Search Results - "Kohara, Atsuyuki"
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Amelioration of neuropathic pain by novel transient receptor potential vanilloid 1 antagonist AS1928370 in rats without hyperthermic effect
Published in The Journal of pharmacology and experimental therapeutics (01-03-2011)“…Transient receptor potential vanilloid 1 (TRPV1) is activated by a variety of stimulations, such as endogenous ligands and low pH, and is believed to play a…”
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2
Allodynia and hyperalgesia in adjuvant-induced arthritic rats: time course of progression and efficacy of analgesics
Published in The Journal of pharmacology and experimental therapeutics (01-08-2003)“…The complete Freund's adjuvant (CFA)-induced arthritic rat model has extensively served as a laboratory model in the study of arthritic pain. However, the time…”
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Neuroprotective effects of the selective type 1 metabotropic glutamate receptor antagonist YM-202074 in rat stroke models
Published in Brain research (29-01-2008)“…Abstract We describe in vitro properties and in vivo neuroprotective effects of a newly synthesized, high-affinity, selective allosteric metabotropic glutamate…”
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4
Radioligand binding properties and pharmacological characterization of 6-amino-N-cyclohexyl-N,3-dimethylthiazolo[3,2-a]benzimidazole-2-carboxamide (YM-298198), a high-affinity, selective, and noncompetitive antagonist of metabotropic glutamate receptor type 1
Published in The Journal of pharmacology and experimental therapeutics (01-10-2005)“…Metabotropic glutamate receptor type 1 (mGluR1) is thought to play important roles in the neurotransmission and pathogenesis of several neurological disorders…”
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5
Antinociceptive profile of a selective metabotropic glutamate receptor 1 antagonist YM-230888 in chronic pain rodent models
Published in European journal of pharmacology (24-09-2007)“…Metabotropic glutamate receptor 1 (mGlu 1 receptor) has been suggested to play an important role in pain transmission. In this study, the effects of a…”
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6
Control of calcium oscillations by phosphorylation of metabotropic glutamate receptors
Published in Nature (London) (05-09-1996)“…Stimulation of two metabotropic glutamate-receptor subtypes, mGluR1 and mGluR5, triggers the release of Ca2+ from intracellular stores through the…”
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Diversity of Calcium Signaling by Metabotropic Glutamate Receptors
Published in The Journal of biological chemistry (10-07-1998)“…During prolonged application of glutamate (20 min), patterns of increase in intracellular Ca 2+ concentration ([Ca 2+ ] i ) were studied in HEK-293 cells…”
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Characterization of YM90K, a selective and potent antagonist of AMPA receptors, in rat cortical mRNA-injected Xenopus oocytes
Published in European journal of pharmacology (15-08-1996)“…The inhibitory potencies of 6-(1 H-imidazol-1-yl)-7-nitro-2,3(1 H,4 H)-quinoxalinedione hydrochloride (YM90K), 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(…”
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9
Synthesis and Biological Evaluation of 3-Biphenyl-4-yl-4-phenyl-4 H -1,2,4-triazoles as Novel Glycine Transporter 1 Inhibitors
Published in Journal of medicinal chemistry (13-01-2011)Get full text
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Synthesis and Biological Evaluation of 3-Biphenyl-4-yl-4-phenyl-4H-1,2,4-triazoles as Novel Glycine Transporter 1 Inhibitors
Published in Journal of medicinal chemistry (13-01-2011)“…We describe the preparation and evaluation of a novel series of glycine transporter 1 (GlyT1) inhibitors derived from a high-throughput screening hit. The SAR…”
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11
Kainate excitotoxicity is mediated by AMPA- but not kainate-preferring receptors in embryonic rat hippocampal cultures
Published in Neurochemistry international (01-11-1997)“…We investigated kainate-induced excitotoxicity in embryonic rat hippocampal cells cultured in a chemically defined medium. Treatment with kainate for 24 h…”
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12
In-vitro Characterization of YM872, a Selective, Potent and Highly Water-soluble α-Amino-3-hydroxy-5-methylisoxazole-4-propionate Receptor Antagonist
Published in Journal of pharmacy and pharmacology (01-07-1998)“…The in‐vitro pharmacological properties of (2,3‐dioxo‐7‐(1H‐imidazol‐***1‐yl)‐6‐nitro‐1,2,3,4‐tetrahydro‐1‐quinoxalinyl)‐acetic acid monohydrate, YM872, a…”
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Characterization of metabotropic glutamate receptors linked to IP3CA2- cascade in trnsfected cells
Published in Neuropharmacology (01-06-1996)Get full text
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Characterization of metabotropic glutamate receptors linked to [formula omitted] cascade in trnsfected cells
Published in Neuropharmacology (1996)Get full text
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15
The unique feature of dog liver cytosolic glutathione S-transferases. An isozyme not retained on the affinity column has the highest activity toward 1,2-dichloro-4-nitrobenzene
Published in The Journal of biological chemistry (15-11-1991)“…In the adult dog liver cytosol we identified four glutathione S-transferase (GST) subunits, Yd1 (Mr 26,000), Yd2 (Mr 27,000), Yd3 (Mr 28,000), and Ydf (Mr…”
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YM872: A Selective, Potent and Highly Water‐Soluble α‐Amino‐3‐Hydroxy‐5‐Methylisoxazole‐4‐Propionic Acid Receptor Antagonist
Published in CNS drug reviews (01-12-2002)“…ABSTRACT This review focuses on the in vitro and in vivo neuropharmacology of YM872, a potential neuroprotective agent currently undergoing clinical trials in…”
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