Purinergic modulation of [3H]GABA release from rat hippocampal nerve terminals

Author:

Cunha Rodrigo A.,Ribeiro J.A.

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Pharmacology

Reference54 articles.

1. Agostinho, P., Caseiro, P., Rego, A.C., Duarte, E.P., Cunha, R.A., Oliveira, C.R., 1999. Adenosine modulation of D-[3H]aspartate release in cultured retina cells exposed to oxidative stress. Neurochem. Int., in press.

2. Phosphorylation of an α1-like subunit of an ω-conotoxin-sensitive brain calcium channel by cAMP-dependent protein kinase A and protein kinase C;Ahlijanian;J. Biol. Chem.,1991

3. Inhibition of N-, P/Q- and other types of Ca2+ channels in rat hippocampal nerve terminals by adenosine Al receptor;Ambrósio;Eur. J. Pharmacol.,1997

4. Evidence for presynaptic adenosine A2a receptors associated with norepinephrine release and their desensitization in the rat nucleus tractus solitarius;Barraco;J. Neurochem.,1995

5. A1, but not A2A, adenosine receptors modulate electrically stimulated [14C]acetylcholine release from rat cortex;Broad;J. Pharmacol. Exp. Ther.,1996

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