An activity-dependent spermine-mediated mechanism that modulates glutamate transmission

Trends in Neurosciences

Volumn 26, Issue 1, 2003, Pages 9-11

  Pellegrini Giampietro, Domenico E ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMPA RECEPTOR; CALCIUM CHANNEL; CALCIUM ION; GLUTAMIC ACID; POLYAMINE; SPERMINE; VOLTAGE GATED CALCIUM CHANNEL;

ANIMAL CELL; CALCIUM TRANSPORT; CELL ACTIVATION; CONTROLLED STUDY; NERVE CELL; NEUROBLAST; NEUROMODULATION; NONHUMAN; OPTIC TECTUM; POLYAMINE SYNTHESIS; PRIORITY JOURNAL; SHORT SURVEY; SYNAPTIC POTENTIAL; SYNAPTIC TRANSMISSION; SYNAPTOGENESIS;

ANIMALS; CALCIUM; CELLS, CULTURED; GLUTAMIC ACID; NEURONS; POLYAMINES; RECEPTORS, AMPA; RECEPTORS, GLUTAMATE; SPERMINE; SUPERIOR COLLICULUS;

EID: 0037213822     PISSN: 01662236     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0166-2236(02)00004-8     Document Type: Short Survey

References (16)

1. Tabor C.W., Tabor H. Polyamines. Annu. Rev. Biochem. 53:1984;749-790.
2. Williams K. Modulation and block of ion channels: a new biology of polyamines. Cell. Signal. 9:1997;1-13.
3. 2+ permeability of KA-AMPA-gated glutamate receptor channels depends on subunit composition. Science. 252:1991;851-853.
4. Verdoorn T.A., et al. Structural determinants of ion flow through recombinant glutamate receptor channels. Science. 252:1991;1715-1718.
5. Sommer B., et al. RNA editing in brain controls a determinant of ion flow in glutamate-gated channels. Cell. 67:1991;11-19.
6. Jonas P., Burnashev N. Molecular mechanisms controlling calcium entry through AMPA-type glutamate receptor channels. Neuron. 15:1995;987-990.
7. 2+-permeable AMPA receptors in neurological disorders. Trends Neurosci. 20:1997;464-470.
8. Bowie D., Mayer M. Inward rectification of both AMPA and kainate subtype glutamate receptors generated by polyamine-mediated ion channel block. Neuron. 15:1995;453-462.
9. Najm I., et al. Seizure activity-induced increase in polyamine metabolism and neuronal pathology during the postnatal period in rat brain. Brain Res. Dev. Brain Res. 69:1992;11-21.
10. Gilad G.M., Gilad V.H. Novel polyamine derivatives as neuroprotective agents. J. Pharmacol. Exp. Ther. 291:1999;39-43.
11. Aizenman C.D., et al. Visually driven modulation of glutamatergic synaptic transmission is mediated by the regulation of intracellular polyamines. Neuron. 34:2002;623-634.
12. Carvalho A.L., et al. Regulation of AMPARs by phosphorylation. Neurochem. Res. 25:2000;1245-1255.
13. Malinow R., et al. LTP mechanisms: from silence to four-lane traffic. Curr. Opin. Neurobiol. 10:2000;352-357.
14. Lawrence J.J., Trussell L.O. Long-term specification of AMPAR properties after synapse formation. J. Neurosci. 20:2000;4864-4870.
15. Liu S.Q., Cull-Candy S.G. Synaptic activity at calcium-permeable AMPARs induces a switch in receptor subtype. Nature. 405:2000;454-458.
16. Adibhatla R.M., et al. Polyamines and central nervous system injury: spermine and spermidine decrease following transient focal cerebral ischemia in spontaneously hypertensive rats. Brain Res. 938:2002;81-86.