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Psychopharmacology|November 11, 1998
Acamprosate suppresses the expression of morphine-induced sensitization in rats but does not affect heroin self-administration or relapse induced by heroin or stressR Spanagel, I Sillaber, W Zieglgänsberger, et al.
Psychopharmacology|December 1, 1995
Anxiety: a potential predictor of vulnerability to the initiation of ethanol self-administration in ratsR Spanagel, A Montkowski, K Allingham, et al.
Behavioural Brain Research|September 4, 1999
Stress- and corticosteroid-induced modulation of the locomotor response to morphine in ratsT Stöhr, O F Almeida, R Landgraf, et al.
Psychopharmacology|May 5, 1999
Assessment of neuroleptic-like properties of progesteroneR Rupprecht, M Koch, A Montkowski, et al.
Neuroscience Letters|April 8, 2000
Autoradiographic distribution of mu-, delta- and kappa 1-opioid stimulated [35S]guanylyl-5'-O-(gamma-thio)-triphosphate binding in human frontal cortex and cerebellumS Platzer, A Winkler, J Schadrack, et al.
The European Journal of Neuroscience|February 13, 2001
Differential role of the nitric oxide pathway on delta(9)-THC-induced central nervous system effects in the mouseS C Azad, G Marsicano, I Eberlein, et al.
Alcoholism, Clinical and Experimental Research|June 11, 1998
Release and accumulation of neurotransmitters in the rat brain: acute effects of ethanol in vitro and effects of long-term voluntary ethanol intakeM Darstein, C Albrecht, L López-Francos, et al.
Brain Research. Molecular Brain Research|November 14, 1998
Long-term alcohol self-administration and alcohol withdrawal differentially modulate microtubule-associated protein 2 (MAP2) gene expression in the rat brainJ Putzke, R De Beun, R Schreiber, et al.
The European Journal of Neuroscience|February 1, 1997
Infusions of tyrosine hydroxylase antisense oligodeoxynucleotide into substantia nigra of the rat: effects on tyrosine hydroxylase mRNA and protein content, striatal dopamine release and behaviourT Skutella, R K Schwarting, J P Huston, et al.
Neuropharmacology|May 23, 2001
The anti-craving compound acamprosate acts as a weak NMDA-receptor antagonist, but modulates NMDA-receptor subunit expression similar to memantine and MK-801G Rammes, B Mahal, J Putzke, et al.
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