Pharmacological Effects of the Metabotropic Glutamate Receptor 1 Antagonist Compared with Those of the Metabotropic Glutamate Receptor 5 Antagonist and Metabotropic Glutamate Receptor 2/3 Agonist in Rodents: Detailed Investigations with a Selective Allosteric Metabotropic Glutamate Receptor 1 Antago

@article{Satow2008PharmacologicalEO,
  title={Pharmacological Effects of the Metabotropic Glutamate Receptor 1 Antagonist Compared with Those of the Metabotropic Glutamate Receptor 5 Antagonist and Metabotropic Glutamate Receptor 2/3 Agonist in Rodents: Detailed Investigations with a Selective Allosteric Metabotropic Glutamate Receptor 1 Antago},
  author={Akio Satow and Shunsuke Maehara and Satoko Ise and Hirohiko Hikichi and Miyuki Fukushima and Gentaroh Suzuki and Toshifumi Kimura and Takeshi Tanaka and Satoru Ito and Hiroshi Kawamoto and Hisashi Ohta},
  journal={Journal of Pharmacology and Experimental Therapeutics},
  year={2008},
  volume={326},
  pages={577 - 586}
}
  • A. Satow, S. Maehara, H. Ohta
  • Published 1 August 2008
  • Biology, Psychology, Chemistry
  • Journal of Pharmacology and Experimental Therapeutics
The functional roles of metabotropic glutamate receptor (mGluR) 1 in integrative brain functions were investigated using a potent and selective mGluR1 allosteric antagonist, FTIDC [4-[1-(2-fluoropyridine-3-yl)-5-methyl-1H-1,2,3-triazol-4-yl]-N-isopropyl-N-methyl-3,6-dihydropyridine-1(2H)-carboxamide], in comparison with the mGluR5 allosteric antagonist and the mGluR2/3 orthosteric agonist in rodents. FTIDC reduced maternal separation-induced ultrasonic vocalization and stress-induced… 

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