Varying levels of pharmaceuticals, including salicylate, ibuprofen, and acetaminophen, have been reported in the aquatic environment, but few studies have actually addressed the impact of these drugs on aquatic organisms. We tested the hypothesis that these pharmaceuticals are endocrine disruptors in fish by examining their impact on interrenal corticosteroidogenesis in rainbow trout. Indeed, acute adrenocorticotrophic hormone (ACTH)-mediated cortisol production in trout interrenal cells in vitro was significantly depressed (20-40%) by these pharmaceutical drugs. Furthermore, we investigated whether this interrenal dysfunction involved inhibition of the steroidogenic capacity in rainbow trout. To this end, we fed trout salicylate-laced feed (100 mg/kg body weight) for 3 days and assessed the transcript levels of key proteins involved in corticosteroidogenesis, including steroidogenic acute regulatory protein (StAR), peripheral-type benzodiazepine receptor (PBR), cytochrome P450 cholesterol side chain cleavage (P450scc), and 11beta-hydroxylase. Salicylate treatment did not affect the resting plasma cortisol or glucose levels, whereas the acute ACTH-stimulated cortisol production was significantly depressed in the interrenal tissue. This disruption of steroidogenesis by salicylate corresponded to a significant drop in the gene expression of StAR and PBR, but not P450scc or 11beta-hydroxylase, compared to the sham-treated fish. Also, brain glucocorticoid receptor (GR) protein content and not GR mRNA level was significantly reduced by salicylate. Taken together, salicylate is a corticosteroid disruptor in trout and the targets include the key rate-limiting step in interrenal steroidogenesis and brain glucocorticoid signaling.
Although it has been reported that adult yellow perch (Perca flavescens) chronically exposed to metals in the environment exhibit endocrine impairment characterized by blunted cortisol secretion, little is known about the vulnerability of early life stages. Young-of-the-year (YOY) and 1+ yellow perch were captured, subjected to a standardized stress test or adrenocorticotropic-hormone stimulation in lakes situated along a contamination gradient of Cd, Cu, and Zn in the mining region of Abitibi, Quebec. For the first time, whole-body cortisol concentrations were measured. The 1+ fish with elevated whole-body Cd, Cu, and Zn concentrations had an impaired capacity to respond to an acute stress challenge. Although YOY perch had similar whole-body Cd concentrations to 1+ perch, no effects on physiological status were detected in relation to body burdens of metals. Metal contamination did not affect whole-body thyroid-hormone concentrations, condition factor, or hepatosomatic index in 1+ or YOY perch. These results indicate that effects of Cd, Cu, and Zn on the functional integrity of the hypothalamo-pituitary-interrenal axis in yellow perch are detectable after only 1 year of environmental exposure.
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