Antagonism by ketanserin of the behavioral effects of quipazine but not l-5-hydroxytryptophan in squirrel monkeys
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[1] E. sanders-Bush,et al. Additional evidence that l-5-hydroxytryptophan discrimination models a unique serotonin receptor , 2004, Psychopharmacology.
[2] E. sanders-Bush,et al. Discriminative stimulus properties of l-5-hydroxytryptophan: Behavioral evidence for multiple serotonin receptors , 2004, Psychopharmacology.
[3] J. Barrett,et al. Effects of serotonin receptor agonists and antagonists on schedule-controlled behavior of squirrel monkeys. , 1985, The Journal of pharmacology and experimental therapeutics.
[4] J. Barrett,et al. Effects of serotonin receptor antagonists on punished responding maintained by stimulus-shock termination or food presentation in squirrel monkeys. , 1985, The Journal of pharmacology and experimental therapeutics.
[5] D. Mokler,et al. The 5HT2 antagonist pirenperone reverses disruption of FR-40 by hallucinogenic drugs , 1985, Pharmacology Biochemistry and Behavior.
[6] K. Cunningham,et al. Differentiation between the stimulus effects of l-5-hydroxytryptophan and LSD. , 1985, European journal of pharmacology.
[7] E. sanders-Bush,et al. Discriminative stimulus properties of quipazine: mediation by serotonin2 binding sites. , 1984, The Journal of pharmacology and experimental therapeutics.
[8] R. Ortmann. The 5‐HT syndrome in rats as tool for the screening of psychoactive drugs , 1984 .
[9] I. Lucki,et al. Differential actions of serotonin antagonists on two behavioral models of serotonin receptor activation in the rat. , 1984, The Journal of pharmacology and experimental therapeutics.
[10] D. Reis,et al. Some neurons of the rat central nervous system contain aromatic-L-amino-acid decarboxylase but not monoamines. , 1983, Science.
[11] C. Niemegeers,et al. A drug discrimination analysis of lysergic acid diethylamide (LSD): in vivo agonist and antagonist effects of purported 5-hydroxytryptamine antagonists and of pirenperone, a LSD-antagonist. , 1982, The Journal of pharmacology and experimental therapeutics.
[12] J. Leander. Antagonism by methysergide of the effects of l-5-hydroxytryptophan and quipazine on schedule-controlled responding , 1981, Neuropharmacology.
[13] S. Snyder,et al. Two distinct central serotonin receptors with different physiological functions. , 1981, Science.
[14] J. Leysen,et al. Receptor binding profile of R 41 468, a novel antagonist at 5-HT2 receptors. , 1981, Life sciences.
[15] R. Fuller. Pharmacology of central serotonin neurons. , 1980, Annual review of pharmacology and toxicology.
[16] F. J. White,et al. Discriminative stimulus properties of quipazine: Direct serotonergic mediation , 1979, Neuropharmacology.
[17] R. B. Carter,et al. Role of peripheral mechanisms in the behavioral effects of 5-hydroxytryptophan , 1978, Pharmacology Biochemistry and Behavior.
[18] K. Davis. Psychopharmacology: A Biochemical and Behavioral Approach , 1978 .
[19] F. J. White,et al. Discriminative stimulus properties of quipazine , 1977, Neuropharmacology.
[20] L. Seiden,et al. Psychopharmacology: A Biochemical and Behavioral Approach , 1977 .
[21] T. Chase,et al. Release of [3H]dopamine byl-5-hydroxytryptophan , 1972 .
[22] T. Chase,et al. Release of ( 3 H)dopamine by L-5-hydroxytryptophan. , 1972, Brain research.
[23] D. Straughan,et al. Excitation and depression of cortical neurones by 5‐hydroxytryptamine , 1967, The Journal of physiology.
[24] L. N. Balaam,et al. Biostatistics -- An Introductory Text , 1965 .
[25] N H AZRIN,et al. An apparatus for delivering pain shock to monkevs. , 1963, Journal of the experimental analysis of behavior.