Decreased mitochondrial function and increased brain inflammation in bipolar disorder and other neuropsychiatric diseases.
Decreased mitochondrial function and increased brain inflammation in bipolar disorder and other neuropsychiatric diseases.
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双相情感障碍和其他神经精神疾病中线粒体功能下降和脑部炎症增加。
DOI:
10.1097/jcp.0b013e318239c190
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发表时间:
2011
影响因子:
2.9
通讯作者:
P. Conti
中科院分区:
文献类型:
--
作者:
T. Theoharides;B. Zhang;P. Conti
Arecent review article by Konradi and coworkers 1 summarized the results of gene expression studies based on analysis of the entire mRNA pool (transcriptome) of brains from patients with bipolar disorder. The transcriptome differs from the genome because it can be shaped by environmental influences. The authors concluded that clusters of genes (a) for energy production were downregulated, (b) for immune responses were up-regulated, and (c) for oligodendrocyte function were mostly down-regulated (Fig. 1). They compared these general outcomes with similar available data from other authors for major depressive disorder and schizophrenia and concluded that there was significant overlap, making it impossible to identify a specific profile unique for bipolar disorder. Konradi and coworkers reviewed 7 published studies between 2003 and 2009 using brain material and 4 studies using peripheral tissue from patients with bipolar disorder. These studies did not all examine the same clusters. Only 3 of the 7 studies using brain tissue investigated ‘‘markers of energy function’’; of these, 2 reported significant decrease, whereas 1 study reported an increase. Only 3 of the 7 studies using brain tissue investigated expression of genes associated with immune response, and all 3 reported significant increase. Only 1 study investigated the expression of oligodendrocyte markers and found decreased expression of some but increased level of others. Four studies using peripheral tissues were reviewed; of these, 2 studies showed decreased expression of genes regulating energy production, and only 1 study investigated genes associated with immune responses and reported significantly increased expression. No particular gene was singled out for discussion. However, the authors proposed that the transcriptome changes observed may be the early stage of an autoimmune process that is more dramatic, but similar to changes in the neuro
影响因子:
2.9
作者:
T. Theoharides;Craig C. Weinkauf;P. Conti
通讯作者:
T. Theoharides;Craig C. Weinkauf;P. Conti