4.5 Article

Functional Coupling between Metabotropic Glutamate Receptors and G-Proteins in Rat Cerebral Cortex Assessed by Guanosine-5'-O-(3-[35S]thio)triphosphate Binding Assay

Journal

BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
Volume 109, Issue 3, Pages 175-185

Publisher

WILEY-BLACKWELL
DOI: 10.1111/j.1742-7843.2011.00705.x

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Stimulation of specific guanosine-5'-O-(3-[S-35]thio) triphosphate ([S-35]GTP gamma S) binding by L-glutamate was pharmacologically characterized in rat cerebral cortical membranes. Optimization of the experimental conditions with respect to the concentrations of GDP, MgCl2 and NaCl in assay buffer prompted us to adopt the incubation of rat cerebral cortical membranes with 0.2 nM [S-35]GTP gamma S at 30 degrees C for 60 min. in the presence of 20 mu M GDP, 5 mM MgCl2 and 100 mM NaCl as a standard condition. Specific [S-35]GTP gamma S binding was stimulated by L-glutamate in a concentration-dependent manner but not by ionotropic glutamate receptor agonists. The stimulatory responses were also elicited by many agonists for metabotropic glutamate (mGlu) receptor, with (-)-2-oxa-4-aminobicyclo[3.1.0] hexane-4,6-dicarboxylic acid (LY379268) being the most potent. L-glutamate-stimulated [S-35]GTP gamma S binding was inhibited by several mGlu antagonists, with (2S)-2-amino-2-[(1S,2S)-2-carboxycycloprop- 1-yl]-3-(xanth-9-yl) propanoic acid (LY341495) being the most potent. The pharmacological properties of a series of agonists and antagonists indicated the involvement of group II mGlu receptors, especially mGlu2. Supportive of this notion was the finding that L-glutamate-stimulated specific [S-35]GTP gamma S binding was augmented by 2,2,2-trifluoro-N-[4-(2-methoxyphenoxy) phenyl]-N-(3-pyridinylmethyl) ethanesulphonamide hydrochloride (LY487379), a reportedly selective allosteric positive modulator for mGlu2, by means of upward and leftward shift of the concentration-response curve. In addition, LY487379 per se stimulated [S-35]GTP gamma S binding, though, through a mechanism different from the stimulation by L-glutamate. Pre-treatment of the membranes with N-ethylmaleimide (NEM) cancelled L-glutamate-stimulated [S-35]GTP gamma S binding in a concentration and incubation time-dependent manner. Taken altogether, L-glutamate-stimulated [S-35]GTP gamma S binding serves as a useful functional assay for the activation of NEM-sensitive G(i/o)-mediated group II mGlu receptors in rat cerebral cortical membranes.

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