The influence of NO-containing ruthenium complexes on mouse hippocampal evoked potentials in vitro

Life Sciences

Volumn 68, Issue 13, 2001, Pages 1535-1544

  Wieraszko, Andrzej ^a   Clarke, Michael J ^b   Lang, Douglas R ^b   Lopes, Luiz G F ^c   Franco, Douglas W ^c  

^a CITY UNIVERSITY OF NEW YORK   (United States)

^b BOSTON COLLEGE   (United States)

^c UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Long term potentiation; Nitric oxide; Ruthenium

Indexed keywords

NITRIC OXIDE; OXYHEMOGLOBIN; RUTHENIUM COMPLEX;

ANIMAL TISSUE; ARTICLE; BRAIN PERFUSION; CHEMICAL STRUCTURE; CONTROLLED STUDY; DRUG EFFECT; DRUG POTENCY; ELECTROSTIMULATION; EVOKED CORTICAL RESPONSE; EXCITATORY POSTSYNAPTIC POTENTIAL; FEMALE; HIPPOCAMPUS; IN VITRO STUDY; LONG TERM POTENTIATION; MALE; NONHUMAN; RAT; REDUCTION; SPIKE WAVE;

ANIMALS; EXCITATORY POSTSYNAPTIC POTENTIALS; FEMALE; HIPPOCAMPUS; MALE; MICE; MICE, INBRED C57BL; NITRIC OXIDE; RUTHENIUM COMPOUNDS; SODIUM NITRITE;

EID: 0035895655     PISSN: 00243205     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0024-3205(01)00951-1     Document Type: Article

References (35)

1. A synaptic model of memory:long-term potentiation in the hippocampus
2. Long-term depression of excitatory synaptic transmission and its relationship to long-term potentiation
3. Possible involvement of NO in long-term potentiation
4. The role of nitric oxide in hippocampal long-term potentiation
5. Tests of the roles of two diffusible substances in LTP: Evidence for NO as a possible early retrograde messenger
6. Nitric oxide inhibitors facilitate the induction of hippocampal long-term potentiation by modulating NMDA responses
7. Induction in the rat hippocampus of long-term potentiation (LTP) and long-term depression (LTD) in the presence of a nitric oxide synthase inhibitor
8. Photolytic release of nitric oxide modulates NMDA receptor-mediated transmission but does not induce long-term potentiation at hippocampal synapses
9. The suppression of long-term potentiation in rat hippocampus by inhibitors of nitric oxide synthase is temperature and age dependent
10. 2+ and its transient 3+ mixed-valence ion
11. Recent chemical studies of sodium nitroprusside relevant to its hypotensive action
12. Peroxynitrate: Reactive, invasive and enigmatic
13. Dual effects of sodium nitroprusside on potentials recorded from mouse hippocampal slices
14. Chemistry relevant to the biological effects of nitric oxide and metallonitrosyls
15. Ruthenium-NO complexes: Promising vasodilators
16. Ruthenium nitrosyl complexes with N-heterocyclic ligands
17. Cis- and trans-nitrosyltetra-ammineruthenium (II). Spectral and electrochemical properties and reactivity
18. Pentammineruthenium salts
19. Crystal and molecular structure of ruthenium-sulfur dioxide coordination compounds. I. Clorotetraammine(sulfur dioxide)ruthenium(II) Chloride
20. 3+
21. Triethyl phosphite as a ligand on ruthenium (II)
22. N-macrocyclic complexes of ruthenium(II) and ruthenium(III)
23. Characterization of LTP induced by the activation of glutamate metabotropic receptors in area CA1 of the hippocampus
24. Activation of glutamate metabotropic receptors induces long-term potentiation
25. Endogenous nitric oxide releases striatal dopamine in vivo via a glutamate-mediated facilitation
26. Potentiation of synaptic transmission in the rat hippocampal slice by exogenous L-glutamate and selective L-glutamate receptor subtype agonists
27. The effect of glutamate uptake inhibitors on hippocampal evoked potentials in vitro
28. Onset and stabilization of NMDA receptor-mediated hippocampal long-term potentiation
29. Quisqualate and N-methyl-D-aspartate (NMDA) receptors in induction of hippocampal long-term facilitation using conditioning solution
30. Photolytically released nitric oxide produces a delayed but persistent suppression of LTP in area CA1 of the rat hippocampal slice
31. Long-term potentiation: Biophysical and biochemical mechanisms
32. Nitric oxide facilitates long-term potentiation, but not long-term depression
33. Nitric oxide synthase-independent long-term potentiation in area CA1 of hippocampus