메뉴 건너뛰기




Volumn 326, Issue 2, 2008, Pages 646-656

Neuroprotective effects of the novel glutamate transporter inhibitor (-)-3-hydroxy-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d]-isoxazole-4-carboxylic acid, which preferentially inhibits reverse transport (glutamate release) compared with glutamate reuptake

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXY 4,5,6,6A TETRAHYDRO 3AH PYRROLO[3,4 D]ISOXAZOLE 4 CARBOXYLIC ACID; 3 HYDROXY 4,5,6,6A TETRAHYDRO 3AH PYRROLO[3,4 D]ISOXAZOLE 6 CARBOXYLIC ACID; ASPARTIC ACID; ASPARTIC ACID DERIVATIVE; EXCITATORY AMINO ACID TRANSPORTER; GLUTAMATE TRANSPORTER; GLUTAMATE TRANSPORTER INHIBITOR; GLUTAMIC ACID; PROTEIN INHIBITOR; THREO BETA BENZYLOXYASPARTIC ACID; TRITIUM;

EID: 47849133459     PISSN: 00223565     EISSN: 15210103     Source Type: Journal    
DOI: 10.1124/jpet.107.135251     Document Type: Article
Times cited : (28)

References (41)
  • 1
    • 0030932152 scopus 로고    scopus 로고
    • Excitatory amino acid transporter 5, a retinal glutamate transporter coupled to a chloride conductance
    • Arriza JL, Eliasof S, Kavanaugh MP, and Amara SG (1997) Excitatory amino acid transporter 5, a retinal glutamate transporter coupled to a chloride conductance. Proc Natl Acad Sci U S A 94:4155-4160.
    • (1997) Proc Natl Acad Sci U S A , vol.94 , pp. 4155-4160
    • Arriza, J.L.1    Eliasof, S.2    Kavanaugh, M.P.3    Amara, S.G.4
  • 3
    • 0037539911 scopus 로고    scopus 로고
    • Neurotoxic and neuroprotective effects of the glutamate transporter inhibitor DL-threo-beta-benzyloxyaspartate (DL-TBOA) during physiological and ischemia-like conditions
    • Bonde C, Sarup A, Schousboe A, Gegelashvili G, Zimmer J, and Noraberg J (2003) Neurotoxic and neuroprotective effects of the glutamate transporter inhibitor DL-threo-beta-benzyloxyaspartate (DL-TBOA) during physiological and ischemia-like conditions. Neurochem Int 43:371-380.
    • (2003) Neurochem Int , vol.43 , pp. 371-380
    • Bonde, C.1    Sarup, A.2    Schousboe, A.3    Gegelashvili, G.4    Zimmer, J.5    Noraberg, J.6
  • 4
    • 33846505059 scopus 로고    scopus 로고
    • Coupling substrate and ion binding to extracellular gate of a sodium-dependent aspartate transporter
    • Boudker O, Ryan RM, Yernool D, Shimamoto K, and Gouaux E (2007) Coupling substrate and ion binding to extracellular gate of a sodium-dependent aspartate transporter. Nature 445:387-393.
    • (2007) Nature , vol.445 , pp. 387-393
    • Boudker, O.1    Ryan, R.M.2    Yernool, D.3    Shimamoto, K.4    Gouaux, E.5
  • 7
    • 0035001341 scopus 로고    scopus 로고
    • Glutamate uptake
    • Danbolt NC (2001) Glutamate uptake. Prog Neurobiol 65:1-105.
    • (2001) Prog Neurobiol , vol.65 , pp. 1-105
    • Danbolt, N.C.1
  • 8
    • 0035498802 scopus 로고    scopus 로고
    • Substrate exchange properties of the high-affinity glutamate transporter EAAT2
    • Dunlop J (2001) Substrate exchange properties of the high-affinity glutamate transporter EAAT2. J Neurosci Res 66:482-486.
    • (2001) J Neurosci Res , vol.66 , pp. 482-486
    • Dunlop, J.1
  • 9
    • 0032748509 scopus 로고    scopus 로고
    • Inducible expression and pharmacology of the human excitatory amino acid transporter 2 subtype of L-glutamate transporter
    • Dunlop J, Lou Z, Zhang Y, and McIlvain HB (1999) Inducible expression and pharmacology of the human excitatory amino acid transporter 2 subtype of L-glutamate transporter. Br J Pharmacol 128:1485-1490.
    • (1999) Br J Pharmacol , vol.128 , pp. 1485-1490
    • Dunlop, J.1    Lou, Z.2    Zhang, Y.3    McIlvain, H.B.4
  • 10
    • 25144521444 scopus 로고    scopus 로고
    • Characterization of novel aryl-ether, biaryl, and fluorene aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT2
    • Dunlop J, McIlvain HB, Carrick TA, Jow B, Lu Q, Kowal D, Lin S, Greenfield A, Grosanu C, Fan K, et al. (2005) Characterization of novel aryl-ether, biaryl, and fluorene aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT2. Mol Pharmacol 68:974-982.
    • (2005) Mol Pharmacol , vol.68 , pp. 974-982
    • Dunlop, J.1    McIlvain, H.B.2    Carrick, T.A.3    Jow, B.4    Lu, Q.5    Kowal, D.6    Lin, S.7    Greenfield, A.8    Grosanu, C.9    Fan, K.10
  • 11
    • 0029076899 scopus 로고
    • An excitatory amino-acid transporter with properties of a ligand-gated chloride channel
    • Fairman WA, Vandenberg RJ, Arriza JL, Kavanaugh MP, and Amara SG (1995) An excitatory amino-acid transporter with properties of a ligand-gated chloride channel. Nature 375:599-603.
    • (1995) Nature , vol.375 , pp. 599-603
    • Fairman, W.A.1    Vandenberg, R.J.2    Arriza, J.L.3    Kavanaugh, M.P.4    Amara, S.G.5
  • 12
    • 4944221304 scopus 로고    scopus 로고
    • 3H]D-aspartate release by 3-hydroxy-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d] isoxazole-4-carboxylic acid and 3-hydroxy-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d]isoxazole-6-carboxylic acid, two conformationally constrained aspartate and glutamate analogs. Mol Pharmacol 66:522-529.
    • 3H]D-aspartate release by 3-hydroxy-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d] isoxazole-4-carboxylic acid and 3-hydroxy-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d]isoxazole-6-carboxylic acid, two conformationally constrained aspartate and glutamate analogs. Mol Pharmacol 66:522-529.
  • 13
    • 0242660419 scopus 로고    scopus 로고
    • The effect of phosphorylation on amphetamine-mediated outward transport
    • Gnegy ME (2003) The effect of phosphorylation on amphetamine-mediated outward transport. Eur J Pharmacol 479:83-91.
    • (2003) Eur J Pharmacol , vol.479 , pp. 83-91
    • Gnegy, M.E.1
  • 15
    • 2342467905 scopus 로고    scopus 로고
    • Pharmacological characterization of human excitatory amino acid transporters EAAT1, EAAT2 and EAAT3 in a fluorescence-based membrane potential assay
    • Jensen AA and Bräuner-Osborne H (2004) Pharmacological characterization of human excitatory amino acid transporters EAAT1, EAAT2 and EAAT3 in a fluorescence-based membrane potential assay. Biochem Pharmacol 67:2115-2127.
    • (2004) Biochem Pharmacol , vol.67 , pp. 2115-2127
    • Jensen, A.A.1    Bräuner-Osborne, H.2
  • 16
    • 0029586025 scopus 로고
    • Neuronal high-affinity glutamate transport in the rat central nervous system
    • Kanai Y, Bhide PG, DiFiglia M, and Hediger MA (1995) Neuronal high-affinity glutamate transport in the rat central nervous system. Neuroreport 6:2357-2362.
    • (1995) Neuroreport , vol.6 , pp. 2357-2362
    • Kanai, Y.1    Bhide, P.G.2    DiFiglia, M.3    Hediger, M.A.4
  • 17
    • 0035012078 scopus 로고    scopus 로고
    • Protein kinase C and intracellular calcium are required for amphetamine-mediated dopamine release via the norepinephrine transporter in undifferentiated PC12 cells
    • Kantor L, Hewlett GH, Park YH, Richardson-Burns SM, Mellon MJ, and Gnegy ME (2001) Protein kinase C and intracellular calcium are required for amphetamine-mediated dopamine release via the norepinephrine transporter in undifferentiated PC12 cells. J Pharmacol Exp Ther 297:1016-1024.
    • (2001) J Pharmacol Exp Ther , vol.297 , pp. 1016-1024
    • Kantor, L.1    Hewlett, G.H.2    Park, Y.H.3    Richardson-Burns, S.M.4    Mellon, M.J.5    Gnegy, M.E.6
  • 19
    • 0032976901 scopus 로고    scopus 로고
    • Nontransportable inhibitors attenuate reversal of glutamate uptake in synaptosomes following a metabolic insult
    • Koch HP, Chamberlin AR, and Bridges RJ (1999a) Nontransportable inhibitors attenuate reversal of glutamate uptake in synaptosomes following a metabolic insult. Mol Pharmacol 55:1044-1048.
    • (1999) Mol Pharmacol , vol.55 , pp. 1044-1048
    • Koch, H.P.1    Chamberlin, A.R.2    Bridges, R.J.3
  • 21
    • 0032194950 scopus 로고    scopus 로고
    • The number of glutamate transporter subtype molecules at glutamatergic synapses: Chemical and stereological quantification in young adult rat brain
    • Lehre KP and Danbolt NC (1998) The number of glutamate transporter subtype molecules at glutamatergic synapses: chemical and stereological quantification in young adult rat brain. J Neurosci 18:8751-8757.
    • (1998) J Neurosci , vol.18 , pp. 8751-8757
    • Lehre, K.P.1    Danbolt, N.C.2
  • 22
    • 0027428320 scopus 로고
    • Carrier-mediated release of neurotransmitters
    • Levi G and Raiteri M (1993) Carrier-mediated release of neurotransmitters. Trends Neurosci 16:415-419.
    • (1993) Trends Neurosci , vol.16 , pp. 415-419
    • Levi, G.1    Raiteri, M.2
  • 23
    • 0025836416 scopus 로고
    • The bioenergetics of neurotransmitter release
    • McMahon HT and Nicholls DG (1991) The bioenergetics of neurotransmitter release. Biochim Biophys Acta 1059:243-264.
    • (1991) Biochim Biophys Acta , vol.1059 , pp. 243-264
    • McMahon, H.T.1    Nicholls, D.G.2
  • 24
    • 0042626560 scopus 로고    scopus 로고
    • Functional changes of glial glutamate transporter GLT-1 during ischemia: An in vivo study in the hippocampal CA1 of normal mice and mutant mice lacking GLT-1
    • Mitani A and Tanaka K (2003) Functional changes of glial glutamate transporter GLT-1 during ischemia: an in vivo study in the hippocampal CA1 of normal mice and mutant mice lacking GLT-1. J Neurosci 23:7176-7182.
    • (2003) J Neurosci , vol.23 , pp. 7176-7182
    • Mitani, A.1    Tanaka, K.2
  • 25
    • 20444371553 scopus 로고    scopus 로고
    • Differential effects of the substrate inhibitor L-trans-pyrrolidine-2, 4-dicarboxylate (PDC) and the non-substrate inhibitor DL-threo-beta- benzyloxyaspartate (DL-TBOA) of glutamate transporters on neuronal damage and extracellular amino acid levels in rat brain in vivo
    • Montiel T, Camacho A, Estrada-Sanchez AM, and Massieu L (2005) Differential effects of the substrate inhibitor L-trans-pyrrolidine-2, 4-dicarboxylate (PDC) and the non-substrate inhibitor DL-threo-beta- benzyloxyaspartate (DL-TBOA) of glutamate transporters on neuronal damage and extracellular amino acid levels in rat brain in vivo. Neuroscience 133:667-678.
    • (2005) Neuroscience , vol.133 , pp. 667-678
    • Montiel, T.1    Camacho, A.2    Estrada-Sanchez, A.M.3    Massieu, L.4
  • 26
    • 0030993144 scopus 로고    scopus 로고
    • EAAT4, a glutamate transporter with properties of a chloride channel, is predominantly localized in Purkinje cell dendrites, and forms parasagittal compartments in rat cerebellum
    • Nagao S, Kwak S, and Kanazawa I (1997) EAAT4, a glutamate transporter with properties of a chloride channel, is predominantly localized in Purkinje cell dendrites, and forms parasagittal compartments in rat cerebellum. Neuroscience 78:929-933.
    • (1997) Neuroscience , vol.78 , pp. 929-933
    • Nagao, S.1    Kwak, S.2    Kanazawa, I.3
  • 27
    • 0030976929 scopus 로고    scopus 로고
    • Glutamate transporter EAAC-1-deficient mice develop dicarboxylic aminoaciduria and behavioral abnormalities but no neurodegeneration
    • Peghini P, Janzen J, and Stoffel W (1997) Glutamate transporter EAAC-1-deficient mice develop dicarboxylic aminoaciduria and behavioral abnormalities but no neurodegeneration. EMBO J 16:3822-3832.
    • (1997) EMBO J , vol.16 , pp. 3822-3832
    • Peghini, P.1    Janzen, J.2    Stoffel, W.3
  • 28
    • 0032824540 scopus 로고    scopus 로고
    • 1-Aminoindan-1,5-dicarboxylic acid and (S)-(+)-2-(3′-carboxybicyclo[1.1.1] pentyl)-glycine, two mGlu1 receptor-preferring antagonists, reduce neuronal death in in vitro and in vivo models of cerebral ischaemia
    • Pellegrini-Giampietro DE, Cozzi A, Peruginelli F, Leonardi P, Meli E, Pellicciari R, and Moroni F (1999) 1-Aminoindan-1,5-dicarboxylic acid and (S)-(+)-2-(3′-carboxybicyclo[1.1.1] pentyl)-glycine, two mGlu1 receptor-preferring antagonists, reduce neuronal death in in vitro and in vivo models of cerebral ischaemia. Eur J Neurosci 11:3637-3647.
    • (1999) Eur J Neurosci , vol.11 , pp. 3637-3647
    • Pellegrini-Giampietro, D.E.1    Cozzi, A.2    Peruginelli, F.3    Leonardi, P.4    Meli, E.5    Pellicciari, R.6    Moroni, F.7
  • 29
    • 0034674519 scopus 로고    scopus 로고
    • Transporter reversal as a mechanism of glutamate release from the ischemic rat cerebral cortex: Studies with DL-threo-beta-benzyloxyaspartate
    • Phillis JW, Ren J, and O'Regan MH (2000) Transporter reversal as a mechanism of glutamate release from the ischemic rat cerebral cortex: studies with DL-threo-beta-benzyloxyaspartate. Brain Res 868:105-112.
    • (2000) Brain Res , vol.868 , pp. 105-112
    • Phillis, J.W.1    Ren, J.2    O'Regan, M.H.3
  • 33
    • 0035176824 scopus 로고    scopus 로고
    • Antisense knockdown of the glial glutamate transporter GLT-1 exacerbates hippocampal neuronal damage following traumatic injury to rat brain
    • Rao VL, Dogan A, Bowen KK, Todd KG, and Dempsey RJ (2001) Antisense knockdown of the glial glutamate transporter GLT-1 exacerbates hippocampal neuronal damage following traumatic injury to rat brain. Eur J Neurosci 13:119-128.
    • (2001) Eur J Neurosci , vol.13 , pp. 119-128
    • Rao, V.L.1    Dogan, A.2    Bowen, K.K.3    Todd, K.G.4    Dempsey, R.J.5
  • 34
    • 0034688312 scopus 로고    scopus 로고
    • Glutamate release in severe brain ischaemia is mainly by reversed uptake
    • Rossi DJ, Oshima T, and Attwell D (2000) Glutamate release in severe brain ischaemia is mainly by reversed uptake. Nature 403:316-321.
    • (2000) Nature , vol.403 , pp. 316-321
    • Rossi, D.J.1    Oshima, T.2    Attwell, D.3
  • 35
    • 0029927773 scopus 로고    scopus 로고
    • Relationships between ATP depletion, membrane potential, and the release of neurotransmitters in rat nerve terminals: An in vitro study under conditions that mimic anoxia, hypoglycemia, and ischemia
    • Santos MS, Moreno AJ, and Carvalho AP (1996) Relationships between ATP depletion, membrane potential, and the release of neurotransmitters in rat nerve terminals: an in vitro study under conditions that mimic anoxia, hypoglycemia, and ischemia. Stroke 27:941-950.
    • (1996) Stroke , vol.27 , pp. 941-950
    • Santos, M.S.1    Moreno, A.J.2    Carvalho, A.P.3
  • 37
    • 21844463566 scopus 로고    scopus 로고
    • Role of the GLT-1 subtype of glutamate transporter in glutamate homeostasis: The GLT-1-preferring inhibitor WAY-855 produces marginal neurotoxicity in the rat hippocampus
    • Selkirk JV, Nottebaum LM, Vana AM, Verge GM, Mackay KB, Stiefel TH, Naeve GS, Pomeroy JE, Petroski RE, Moyer J, et al. (2005) Role of the GLT-1 subtype of glutamate transporter in glutamate homeostasis: the GLT-1-preferring inhibitor WAY-855 produces marginal neurotoxicity in the rat hippocampus. Eur J Neurosci 21:3217-3228.
    • (2005) Eur J Neurosci , vol.21 , pp. 3217-3228
    • Selkirk, J.V.1    Nottebaum, L.M.2    Vana, A.M.3    Verge, G.M.4    Mackay, K.B.5    Stiefel, T.H.6    Naeve, G.S.7    Pomeroy, J.E.8    Petroski, R.E.9    Moyer, J.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.