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Am J Physiol Regul Integr Comp Physiol (November 21, 2002). doi:10.1152/ajpregu.00512.2002
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Articles in PresS, published online ahead of print November 21, 2002
Am J Physiol Regu Physiol, 10.1152/ajpregu.00512.2002
Submitted on August 26, 2002
Accepted on November 18, 2002

The Rainbow Trout Skeletal Muscle {beta}-Adrenergic System: Characterization and Signaling

Michel B Lortie1 and Thomas W Moon1*

1 Biology, University of Ottawa, Ottawa, Ontario, Canada

* To whom correspondence should be addressed. E-mail: tmoon{at}science.uottawa.ca.

The presence and functionality of {beta}-adrenoceptors ({beta}-ARs) were examined in red (RM) and white (WM) muscle membranes isolated from the rainbow trout, Oncorhynchus mykiss. Specific binding assays revealed the presence of a single class of binding sites with similar affinities in both muscle types (Kd in nM, 0.14 ± 0.03 and 0.18 ± 0.03 for RM and WM, respectively) but with a significant higher number of binding sites in RM compared with WM (Bmax in fmol/mg protein, 3.22 ± 0.11 and 2.60 ± 0.13, respectively). Selective and non-selective {beta}-adrenergic agonists ({beta}-AAs) and antagonists indicated an "atypical" {beta}-AR pharmacology. This result may represent a non-mammalian {beta}-AR classification or, more likely, the presence of more than one {beta}-AR subtype in trout muscles with similar affinities that could not be kinetically resolved. Adenylyl cyclase (ACase) assays showed a dose-dependent increase in cAMP production as concentrations of {beta}2-AAs increased in both muscle membranes with significantly higher basal cAMP production in RM compared with WM (cAMP production in pmol cAMP/mg protein/10 min, 24.67 ± 3.06 and 9.64 ± 3.45, respectively). The agonist-induced increase in cAMP production was blocked by the {beta}-adrenergic antagonist propranolol (PROP) while the ACase activator forskolin increased cAMP production by 7- to 14-fold above basal and approximately 3-fold above all {beta}-AAs tested. This study demonstrated the presence of "atypical" {beta}2-ARs on RM and WM membranes of trout, suggesting that {beta}2-AA may be a tool to enhance protein accretion through this signaling pathway.




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