rdf:type |
|
lifeskim:mentions |
umls-concept:C0004083,
umls-concept:C0032659,
umls-concept:C0085228,
umls-concept:C0206529,
umls-concept:C0525045,
umls-concept:C0871261,
umls-concept:C0936012,
umls-concept:C1257890,
umls-concept:C1335671,
umls-concept:C1415306,
umls-concept:C1415307,
umls-concept:C1556094,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
|
pubmed:issue |
5
|
pubmed:dateCreated |
2009-7-1
|
pubmed:abstractText |
Several lines of evidence implicate abnormalities in glutamate neural transmission in the pathophysiology of mood disorders, including major depressive disorder (MDD) and bipolar disorder (BP). Preclinical antidepressant effects were also reported for group II metabotropic glutamate receptor (Group II mGluRs) antagonists show dose-dependent antidepressant-like effects in murine models of depression. Also, it has been suggested that abnormalities in the hypothalamic-pituitary-adrenal axis and serotonergic neural transmission are important mechanisms in the pathophysiology of mood disorders. Group II mGluRs play an important role in regulating the function of these mechanisms. From these results, it has been suggested that abnormalities in Group II mGluRs might be involved in the pathophysiology of mood disorders, including MDD) and BP, and may influence the clinical response to treatment with SSRIs in MDD. Therefore, we studied the association between Group II mGluR genes (GRM2 and GRM3) and mood disorders and the efficacy of fluvoxamine treatment in Japanese MDD patients.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
1878-4216
|
pubmed:author |
pubmed-author:IkedaMasashiM,
pubmed-author:InadaToshiyaT,
pubmed-author:IwataNakaoN,
pubmed-author:KawashimaKunihiroK,
pubmed-author:KinoshitaYokoY,
pubmed-author:KishiTaroT,
pubmed-author:KitajimaTsuyoshiT,
pubmed-author:OkochiTomoT,
pubmed-author:OkumuraTakenoriT,
pubmed-author:OzakiNorioN,
pubmed-author:TsunokaTomokoT,
pubmed-author:YamanouchiYoshioY
|
pubmed:issnType |
Electronic
|
pubmed:day |
1
|
pubmed:volume |
33
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
875-9
|
pubmed:meshHeading |
pubmed-meshheading:19386277-Adult,
pubmed-meshheading:19386277-Asian Continental Ancestry Group,
pubmed-meshheading:19386277-Case-Control Studies,
pubmed-meshheading:19386277-Female,
pubmed-meshheading:19386277-Fluvoxamine,
pubmed-meshheading:19386277-Gene Frequency,
pubmed-meshheading:19386277-Genome-Wide Association Study,
pubmed-meshheading:19386277-Genotype,
pubmed-meshheading:19386277-Haplotypes,
pubmed-meshheading:19386277-Humans,
pubmed-meshheading:19386277-Male,
pubmed-meshheading:19386277-Middle Aged,
pubmed-meshheading:19386277-Mood Disorders,
pubmed-meshheading:19386277-Receptors, Metabotropic Glutamate,
pubmed-meshheading:19386277-Young Adult
|
pubmed:year |
2009
|
pubmed:articleTitle |
Association analysis of group II metabotropic glutamate receptor genes (GRM2 and GRM3) with mood disorders and fluvoxamine response in a Japanese population.
|
pubmed:affiliation |
Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Aichi, 470-1192, Japan.
|
pubmed:publicationType |
Journal Article,
Comparative Study
|