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Protein kinase A and Ca(v)1 (L-type) channels are common targets to facilitatory adenosine A(2A) and muscarinic M-1 receptors on rat motoneurons

Title
Protein kinase A and Ca(v)1 (L-type) channels are common targets to facilitatory adenosine A(2A) and muscarinic M-1 receptors on rat motoneurons
Type
Article in International Scientific Journal
Year
2005
Authors
Paulo Correia de Sá
(Author)
ICBAS
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Journal
Title: NeuroSignalsImported from Authenticus Search for Journal Publications
Vol. 14
Pages: 262-272
ISSN: 1424-862X
Other information
Authenticus ID: P-000-6BD
Abstract (EN): At the rat motor endplate, pre-synaptic facilitatory adenosine A(2A) and muscarinic M-1 receptors are mutually exclusive. We investigated whether these receptors share a common intracellular signalling pathway. Suppression of McN-A-343-induced M-1 facilitation of [H-3] ACh release was partially recovered when CGS21680C ( an A(2A) agonist) was combined with the cyclic AMP antagonist Rp- cAMPS. Forskolin, rolipram and 8-bromo-cyclic AMP mimicked CGS21680C blockade of M 1 facilitation. Both Rp-cAMPs and nifedipine reduced augmentation of [H-3] ACh release by McN-A-343 and CGS21680C. Activation of M-1 and A(2A) receptors enhanced Ca2+ recruitment through nifedipine-sensitive channels. Nifedipine inhibition revealed by McN-A-343 was prevented by chelerythrine (a PKC inhibitor) and Rp-cAMPS, suggesting that Ca(v)1 (L-type) channels phosphorylation by PKA and PKC is required. Rp- cAMPS inhibited [H-3] ACh release in the presence of phorbol 12-myristate 13-acetate, but PKC inhibition by chelerythrine had no effect on release in the presence of 8-bromo-cyclic AMP. This suggests that the involvement of PKA may be secondary to M-1-induced PKC activation. In conclusion, competition of M-1 and A(2A) receptors to facilitate ACh release from motoneurons may occur by signal convergence to a common pathway involving PKA activation and Ca2+ influx through Ca(v)1 (L-type) channels. Copyright (C) 2005 S. Karger AG, Basel.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 11
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