Comparative effects of the dopaminergic agonists piribedil and bromocriptine in three different memory paradigms in rodents

被引:14
作者
Marighetto, A. [1 ]
Valerio, S. [1 ]
Philippin, J. N. [1 ]
Bertaina-Anglade, V. [2 ]
la Rochelle, C. Drieu [2 ]
Jaffard, R. [1 ]
Morain, P. [3 ]
机构
[1] Univ Bordeaux 1, CNRS UMR 5228, Ctr Neurosci Integrat & Cognit, F-33405 Talence, France
[2] Preclin Pharmacol Dept, Rennes, France
[3] Inst Rech Int Servier, F-92415 Courbevoie, France
关键词
spontaneous object recognition; relational/declarative memory; working memory; rat; mouse; aging;
D O I
10.1177/0269881107083836
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The potential memory-enhancing properties of two dopamine agonists currently used in patients with Parkinson's disease, piribedil (1, 10 mg/kg/day, subcutaneously) and bromocriptine (5 mg/kg/day, subcutaneously), were evaluated in three experiments. Although piribedil (10 mg/kg) and bromocriptine equally enhanced spontaneous object recognition in young adult rats (experiment A), only piribedil displayed beneficial effects against aging-related memory impairments in two radial-maze experiments in mice. First (experiment B), a two-stage paradigm of spatial discrimination was used to assess relational/declarative memory in aged mice; piribedil (1 and 10 mg/kg) selectively and significantly improved the performances of aged mice in the critical tests for relational/declarative memory, whereas bromocriptine had no effect. Second, in a novel working memory task (experiment C), vehicle- or bromocriptine-treated aged mice displayed, compared with (vehicle) younger controls, a severe and persistent deficit in short-term retention of successive arm-visits, performing close to chance whichever the retention interval. Performances of piribedil (10 mg/kg) group remarkably improved across testing-days and reached young adults' level. The restoration of specific mnemonic impairments, in aged mice, highlights the memory-enhancing properties of piribedil. The efficacy of this drug in treating cognitive impairment of Parkinson's disease should now be assessed in more specific models. This work was published in an abstract form: ECNP Abstracts, 2005 (P8060 & P8065).
引用
收藏
页码:511 / 521
页数:11
相关论文
共 53 条
[1]   The modulatory effects of dopamine D1 and D2 receptor function on object working memory in humans [J].
Bartholomeusz, CF ;
Box, G ;
Van Rooy, C ;
Nathan, PJ .
JOURNAL OF PSYCHOPHARMACOLOGY, 2003, 17 (01) :9-15
[2]   COGNITIVE FUNCTION IN PARKINSONS-DISEASE - FROM DESCRIPTION TO THEORY [J].
BROWN, RG ;
MARSDEN, CD .
TRENDS IN NEUROSCIENCES, 1990, 13 (01) :21-29
[3]   In vitro affinity of piribedil for dopamine D-3 receptor subtypes, an autoradiographic study [J].
Cagnotto, A ;
Parotti, L ;
Mennini, T .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 313 (1-2) :63-67
[4]   The Parkinson-control study: A 1-year randomized, double-blind trial comparing piribedil (150 mg/day) with bromocriptine (25 mg/day) in early combination with levodopa in Parkinson's disease [J].
Castro-Caldas, A ;
Delwaide, P ;
Jost, W ;
Merello, M ;
Williams, A ;
Lamberti, P ;
Aguilar, M ;
Del Signore, S ;
Cesaro, P .
MOVEMENT DISORDERS, 2006, 21 (04) :500-509
[5]   DIFFERENT MEMORY-SYSTEMS UNDERLYING ACQUISITION OF PROCEDURAL AND DECLARATIVE KNOWLEDGE [J].
COHEN, NJ ;
EICHENBAUM, H ;
DEACEDO, BS .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1985, 444 (MAY) :54-71
[6]   BEHAVIORAL EVIDENCE OF DOPAMINE RECEPTOR STIMULATION BY PIRIBEDIL (ET495) AND ITS METABOLITE S584 [J].
CREESE, I .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1974, 28 (01) :55-58
[7]   DIFFERENTIAL EFFECT OF SYSTEMIC ADMINISTRATION OF BROMOCRIPTINE AND L-DOPA ON THE RELEASE OF ACETYLCHOLINE FROM STRIATUM OF INTACT AND 6-OHDA-TREATED RATS [J].
DEBOER, P ;
ABERCROMBIE, ED ;
HEERINGA, M ;
WESTERINK, BHC .
BRAIN RESEARCH, 1993, 608 (02) :198-203
[8]   IMPAIRED EXTRA-DIMENSIONAL SHIFT PERFORMANCE IN MEDICATED AND UNMEDICATED PARKINSONS-DISEASE - EVIDENCE FOR A SPECIFIC ATTENTIONAL DYSFUNCTION [J].
DOWNES, JJ ;
ROBERTS, AC ;
SAHAKIAN, BJ ;
EVENDEN, JL ;
MORRIS, RG ;
ROBBINS, TW .
NEUROPSYCHOLOGIA, 1989, 27 (11-12) :1329-1343
[9]   Hippocampus: Cognitive processes and neural representations that underlie declarative memory [J].
Eichenbaum, H .
NEURON, 2004, 44 (01) :109-120
[10]   THE HIPPOCAMPUS - WHAT DOES IT DO [J].
EICHENBAUM, H ;
OTTO, T ;
COHEN, NJ .
BEHAVIORAL AND NEURAL BIOLOGY, 1992, 57 (01) :2-36