The 2-phenyl-imidazo[1,2-a]pyridine derivative CB 34 is a ligand for peripheral benzodiazepine receptors. The binding of [3H]CB 34 to rat cerebrocortical membranes was characterized. Specific binding was rapid, reversible, saturable and of high affinity. Kinetic analysis yielded association and dissociation rate constants of 0.2 × 108 M-1 min-1 and 0.29 min-1, respectively. Saturation binding experiments revealed a single class of binding sites with a total binding capacity of 188 ± 8 fmol/mg protein and an apparent dissociation constant of 0.19 ± 0.02 nM. Specific [3H]CB 34 binding was inhibited by ligands selective for peripheral benzodiazepine receptors, whereas, with the exception of flunitrazepam and diazepam, ligands for central benzodiazepine receptors were inactive. Of the brain regions examined, the density of the [3H]CB 34-binding sites was greatest in the hypothalamus and lowest in the cerebral cortex. [3H]CB 34 is thus a potent and selective ligand for peripheral benzodiazepine receptors and should be proven useful for studies of the roles of these receptors. © 2001 Elsevier B.V. All rights reserved.

Binding of [3H]CB 34, a selective ligand for peripheral benzodiazepine receptors, to rat brain membranes

Pisu;Porcu;Pa;
2001

Abstract

The 2-phenyl-imidazo[1,2-a]pyridine derivative CB 34 is a ligand for peripheral benzodiazepine receptors. The binding of [3H]CB 34 to rat cerebrocortical membranes was characterized. Specific binding was rapid, reversible, saturable and of high affinity. Kinetic analysis yielded association and dissociation rate constants of 0.2 × 108 M-1 min-1 and 0.29 min-1, respectively. Saturation binding experiments revealed a single class of binding sites with a total binding capacity of 188 ± 8 fmol/mg protein and an apparent dissociation constant of 0.19 ± 0.02 nM. Specific [3H]CB 34 binding was inhibited by ligands selective for peripheral benzodiazepine receptors, whereas, with the exception of flunitrazepam and diazepam, ligands for central benzodiazepine receptors were inactive. Of the brain regions examined, the density of the [3H]CB 34-binding sites was greatest in the hypothalamus and lowest in the cerebral cortex. [3H]CB 34 is thus a potent and selective ligand for peripheral benzodiazepine receptors and should be proven useful for studies of the roles of these receptors. © 2001 Elsevier B.V. All rights reserved.
2001
6
8 dichloro 2 (4 chlorophenyl) n
n diisopropylimidazo[1
2 a
benzodiazepine receptor
diazepam
flunitrazepam
ligand
pyridine derivative
tritium
4 aminobutyric acid A receptor
4' chlorodiazepam
4'-chlorodiazepam
Anti Anxiety Agents
Benzodiazepine
anxiolytic agent
benzodiazepine derivative
delorazepam
diagnostic agent
drug derivative
flumazenil
imidazole derivative
indoleacetic acid derivative
isoquinoline derivative
ligand
membrane protein
n sec butyl 1 (2 chlorophenyl) n methyl 3 isoquinolinecarboxamide
N
N di n hexyl 2 (4 fluorophenyl)indole 3 acetamide
N
N-di-n-hexyl-2-(4-fluorophenyl)indole-3-acetamide
nordazepam
pyridine derivative
Receptors
GABA A
animal tissue
article
brain cortex
brain membrane
brain region
controlled study
dissociation
drug binding site
drug mechanism
drug
female
hypothalamus
ligand binding
nonhuman
priority journal
rat
receptor affinity
animal
binding competition
brain
dose response
drug effect
membrane
metabolism
rat strain
Animal
Anti-Anxiety Agents
Benzodiazepine
Benzodiazepinones
Binding
Competitive
Brain
Dose-Response Relationship
Drug
Female
Flumazenil
Imidazoles
Indoleacetic Acids
Isoquinolines
Ligands
Membrane Proteins
Membranes
Nordazepam
Pyridines
Rats
Rats
Sprague-Dawley
Receptors
GABA-A
Tritium
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/198731
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