Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Christian Renault"'
Autor:
F. Marquis, C. Gueremy, Christian Renault, G. Le Fur, Marie-Christine Dubroeucq, F. Imbault, N. Mitrani, Andre Uzan
Publikováno v:
Neuropharmacology. 23:169-173
Summary Two epimer quinoline derivatives, PK 5078 and PK 7059, have been shown to be potent at releasing 5-HT from blood platelets. Moreover PK 5078 was also a potent and selective inhibitor of the uptake of 5-HT, being about 20 times as active as cl
Autor:
J. Benavides, Andre Uzan, C. Gueremy, G. Le Fur, Nadine Vaucher, Marie-Christine Dubroeucq, A. Flamier, F. Imbault, Christian Renault, M.L. Perrier
Publikováno v:
Life Sciences. 32:1839-1847
Autor:
J. Benavides, G. Le Fur, C. Gueremy, T. Phan, Andre Uzan, C. Tur, Christian Renault, Marie-Christine Dubroeucq, F. Begassat
Publikováno v:
Life Sciences. 35:1249-1256
[3H]PK 11195 binding to peripheral type benzodiazepine binding sites in kidney membranes is inhibited by the histidine blocking agent diethylpyrocarbonate. This reagent irreversibly decreases the Bmax for [3H]PK 11195 without affecting the affinity.
Autor:
J. Benavides, Andre Uzan, Christian Renault, Marie-Christine Dubroeucq, D.E. Allam, C. Gueremy, Francoise Guilloux, J. Mizoule, G. Le Fur
Publikováno v:
Life Sciences. 34:2613-2620
Two compounds with high affinity for the "peripheral type" benzodiazepine binding sites, PK 11195 (an isoquinoline derivative) and RO5-4864 (a benzodiazepine derivative) can modify the sensitivity of DBA/2J mice to audiogenic seizures. RO5-4864 (1-15
Autor:
Nadine Vaucher, Adam Doble, Claude Gueremy, Philippe Bertrand, Marie-Christine Dubroeucq, J. Benavides, Christian Renault, Andre Uzan, Gérard Le Fur, Djamal Allam, Francoise Guilloux
Publikováno v:
European Journal of Pharmacology. 128:269-272
The specific binding of [3H]PK 11195 to the peripheral-type benzodiazepine binding site is inhibited by the 1-enantiomer of N,N-diethyl-α-methyl-2-phenyl-4-quinolinepropanamide ((−)Q1) but not by its d-enantiomer ((+)Q1). (−)Q1 inhibited [3H]PK
Autor:
J. Benavides, A. Flamier, F. Imbault, Christian Renault, Marie-Christine Dubroeucq, C. Gueremy, Andre Uzan, G. Le Fur, Nadine Vaucher, M.L. Perrier
Publikováno v:
Life Sciences. 32:1849-1856
Peripheral type of benzodiazepine binding sites were labelled in the kidney, the heart and the brain with [ 3 H] R05-4864 following intravenous injection in mice. The regional distribution of this in vivo binding parallels the in vitro binding: heart
Autor:
G. Le Fur, Nadine Vaucher, J. Benavides, A. Flamier, Marie-Christine Dubroeucq, Andre Uzan, Christian Renault, M.L. Perrier, C. Gueremy
Publikováno v:
Life Sciences. 33:449-457
The [3H]PK 11195, 1-(2-chlorophenyl)-N-methyl-N-(1-methyl-propyl)-3-isoquinolinecarboxamide, binding sites in rat cardiac membranes are saturable, with high affinity, specific GABA-independent and correspond to the peripheral type of benzodiazepine.
Autor:
Gervais Neliat, G. Le Fur, C. Gueremy, Marie-Christine Dubroeucq, Adam Doble, Andre Uzan, T. Carriot, M. Mestre, Christian Renault
Publikováno v:
Life Sciences. 39:329-339
In a partially depolarized guinea pig papillary muscle preparation, BAY K8644 stimulated voltage-operated calcium channels, promoting slow action potentials; this effect was dose-dependent over a concentration range of 3 × 10 −7 M to 3 × 10 −6
Autor:
A. Doble, Christian Renault, Andre Uzan, Jean Menager, C. Gueremy, G. Le Fur, F. Begassat, Marie-Christine Dubroeucq, O. Ferris, Marie-Claude Burgevin
Publikováno v:
Journal of Receptor Research. 7:55-70
This report describes the results obtained with a new photoaffinity ligand for the "peripheral-type" benzodiazepine binding site (PBS), using a digitonin solubilized preparation from rat heart or adrenals. The specific binding activity of the solubil
Autor:
G. Le Fur, Andre Uzan, M. Mestre, Marie-Christine Dubroeucq, C. Belin, C. Gueremy, Christian Renault, T. Carriot, Adam Doble
Publikováno v:
Life Sciences. 36:391-400
PK 11195, an antagonist of the peripheral type benzodiazepine receptor, does not affect either the duration of the action potential or the tension of the guinea pig papillary muscle. However, it antagonized the effects of the calcium channel blockers