All Relations between Haloperidol and dopaminergic

Publication Sentence Publish Date Extraction Date Species
Andrzej Dekundy, Malgorzata Pietraszek, Daniela Schaefer, M Angela Cenci, Wojciech Danys. Effects of group I metabotropic glutamate receptors blockade in experimental models of Parkinson's disease. Brain research bulletin. vol 69. issue 3. 2006-07-06. PMID:16564428. the present study was devoted to investigate the effects of the metabotropic glutamate receptor(mglur)5 antagonist [(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine (mtep) and the mglur1 antagonist, (3-ethyl-2-methyl-quinolin-6-yl)-(4-methoxy-cyclohexyl)-methanone methanesulfonate (emqmcm), in animal studies indicative of antiparkinsonian-like activity such as haloperidol-induced catalepsy, hypoactivity in open field following haloperidol, and rotation in rats with unilateral 6-hydroxydopamine(ohda)-induced lesions of the midbrain dopaminergic system (alone and in combination with l-dopa). 2006-07-06 2023-08-12 rat
Christopher J MacDonald, Warren H Mec. Differential effects of clozapine and haloperidol on interval timing in the supraseconds range. Psychopharmacology. vol 182. issue 2. 2006-01-18. PMID:16001114. these results support the proposal that typical antipsychotic drugs such as haloperidol and atypical antipsychotic drugs such as clozapine exert differential effects on dopaminergic, serotonergic, and glutamatergic systems within the cortex and striatum, two brain regions shown to be crucial for interval timing. 2006-01-18 2023-08-12 rat
C L Parish, J Nunan, D I Finkelstein, F N McNamara, J Y Wong, J L Waddington, R M Brown, A J Lawrence, M K Horne, J Drag. Mice lacking the alpha4 nicotinic receptor subunit fail to modulate dopaminergic neuronal arbors and possess impaired dopamine transporter function. Molecular pharmacology. vol 68. issue 5. 2005-11-28. PMID:16077034. given the known effects of nachrs on dopaminergic neurotransmission, we assessed the ability of the alpha4 nachr subunit to regulate arbor size of dopaminergic neurons by comparing responses of wild-type and alpha4 nachr subunit knockout [alpha4(-/-)] mice to long-term exposure to cocaine, amphetamine, nicotine, and haloperidol, and after substantia nigra neurotoxic lesioning. 2005-11-28 2023-08-12 mouse
E A Del Bel, F S Guimarães, M Bermúdez-Echeverry, M Z Gomes, A Schiaveto-de-souza, F E Padovan-Neto, V Tumas, A P Barion-Cavalcanti, M Lazzarini, L P Nucci-da-Silva, D de Paula-Souz. Role of nitric oxide on motor behavior. Cellular and molecular neurobiology. vol 25. issue 2. 2005-09-01. PMID:16047547. considering these results we suggest that (i) no may modulate motor behavior, probably by interfering with dopaminergic, serotonergic, and cholinergic neurotransmission in the striatum; (ii) subchronic no synthesis inhibition induces plastic changes in no-producing neurons in brain areas related to motor control and causes cross-tolerance to the cataleptic effect of haloperidol, raising the possibility that such treatments could decrease motor side effects associated with antipsychotic medications. 2005-09-01 2023-08-12 mouse
Johan P Rung, Arvid Carlsson, Katarina Rydén Markinhuhta, Maria L Carlsso. The dopaminergic stabilizers (-)-OSU6162 and ACR16 reverse (+)-MK-801-induced social withdrawal in rats. Progress in neuro-psychopharmacology & biological psychiatry. vol 29. issue 5. 2005-08-26. PMID:15913873. in this study we aimed to evaluate the dopaminergic stabilizers (-)-osu6162 and acr16, compared to haloperidol and clozapine, in a rat model for schizophrenia, focusing on (+)-mk-801 induced social withdrawal. 2005-08-26 2023-08-12 rat
Tomohisa Mori, Shinobu Ito, Minoru Narita, Tsutomu Suzuki, Toshiko Sawaguch. Combined effects of psychostimulants and morphine on locomotor activity in mice. Journal of pharmacological sciences. vol 96. issue 4. 2005-04-28. PMID:15599100. it is well known that psychostimulants- and opioids-induced hyperlocomotion is mediated by the activation of the dopaminergic system, however, haloperidol (a dopamine receptor antagonist) and u50,488h (which attenuates dopamine release from nerve terminals) significantly increased the effects of methamphetamine and morphine on the locomotor activity. 2005-04-28 2023-08-12 mouse
Hidekazu Kawashima, Yasuhiko Iida, Youji Kitamura, Hideo Saj. Binding of 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]pyridinium ion (HPP+), a metabolite of haloperidol, to synthetic melanin: implications for the dopaminergic neurotoxicity of HPP+. Neurotoxicity research. vol 6. issue 7-8. 2005-04-08. PMID:15639785. binding of 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]pyridinium ion (hpp+), a metabolite of haloperidol, to synthetic melanin: implications for the dopaminergic neurotoxicity of hpp+. 2005-04-08 2023-08-12 rat
Hidekazu Kawashima, Yasuhiko Iida, Youji Kitamura, Hideo Saj. Binding of 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]pyridinium ion (HPP+), a metabolite of haloperidol, to synthetic melanin: implications for the dopaminergic neurotoxicity of HPP+. Neurotoxicity research. vol 6. issue 7-8. 2005-04-08. PMID:15639785. the toxicity of 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]pyridinium ion (hpp+), a metabolite of haloperidol, toward dopaminergic neurons was investigated. 2005-04-08 2023-08-12 rat
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
A Gepdiremen, N Aydin, Z Halici, O S Ahin, B Unal, M D Aydin, K Bakuridz. Chronic treatment of haloperidol causes vasoconstriction on basilar arteries of rats, dose dependently. Pharmacological research. vol 50. issue 6. 2005-03-23. PMID:15501694. haloperidol is a widely used antipsychotic drug, which exerts its effects via antagonizing the dopaminergic d2 receptors. 2005-03-23 2023-08-12 rat
Iluminada Corripio, Ana M Catafau, Víctor Perez, Dolors Puigdemont, Esther Mena, Yolanda Aguilar, Ignasi Carrió, Enric Alvare. Striatal dopaminergic D2 receptor occupancy and clinical efficacy in psychosis exacerbation: a 123I-IBZM study with ziprasidone and haloperidol. Progress in neuro-psychopharmacology & biological psychiatry. vol 29. issue 1. 2005-02-15. PMID:15610950. striatal dopaminergic d2 receptor occupancy and clinical efficacy in psychosis exacerbation: a 123i-ibzm study with ziprasidone and haloperidol. 2005-02-15 2023-08-12 Not clear
Iluminada Corripio, Ana M Catafau, Víctor Perez, Dolors Puigdemont, Esther Mena, Yolanda Aguilar, Ignasi Carrió, Enric Alvare. Striatal dopaminergic D2 receptor occupancy and clinical efficacy in psychosis exacerbation: a 123I-IBZM study with ziprasidone and haloperidol. Progress in neuro-psychopharmacology & biological psychiatry. vol 29. issue 1. 2005-02-15. PMID:15610950. the aim of this study was to compare striatal dopaminergic d2 receptor occupancy (d2 ro) induced by ziprasidone and haloperidol and its relationship with clinical response and extrapyramidal side effects (eps) in patients with acute psychosis exacerbation. 2005-02-15 2023-08-12 Not clear
Matteo Marti, Flora Mela, Remo Guerrini, Girolamo Calò, Clementina Bianchi, Michele Morar. Blockade of nociceptin/orphanin FQ transmission in rat substantia nigra reverses haloperidol-induced akinesia and normalizes nigral glutamate release. Journal of neurochemistry. vol 91. issue 6. 2005-01-21. PMID:15584926. to investigate whether such motor-stimulating action was dependent on functional dopaminergic transmission, the selective nop receptor peptide antagonist [nphe1,arg14,lys15]n/ofq-nh2 (ufp-101) was microinjected into the substantia nigra reticulata of rats made cataleptic by systemic haloperidol administration. 2005-01-21 2023-08-12 rat
Ingmar H A Franken, Vincent M Hendriks, Cornelis J Stam, Wim Van den Brin. A role for dopamine in the processing of drug cues in heroin dependent patients. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. vol 14. issue 6. 2005-01-13. PMID:15589390. the present study tests the hypothesis that enhanced attention for heroin cues is mediated by the dopaminergic system using haloperidol as dopamine antagonist. 2005-01-13 2023-08-12 Not clear
Bob Oranje, René S Kahn, Chantal Kemner, Marinus N Verbate. Modulating sensorimotor gating in healthy volunteers: the effects of desipramine and haloperidol. Psychiatry research. vol 127. issue 3. 2004-12-14. PMID:15296819. both desipramine and haloperidol reduced ppi, which suggests that an enhanced noradrenergic activity and a reduced dopaminergic activity lead to a reduction in sensorimotor gating. 2004-12-14 2023-08-12 human
Petra Dirks, Silke Tieding, Ilka Schneider, Jörg Mey, Reto Weile. Characterization of retinoic acid neuromodulation in the carp retina. Journal of neuroscience research. vol 78. issue 2. 2004-11-15. PMID:15378613. the action of at-ra, however, seems independent of the dopaminergic system, known for its light-signaling role in the retina, because at-ra effects on spinule formation persisted in retina depleted of dopaminergic neurons or in the presence of haloperidol. 2004-11-15 2023-08-12 Not clear
Il-Woong Seol, Na Youn Kuo, Kyeong Man Ki. Effects of dopaminergic drugs on the mast cell degranulation and nitric oxide generation in RAW 264.7 cells. Archives of pharmacal research. vol 27. issue 1. 2004-11-02. PMID:14969346. among the dopaminergic agonists and antagonists tested, bromocriptine, 7-oh-dpat, haloperidol, and clozapine showed potent inhibitions of mast cell degranualtion (ic50 value, 5 microm). 2004-11-02 2023-08-12 Not clear
Kerstin Håkansson, Laura Pozzi, Alessandro Usiello, John Haycock, Emiliana Borrelli, Gilberto Fison. Regulation of striatal tyrosine hydroxylase phosphorylation by acute and chronic haloperidol. The European journal of neuroscience. vol 20. issue 4. 2004-10-14. PMID:15305880. according to this model, haloperidol increases th activity via blockade of dopamine d2 receptors, disinhibition of dopaminergic projection neurons and erk1/2-dependent phosphorylation of th at ser31 and ser40. 2004-10-14 2023-08-12 mouse
Giorgio Marchese, Francesco Bartholini, Stefania Ruiu, Paola Casti, Gian Luca Casu, Luca Pan. Ritanserin counteracts both rat vacuous chewing movements and nigro-striatal tyrosine hydroxylase-immunostaining alterations induced by haloperidol. European journal of pharmacology. vol 483. issue 1. 2004-09-07. PMID:14709327. furthermore, ritanserin prevented the reduction of striatal tyrosine hydroxylase-immunostaining and the shrinkage of nigral dopaminergic cell bodies induced by haloperidol. 2004-09-07 2023-08-12 rat
Giorgio Marchese, Francesco Bartholini, Stefania Ruiu, Paola Casti, Gian Luca Casu, Luca Pan. Ritanserin counteracts both rat vacuous chewing movements and nigro-striatal tyrosine hydroxylase-immunostaining alterations induced by haloperidol. European journal of pharmacology. vol 483. issue 1. 2004-09-07. PMID:14709327. the present results indicate that ritanserin may possess protective properties on both dopaminergic nigro-striatal neuron alterations and vacuous chewing movements induced by haloperidol, and provide further evidence indicating a possible association between these two haloperidol-induced effects. 2004-09-07 2023-08-12 rat