitative changes between December and May in SNP fish during the two investigations. However, when these differences were compared with the contemporary controls in the 6MA and 8MA studies, the changes did not appear to be specific to smolting. © 1989

Intestinal uptake of lipovitellin from brine shrimp (Artemia franciscana) by larval inland silversides (Menidia beryllina) and striped bass (Morone saxatilis)

Intestinal uptake of lipovitellin (LV) from brine shrimp (Artemia franciscana) in larval inland silversides (Menidida beryllina) and striped bass (Morone saxatilis) was described using immunocytochemistry. Polyclonal antisera were raised against two subunits of LV (LV68 and LV190). When tested by immunocytochemistry, anti-LV68 showed cross-reactivity with some of the pancreatic cells especially in inland silversides. Therefore anti-LV190 was used to localize immunoreactive LV. Inland silversides at 14 days after hatching were fed Artemia nauplii and then sampled 4, 8, 12 hr after feeding. Similar experiments were carried out by using striped bass at 5 days and 15 days of age. They were sampled at 2, 4, 8, and 12 hr after feeding. Anterior enterocytes showed no evidence of uptake; however, the brush border of the cells of inland silversides reacted with the antiserum. Posterior enterocytes took up the LV and/or, possibly, their immunoreactive breakdown products. The pattern of uptake included accumulation in supranuclear vacuoles and digestion in supranuclear vacuoles, as suggested by the decay of the immunoreactivity over time. Thus, the posterior intestine of these larval fishes is the site of uptake and digestion of LV, an important nutritive component in the food of many larval fishes; this supports earlier findings using non-nutritive marker proteins

Protein and lipid binding parameters in rainbow trout (Oncorhynchus mykiss) blood and liver fractions to extrapolate from an in vitro metabolic degradation assay to in vivo bioaccumulation potential of hydrophobic organic chemicals

Binding of hydrophobic chemicals to colloids such as proteins or lipids is difficult to measure using classical microdialysis methods due to low aqueous concentrations, adsorption to dialysis membranes and test vessels, and slow kinetics of equilibration. Here, we employed a three-phase partitioning system where silicone (polydimethylsiloxane, PDMS) serves as a third phase to determine partitioning between water and colloids and acts at the same time as a dosing device for hydrophobic chemicals. The applicability of this method was demonstrated with bovine serum albumin (BSA). Measured binding constants (K(BSAw)) for chlorpyrifos, methoxychlor, nonylphenol, and pyrene were in good agreement with an established quantitative structure-activity relationship (QSAR). A fifth compound, fluoxypyr-methyl-heptyl ester, was excluded from the analysis because of apparent abiotic degradation. The PDMS depletion method was then used to determine partition coefficients for test chemicals in rainbow trout (Oncorhynchus mykiss) liver S9 fractions (K(S9w)) and blood plasma (K(bloodw)). Measured K(S9w) and K(bloodw) values were consistent with predictions obtained using a mass-balance model that employs the octanol-water partition coefficient (K(ow)) as a surrogate for lipid partitioning and K(BSAw) to represent protein binding. For each compound, K(bloodw) was substantially greater than K(S9w), primarily because blood contains more lipid than liver S9 fractions (1.84% of wet weight vs 0.051%). Measured liver S9 and blood plasma binding parameters were subsequently implemented in an in vitro to in vivo extrapolation model to link the in vitro liver S9 metabolic degradation assay to in vivo metabolism in fish. Apparent volumes of distribution (V(d)) calculated from the experimental data were similar to literature estimates. However, the calculated binding ratios (f(u)) used to relate in vitro metabolic clearance to clearance by the intact liver were 10 to 100 times lower than values used in previous modeling efforts. Bioconcentration factors (BCF) predicted using the experimental binding data were substantially higher than the predicted values obtained in earlier studies and correlated poorly with measured BCF values in fish. One possible explanation for this finding is that chemicals bound to proteins can desorb rapidly and thus contribute to metabolic turnover of the chemicals. This hypothesis remains to be investigated in future studies, ideally with chemicals of higher hydrophobicity