Zobrazeno 1 - 10
of 90
pro vyhledávání: '"C J, Niemegeers"'
Autor:
C J, Niemegeers
Publikováno v:
Ceskoslovenska psychiatrie. 89(1)
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 260(1)
The mixed serotonin-2/dopamine-D2 antagonists risperidone and ocaperidone were compared with the specific D2 antagonist haloperidol for their ability to antagonize amphetamine (10 mg/kg, s.c.)-induced stereotypy in rats. Four successive stages of amp
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 260(1)
Ocaperidone, a new benzisoxazolyl piperidine neuroleptic, was compared with haloperidol, risperidone and ritanserin in a large series of pharmacological tests. Ocaperidone inhibited dopamine agonist (apomorphine, amphetamine or cocaine)-induced behav
Publikováno v:
Arzneimittel-Forschung. 41(6)
The pharmacological profile of bethanechol (CAS 674-38-4), metoclopramide (CAS 364-62-5), trimebutine (CAS 39133-31-8) and cisapride (CAS 81098-60-4) was studied in a series of simple pharmacological tests in rats and dogs. Bethanechol stimulated bot
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 254(3)
The functional significance of the interaction between serotonergic and dopaminergic neurotransmission is still uncertain. To document this interaction further, specific behavioral responses of rats to tryptamine and apomorphine were studied. The seq
Publikováno v:
L'Encephale. 16(2)
Shortly after the introduction of the first neuroleptics a serotonin hypothesis of schizophrenia has been proposed. But neuroleptics in animals and in man were found to produce effects more consistently related to inhibition of the dopaminergic than
Autor:
C J, Niemegeers
Publikováno v:
Acta psiquiatrica y psicologica de America latina. 36(1-2)
Autor:
A, Wauquier, C J, Niemegeers
Publikováno v:
Psychopharmacologia. 34:265-274
Autor:
A, Wauquier, C J, Niemegeers
Publikováno v:
Arzneimittel-Forschung. 26(7)
Bromperidol, a new potent and long-acting neuroleptic of the butyrophenone series, and haloperidol were injected s.c. at the doses 0.01, 0.02, 0.04 and 0.08 mg/kg, in rats implanted with electrodes in the lateral hypothalamic region of the medial for
Publikováno v:
Archives internationales de pharmacodynamie et de therapie. 218(2)
Various non-narcotic drugs with intrinsic stimulus properties were found not to be generalized with fentanyl treatment in rats trained to discriminate fentanyl (0.04 mg/kg, s.c., t-30') from its solvent (s.c., t-30'). In contrast, five typical narcot