All Relations between conditioned response and suprachiasmatic nucleus

Reference Sentence Publish Date Extraction Date Species
Tianyi Yang, Guang Yue, Yu Ge, Yue Zhang, Peng Xu, Youmei Wang, Bo Li, Bin D. SCH 23390 inhibits the acquisition of nitrous oxide-induced conditioned place preference and the changes in ERK phosphorylation expression in nucleus accumbens of mice. Neuroscience letters vol issue 2022 35525502 sch 23390 inhibits the acquisition of nitrous oxide-induced conditioned place preference and the changes in erk phosphorylation expression in nucleus accumbens of mice. 2022-05-07 2022-05-09 Not clear
L. Marrow, P. Overton, D. Clar. Disruption of conditioned reaction time performance by dopamine receptor antagonists in the rat. Behavioural pharmacology vol 4 issue 1 2019 11224167 the effects of the neuroleptics haloperidol, cis-flupenthixol and chlorpromazine, and the selective dopamine (da) receptor antagonists raclopride and sch 23390, were assessed in a conditioned reaction time task. 2019-11-20 2022-01-11 Not clear
D. Fontana, R.M. Post, S.R.B. Weiss, A. Per. The role of D1 and D2 dopamine receptors in the acquisition and expression of cocaine-induced conditioned increases in locomotor behavior. Behavioural pharmacology vol 4 issue 4 2019 11224206 however, pretreatment with raclopride or sch 23390 on day 2, prior to cocaine injections, did not eliminate the differences in behavior between the conditioned and non-conditioned groups. 2019-11-20 2022-01-11 Not clear
Anthony S Rauhu. Timing of SCH 23390 administration influences extinction of conditioned hyperactivity in mice. Behavioural pharmacology vol 27 issue 1 2016 26292185 timing of sch 23390 administration influences extinction of conditioned hyperactivity in mice. 2016-09-19 2022-01-12 Not clear
Anthony S Rauhu. Timing of SCH 23390 administration influences extinction of conditioned hyperactivity in mice. Behavioural pharmacology vol 27 issue 1 2016 26292185 thus, the present experiments determined the effect of a selective d1 receptor antagonist, sch 23390, on extinction of conditioned hyperactivity when sch 23390 was administered immediately after (memory reconsolidation; experiment 1) or before (memory retrieval; experiment 2) extinction sessions. 2016-09-19 2022-01-12 Not clear
Anthony S Rauhu. Timing of SCH 23390 administration influences extinction of conditioned hyperactivity in mice. Behavioural pharmacology vol 27 issue 1 2016 26292185 furthermore, sch 23390 (0.05\xe2\x80\x89mg/kg) blocked expression of conditioned hyperactivity, without nonspecifically impairing locomotor activity, when administered before the extinction session, but did not alter the rate of extinction when administered immediately following the sessions. 2016-09-19 2022-01-12 Not clear
Elizabeth Glenn Guy, Paul J Fletche. Responding for a conditioned reinforcer, and its enhancement by nicotine, is blocked by dopamine receptor antagonists and a 5-HT(2C) receptor agonist but not by a 5-HT(2A) receptor antagonist. Pharmacology, biochemistry, and behavior vol 125 issue 2015 25158104 to examine potential roles for dopamine (da) and serotonin (5-ht) receptors in this effect, separate groups of animals were used to assess the impact of administering the d1 receptor antagonist sch 23390, d2 receptor antagonist eticlopride, 5-ht2c receptor agonist ro 60-0175, or 5-ht2a receptor antagonist m100907 on nicotine-enhanced responding for conditioned reinforcement. 2015-07-28 2022-01-12 Not clear
Elizabeth Glenn Guy, Paul J Fletche. Responding for a conditioned reinforcer, and its enhancement by nicotine, is blocked by dopamine receptor antagonists and a 5-HT(2C) receptor agonist but not by a 5-HT(2A) receptor antagonist. Pharmacology, biochemistry, and behavior vol 125 issue 2015 25158104 sch 23390, eticlopride, and ro 60-0175 all reduced responding for conditioned reinforcement, and the ability of nicotine to enhance this effect. 2015-07-28 2022-01-12 Not clear
Emilio Dom\\xc3\\xadnguez-Salazar, Hishan F Naser, Javier Vel\\xc3\\xa1zquez-Moctezum. D1-like antagonist blocks conditioned place preference induced by ejaculation in male rats. Behavioural brain research vol 269 issue 2015 24768642 we show that a dose of sch 23390 (a specific dopamine d1-like receptor antagonist), which does not modify locomotion, blocks the conditioned place preference induced by ejaculation and the conditioned place preference induced by skf 38393 (d1-like agonist). 2015-01-15 2022-01-12 Not clear
Tamar T Kraft, Yakov Yakubov, Donald Huang, Gregory Fitzgerald, Vanessa Acosta, Elona Natanova, Khalid Touzani, Anthony Sclafani, Richard J Bodna. Dopamine D1 and opioid receptor antagonism effects on the acquisition and expression of fat-conditioned flavor preferences in BALB/c and SWR mice. Pharmacology, biochemistry, and behavior vol 110 issue 2014 23831446 in balb and swr mice, acquisition and expression of sucrose conditioned flavor preferences (cfp) are differentially affected by systemic da d1 (sch23390: sch) and opioid (naltrexone: ntx) antagonism. 2014-07-15 2022-01-12 Not clear
Tomek J Banasikowski, Richard J Beninge. Haloperidol conditioned catalepsy in rats: a possible role for D1-like receptors. The international journal of neuropsychopharmacology vol 15 issue 10 2013 22093169 when rats were injected and tested with saline following haloperidol sensitization they exhibited conditioned catalepsy in the test environment; conditioned catalepsy was not seen following sch 23390. 2013-07-15 2022-01-12 Not clear
Tomek J Banasikowski, Richard J Beninge. Haloperidol conditioned catalepsy in rats: a possible role for D1-like receptors. The international journal of neuropsychopharmacology vol 15 issue 10 2013 22093169 rats treated with 0.05 mg/kg sch 23390+0.25 mg/kg haloperidol showed catalepsy sensitization but failed to show conditioned catalepsy. 2013-07-15 2022-01-12 Not clear
Tomek J Banasikowski, Richard J Beninge. Haloperidol conditioned catalepsy in rats: a possible role for D1-like receptors. The international journal of neuropsychopharmacology vol 15 issue 10 2013 22093169 conversely, sch 23390 (0.05 mg/kg) given on the test day after sensitization to haloperidol (0.25 mg/kg) failed to block conditioned catalepsy. 2013-07-15 2022-01-12 Not clear
Mohammad-Hossein Esmaeili, Mojtaba Kermani, Asghar Parvishan, Abbas Haghparas. Role of D1/D2 dopamine receptors in the CA1 region of the rat hippocampus in the rewarding effects of morphine administered into the ventral tegmental area. Behavioural brain research vol 231 issue 1 2012 22426507 the current study assessed the ability of the selective d1 receptor antagonist sch 23390 and d2 receptor antagonist sulpiride administrated into the ca1 region of hippocampus (dorsal hippocampus) to alter the rewarding effects of intra-vta administration of morphine using the conditioned place preference (cpp). 2012-08-20 2022-01-12 Not clear
J A D Dela Cruz, D Icaza-Cukali, H Tayabali, C Sampson, V Galanopoulos, D Bamshad, K Touzani, A Sclafani, R J Bodna. Roles of dopamine D1 and D2 receptors in the acquisition and expression of fat-conditioned flavor preferences in rats. Neurobiology of learning and memory vol 97 issue 3 2012 22390857 systemic dopamine (da) d1 (sch23390: sch) and d2 (raclopride: rac), but not opioid antagonists blocked the acquisition and expression of flavor-flavor preferences conditioned by sugars. 2012-07-30 2022-01-12 Not clear
Sherry X Lu, Guy A Higgins, Robert A Hodgson, Lynn A Hyde, Robert A Del Vecchio, Donald H Guthrie, Tatiana Kazdoba, Martha F McCool, Cynthia A Morgan, Ana Bercovici, Ginny D Ho, Deen Tulshian, Eric M Parker, John C Hunter, Geoffrey B Vart. The anxiolytic-like profile of the nociceptin receptor agonist, endo-8-[bis(2-chlorophenyl)methyl]-3-phenyl-8-azabicyclo[3.2.1]octane-3-carboxamide (SCH 655842): comparison of efficacy and side effects across rodent species. European journal of pharmacology vol 661 issue 1-3 2011 21545797 specifically, sch 655842 was effective in rat conditioned lick suppression (3-10 mg/kg) and fear-potentiated startle (3-10 mg/kg) tests, a guinea pig pup vocalization test (1-3 mg/kg), as well as in mouse geller-seifter (30 mg/kg) and marble burying (30 mg/kg) tests. 2011-09-20 2022-01-12 Not clear
Sherry X Lu, Guy A Higgins, Robert A Hodgson, Lynn A Hyde, Robert A Del Vecchio, Donald H Guthrie, Tatiana Kazdoba, Martha F McCool, Cynthia A Morgan, Ana Bercovici, Ginny D Ho, Deen Tulshian, Eric M Parker, John C Hunter, Geoffrey B Vart. The anxiolytic-like profile of the nociceptin receptor agonist, endo-8-[bis(2-chlorophenyl)methyl]-3-phenyl-8-azabicyclo[3.2.1]octane-3-carboxamide (SCH 655842): comparison of efficacy and side effects across rodent species. European journal of pharmacology vol 661 issue 1-3 2011 21545797 the anxiolytic-like effect of sch 655842 in the conditioned lick suppression test was attenuated by the nop antagonist, j-113397. 2011-09-20 2022-01-12 Not clear
Cameron L Adams, Michael S Cowen, Jennifer L Short, Andrew J Lawrenc. Combined antagonism of glutamate mGlu5 and adenosine A2A receptors interact to regulate alcohol-seeking in rats. The international journal of neuropsychopharmacology vol 11 issue 2 2008 17517168 moreover, this combination of sch 58261 and mtep also prevented the conditioned reinstatement of alcohol-seeking elicited by the re-presentation of cues previously paired with alcohol availability. 2008-05-08 2022-01-12 Not clear
Ma\\xc5\\x82gorzata Filip, Ma\\xc5\\x82gorzata Frankowsk. Effects of GABA(B) receptor agents on cocaine priming, discrete contextual cue and food induced relapses. European journal of pharmacology vol 571 issue 2-3 2007 17610868 sch 50911 (3-10 mg/kg) dose-dependently attenuated responding on the previously cocaine-paired lever during both reinstatement conditions, with slightly greater efficacy at reducing conditioned cue reinstatement. 2007-10-25 2022-01-12 Not clear
Fl\\xc3\\xa1via Regina Cruz Dias, Robert J Carey, Marinete Pinheiro Carrer. Conditioned locomotion induced by unilateral intrastriatal administration of apomorphine: D(2) receptor activation is critical but not the expression of the unconditioned response. Brain research vol 1083 issue 1 2006 16530737 pretreatment with the d(1) antagonist sch 23390 also blocked the apomorphine-induced behavioral response during the induction phase but did not block the apomorphine conditioned response. 2006-07-03 2022-01-12 Not clear
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