In vivo binding of (/sup 3/H)Ro 15-1788 in mice: comparison with the in vivo binding of (/sup 3/H)flunitrazepam
Benzodiazepine binding sites have generally been labelled with benzodiazepine agonists: (/sup 3/H)flunitrazepam and (/sup 3/H)diazepam in vivo. The authors studied the in vivo binding of the antagonist (/sup 3/H)Ro 15-1788 in mice and compared it to the in vivo binding of (/sup 3/H)flunitrazepam. For this in vivo labelling, mice were injected with labelled and unlabelled ligands. Animals were then sacrificed and bound radioactivity was measured after homogenization of the excised brain and filtration of the homogenate. (/sup 3/H)Ro 15-1788 is a better tool than (/sup 3/H)flunitrazepam for in vivo labelling of benzodiazepine receptors since 1) it labels specifically the central type binding sites, 2) injection of 4 times less (/sup 3/H)Ro 15-1788 than (/sup 3/H)flunitrazepam produced the same amount of bound radioactivity, 3) 70-90% of the total (/sup 3/H)Ro 15-1788 present in the brain is membrane bound instead of 45-55% with (/sup 3/H)flunitrazepam, 4) maximal binding of (/sup 3/H)Ro 15-1788 is reached within 3 min, 5) only 5% of the membrane bound (/sup 3/H)Ro 15-1788 is nonspecific instead of 15% for (/sup 3/H)flunitrazepam.
- Research Organization:
- C.N.R.S. Gif-sur-Yvette (France)
- OSTI ID:
- 6703136
- Journal Information:
- Life Sci.; (United States), Vol. 43:16
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
TRANQUILIZERS
BIOCHEMICAL REACTION KINETICS
BRAIN
CELL MEMBRANES
COMPARATIVE EVALUATIONS
IN VIVO
LIGANDS
MICE
RECEPTORS
TRACER TECHNIQUES
TRITIUM COMPOUNDS
ANIMALS
BODY
CELL CONSTITUENTS
CENTRAL NERVOUS SYSTEM
CENTRAL NERVOUS SYSTEM AGENTS
DRUGS
ISOTOPE APPLICATIONS
KINETICS
LABELLED COMPOUNDS
MAMMALS
MEMBRANE PROTEINS
MEMBRANES
NERVOUS SYSTEM
ORGANIC COMPOUNDS
ORGANS
PROTEINS
PSYCHOTROPIC DRUGS
REACTION KINETICS
RODENTS
VERTEBRATES
550201* - Biochemistry- Tracer Techniques