创伤性脑损伤
线粒体生物发生
免疫印迹
内分泌学
大脑皮层
激活剂(遗传学)
氧化应激
内科学
免疫染色
医学
脑损伤
线粒体
受体
免疫组织化学
生物
基因
生物化学
精神科
作者
Youwu Fan,Kangjian Sun,Lei Mao,Hong Liao,Handong Wang
出处
期刊:Brain Injury
[Informa]
日期:2012-05-29
卷期号:26 (10): 1267-1272
被引量:3
标识
DOI:10.3109/02699052.2012.672789
摘要
Peroxisome proliferator activated receptor γ co-activator-1α (PGC-1α) is a transcriptional co-activator that co-ordinately regulates genes required for mitochondrial biogenesis and is a key contributor to the up-regulation of antioxidant activities in response to oxidative stress. The expression pattern of PGC-1α after traumatic brain injury (TBI) has not been studied.Ninety male ICR mice (28-32 g) were randomly assigned to six groups: sham, 3, 6, 12, 24 and 48 hours after TBI. PGC-1α mRNA levels in mice brain were detected by reverse-transcriptase polymerase chain reaction and its nuclear protein levels by Western blot from 3-48 hours after TBI. PGC-1α distribution in the cerebral cortex after TBI was investigated by immunohistochemistry.The PGC-1α mRNA level significantly increased from 3 hours after TBI, peaked at 6 hours and gradually decreased from 12 to 48 hours. The nuclear PGC-1α protein level increased from 6 to 24 hours after TBI and decreased at 48 hours after TBI. Increased PGC-1α immunostaining was detected in the neurons of the cerebral cortex at 12 hours after TBI.PGC-1α may play an important role in the brain after TBI.
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