Comparative autoradiographic distribution of central ω (benzodiazepine) modulatory site subtypes with high, intermediate and low affinity for zolpidem and alpidem

Author:

Benavides J.,Peny B.,Ruano D.,Vitorica J.,Scatton B.

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference32 articles.

1. High affinity [3H] zolpidem binding in the rat brain: an imidazopyridine with agonist properties at central benzodiazepine receptors;Arbilla;Eur. J. Pharmacol.,1986

2. In vivo interaction of zolpidem with central benzodiazepine (BZD) binding sites (as labeled by [3H] Ro 15–1788) in the mouse brain. Preferential affinity of zolpidem for the ω1 (BZD)1) subtype;Benavides;J. Pharmacol. Exp. Ther.,1988

3. Selective affinity of the benzodiazepines quazepam and 2-oxoquazepam for BZ1 binding site and demonstration [3H]2-oxoquazepam as BZ1 selective radioligand;Billard;Life Sci.,1988

4. Interaction of convulsive ligands with benzodiazepine receptors;Braestrup;Science,1982

5. [3H Propyl β-carboline-3-carboxylate as a selective radioligand for the BZD1 benzodiazepine receptors subclass;Braestrup;J. Neurochem.,1981

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