Výsledky vyhledávání - "L Prado de Carvalho"

Kinetics properties of the alpha2 homo-oligomeric glycine receptor impairs a proper synaptic functioning

Autor: Pascal Legendre, M. Baloul, L. Prado de Carvalho, Bernard Rogister, Jean-Marie Mangin, Jean-Michel Rigo

Publikováno v: The Journal of Physiology
The Journal of Physiology, Wiley, 2003, 553, pp.369-386. ⟨10.1113/jphysiol.2003.052142⟩
The Journal of Physiology, 2003, 553, pp.369-386. ⟨10.1113/jphysiol.2003.052142⟩

Ionotropic glycine receptors (GlyRs) are present in the central nervous system well before the establishment of synaptic contacts. Immature nerve cells are known, at least in the spinal cord, to express alpha2 homomeric GlyRs, the properties of which

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ca1e76d9e0d6e08768db88c9ac9e8cc
https://hal.archives-ouvertes.fr/hal-00079733

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A novel Glycine Receptor aZ1 Subunit Variant in the Zebrafish Brain

Autor: V Devignot, C Goblet, L Prado de Carvalho, Piotr Bregestovski

Publikováno v: Neuroscience
Neuroscience, 2003, 122, pp.449-457. ⟨10.1016/S0306-4522(03)00171-4⟩
Neuroscience, Elsevier-International Brain Research Organization, 2003, 122, pp.449-457. ⟨10.1016/S0306-4522(03)00171-4⟩

Alpha subunits of the inhibitory glycine receptor (GlyR) display genetic heterogeneity in mammals and zebrafish. This diversity is increased in mammals by the alternative splicing mechanism. We report here in zebrafish, the characterization of a new

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6789bdfd2c2e92a9dde0e6b40779f0bc
https://hal.science/hal-00079769

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Evoked acetylcholine release by immortalized brain endothelial cells genetically modified to express choline acetyltransferase and/or the vesicular acetylcholine transporter

Autor: L. Prado de Carvalho, Michel Malo, François-Marie Meunier, Yves Dunant, Marie-Françoise Diebler, Pierre-Olivier Couraud, Monique Tomasi, Jean-Léon Tchelingerian, Maurice Israël, Alain Bloc, Jacques Stinnakre

Publikováno v: Journal of neurochemistry. 73(4)

Immortalized rat brain endothelial RBE4 cells do not express choline acetyltransferase (ChAT), but they do express an endogenous machinery that enables them to release specifically acetylcholine (ACh) on calcium entry when they have been passively lo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9519411b909a4c810a1fd8473d54069d
https://pubmed.ncbi.nlm.nih.gov/10501193

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ChemInform Abstract: Synthesis and Benzodiazepine Receptor Affinities of Rigid Analogues of 3-Carboxy-β-carbolines: Demonstration that the Benzodiazepine Receptor Recognizes Preferentially the s-Cis Conformation of the 3-Carboxy Group

Autor: Pierre Jean-Paul Potier, Georges Chapouthier, Patrice Venault, G. Dorey, Guillaume Poissonnet, Robert H. Dodd, J. Rossier, Marie-Claude Potier, L. Prado De Carvalho

Publikováno v: ChemInform. 21

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e082f468967c8f3e4905d481f1a54b29
https://doi.org/10.1002/chin.199002206

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Akademický článek

An H-bond between two residues from different loops of the acetylcholine binding site contributes to the activation mechanism of nicotinic receptors.

Autor: T. Grutter, L. Prado de Carvalho, N. Le Novère, P.J. Corringer, S. Edelstein, J-P. Changeux

Publikováno v: EMBO Journal; 5/1/2003, Vol. 22 Issue 9, p1990-2003, 14p

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In vivo binding of (3H) Ro 15-1788 in mice: Comparison with the in vivo binding of (3H) flunitrazepam

Autor: J. Rossier, Robert H. Dodd, Marie-Claude Potier, ChloëL. Brown, L. Prado De Carvalho

Publikováno v: Life Sciences. 43:1287-1296

Benzodiazepine binding sites have generally been labelled with benzodiazepine agonists: (3H) flunitrazepam and (3H) diazepam in vivo . We studied the in vivo binding of the antagonist (3H) Ro 15-1788 in mice and compared it to the in vivo binding of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ba7ca38449002e659b8df815f1f60ab
https://doi.org/10.1016/0024-3205(88)90583-8

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ChemInform Abstract: Synthesis of β-Carboline-Benzodiazepine Hybrid Molecules: Use of the Known Structural Requirements for Benzodiazepine and β-Carboline Binding in Designing a Novel, High-Affinity Ligand for the Benzodiazepine Receptor

Autor: C. Ouannes, Robert H. Dodd, Marie-Claude Potier, J. Rossier, Pierre Jean-Paul Potier, L. Prado De Carvalho

Publikováno v: ChemInform. 18

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::528f4def9b719bc4c537e4ed96ae4952
https://doi.org/10.1002/chin.198750244

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Electroencephalographic and behavioral observations in rats during chronic ethanol ingestion and after abstinence

Autor: L, Prado de Carvalho, I, Izquierdo

Publikováno v: Archives internationales de pharmacodynamie et de therapie. 235(2)

Increasing aqueous solutions of ethanol were given to rats, starting immediately after weaning, instead of drinking water. A 12% v/v concentration was reached on day 81 of age and maintained from then on. Animals drinking 12% ethanol had a median blo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::24d5e3c8fba792579b6899420c485495
https://pubmed.ncbi.nlm.nih.gov/570025

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