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1.
Artigo em Inglês | MEDLINE | ID: mdl-17215158

RESUMO

While studies clearly point to a role for cortisol signaling in seawater adaptation, very little is known about salinity impact on glucocorticoid receptor (GR) expression in fish. To this end, we investigated the temporal GR expression in the gill and liver of rainbow trout (Oncorhynchus mykiss) to salinity exposure. Trout were subjected to gradual salinity increases (11 ppt for 1 d, 17 ppt for 2 d and 23 ppt for 2 d) over a five day period. Gill Na(+), K(+)-ATPase alpha-subunit mRNA showed a transient elevation with salinity exposure, while gill cystic fibrosis transmembrane conductance regulator mRNA was not significantly affected by salinity. Liver PEPCK transcript levels showed a transient increase at day 1, but not at day 3 or day 5 of salinity exposure, while the activity of this enzyme was significantly depressed at all time points. Liver glycogen content was also significantly reduced by salinity exposure compared to the freshwater group. Gill GR transcript levels were 3-fold greater upon salinity exposure and this level was maintained over the 5 day period, while gill GR protein content remained unchanged except for a significant drop at day 1 of salinity exposure. Liver GR transcript levels showed no significant change with salinity exposure, while GR protein content was transiently elevated at day 3, but not at day 1 or day 5 of salinity exposure. The tissue-specific GR transcript response in the gill leads us to hypothesize a role for osmosensory signal transduction pathway in the regulation of GR expression in fish. Collectively, salinity exposure modulates GR expression and glucocorticoid signaling in rainbow trout.


Assuntos
Perfilação da Expressão Gênica , Oncorhynchus mykiss/genética , Receptores de Glucocorticoides/genética , Cloreto de Sódio/farmacologia , Aclimatação/efeitos dos fármacos , Aclimatação/genética , Aclimatação/fisiologia , Animais , Regulador de Condutância Transmembrana em Fibrose Cística/genética , Regulação da Expressão Gênica/genética , Brânquias/efeitos dos fármacos , Brânquias/metabolismo , Fígado/efeitos dos fármacos , Fígado/metabolismo , Glicogênio Hepático/metabolismo , Oncorhynchus mykiss/fisiologia , Fosfoenolpiruvato Carboxilase/genética , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Receptores de Glucocorticoides/metabolismo , ATPase Trocadora de Sódio-Potássio/metabolismo , Fatores de Tempo
2.
Aquat Toxicol ; 78(3): 253-61, 2006 Jun 30.
Artigo em Inglês | MEDLINE | ID: mdl-16675040

RESUMO

To help extend the freshwater based biotic ligand model for silver (Ag) into brackish and saltwater conditions, 50g Gulf toadfish (Opsanus beta) were acclimated to 2.5%, 5%, 10%, 20%, 40%, 80%, or 100% salt water and exposed for 6d to 1.0microM AgNO(3), with or without 10mg C/L organic matter. Suwannee River natural organic matter collected by reverse osmosis was used. Silver accumulation in toadfish gills and plasma decreased as salinity increased, indicating low bioavailability of AgCl complexes. Complexation of Ag by organic matter, normally important in freshwater conditions, was less important as salinity increased. Although relatively little intestinal Ag uptake was observed, both liver and bile accumulated Ag from water imbibed past the isosmotic salinity point ( approximately 1/3 salt water). Toadfish also produced intestinal carbonate pellets, minerals which did not influence Ag accumulation. Our results further stress the importance of Ag speciation, physiological mechanisms, and intestinal Ag uptake when modelling Ag uptake and toxicity beyond freshwater conditions.


Assuntos
Batracoidiformes/metabolismo , Prata/farmacocinética , Cloreto de Sódio/farmacologia , Poluentes Químicos da Água/farmacocinética , Animais , Bile/química , Disponibilidade Biológica , Carbonatos/análise , Brânquias/química , Brânquias/metabolismo , Mucosa Intestinal/metabolismo , Intestinos/química , Água do Mar/análise , Prata/análise , Nitrato de Prata/farmacocinética
3.
Am J Physiol Regul Integr Comp Physiol ; 288(5): R1385-95, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-15604305

RESUMO

In this study, we set out to examine the role of the somatotropic axis in the ion-regulation process in rainbow trout. Specifically, our objective was to examine whether plasma insulin-like growth factor-binding proteins (IGFBPs) are modulated by gradual salinity exposure. To this end, freshwater (FW)-adapted rainbow trout were subjected to gradual salinity increases, up to 66% seawater, over a period of 5 days. During this acclimation process, minimal elevations in plasma Ca2+ and Cl- were seen in the salinity-acclimated groups compared with FW controls. There were no changes in plasma Na+ levels, and only a minor transient change in plasma cortisol levels was seen with salinity exposure. The salinity challenged animals responded with elevations in plasma growth hormone (GH) and IGF-I levels and gill Na+-K+-ATPase activity. We identified IGFBPs of 21, 32, 42, and 50 kDa in size in the plasma of these animals, and they were consistently higher with salinity. Despite the overall increase in IGFBPs with salinity, transient changes in individual BPs over the 5-day period were noted in the FW and salinity-exposed fish. Specifically, the transient changes in plasma levels of the 21-, 42-, and 50-kDa IGFBPs were different between the FW and salinity groups, while the 32-kDa IGFBP showed a similar trend (increases with sampling time) in both groups. Considered together, the elevated plasma IGFBPs suggest a key role for these binding proteins in the regulation of IGF-I during salinity acclimation in salmonids.


Assuntos
Aclimatação/fisiologia , Proteínas de Ligação a Fator de Crescimento Semelhante a Insulina/sangue , Oncorhynchus mykiss/sangue , Oncorhynchus mykiss/fisiologia , Cloreto de Sódio , Equilíbrio Hidroeletrolítico/fisiologia , Animais , Cálcio/sangue , Cloretos/sangue , Regulação da Expressão Gênica/fisiologia , Hormônio do Crescimento/sangue , Hidrocortisona/sangue , Proteínas de Ligação a Fator de Crescimento Semelhante a Insulina/metabolismo , Fator de Crescimento Insulin-Like I/fisiologia , Sódio/sangue , Cloreto de Sódio/química , Água/química
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