Source:http://linkedlifedata.com/resource/pubmed/id/19410634
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rdf:type | |
lifeskim:mentions |
umls-concept:C0026336,
umls-concept:C0027882,
umls-concept:C0030567,
umls-concept:C0034693,
umls-concept:C0034721,
umls-concept:C0162783,
umls-concept:C0205098,
umls-concept:C0441655,
umls-concept:C0597357,
umls-concept:C0871261,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1948023,
umls-concept:C2911692
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pubmed:issue |
4
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pubmed:dateCreated |
2009-8-7
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pubmed:abstractText |
The changes in the firing rate and firing pattern of pyramidal neurons in medial prefrontal cortex (mPFC) and the effects of selective 5-hydroxytryptamine-(1A) (5-HT(1A)) receptor agonist (R)-(+)-8-hydroxy-2-(dipropylamino)tetralin hydrobromide (8-OH-DPAT) and antagonist N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-2-pyridylcyclohexane carboxamide maleate salt (WAY-100635) on the firing activity of the neurons were studied in sham-lesioned rats and rats with 6-hydroxydopamine lesions of the substantia nigra pars compacta (SNc). The lesion of the SNc increased the firing rate of pyramidal neurons significantly compared to sham-lesioned rats, and the firing pattern of these neurons also changed significantly towards a more burst-firing. The systemic administration of 8-OH-DPAT at doses in the range of 0.5-128 microg/kg showed an excitatory-inhibitory effect on the firing rate of pyramidal neurons in mPFC of sham-lesioned rats. At lower doses, 0.5-32 microg/kg, it evoked excitation of the neurons, and at a high dose, i.e. 128 microg/kg, inhibited the activity of the neurons. In contrast to sham-lesioned rats, 8-OH-DPAT, at the same doses, showed no excitatory effect in the lesioned rats although the inhibitory phase of the effect of 8-OH-DPAT on the firing rate of pyramidal neurons in mPFC was still present. Furthermore, the local application of 8-OH-DPAT, 5 microg, in mPFC inhibited the firing rate of pyramidal neurons in sham-lesioned rats, while having no effect on firing rate in the lesioned rats. The excitatory or inhibitory effects of 8-OH-DPAT were reversed by WAY-100635, indicating that these effects are mediated by 5-HT(1A) receptor. Altogether, these results indicate that the lesion of the SNc leads to hyperactivity of pyramidal neurons in mPFC and the abnormality of response of these neurons to 5-HT(1A) receptor stimulation, suggesting that mPFC may be involved in the pathophysiology of the psychiatric disturbance of Parkinson's disease.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/8-Hydroxy-2-(di-n-propylamino)tetral...,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidopamine,
http://linkedlifedata.com/resource/pubmed/chemical/Piperazines,
http://linkedlifedata.com/resource/pubmed/chemical/Pyridines,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin 5-HT1 Receptor Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/WAY 100635
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1873-7544
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
162
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1091-100
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:19410634-8-Hydroxy-2-(di-n-propylamino)tetralin,
pubmed-meshheading:19410634-Action Potentials,
pubmed-meshheading:19410634-Animals,
pubmed-meshheading:19410634-Cell Count,
pubmed-meshheading:19410634-Male,
pubmed-meshheading:19410634-Oxidopamine,
pubmed-meshheading:19410634-Parkinson Disease, Secondary,
pubmed-meshheading:19410634-Piperazines,
pubmed-meshheading:19410634-Prefrontal Cortex,
pubmed-meshheading:19410634-Pyramidal Cells,
pubmed-meshheading:19410634-Pyridines,
pubmed-meshheading:19410634-Rats,
pubmed-meshheading:19410634-Rats, Sprague-Dawley,
pubmed-meshheading:19410634-Serotonin 5-HT1 Receptor Agonists
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pubmed:year |
2009
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pubmed:articleTitle |
The firing activity of pyramidal neurons in medial prefrontal cortex and their response to 5-hydroxytryptamine-1A receptor stimulation in a rat model of Parkinson's disease.
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pubmed:affiliation |
Department of Physiology and Pathophysiology, School of Medicine, Xi'an Jiaotong University, Yan Ta Xi Lu 76, Xi'an 710061, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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