All Relations between dat and dopamine

Publication Sentence Publish Date Extraction Date Species
George R Uhl, Zhicheng Li. The top 20 dopamine transporter mutants: structure-function relationships and cocaine actions. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612139. our laboratory and others elucidated the primary amino acid sequences of the dopamine transporter (dat) by cloning its cdna and genomic sequences more than 12 years ago. 2004-07-20 2023-08-12 mouse
Beatriz A Roch. Stimulant and reinforcing effects of cocaine in monoamine transporter knockout mice. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612142. a large body of evidence supports the hypothesis that the reinforcing effects of cocaine depend on its ability to block the dopamine transporter (dat), thereby increasing dopamine extracellular concentration within the mesocorticolimbic system. 2004-07-20 2023-08-12 mouse
Phillip G Greco, Paul A Garri. In vivo interaction of cocaine with the dopamine transporter as measured by voltammetry. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612143. the goal of this review is to describe what the voltammetry technique tells us about cocaine-dopamine transporter (dat) interactions and the subsequent changes in extracellular dopamine levels in the brain. 2004-07-20 2023-08-12 Not clear
Kristopher M Kahlig, Aurelio Gall. Regulation of dopamine transporter function and plasma membrane expression by dopamine, amphetamine, and cocaine. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612146. pharmacological alterations in dopamine transporter (dat) function not only modulate dopamine reuptake, but they can induce rapid changes in the plasmalemmal expression of the transporter. 2004-07-20 2023-08-12 Not clear
Ole V Mortensen, Susan G Amar. Dynamic regulation of the dopamine transporter. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612147. in the mammalian central nervous system the dopamine transporter (dat) is the primary mechanism for clearance of dopamine from the extracellular space. 2004-07-20 2023-08-12 Not clear
Claus Juul Loland, Kristine Norgaard-Nielsen, Ulrik Gethe. Probing dopamine transporter structure and function by Zn2+-site engineering. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612149. the biogenic amine transporters belong to the class of na+/cl--coupled solute carriers and include the transporters for dopamine (dat), norepinephrine (net), and serotonin (sert). 2004-07-20 2023-08-12 human
Jean-Jacques Bonne. Interactions of cations and anions with the binding of uptake blockers to the dopamine transporter. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612150. uptake blockers and substrates are likely to recognise a common binding domain on the dopamine neuronal transporter (dat). 2004-07-20 2023-08-12 Not clear
Jean-Jacques Bonne. Interactions of cations and anions with the binding of uptake blockers to the dopamine transporter. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612150. several metals impair binding to the dat and/or the dopamine transport, but, under specific conditions, some of them, and chiefly zn2+, stimulate binding. 2004-07-20 2023-08-12 Not clear
Jean-Jacques Bonne. Interactions of cations and anions with the binding of uptake blockers to the dopamine transporter. European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612150. the dependence of the binding of dopamine on ions could be involved in its preferential inward transport and used by uptake blockers for their own binding to the dat. 2004-07-20 2023-08-12 Not clear
James O Schenk, Shannon E George, Paul Dietrich Schumache. What can be learned from studies of multisubstrate mechanisms of neuronal dopamine transport? European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612152. the dopamine transporter (dat) is a na+- and cl--dependent transporter and, with respect to its three apparent substrates, both partially random sequential as well as ordered mechanisms have been reported. 2004-07-20 2023-08-12 Not clear
James O Schenk, Shannon E George, Paul Dietrich Schumache. What can be learned from studies of multisubstrate mechanisms of neuronal dopamine transport? European journal of pharmacology. vol 479. issue 1-3. 2004-07-20. PMID:14612152. here we describe some of the features of dat, such as the coupling of energy to concentrate dopamine and the properties of slippage and leakage. 2004-07-20 2023-08-12 Not clear
Hans J C Berger, Alexander R Cools, Martin W I M Horstink, Wim J G Oyen, Elisabeth W M Verhoeven, Sieberen P van der Wer. Striatal dopamine and learning strategy-an (123)I-FP-CIT SPECT study. Neuropsychologia. vol 42. issue 8. 2004-07-19. PMID:15093146. the aim of this study was to assess the relation between striatal dopamine activity as revealed by single photon emission computed tomography (spect) with (123)i-fp-cit, a ligand for the dopamine transporter (dat), and type of learning strategy, as identified by the california verbal learning task (cvlt) in 19 patients with probable pd. 2004-07-19 2023-08-12 human
Hans J C Berger, Alexander R Cools, Martin W I M Horstink, Wim J G Oyen, Elisabeth W M Verhoeven, Sieberen P van der Wer. Striatal dopamine and learning strategy-an (123)I-FP-CIT SPECT study. Neuropsychologia. vol 42. issue 8. 2004-07-19. PMID:15093146. the results showed a robust inverse correlation between striatal dopamine dat binding and the externally guided, serial learning strategy: the lower the dat in caudate nucleus as well as in putamen, the more the patient group appeared to rely on externally structured learning. 2004-07-19 2023-08-12 human
Margaret E Gnegy, Habibeh Khoshbouei, Kelly A Berg, Jonathan A Javitch, William P Clarke, Minjia Zhang, Aurelio Gall. Intracellular Ca2+ regulates amphetamine-induced dopamine efflux and currents mediated by the human dopamine transporter. Molecular pharmacology. vol 66. issue 1. 2004-07-15. PMID:15213305. although it is clear that amphetamine-induced dopamine (da) release mediated by the dopamine transporter (dat) is integral to the behavioral actions of this psychostimulant, the mechanism of this release is not clear. 2004-07-15 2023-08-12 human
Margaret E Gnegy, Habibeh Khoshbouei, Kelly A Berg, Jonathan A Javitch, William P Clarke, Minjia Zhang, Aurelio Gall. Intracellular Ca2+ regulates amphetamine-induced dopamine efflux and currents mediated by the human dopamine transporter. Molecular pharmacology. vol 66. issue 1. 2004-07-15. PMID:15213305. these studies demonstrate that amphetamine-induced dat-mediated currents and substrate efflux require internal ca(2+) and that amphetamine can stimulate dopamine efflux by regulating cytoplasmic ca(2+) levels through its interaction with dat. 2004-07-15 2023-08-12 human
Elzbieta Lorenc-Koci, Lucyna Antkiewicz-Michaluk, Jadwiga Wardas, Małgorzata Zapała, Joanna Wierońsk. Effect of 1,2,3,4,-tetrahydroisoquinoline administration under conditions of CYP2D inhibition on dopamine metabolism, level of tyrosine hydroxylase protein and the binding of [3H]GBR 12,935 to dopamine transporter in the rat nigrostriatal, dopaminergic system. Brain research. vol 1009. issue 1-2. 2004-07-12. PMID:15120584. twice daily for 14 days) markedly decreased the level of tyrosine hydroxylase protein (th) in the str; however, this effect was not accompanied by reduction of dopamine (da) concentration and [(3)h]gbr 12,935 binding to dopamine transporter (dat). 2004-07-12 2023-08-12 rat
John G Nutt, Julie H Carter, Gary J Sexto. The dopamine transporter: importance in Parkinson's disease. Annals of neurology. vol 55. issue 6. 2004-07-12. PMID:15174010. the dopamine transporter (dat) may be the single most important determinant of extracellular dopamine concentrations. 2004-07-12 2023-08-12 Not clear
Santosh S Kulkarni, Peter Grundt, Theresa Kopajtic, Jonathan L Katz, Amy Hauck Newma. Structure-activity relationships at monoamine transporters for a series of N-substituted 3alpha-(bis[4-fluorophenyl]methoxy)tropanes: comparative molecular field analysis, synthesis, and pharmacological evaluation. Journal of medicinal chemistry. vol 47. issue 13. 2004-07-09. PMID:15189035. one of the most potent and dopamine transporter (dat) selective n-substituted benztropine analogues (n-(4-phenyl-n-butyl)-3alpha-(bis[4-fluorophenyl]methoxy)tropane, 1c) is devoid of cocaine-like behaviors in rodent models but is also highly lipophilic (clogd = 5.01), which compromises its water solubility and may adversely affect its pharmacokinetic properties. 2004-07-09 2023-08-12 rat
Santosh S Kulkarni, Peter Grundt, Theresa Kopajtic, Jonathan L Katz, Amy Hauck Newma. Structure-activity relationships at monoamine transporters for a series of N-substituted 3alpha-(bis[4-fluorophenyl]methoxy)tropanes: comparative molecular field analysis, synthesis, and pharmacological evaluation. Journal of medicinal chemistry. vol 47. issue 13. 2004-07-09. PMID:15189035. most of the analogues showed high dat affinity (12-50 nm), selectivity (10- to 120-fold), potent inhibition of dopamine uptake, and lower lipophilicities as predicted by clogd values. 2004-07-09 2023-08-12 rat
Peter C Meltzer, Mark McPhee, Bertha K Madra. Synthesis and biological activity of 2-carbomethoxy-3-catechol-8-azabicyclo[3.2.1]octanes. Bioorganic & medicinal chemistry letters. vol 13. issue 22. 2004-07-06. PMID:14592523. tropane analogues of cocaine, targeted to the dopamine transporter (dat), are a significant focus of drug design for cocaine addiction medications. 2004-07-06 2023-08-12 rat