NPI-031G (puerarin) reduces anxiogenic effects of alcohol withdrawal or benzodiazepine inverse or 5-HT2C agonists

Author:

Overstreet David H.,Kralic Jason E.,Morrow A.Leslie,Ma Zhong Z.,Zhang Y.W.,Lee David Y.W.

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Biological Psychiatry,Clinical Biochemistry,Pharmacology,Toxicology,Biochemistry

Reference41 articles.

1. Acamprosate is neuroprotective against glutamate-induced excitotoxicity when enhanced by alcohol withdrawal in neocortical cultures of fetal rat brain;Al Qatari;Alcohol Clin. Exp. Res.,2001

2. Anxiety-like effects induced by acute fluoxetine, sertraline or m-CPP treatment are reversed by pretreatment with the 5-HT2C receptor antagonist SB-242084 but not the 5-HT1A receptor antagonist WAY-100635;Bagdy;Int. J. Neuropsychopharmacol.,2001

3. Evidence for accelerated desensitisation of 5-HT2C receptors following combined treatment with fluoxetine and the 5-HT1A receptor antagonist, WAY 100635, in the rat;Bristow;Neuropharmacology,2000

4. Effects of the calcium channel antagonist darodipine on ethanol withdrawal in rats;Colombo;Alcohol. Alcohol,1995

5. Effects of NPI-031G against glutamate excitotoxicity on cultured mouse cerebral cortical neurons;Dong;Acta Pharmacol. Sin.,1998

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