The 5-HT1A and 5-HT2A/2C receptor antagonists WAY-100635 and ritanserin do not attenuate d-fenfluramine-induced Fos expression in the brain

Author:

Javed A,Van de Kar L.D,Gray T.S

Publisher

Elsevier BV

Subject

Developmental Biology,Clinical Neurology,Molecular Biology,General Neuroscience

Reference65 articles.

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2. Autoradiographic characterization of (±)-1-(2,5-dimethoxy-4-[125I]iodophenyl)-2-aminopropane ([125I]DOI) binding to 5-HT2 and 5-HT1C receptors in rat brain;Appel;J. Pharmacol. Exp. Ther.,1990

3. The neuroendocrine response to d-fenfluramine in women with premenstrual depression;Bancroft;J. Affect. Disord.,1995

4. 8-Hydroxy-2-(di-n-propylamino)tetralin-responsive 5-hydroxytryptamine4-like receptor expressed in bovine pulmonary artery smooth muscle cells;Becker;Mol. Pharmacol.,1992

5. Expression of c-fos-like protein as a marker for neuronal activity following noxious stimulation in the rat;Bullitt;J. Comp. Neurol.,1990

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