Source:http://linkedlifedata.com/resource/pubmed/id/19578995
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2010-3-23
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pubmed:abstractText |
Parkinson's disease is the second most common neurodegenerative disorder and remains incurable. Many potential compensatory mechanisms have now been proposed; these are both dopaminergic, focused on enhancing effects or exposure to existing dopamine, and non-dopaminergic, being focused on reducing activity of the indirect striatal output pathway. In the present study, the effects of serotonin, gamma-aminobutyric acid, and bone marrow cell supplementation intranigrally to the substantia nigra on unilateral 6-hydroxydopamine-infused rats were analyzed individually. Dopaminergic binding parameters were done by Scatchard analysis of dopamine D(1) receptor-binding assay using [(3)H]SCH 23390. In the corpus striatum, 6-hydroxydopamine-infused rats showed a significant decrease in B (max) (P < 0.001), and in cerebral cortex, they showed a significant increase in B (max) (P < 0.001) compared to control. Real-time polymerase chain reaction amplification of dopamine D(1) was downregulated (P < 0.001) in the corpus striatum of 6-hydroxydopamine-infused rats compared to control, whereas in the cerebral cortex, it showed a significant upregulation (P < 0.001). Behavioral studies were carried out to confirm the biochemical and molecular studies. Serotonin and gamma-aminobutyric acid supplementation reversed these changes to control. The bone marrow cell-treated group of our studies does not show much significant change as compared to the serotonin and gamma-aminobutyric acid-supplemented groups. The alterations in dopamine D(1) receptor-binding parameters and gene expression during Parkinson's model were reversed by serotonin and gamma-aminobutyric acid supplementation in our experiments, which has clinical significance in the management of the 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/Adrenergic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidopamine,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D1,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/gamma-Aminobutyric Acid
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1559-1166
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
41
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1-11
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pubmed:meshHeading |
pubmed-meshheading:19578995-Adrenergic Agents,
pubmed-meshheading:19578995-Animals,
pubmed-meshheading:19578995-Bone Marrow Transplantation,
pubmed-meshheading:19578995-Brain,
pubmed-meshheading:19578995-Dopamine,
pubmed-meshheading:19578995-Male,
pubmed-meshheading:19578995-Oxidopamine,
pubmed-meshheading:19578995-Parkinsonian Disorders,
pubmed-meshheading:19578995-Radioligand Assay,
pubmed-meshheading:19578995-Rats,
pubmed-meshheading:19578995-Rats, Wistar,
pubmed-meshheading:19578995-Receptors, Dopamine D1,
pubmed-meshheading:19578995-Serotonin,
pubmed-meshheading:19578995-gamma-Aminobutyric Acid
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pubmed:year |
2010
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pubmed:articleTitle |
Dopamine D1 receptor gene expression studies in unilateral 6-hydroxydopamine-lesioned Parkinson's rat: effect of 5-HT, GABA, and bone marrow cell supplementation.
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pubmed:affiliation |
Molecular Neurobiology and Cell Biology Unit, Centre for Neuroscience, Department of Biotechnology, Cochin University of Science and Technology, Kochi, 682 022, Kerala, India.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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