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Granule cells glutamate

In cerebellar granule cells, glutamate-triggered, Ca -mediated cell death is independent of endogenous NO production (Lafon-Cazal et al. 1993). A rather inverted mechanism has been demonstrated in these neurones exposure to NO donors leads to stimulation of N-methyl-D-aspartate receptors, probably because NO-related species stimulate the release of endogenous agonists (Leist et al. 1997). This sort of stimulation eventually causes apoptosis (Bonfoco et al. 1996). [Pg.540]

Isokawa, M, Levesque, M, Fried, I and Engel, J Jr (1997) Glutamate currents in morphologically identified human dentate granule cells in temporal lobe epilepsy. J. Neurophysiol. 77 3355-3369. [Pg.350]

Fig. 5.12 (a) Synaptic types along dendritic spines of M/T and GC units uni-, and bi-directional junctions, (b) Transmitter systems at a reciprocal synapse, Mitral-Granule cell junction. [Glu, glutamate (R, receptor) GABA, y-aminobutyric acid (R, receptor) E, intracellular effector and aAR, alpha-adrenergic receptor.]. (From Hayashi et al., 1993.)... [Pg.121]

Kawasaki, H., Morooka, T., Shimohama, S., Kimura, J., Hirano, T., Gotoh, Y., and Nishida, E., Activation and involvement of p38 mitogen-activated protein kinase in glutamate-induced apoptosis in rat cerebellar granule cells. J. Biol. Chem. Ill, 18518-18521 (1997). [Pg.102]

Chuang DM, Gao X-M, Paul SM N-methyl-D-aspartate exposure blocks glutamate toxicity in cultured cerebellar granule cells. Mol Pharmacol 42 210-216, 1992 Chugh Y, Saha N, Sankaranarayanan A, et al Enhancement of memory retrieval and attenuation of scopolamine-induced amnesia following administration of S-HTj antagonist ICS 205-930. Pharmacol Toxicol 69 105-106, 1991 Ciraulo DA, Jaffe JH Tricyclic antidepressants in the treatment of depression associated with alcoholism. Clin Psychopharmacol 1 146, 1981 Ciraulo DA, Barnhill JG, Jaffe JH Clinical pharmacokinetics of imipramine and desipramine in alcoholics and normal volunteers. Pharmacol Ther 43 539-548, 1988... [Pg.612]

Holopainen I., Enkvist M. O. K., and Akerman K. E. O. (1989). Glutamate receptor agonists increase intracellular Ca2+ independently of voltage-gated Ca2+ channels in rat cerebellar granule cells. Neurosci. Lett. 98 57-62. [Pg.35]

Lazarewicz J. W., Wroblewski J. T., and Costa E. (1990). N-methyl-D-aspartate-sensitive glutamate receptors induce calcium-mediated arachidonic acid release in primary cultures of cerebellar granule cells. J. Neurochem. 55 1875-1881. [Pg.100]

Atlante A., Gagliardi S., Minervini G. M., Ciotti M. T., Marra E., and Calissano P. (1997). Glutamate neurotoxicity in rat cerebellar granule cells A major role for xanthine oxidase in oxygen radical formation. J. Neurochem. 68 2038-2045. [Pg.129]

Aronica E, Dell Albani P, Condorelli DF et al (1993) Mechanisms underlying developmental changes in the expression of metabotropic glutamate receptors in cultured cerebellar granule cells homologous desensitization and interactive effects involving N-methyl-D-aspartate receptors. Mol Pharmacol 44 981-9... [Pg.400]

Vale, C., Alfonso, A., Sunol, C., Vieytes, M.R., and Botana, L.M. 2006. Modulation of calcium entry and glutamate release in cultured cerebellar granule cells by palytoxin. Journal of Neuroscience Research 83, 1393—1406. [Pg.117]

Bouchelouche, P., Belhage, B., Frandsen, A., Drejer, J., Schousboe, A. (1989). Glutamate receptor activation in cultured cerebellar granule cells increases cytosolic free Ca by mobilization of cellular Ca and activation of Ca influx. Exp. Brain Res. 76 281-91. [Pg.646]

Cehers, G., Cehere, A., Wagner, A., Liljequist, S. (1999). Prolonged inhibition of glutamate reuptake down-regulates NMDA receptor fimctions in cultured cerebellar granule cells. J. Neurochem. 72 2181-90. [Pg.646]

Bachis A, Colangelo AM, Vicini S, Doe PP, De Bernardi MA, Brooker G, Mocchetti I (2001) Interleukin-10 prevents glutamate-mediated cerebellar granule cell death by blocking caspase-3-like activity. J Neurosci 21 3104—3112. [Pg.198]

F. Sureda et al.. Effects of U-83836E on glutamate-induced neurotoxicity in dissociated rat cerebellar granule cells. Toxicol. Appl. Pharmacol. 156 (1999) 1-5. [Pg.168]

Huh K-H, Wenthold RJ. 1999. Turnover analysis of glutamate receptors identifies a rapidly degraded pool of the N-methyl-D-aspartate receptor subunit, NRl, in cultured cerebellar granule cells. J. Biol. Chem. 274 151-57... [Pg.352]

Heinbockel T, Ennis M. 2003. Granule cell-mediated lateral inhibition can be driven by metabotropic glutamate receptors. AchemS Abstr XXV 201. [Pg.190]

Fig. 5. Drawing of the brainstem depicting neurons and pathways likely to use glutamate as a neurotransmitter. 1 = primary afferent inputs to the dorsal column nuclei (a), the solitary tract nucleus (b), and the cochlear nucleus (c) 2 = granule cell/parallel fibers in the dorsal cochlear nucleus 3 = calyces of Held in the medial nucleus of the trapezoid body 4 = cochlear nucleus inputs to the lateral superior olive 5 = input to the oculomotor nucleus from the ventral lateral vestibular nucleus 6 = input to the oculomotor nucleus from the abducens nucleus 7 = corticocollieular inputs 8 = spinal input to the periaqueductal gray 9 = inputs to the red nucleus and pontine nuclei from the cerebellar nuclei. For further details, see Section 3.3. Fig. 5. Drawing of the brainstem depicting neurons and pathways likely to use glutamate as a neurotransmitter. 1 = primary afferent inputs to the dorsal column nuclei (a), the solitary tract nucleus (b), and the cochlear nucleus (c) 2 = granule cell/parallel fibers in the dorsal cochlear nucleus 3 = calyces of Held in the medial nucleus of the trapezoid body 4 = cochlear nucleus inputs to the lateral superior olive 5 = input to the oculomotor nucleus from the ventral lateral vestibular nucleus 6 = input to the oculomotor nucleus from the abducens nucleus 7 = corticocollieular inputs 8 = spinal input to the periaqueductal gray 9 = inputs to the red nucleus and pontine nuclei from the cerebellar nuclei. For further details, see Section 3.3.

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See also in sourсe #XX -- [ Pg.58 ]




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