| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Takeshi Inoue, Takeshi Izumi, Xiao Bai Li, Yuji Kitaichi, Shin Nakagawa, Tsukasa Koyam. Effect of a dopamine D1/5 receptor antagonist on haloperidol-induced inhibition of the acquisition of conditioned fear. European journal of pharmacology. vol 519. issue 3. 2005-10-25. PMID:16135362. |
rats were treated subcutaneously with haloperidol (3 mg/kg) combined with sch 23390 (0.03 mg/kg) and were given fear conditioning by 5 min footshocks in shock chambers 30 min after the injection. |
2005-10-25 |
2023-08-12 |
rat |
| Takeshi Inoue, Takeshi Izumi, Xiao Bai Li, Yuji Kitaichi, Shin Nakagawa, Tsukasa Koyam. Effect of a dopamine D1/5 receptor antagonist on haloperidol-induced inhibition of the acquisition of conditioned fear. European journal of pharmacology. vol 519. issue 3. 2005-10-25. PMID:16135362. |
sch 23390 combined with haloperidol inhibited the acquisition of conditioned freezing more than either drug alone did. |
2005-10-25 |
2023-08-12 |
rat |
| Monica Levy Andersen, Ligia Assumpção Papale, Débora Cristina Hipólide, José N Nobrega, Sergio Tufi. Involvement of dopamine receptors in cocaine-induced genital reflexes after paradoxical sleep deprivation. Behavioural brain research. vol 160. issue 1. 2005-07-05. PMID:15836899. |
separate groups of psd rats received saline, haloperidol (0.4, 0.8 or 1.6 mg/kg), sch 23390 (0.25, 0.5, 1 mg/kg) or sulpiride (50, 100, 200 mg/kg) 60 min prior to acute cocaine (7 mg/kg). |
2005-07-05 |
2023-08-12 |
rat |
| Monica Levy Andersen, Ligia Assumpção Papale, Débora Cristina Hipólide, José N Nobrega, Sergio Tufi. Involvement of dopamine receptors in cocaine-induced genital reflexes after paradoxical sleep deprivation. Behavioural brain research. vol 160. issue 1. 2005-07-05. PMID:15836899. |
this percentage was not significantly reduced by haloperidol at any dose, but was significantly reduced in rats pretreated with sch 23390 (1 mg/kg) or sulpiride (100 or 200 mg/kg). |
2005-07-05 |
2023-08-12 |
rat |
| Monica Levy Andersen, Ligia Assumpção Papale, Débora Cristina Hipólide, José N Nobrega, Sergio Tufi. Involvement of dopamine receptors in cocaine-induced genital reflexes after paradoxical sleep deprivation. Behavioural brain research. vol 160. issue 1. 2005-07-05. PMID:15836899. |
this effect was not affected by haloperidol at any dose, but was significantly reduced by all doses of sch 23390 and by the 200 mg/kg dose of sulpiride. |
2005-07-05 |
2023-08-12 |
rat |
| Marco Bortolato, Gian Nicola Aru, Mauro Fà, Roberto Frau, Marco Orrù, Paola Salis, Alberto Casti, Grant Christopher Luckey, Giampaolo Mereu, Gian Luigi Gess. Activation of D1, but not D2 receptors potentiates dizocilpine-mediated disruption of prepulse inhibition of the startle. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. vol 30. issue 3. 2005-04-21. PMID:15328529. |
furthermore, this effect was reversed by sch 23390, but not by haloperidol or clozapine. |
2005-04-21 |
2023-08-12 |
rat |
| Carmen Manzanedo, María A Aguilar, Marta Rodríguez-Arias, José Miñarr. Sensitization to the rewarding effects of morphine depends on dopamine. Neuroreport. vol 16. issue 2. 2005-04-14. PMID:15671878. |
the effects of pre-treatment with saline or morphine plus naloxone, cgs 10746b, haloperidol, sch 23390 and raclopride, on the place conditioning induced by 2 mg/kg morphine were evaluated. |
2005-04-14 |
2023-08-12 |
mouse |
| Carmen Manzanedo, María A Aguilar, Marta Rodríguez-Arias, José Miñarr. Sensitization to the rewarding effects of morphine depends on dopamine. Neuroreport. vol 16. issue 2. 2005-04-14. PMID:15671878. |
conversely, animals pre-treated with morphine plus naloxone, cgs 10746b, sch 23390, raclopride and the high dose of haloperidol did not acquire place preference. |
2005-04-14 |
2023-08-12 |
mouse |
| B Ribeiro Do Couto, M A Aguilar, C Manzanedo, M Rodríguez-Arias, J Miñarr. NMDA glutamate but not dopamine antagonists blocks drug-induced reinstatement of morphine place preference. Brain research bulletin. vol 64. issue 6. 2005-04-01. PMID:15639545. |
following extinction of a place preference induced by morphine (40 mg/kg), a non-contingent injection of the dopaminergic antagonists sch 23390 (0.125, 0.5 mg/kg), raclopride (0.3, 1.2 mg/kg), haloperidol (0.1, 0.2 mg/kg) and the dopamine (da) release inhibitor cgs 10746b (1, 10 mg/kg) or glutamatergic nmda antagonists memantine (10, 20, 40 mg/kg) and mk-801 (0.1, 0.2, 0.3 mg/kg) alone or with 10 mg/kg morphine was given. |
2005-04-01 |
2023-08-12 |
mouse |
| Renata C H Barros, Luiz G S Branco, Evelin C Cárni. Evidence for thermoregulation by dopamine D1 and D2 receptors in the anteroventral preoptic region during normoxia and hypoxia. Brain research. vol 1030. issue 2. 2005-03-08. PMID:15571666. |
thus, we predicted that injection of sch 23390 and haloperidol, d1 and partly d2 receptor antagonists, respectively, into the anteroventral preoptic region (avpo, the thermointegrative region of the cns) would lessen the hypoxia-induced anapyrexia. |
2005-03-08 |
2023-08-12 |
rat |
| Renata C H Barros, Luiz G S Branco, Evelin C Cárni. Evidence for thermoregulation by dopamine D1 and D2 receptors in the anteroventral preoptic region during normoxia and hypoxia. Brain research. vol 1030. issue 2. 2005-03-08. PMID:15571666. |
we measured tb of conscious wistar rats before and after injection of sch 23390 (50 and 100 ng/100 nl) or haloperidol (50 e 500 ng/100 nl) or their respective vehicles (saline and dmso 5%) into the avpo followed by 30 min of hypoxia (7% o2). |
2005-03-08 |
2023-08-12 |
rat |
| Renata C H Barros, Luiz G S Branco, Evelin C Cárni. Evidence for thermoregulation by dopamine D1 and D2 receptors in the anteroventral preoptic region during normoxia and hypoxia. Brain research. vol 1030. issue 2. 2005-03-08. PMID:15571666. |
vehicles and the lower doses of sch 23390 and haloperidol had no effect on tb during normoxia or hypoxia. |
2005-03-08 |
2023-08-12 |
rat |
| Renata C H Barros, Luiz G S Branco, Evelin C Cárni. Evidence for thermoregulation by dopamine D1 and D2 receptors in the anteroventral preoptic region during normoxia and hypoxia. Brain research. vol 1030. issue 2. 2005-03-08. PMID:15571666. |
the higher doses of sch 23390 and haloperidol attenuated (p<0.05) the drop in tb elicited by hypoxia. |
2005-03-08 |
2023-08-12 |
rat |
| Rui D S Prediger, Luciano C Batista, Edmar Miyoshi, Reinaldo N Takahash. Facilitation of short-term social memory by ethanol in rats is mediated by dopaminergic receptors. Behavioural brain research. vol 153. issue 1. 2004-09-27. PMID:15219716. |
the facilitatory effect of ethanol on social memory was inhibited by the pretreatment with reserpine and it was antagonized by the administration of haloperidol or sulpiride, but not by sch 23390. |
2004-09-27 |
2023-08-12 |
rat |
| Pattipati S Naidu, Amanpreet Singh, Shrinivas K Kulkarn. D2-dopamine receptor and alpha2-adrenoreceptor-mediated analgesic response of quercetin. Indian journal of experimental biology. vol 41. issue 12. 2004-09-23. PMID:15320492. |
prior treatment with haloperidol (1 mg/kg), d1/d2 receptor antagonist haloperidol, sulpiride (50 mg/kg), a selective d2 receptor antagonist, yohimbine (5 mg/kg), a alpha2-adrenoreceptor antagonist but not by sch 23390 a, selective d1 receptor antagonist blocked this response. |
2004-09-23 |
2023-08-12 |
Not clear |
| Emilia Díaz, María Silva, Anita Israe. Role of brain dopaminergic system in the adrenomedullin-induced diuresis and natriuresis. Pharmacological research. vol 48. issue 5. 2004-06-17. PMID:12967595. |
selective d(2) da receptor antagonism with haloperidol, sulpiride, and remoxipride; or with the d(1) da receptor antagonist, sch 23390, blunted the increase in urinary volume and sodium excretion induced by ivt-am. |
2004-06-17 |
2023-08-12 |
rat |
| George C Wagner, Nicole Avena, Taizo Kita, Toshikatsu Nakashima, Hans Fisher, Alycia K Hallada. Risperidone reduction of amphetamine-induced self-injurious behavior in mice. Neuropharmacology. vol 46. issue 5. 2004-06-15. PMID:14996547. |
the behavioral and neurochemical effects of high doses of amphetamine administered to balb/c mice were examined in the presence and absence of co-administered haloperidol (a d2 antagonist), sch 23390 (a d1 antagonist) and risperidone (a mixed 5-ht2/d2 antagonist). |
2004-06-15 |
2023-08-12 |
mouse |
| Cristina Colombo, Marco Cosentino, Franca Marino, Emanuela Rasini, Maria Ossola, Fabio Blandini, Anna Mangiagalli, Alberta Samuele, Marco Ferrari, Raffaella Bombelli, Sergio Lecchini, Giuseppe Nappi, Gianmario Frig. Dopaminergic modulation of apoptosis in human peripheral blood mononuclear cells: possible relevance for Parkinson's disease. Annals of the New York Academy of Sciences. vol 1010. 2004-06-15. PMID:15033811. |
da 1 x 310(-6) m was inhibited by the d1-like receptor antagonist sch 23390 1 x 310(-6) m, but not by the d2-like receptor antagonists domperidone 1 x 3 10(-6) m or haloperidol 1 x 3 10(-6) m, while the effect of da 5 x 3 10(-4) m was prevented by the antioxidants glutathione 5-10 mm or n-acetyl-l-cysteine 1-10 mm. |
2004-06-15 |
2023-08-12 |
human |
| Yurie Akimoto, Takahiro Horinouchi, Yoshio Tanaka, Katsuo Koik. The beta3-adrenoceptor-mediated relaxation induced by dopamine in guinea pig taenia caecum. Journal of smooth muscle research = Nihon Heikatsukin Gakkai kikanshi. vol 39. issue 3. 2004-06-02. PMID:14572171. |
atenolol (3 x 10(-7)-3 x 10(-4) m), butoxamine (10(-7)-10(-4) m), prazosin (10(-8)-10(-5) m), yohimbine (10(-8)-10(-5) m), sch 23390 (10(-8)-10(-5) m) and haloperidol (10(-8)-10(-5) m) had no effect on the potency of dopamine. |
2004-06-02 |
2023-08-12 |
Not clear |
| A Fredriksson, T Arche. Functional alteration by NMDA antagonist: effects of L-Dopa, neuroleptics drug and postnatal administration. Amino acids. vol 23. issue 1-3. 2004-02-26. PMID:12373526. |
in rats, mk-801 induced marked increases in locomotor activity and disruptions of circular swim maze acquisition that were to greater or lesser extents blocked or potentiated by neuroleptic compounds: sch 23390 (0.005 and 0.05 mg/kg) and clozapine (5.0 and 10.0 mg/kg) dose-dependently antagonised mk-801 (0.3 mg/kg) induced locomotor activity whereas raclopride (0.1 mg/kg) and haloperidol (0.1 mg/kg) attenuated it dose-specifically. |
2004-02-26 |
2023-08-12 |
mouse |