The catecholamine uptake inhibitor nomifensine depresses impulse activity of dopamine neurons in mouse substantia nigra

[1]  M. Dubocovich,et al.  Quantitative autoradiography of 3H-nomifensine binding sites in rat brain. , 1985, Life sciences.

[2]  W. Schultz,et al.  The activity of pars compacta neurons of the monkey substantia nigra is depressed by apomorphine , 1984, Neuroscience Letters.

[3]  M. Sanghera,et al.  Electrophysiological properties of mouse dopamine neurons: In vivo and in vitro studies , 1984, Neuroscience.

[4]  W. Schultz,et al.  Dopaminergic activation of reticulata neurones in the substantia nigra , 1980, Nature.

[5]  A. Grace,et al.  Dopamine auto- and postsynaptic receptors: electrophysiological evidence for differential sensitivity to dopamine agonists. , 1979, Science.

[6]  R. Ings,et al.  Kinetics and metabolism of nomifensine in animals. , 1977, British journal of clinical pharmacology.

[7]  J. Glowinski,et al.  Release of dopamine in vivo from cat substantia nigra , 1977, Nature.

[8]  J. Scheel-Krüger,et al.  Methylphenidate-like effects of the new antidepressant drug nomifensine (HOE 984). , 1976, European journal of pharmacology.

[9]  O. Lindvall,et al.  Dopamine in dendrites of substantia nigra neurons: suggestions for a role in dendritic terminals , 1975, Brain Research.

[10]  U. Schacht,et al.  Effect of nomifensine (HOE 984), a new antidepressant, on uptake of noradrenaline and serotonin and on release of noradrenaline in rat brain synaptosomes. , 1974, Biochemical pharmacology.

[11]  J. Raynaud,et al.  Nomifensine: a new potent inhibitor of dopamine uptake into synaptosomes from rat brain corpus striatum , 1974, The Journal of pharmacy and pharmacology.

[12]  R. Roth,et al.  Comparison of effects of L-dopa, amphetamine and apomorphine on firing rate of rat dopaminergic neurones. , 1973, Nature: New biology.

[13]  I. Hoffmann.  8-Amino-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline, a new antidepressant. , 1973, Arzneimittel-Forschung.