Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-7-21
pubmed:abstractText
The activation of alpha2-adrenoceptors has been reported to impair memory functions in both rats and humans. The alpha2-adrenoceptor subtype responsible for this detrimental effect is still unknown. The effect of the alpha2-agonists clonidine and guanabenz on memory processes, in dependence to the time of administration, was evaluated in the mouse passive avoidance test. Clonidine (0.02-0.2 mg kg(-1) i.p.) and guanabenz (0.1-0.3 mg kg(-1) i.p.) induced amnesia in a dose-dependent manner. From time-course experiments emerged that the impairment of memory function was detectable only when clonidine and guanabenz were administered 60 min before or immediately after the training test, respectively. This detrimental effect was prevented by pretreatment with the alpha2-antagonist yohimbine (1-3 mg kg(-1) i.p.) and by the alpha2A-antagonist BRL-44408 (0.3-1 mg kg(-1) i.p.). By contrast, the alpha(2B,C) antagonists ARC-239 (10 mg kg(-1) i.p.) and prazosin (1 mg kg(-1) i.p.) did not revert the amnesia induced by both clonidine and guanabenz. At the highest effective doses, clonidine and guanabenz were devoid of behavioral side-effects as well as maintained unaltered the motor coordination, as revealed by the rota-rod test. Furthermore, none of the compounds used modified the spontaneous motility as indicated by the Animex apparatus. These results indicate that clonidine and guanabenz impaired memory processes in a mouse passive avoidance paradigm through the selective activation of the alpha2A-adrenoceptor subtype.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/ADRA2A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Adra2a protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Adrenergic alpha-2 Receptor Agonists, http://linkedlifedata.com/resource/pubmed/chemical/Adrenergic alpha-2 Receptor..., http://linkedlifedata.com/resource/pubmed/chemical/BRL 44408, http://linkedlifedata.com/resource/pubmed/chemical/Clonidine, http://linkedlifedata.com/resource/pubmed/chemical/Guanabenz, http://linkedlifedata.com/resource/pubmed/chemical/Imidazoles, http://linkedlifedata.com/resource/pubmed/chemical/Indoles, http://linkedlifedata.com/resource/pubmed/chemical/Isoindoles, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Adrenergic, alpha-2, http://linkedlifedata.com/resource/pubmed/chemical/Yohimbine
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0166-4328
pubmed:author
pubmed:issnType
Print
pubmed:day
31
pubmed:volume
153
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
409-17
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:15265636-Adrenergic alpha-2 Receptor Agonists, pubmed-meshheading:15265636-Adrenergic alpha-2 Receptor Antagonists, pubmed-meshheading:15265636-Animals, pubmed-meshheading:15265636-Avoidance Learning, pubmed-meshheading:15265636-Brain, pubmed-meshheading:15265636-Clonidine, pubmed-meshheading:15265636-Dose-Response Relationship, Drug, pubmed-meshheading:15265636-Electroshock, pubmed-meshheading:15265636-Fear, pubmed-meshheading:15265636-Guanabenz, pubmed-meshheading:15265636-Imidazoles, pubmed-meshheading:15265636-Indoles, pubmed-meshheading:15265636-Injections, Intraperitoneal, pubmed-meshheading:15265636-Isoindoles, pubmed-meshheading:15265636-Male, pubmed-meshheading:15265636-Mental Recall, pubmed-meshheading:15265636-Mice, pubmed-meshheading:15265636-Motor Activity, pubmed-meshheading:15265636-Motor Skills, pubmed-meshheading:15265636-Reaction Time, pubmed-meshheading:15265636-Receptors, Adrenergic, alpha-2, pubmed-meshheading:15265636-Yohimbine
pubmed:year
2004
pubmed:articleTitle
Alpha-2 agonist-induced memory impairment is mediated by the alpha-2A-adrenoceptor subtype.
pubmed:affiliation
Department of Preclinical and Clinical Pharmacology, Viale G. Pieraccini 6, I-50139 Florence, Italy.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't