Source:http://linkedlifedata.com/resource/pubmed/id/16256213
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-1-23
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pubmed:abstractText |
The serotonin 1A (5-HT(1A)) receptor is one of the best described receptor subtypes of the serotonergic system. Due to the complex distribution pattern, the pre- and postsynaptic localisation, the impact on various monoamines, as well as the influence on a wide range of physiological functions, the contribution of 5-HT(1A) receptors to behavioural outcomes is difficult to define. In this study, we present a new transgenic mouse model with a prominent over-expression of the 5-HT(1A) receptor in the outer cortical layers (I-III) and the dentate gyrus. Behavioural studies revealed a slight decrease in baseline motor activity of homozygous mice during the open field test. Moreover, core body temperature of male transgenic mice was significantly lower than that of wild-type mice. Pharmacological studies with the 5-HT(1A) receptor agonist 8-OH-DPAT (0.1-2.5 mg/kg, i.p.) revealed an exaggerated drug response in mutant mice. 8-OH-DPAT led to a drastic decrease in motor activity in the open field and elevated plus maze test. This significant effect on motor activity became more apparent by investigating the serotonergic syndrome induced by 8-OH-DPAT. Concentration as low as 0.5 mg/kg 8-OH-DPAT caused immobility in transgenic mice for 30 min, head weaving behaviour, and backward walking, whereas in wild-type animals, typical behaviours of the serotonin syndrome were first observed at concentrations of 1.5 mg/kg and more. In addition, the 8-OH-DPAT induced hypothermia was more pronounced in mutant mice than in wild-type animals. Therefore, these genetically modified mice represent a promising model for further investigations of the role of 5-HT(1A) receptors.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0166-4328
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:volume |
167
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
328-41
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:16256213-8-Hydroxy-2-(di-n-propylamino)tetralin,
pubmed-meshheading:16256213-Animals,
pubmed-meshheading:16256213-Cerebral Cortex,
pubmed-meshheading:16256213-Dentate Gyrus,
pubmed-meshheading:16256213-Dose-Response Relationship, Drug,
pubmed-meshheading:16256213-Exploratory Behavior,
pubmed-meshheading:16256213-Female,
pubmed-meshheading:16256213-Hypothermia,
pubmed-meshheading:16256213-Immobility Response, Tonic,
pubmed-meshheading:16256213-Male,
pubmed-meshheading:16256213-Mice,
pubmed-meshheading:16256213-Mice, Transgenic,
pubmed-meshheading:16256213-Motor Activity,
pubmed-meshheading:16256213-Receptor, Serotonin, 5-HT1A,
pubmed-meshheading:16256213-Serotonin Receptor Agonists,
pubmed-meshheading:16256213-Serotonin Syndrome
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pubmed:year |
2006
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pubmed:articleTitle |
Mice over-expressing the 5-HT(1A) receptor in cortex and dentate gyrus display exaggerated locomotor and hypothermic response to 8-OH-DPAT.
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pubmed:affiliation |
Institute of Pharmacology and Toxicology, School of Veterinary Medicine, Freie Universität Berlin, Koserstrasse 20, 14195 Berlin, Germany. bert.bettina@vetmed.fu-berlin.de
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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