| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| R A Duffy, M A Hunt, J K Wamsley, R D McQuad. In vivo autoradiography of [3H]SCH 39166 in rat brain: selective displacement by D1/D5 antagonists. Journal of chemical neuroanatomy. vol 19. issue 1. 2000-11-03. PMID:10882836. |
neither haloperidol nor ketanserin displaced [3h]sch 39166 in any of the regions examined. |
2000-11-03 |
2023-08-12 |
rat |
| A E Kelley, V P Bakshi, S Fleming, M R Holaha. A pharmacological analysis of the substrates underlying conditioned feeding induced by repeated opioid stimulation of the nucleus accumbens. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. vol 23. issue 4. 2000-11-01. PMID:10989273. |
in the second experiment, co-treatment with either a d-1 (sch 23390, 0.1 mg/kg) or d-2 (haloperidol, 0.25 mg/kg) antagonist did not block the development of conditioned feeding, nor did these drugs block morphine-induced feeding. |
2000-11-01 |
2023-08-12 |
rat |
| C F Wu, H L Zhang, W Li. Potentiation of ethanol-induced loss of the righting reflex by ascorbic acid in mice: interaction with dopamine antagonists. Pharmacology, biochemistry, and behavior. vol 66. issue 2. 2000-08-28. PMID:10880698. |
to test the effect of each drug on ethanol-induced lorr, ascorbic acid (31.25, 62.5, 125, 250, 500, 1000 mg/kg intraperitoneally [ip]) and dopamine receptor antagonists (haloperidol 0.5, 1.0 mg/kg; l-sulpiride 20, 40, 80 mg/kg; clozapine 0.625, 1.25, 2.5 mg/kg; sch 23390 0.5, 1.0, 2.0 mg/kg subcutaneously [sc]) were administered, respectively, 30 min before ethanol (4.0 g/kg ip) administration. |
2000-08-28 |
2023-08-12 |
mouse |
| C F Wu, H L Zhang, W Li. Potentiation of ethanol-induced loss of the righting reflex by ascorbic acid in mice: interaction with dopamine antagonists. Pharmacology, biochemistry, and behavior. vol 66. issue 2. 2000-08-28. PMID:10880698. |
in the interaction study, the synergistic effect of ascorbic acid (1000 mg/kg ip) on ethanol-induced lorr was significantly enhanced by dopamine d(2) antagonists haloperidol, l-sulpiride, and clozapine, and the highest dose of dopamine d(1) antagonist sch 23390. |
2000-08-28 |
2023-08-12 |
mouse |
| M Imaizumi, M Takeda, T Fushik. Effects of oil intake in the conditioned place preference test in mice. Brain research. vol 870. issue 1-2. 2000-08-21. PMID:10869512. |
injection of sch 23390 (0.03 mg/kg) and haloperidol (0.1 mg/kg), but not by that of (+/-)-sulpiride (100 mg/kg), (-)-sulpiride (100 mg/kg), and l-741, 626 (1 mg/kg) 15 min before conditioning. |
2000-08-21 |
2023-08-12 |
mouse |
| C Nath, R C Saxena, M B Gupt. Effect of dopamine agonists and antagonists on the lorazepam withdrawal syndrome in rats. Clinical and experimental pharmacology & physiology. vol 27. issue 3. 2000-06-21. PMID:10744342. |
the remaining groups received one of the following dopamine antagonists: (i) 0.1 mg/kg per day, i.m., sch 23390; (ii) 0.5 mg/kg per day, i.m., haloperidol; (iii) 0.5 mg/kg per day, i.m., centbutindol; and (iv) either 1 or 20 mg/kg per day, i.m., clozapine. |
2000-06-21 |
2023-08-12 |
rat |
| D Boulay, R Depoortere, A Oblin, D J Sanger, H Schoemaker, G Perraul. Haloperidol-induced catalepsy is absent in dopamine D(2), but maintained in dopamine D(3) receptor knock-out mice. European journal of pharmacology. vol 391. issue 1-2. 2000-05-11. PMID:10720636. |
also, dopamine d(3) receptor mutant mice were no more responsive than wild-type controls when co-administered subthreshold doses of haloperidol (0.125 mg/kg) and sch 23390 (0.03 mg/kg), suggesting that dopamine d(3) receptor knock-out mice are not more sensitive than wild-types to the synergistic effects of concurrent blockade of dopamine d(2) and dopamine d(1) receptors in this model. |
2000-05-11 |
2023-08-12 |
mouse |
| A Parra, M C Arenas, S Monleón, C Vinader-Caerols, V M Simó. Sex differences in the effects of neuroleptics on escape-avoidance behavior in mice: a review. Pharmacology, biochemistry, and behavior. vol 64. issue 4. 1999-12-21. PMID:10593205. |
the acute administration of haloperidol, raclopride, clozapine, and sch 23390 impaired escape-avoidance behavior more in males than in females, and the subchronic administration of haloperidol had a similar effect. |
1999-12-21 |
2023-08-12 |
mouse |
| E Jakubowska-Doğr. Modification of avoidance responding by amphetamine and dopamine receptor antagonists. Polish journal of pharmacology. vol 51. issue 4. 1999-11-30. PMID:10540961. |
this study was designed to investigate the effects of preferential d1 (sch 23390) and d2 (haloperidol) dopamine (da) receptor antagonists and their interaction with low-dose (1 mg kg) d-amphetamine during the acquisition of two-way shuttle avoidance in rats. |
1999-11-30 |
2023-08-12 |
rat |
| S J Gladwell, J H Coot. Fast excitatory post synaptic potentials and their response to catecholaminergic antagonists in rat sympathetic preganglionic neurones in vitro. Neuroscience letters. vol 268. issue 2. 1999-11-22. PMID:10400085. |
the latter potential was blocked with the dopamine d2 antagonist haloperidol but not with the dopamine d1 antagonist sch 23390. |
1999-11-22 |
2023-08-12 |
rat |
| M Rodríguez-Arias, J Pinazo, J Miñarro, L Stinu. Effects of SCH 23390, raclopride, and haloperidol on morphine withdrawal-induced aggression in male mice. Pharmacology, biochemistry, and behavior. vol 64. issue 1. 1999-10-21. PMID:10495006. |
effects of sch 23390, raclopride, and haloperidol on morphine withdrawal-induced aggression in male mice. |
1999-10-21 |
2023-08-12 |
mouse |
| M Rodríguez-Arias, J Pinazo, J Miñarro, L Stinu. Effects of SCH 23390, raclopride, and haloperidol on morphine withdrawal-induced aggression in male mice. Pharmacology, biochemistry, and behavior. vol 64. issue 1. 1999-10-21. PMID:10495006. |
the effect of sch 23390 (0.5 mg/kg), raclopride (0.3 mg/kg), and haloperidol (0.1 mg/kg) on morphine withdrawal-induced aggression has been studied in this work. |
1999-10-21 |
2023-08-12 |
mouse |
| M Rodríguez-Arias, J Pinazo, J Miñarro, L Stinu. Effects of SCH 23390, raclopride, and haloperidol on morphine withdrawal-induced aggression in male mice. Pharmacology, biochemistry, and behavior. vol 64. issue 1. 1999-10-21. PMID:10495006. |
the three neuroleptics counteracted this aggression, but when sch 23390 (selective d1 antagonist) and haloperidol (mixed d1/d2 antagonist) were administered in naloxone-induced withdrawal, the effect was greater in comparison to the spontaneous withdrawal. |
1999-10-21 |
2023-08-12 |
mouse |
| S Cho, A M Duchemin, N H Neff, M Hadjiconstantino. Tyrosine hydroxylase, aromatic L-amino acid decarboxylase and dopamine metabolism after chronic treatment with dopaminergic drugs. Brain research. vol 830. issue 2. 1999-08-11. PMID:10366680. |
at the same time interval, there was tolerance to the enhancing effects of haloperidol and sch 23390 on da metabolism. |
1999-08-11 |
2023-08-12 |
mouse |
| S Cho, A M Duchemin, N H Neff, M Hadjiconstantino. Tyrosine hydroxylase, aromatic L-amino acid decarboxylase and dopamine metabolism after chronic treatment with dopaminergic drugs. Brain research. vol 830. issue 2. 1999-08-11. PMID:10366680. |
the induction of aaad by haloperidol or sch 23990 did not appear to develop tolerance after chronic administration. |
1999-08-11 |
2023-08-12 |
mouse |
| H Moore, J Fadel, M Sarter, J P Brun. Role of accumbens and cortical dopamine receptors in the regulation of cortical acetylcholine release. Neuroscience. vol 88. issue 3. 1999-08-02. PMID:10363819. |
infusions of haloperidol and sulpiride significantly blocked fg 7142-stimulated acetylcholine efflux while sch 23390 did not. |
1999-08-02 |
2023-08-12 |
rat |
| X Shi, R Yin, D Dow-Edward. Chronic haloperidol alters dopamine receptors: effects of cocaine exposure during the preweaning period. European journal of pharmacology. vol 370. issue 3. 1999-07-16. PMID:10334498. |
for sch 23390 binding, most regions showed a significant interaction between haloperidol, sex and preweaning treatment group. |
1999-07-16 |
2023-08-12 |
rat |
| X Shi, R Yin, D Dow-Edward. Chronic haloperidol alters dopamine receptors: effects of cocaine exposure during the preweaning period. European journal of pharmacology. vol 370. issue 3. 1999-07-16. PMID:10334498. |
these data suggest that inhibition of the dopamine transporter during ontogeny produces long-term alterations in dopamine receptor regulation but that selective inhibitors of the dopamine transporter produced greater effects than cocaine on both raclopride and sch 23390 binding following chronic haloperidol injection. |
1999-07-16 |
2023-08-12 |
rat |
| K Huda, T L Salunga, S A Chowdhury, T Kawashima, K Matsunam. Dopaminergic modulation of transcallosal activity of cat motor cortical neurons. Neuroscience research. vol 33. issue 1. 1999-05-17. PMID:10096469. |
the effects of dopamine (da) and its antagonists on the transcallosal activity of pyramidal tract neurons (ptns) and non-ptns in the anesthetized cat motor cortex were studied with iontophoretic applications; dopamine, sch 23390 (d1 antagonist), sulpiride (d2 antagonist) and haloperidol. |
1999-05-17 |
2023-08-12 |
cat |
| K Huda, T L Salunga, S A Chowdhury, T Kawashima, K Matsunam. Dopaminergic modulation of transcallosal activity of cat motor cortical neurons. Neuroscience research. vol 33. issue 1. 1999-05-17. PMID:10096469. |
the number of spikes thus activated was counted for the control and test conditions after application of each drug: (1) dopamine application decreased the number of spikes evoked by transcallosal stimulation; (2) application of sch 23390, sulpiride and haloperidol restored these decreased spike numbers to the control level; (3) latency of neuronal response to transcallosal stimulation was not affected by the application of either da, sch 23390, sulpiride or haloperidol; and (4) there was no significant difference between ptns and non-ptns in the manner of response to da and its antagonist applications. |
1999-05-17 |
2023-08-12 |
cat |