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Regulation of Neurotransmitter Release by Metabotropic Glutamate Receptors

Journal of neurochemistry, 2000-09, Vol.75 (3), p.889-907

2000

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A-317491, a novel potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat

Proceedings of the National Academy of Sciences - PNAS, 2002-12, Vol.99 (26), p.17179-17184

2002

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The metabotropic glutamate 2/3 receptor agonists LY354740 and LY379268 selectively attenuate phencyclidine versus d-amphetamine motor behaviors in rats

The Journal of pharmacology and experimental therapeutics, 1999-10, Vol.291 (1), p.161

1999

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[3H]A-317491, a novel high-affinity non-nucleotide antagonist that specifically labels human P2X2/3 and P2X3 receptors

The Journal of pharmacology and experimental therapeutics, 2004-07, Vol.310 (1), p.407

2004

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The Potent, Selective mGlu2/3 Receptor Agonist LY379268 Increases Extracellular Levels of Dopamine, 3,4‐Dihydroxyphenylacetic Acid, Homovanillic Acid, and 5‐Hydroxyindole‐3‐Acetic Acid in the Medial Prefrontal Cortex of the Freely Moving Rat

Journal of neurochemistry, 2000-09, Vol.75 (3), p.1147-1154

2000

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In Vitro Binding Characteristics of a New Selective Group II Metabotropic Glutamate Receptor Radioligand, [3H]LY354740, in Rat Brain

Molecular pharmacology, 1998-02, Vol.53 (2), p.228-233

1998

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The mGlu2/3 receptor agonist LY379268 selectively blocks amphetamine ambulations and rearing

European journal of pharmacology, 2000-07, Vol.400 (2-3), p.221-224

2000

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Attenuation of specific PCP-evoked behaviors by the potent mGlu2/3 receptor agonist, LY379268 and comparison with the atypical antipsychotic, clozapine

Psychopharmacologia, 2000-03, Vol.148 (4), p.423-429

2000

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The mGlu(2/3) receptor agonist LY379268 selectively blocks amphetamine ambulations and rearing

European journal of pharmacology, 2000-07, Vol.400 (2-3), p.221

2000

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TNP-ATP, a potent P2X3 receptor antagonist, blocks acetic acid-induced abdominal constriction in mice: comparison with reference analgesics

Pain (Amsterdam), 2002-03, Vol.96 (1-2), p.99-105

2002

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Characterization of [ 3 H]‐(2S,2′R,3′R)‐2‐(2′,3′‐dicarboxy‐ cyclopropyl)glycine ([ 3 H]‐DCG IV) binding to metabotropic mGlu 2 receptor‐transfected cell membranes

British journal of pharmacology, 2009-02, Vol.123 (3), p.497-504

2009

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Dopamine and 5-HT turnover are increased by the mGlu2/3 receptor agonist LY379268 in rat medial prefrontal cortex, nucleus accumbens and striatum

Brain research, 2000-12, Vol.887 (2), p.378-384

2000

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Acute increases in monoamine release in the rat prefrontal cortex by the mGlu2/3 agonist LY379268 are similar in profile to risperidone, not locally mediated, and can be elicited in the presence of uptake blockade

Neuropharmacology, 2001-06, Vol.40 (7), p.847-855

2001

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Tolerance to the motor impairment, but not to the reversal of PCP-induced motor activities by oral administration of the mGlu2/3 receptor agonist, LY379268

Naunyn-Schmiedeberg's archives of pharmacology, 2000-01, Vol.361 (1), p.39-46

2000

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Characterization of [3H]‐(2S,2′R,3′R)‐2‐(2′,3′‐dicarboxy‐ cyclopropyl)glycine ([3H]‐DCG IV) binding to metabotropic mGlu2 receptor‐transfected cell membranes

British journal of pharmacology, 1998-02, Vol.123 (3), p.497-504

1998

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[ 3 H]A-317491, a Novel High-Affinity Non-Nucleotide Antagonist That Specifically Labels Human P2X 2/3 and P2X 3 Receptors

The Journal of pharmacology and experimental therapeutics, 2004-07, Vol.310 (1), p.407-416

2004

Volltextzugriff (PDF)

TNP-ATP, a potent P2X 3 receptor antagonist, blocks acetic acid-induced abdominal constriction in mice: comparison with reference analgesics

Pain (Amsterdam), 2002, Vol.96 (1), p.99-105

2002

Volltextzugriff (PDF)

The mGlu 2/3 receptor agonist LY379268 selectively blocks amphetamine ambulations and rearing

European journal of pharmacology, 2000, Vol.400 (2), p.221-224

2000

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Potent desensitization of human P2X3 receptors by diadenosine polyphosphates

European journal of pharmacology, 2002-01, Vol.435 (2-3), p.135-142

2002

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Multiple pathways for regulation of the KCl-induced [ 3H]-GABA release by metabotropic glutamate receptors, in primary rat cortical cultures

Brain research, 1998-01, Vol.782 (1), p.91-104

1998

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mGluR‐evoked augmentation of receptor‐mediated cyclic AMP formation in neonatal and adult rat striatum

British journal of pharmacology, 1997-08, Vol.121 (7), p.1263-1268

1997

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Potent desensitization of human P2X 3 receptors by diadenosine polyphosphates

European journal of pharmacology, 2002, Vol.435 (2), p.135-142

2002

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A-317491, a Novel Potent and Selective Non-Nucleotide Antagonist of P2X3and P2X2/3Receptors, Reduces Chronic Inflammatory and Neuropathic Pain in the Rat

Proceedings of the National Academy of Sciences - PNAS, 2002-12, Vol.99 (26), p.17179-17184

2002

Volltextzugriff (PDF)

A-317491, a novel potent and selective non-nucleotide antagonist of P2X 3 and P2X 2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat

Proceedings of the National Academy of Sciences - PNAS, 2002-12, Vol.99 (26), p.17179-17184

2002

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Effect of metabotropic glutamate receptor activation on receptor-mediated cyclic AMP responses in primary cultures of rat striatal neurones

Brain research, 1998-04, Vol.791 (1), p.191-199

1998

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Regulation of Neurotransmitter Release by Metabotropic Glutamate Receptors

A-317491, a novel potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat

The metabotropic glutamate 2/3 receptor agonists LY354740 and LY379268 selectively attenuate phencyclidine versus d-amphetamine motor behaviors in rats

[3H]A-317491, a novel high-affinity non-nucleotide antagonist that specifically labels human P2X2/3 and P2X3 receptors

The Potent, Selective mGlu2/3 Receptor Agonist LY379268 Increases Extracellular Levels of Dopamine, 3,4‐Dihydroxyphenylacetic Acid, Homovanillic Acid, and 5‐Hydroxyindole‐3‐Acetic Acid in the Medial Prefrontal Cortex of the Freely Moving Rat

In Vitro Binding Characteristics of a New Selective Group II Metabotropic Glutamate Receptor Radioligand, [3H]LY354740, in Rat Brain

The mGlu2/3 receptor agonist LY379268 selectively blocks amphetamine ambulations and rearing

Attenuation of specific PCP-evoked behaviors by the potent mGlu2/3 receptor agonist, LY379268 and comparison with the atypical antipsychotic, clozapine

The mGlu(2/3) receptor agonist LY379268 selectively blocks amphetamine ambulations and rearing

TNP-ATP, a potent P2X3 receptor antagonist, blocks acetic acid-induced abdominal constriction in mice: comparison with reference analgesics

Characterization of [ 3 H]‐(2S,2′R,3′R)‐2‐(2′,3′‐dicarboxy‐ cyclopropyl)glycine ([ 3 H]‐DCG IV) binding to metabotropic mGlu 2 receptor‐transfected cell membranes

Dopamine and 5-HT turnover are increased by the mGlu2/3 receptor agonist LY379268 in rat medial prefrontal cortex, nucleus accumbens and striatum

Acute increases in monoamine release in the rat prefrontal cortex by the mGlu2/3 agonist LY379268 are similar in profile to risperidone, not locally mediated, and can be elicited in the presence of uptake blockade

Tolerance to the motor impairment, but not to the reversal of PCP-induced motor activities by oral administration of the mGlu2/3 receptor agonist, LY379268

Characterization of [3H]‐(2S,2′R,3′R)‐2‐(2′,3′‐dicarboxy‐ cyclopropyl)glycine ([3H]‐DCG IV) binding to metabotropic mGlu2 receptor‐transfected cell membranes

[ 3 H]A-317491, a Novel High-Affinity Non-Nucleotide Antagonist That Specifically Labels Human P2X 2/3 and P2X 3 Receptors

TNP-ATP, a potent P2X 3 receptor antagonist, blocks acetic acid-induced abdominal constriction in mice: comparison with reference analgesics

The mGlu 2/3 receptor agonist LY379268 selectively blocks amphetamine ambulations and rearing

Potent desensitization of human P2X3 receptors by diadenosine polyphosphates

Multiple pathways for regulation of the KCl-induced [ 3H]-GABA release by metabotropic glutamate receptors, in primary rat cortical cultures

mGluR‐evoked augmentation of receptor‐mediated cyclic AMP formation in neonatal and adult rat striatum

Potent desensitization of human P2X 3 receptors by diadenosine polyphosphates

A-317491, a Novel Potent and Selective Non-Nucleotide Antagonist of P2X3and P2X2/3Receptors, Reduces Chronic Inflammatory and Neuropathic Pain in the Rat

A-317491, a novel potent and selective non-nucleotide antagonist of P2X 3 and P2X 2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat

Effect of metabotropic glutamate receptor activation on receptor-mediated cyclic AMP responses in primary cultures of rat striatal neurones

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