Paradoxical locomotor behavior of dopamine D1 receptor transgenic mice

被引:28
作者
Dracheva, S [1 ]
Xu, M
Kelley, KA
Haroutunian, V
Holstein, GR
Haun, S
Silverstein, JH
Sealfon, SC
机构
[1] CUNY Mt Sinai Sch Med, Dr Arthur M Fishberg Res Ctr Neurobiol, New York, NY 10029 USA
[2] CUNY Mt Sinai Sch Med, Dept Psychiat, New York, NY 10029 USA
[3] CUNY Mt Sinai Sch Med, Dept Neurol, New York, NY 10029 USA
[4] CUNY Mt Sinai Sch Med, Dept Cell Biol Anat, New York, NY 10029 USA
[5] CUNY Mt Sinai Sch Med, Dept Anesthesiol, New York, NY 10029 USA
[6] Univ Cincinnati, Med Ctr, Dept Cell Biol Neurobiol & Anat, Cincinnati, OH 45267 USA
关键词
dopamine; D1; receptor; transgenic mice; Parkinson's disease; SKF81297; locomotion;
D O I
10.1006/exnr.1999.7037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The behavioral effects of augmenting dopamine D1 receptor expression in the brain were investigated in mice incorporating additional copies of the mouse D1 receptor gene. Two transgenic lines showed increases in brain D1 receptor binding sites, which were greatest in extrastriatal regions. The full D1 agonist SKF 81297, when administered systemically to control animals, stimulated a dose-dependent increase in locomotor activity. In contrast, in D1 receptor overexpressing transgenic mice, this drug caused a marked suppression of locomotion due to a decrease in the frequency of movement initiation Amphetamine and cocaine induced comparable locomotor activation in both transgenic animals and their control littermates. In the transgenic animals, D1 agonist-induced rearing and climbing behaviors were suppressed. However, on rotarod testing, the agonist-treated transgenic and control mice performed comparably, indicating that sensorimotor coordination was unaffected. These studies demonstrate that altering the levels of D1 receptor expression reverses the effects of D1 agonism on locomotor initiation and rearing. (C) 1999 Academic Press.
引用
收藏
页码:169 / 179
页数:11
相关论文
共 50 条
[41]   Dopamine D1 receptor modulation of set shifting: the role of stress exposure [J].
Nikiforuk, Agnieszka .
BEHAVIOURAL PHARMACOLOGY, 2012, 23 (04) :434-438
[42]   Dopamine D1 receptor activation maintains motor coordination and balance in rats [J].
Avila-Luna, Alberto ;
Galvez-Rosas, Arturo ;
Durand-Rivera, Alfredo ;
Ramos-Languren, Laura-Elisa ;
Rios, Camilo ;
Arias-Montano, Jose-Antonio ;
Bueno-Nava, Antonio .
METABOLIC BRAIN DISEASE, 2018, 33 (01) :99-105
[43]   The D1 family dopamine receptor, DopR, potentiates hind leg grooming behavior in Drosophila [J].
Pitmon, E. ;
Stephens, G. ;
Parkhurst, S. J. ;
Wolf, F. W. ;
Kehne, G. ;
Taylor, M. ;
Lebestky, T. .
GENES BRAIN AND BEHAVIOR, 2016, 15 (03) :327-334
[44]   Dihydrexidine -: The first full dopamine D1 receptor agonist [J].
Salmi, P ;
Isacson, R ;
Kull, B .
CNS DRUG REVIEWS, 2004, 10 (03) :230-242
[45]   D1 dopamine receptor signalling defect in spontaneous hypertension [J].
Felder, RA ;
Eisner, GM ;
Jose, PA .
ACTA PHYSIOLOGICA SCANDINAVICA, 2000, 168 (01) :245-250
[46]   Dopamine D1 receptor involvement in latent inhibition and overshadowing [J].
Nelson, Andrew J. D. ;
Thur, Karen E. ;
Cassaday, Helen J. .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2012, 15 (10) :1513-1523
[47]   Dopamine D1 and D2 receptor antagonism during development alters later behavior in zebrafish [J].
Oliveri, Anthony N. ;
Levin, Edward D. .
BEHAVIOURAL BRAIN RESEARCH, 2019, 356 :250-256
[48]   Intrastriatal dopamine D1 receptor agonist-mediated motor behavior is reduced by local neurokinin 1 receptor antagonism [J].
Krolewski, DM ;
Bishop, C ;
Walker, PD .
SYNAPSE, 2005, 57 (01) :1-7
[49]   Receptor affinities of dopamine D1 receptor-selective novel phenylbenzazepines [J].
Neumeyer, JL ;
Kula, NS ;
Bergman, J ;
Baldessarini, RJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2003, 474 (2-3) :137-140
[50]   Retinoic acid receptor antagonist LE540 attenuates wakefulness via the dopamine D1 receptor in mice [J].
Kitaoka, Kazuyoshi ;
Shimizu, Mika ;
Shimizu, Noriyuki ;
Chikahisa, Sachiko ;
Nakagomi, Madoka ;
Shudo, Koichi ;
Yoshizaki, Kazuo ;
Sei, Hiroyoshi .
BRAIN RESEARCH, 2011, 1423 :10-16