All Relations between Haloperidol and dopamine

Publication Sentence Publish Date Extraction Date Species
M Reimold, C Solbach, S Noda, J-E Schaefer, M Bartels, M Beneke, H-J Machulla, R Bares, T Glaser, H Wormstal. Occupancy of dopamine D(1), D (2) and serotonin (2A) receptors in schizophrenic patients treated with flupentixol in comparison with risperidone and haloperidol. Psychopharmacology. vol 190. issue 2. 2007-03-30. PMID:17111172. occupancy of dopamine d(1), d (2) and serotonin (2a) receptors in schizophrenic patients treated with flupentixol in comparison with risperidone and haloperidol. 2007-03-30 2023-08-12 Not clear
Philip Seema. Targeting the dopamine D2 receptor in schizophrenia. Expert opinion on therapeutic targets. vol 10. issue 4. 2007-03-13. PMID:16848689. of the various neurotransmitters, dopamine was the most potent in inhibiting the binding of [3h]haloperidol, indicating that the antipsychotic receptor was a dopamine receptor, now named the dopamine d2 receptor, a major targeting site in schizophrenia. 2007-03-13 2023-08-12 Not clear
Sandra Schäble, Gerd Poeggel, Katharina Braun, Michael Grus. Long-term consequences of early experience on adult avoidance learning in female rats: role of the dopaminergic system. Neurobiology of learning and memory. vol 87. issue 1. 2007-02-22. PMID:16938473. in addition, the pharmacological blockade of dopamine receptors during preweaning avoidance training via systemic application of haloperidol impaired preweaning avoidance performance in a dose-dependent manner. 2007-02-22 2023-08-12 rat
A Lazou, T Markou, M Zioga, E Vasara, A Efstathiou, C Gaitanak. Dopamine mimics the cardioprotective effect of ischemic preconditioning via activation of alpha1-adrenoceptors in the isolated rat heart. Physiological research. vol 55. issue 1. 2007-01-30. PMID:15857158. pretreatment with the mixed d1/d2 dopaminergic receptor antagonist haloperidol or the beta-adrenoceptor selective antagonist propranolol did not attenuate the protective effect of pharmacological preconditioning with 10 microm dopamine with respect to both functional recovery and infarct size reduction. 2007-01-30 2023-08-12 rat
Hyeon Soo Kim, Minseok Song, Sanatombi Yumkham, Jang Hyun Choi, Taehoon Lee, Joseph Kwon, Sung Jae Lee, Jong-In Kim, Kang-Woo Lee, Pyung-Lim Han, Seung Woo Shin, Ja-Hyun Baik, Yong Sik Kim, Sung Ho Ryu, Pann-Ghill Su. Identification of a new functional target of haloperidol metabolite: implications for a receptor-independent role of 3-(4-fluorobenzoyl) propionic acid. Journal of neurochemistry. vol 99. issue 2. 2007-01-08. PMID:17029599. haloperidol, a dopamine d2 receptor blocker, is a classical neuroleptic drug that elicits extrapyramidal symptoms. 2007-01-08 2023-08-12 mouse
Mahendra Bishnoi, Kanwaljit Chopra, Shrinivas K Kulkarn. Involvement of adenosinergic receptor system in an animal model of tardive dyskinesia and associated behavioural, biochemical and neurochemical changes. European journal of pharmacology. vol 552. issue 1-3. 2007-01-04. PMID:17064683. on chronic administration of haloperidol there was a decrease in dopamine and norepinephrine turnover which was dose-dependently reversed by treatment with adenosine or caffeine. 2007-01-04 2023-08-12 rat
A Fredriksson, T Arche. Subchronic administration of haloperidol influences the functional deficits of postnatal iron administration in mice. Neurotoxicity research. vol 10. issue 2. 2007-01-03. PMID:17062374. in the context of these and other observations, it is suggested that subchronic administration of haloperidol interacting with postnatal iron induces different expressions of dopamine neuron comorbidity underlying movement disorder. 2007-01-03 2023-08-12 mouse
Huma Saeedi, Gary Remington, Bruce K Christense. Impact of haloperidol, a dopamine D2 antagonist, on cognition and mood. Schizophrenia research. vol 85. issue 1-3. 2006-12-28. PMID:16679001. impact of haloperidol, a dopamine d2 antagonist, on cognition and mood. 2006-12-28 2023-08-12 human
Dineshree V Naiker, Stanley V Catts, Vibeke S Catts, Kuldip S Bedi, Lesley J Bryan-Lluk. Dose determination of haloperidol, risperidone and olanzapine using an in vivo dopamine D2-receptor occupancy method in the rat. European journal of pharmacology. vol 540. issue 1-3. 2006-12-11. PMID:16730699. dose determination of haloperidol, risperidone and olanzapine using an in vivo dopamine d2-receptor occupancy method in the rat. 2006-12-11 2023-08-12 rat
Dineshree V Naiker, Stanley V Catts, Vibeke S Catts, Kuldip S Bedi, Lesley J Bryan-Lluk. Dose determination of haloperidol, risperidone and olanzapine using an in vivo dopamine D2-receptor occupancy method in the rat. European journal of pharmacology. vol 540. issue 1-3. 2006-12-11. PMID:16730699. the purpose of the present study was to determine antipsychotic doses that achieve 80% striatal dopamine d2-receptor occupancy for haloperidol, risperidone and olanzapine in rats. 2006-12-11 2023-08-12 rat
Dineshree V Naiker, Stanley V Catts, Vibeke S Catts, Kuldip S Bedi, Lesley J Bryan-Lluk. Dose determination of haloperidol, risperidone and olanzapine using an in vivo dopamine D2-receptor occupancy method in the rat. European journal of pharmacology. vol 540. issue 1-3. 2006-12-11. PMID:16730699. the doses required to achieve dopamine d2-receptor occupancy of 80% in 11- and 24-week old rats were: haloperidol 0.25 mg/kg/day, risperidone 5 mg/kg/day and olanzapine 10 mg/kg/day. 2006-12-11 2023-08-12 rat
Ella H Sklan, Amit Berson, Klara R Birikh, Amos Gutnick, Or Shahar, Shai Shoham, Hermona Sore. Acetylcholinesterase modulates stress-induced motor responses through catalytic and noncatalytic properties. Biological psychiatry. vol 60. issue 7. 2006-11-07. PMID:16904653. more specifically, we induced stress-associated hypofunction of dopaminergic, mainly d2 dopamine receptor-mediated neurotransmission by haloperidol and explored stress induced hyperlocomotion and catalepsy, an extreme form of immobility, induced in mice with ache deficiencies. 2006-11-07 2023-08-12 mouse
C R Maxwell, Y Liang, M P Kelly, S J Kanes, T Abel, S J Siege. Mice expressing constitutively active Gsalpha exhibit stimulus encoding deficits similar to those observed in schizophrenia patients. Neuroscience. vol 141. issue 3. 2006-10-18. PMID:16750890. n40 deficits in transgenic animals were ameliorated with low dose haloperidol and reversed with higher dose, suggesting dopamine d2 receptor-linked gi activity contributes to the impairment. 2006-10-18 2023-08-12 mouse
Jeffrey B Eells, Jaime A Misler, Vera M Nikode. Reduced tyrosine hydroxylase and GTP cyclohydrolase mRNA expression, tyrosine hydroxylase activity, and associated neurochemical alterations in Nurr1-null heterozygous mice. Brain research bulletin. vol 70. issue 2. 2006-10-10. PMID:16782508. furthermore, dopamine levels in the striatum of +/- mice were significantly reduced after inhibition of dopamine synthesis or after haloperidol treatment but not under basal conditions while dopamine levels in the nucleus accumbens were reduced under basal conditions. 2006-10-10 2023-08-12 mouse
Ellen R A de Bruijn, Bernard G C Sabbe, Wouter Hulstijn, Gé S F Ruigt, Robbert J Verke. Effects of antipsychotic and antidepressant drugs on action monitoring in healthy volunteers. Brain research. vol 1105. issue 1. 2006-09-29. PMID:16499887. the attenuated erns after the dopamine antagonist haloperidol are in line with the presumed role of dopamine in action monitoring. 2006-09-29 2023-08-12 human
Tim Karl, Liesl Duffy, Elizabeth O'brien, Izuru Matsumoto, Irina Dedov. Behavioural effects of chronic haloperidol and risperidone treatment in rats. Behavioural brain research. vol 171. issue 2. 2006-09-25. PMID:16697060. the therapeutic properties of typical antipsychotic drugs (apds) such as haloperidol in schizophrenia treatment are mainly associated with their ability to block dopamine d2 receptors. 2006-09-25 2023-08-12 rat
S J Chrapusta, M F Ega. Poor evidence for depolarization block but uncoupling of nigral from striatal dopamine metabolism after chronic haloperidol treatment in the rat. Journal of neural transmission (Vienna, Austria : 1996). vol 113. issue 5. 2006-09-19. PMID:16082510. poor evidence for depolarization block but uncoupling of nigral from striatal dopamine metabolism after chronic haloperidol treatment in the rat. 2006-09-19 2023-08-12 rat
S J Chrapusta, M F Ega. Poor evidence for depolarization block but uncoupling of nigral from striatal dopamine metabolism after chronic haloperidol treatment in the rat. Journal of neural transmission (Vienna, Austria : 1996). vol 113. issue 5. 2006-09-19. PMID:16082510. chronic haloperidol treatment induces depolarization block in midbrain dopamine neuronal systems. 2006-09-19 2023-08-12 rat
S J Chrapusta, M F Ega. Poor evidence for depolarization block but uncoupling of nigral from striatal dopamine metabolism after chronic haloperidol treatment in the rat. Journal of neural transmission (Vienna, Austria : 1996). vol 113. issue 5. 2006-09-19. PMID:16082510. haloperidol pretreatment significantly modified haloperidol challenge effect on regional dopamine metabolite contents. 2006-09-19 2023-08-12 rat
S J Chrapusta, M F Ega. Poor evidence for depolarization block but uncoupling of nigral from striatal dopamine metabolism after chronic haloperidol treatment in the rat. Journal of neural transmission (Vienna, Austria : 1996). vol 113. issue 5. 2006-09-19. PMID:16082510. these results suggest that chronic haloperidol treatment uncouples somatodendritic dopamine turnover and release from those in the axon terminals of nigrostriatal dopamine neurons. 2006-09-19 2023-08-12 rat