Effect of Butylphthalide Injection on Neural Protection in Focal Cerebral Ischemia-reperfusion Rats
10.3969/j.issn.1006-9771.2016.01.007
- VernacularTitle:丁苯酞注射液对局灶性脑缺血再灌注大鼠的脑保护作用及机制
- Author:
Xiuqin ZHAO
;
Wenjing MAO
;
Shiying LI
;
Jinxia ZHANG
;
Yonggui HE
;
Hong YU
;
Bin LIU
- Publication Type:Journal Article
- Keywords:
cerebral ischemia-reperfuson;
Butylphthalide;
apoptosis;
silent information regulation 2 homolog 1;
peroxisome prolifera-tor-activated receptorγcoactivator-1α
- From:
Chinese Journal of Rehabilitation Theory and Practice
2016;22(1):32-37
- CountryChina
- Language:Chinese
-
Abstract:
Objective To observe the neural protection of 3-n-butylphthalide (NBP) injection in focal cerebral ischemia-reperfusion rats. Methods 160 male Sprague-Dawley rats were randomly divided into sham group (n=10), ischemia-reperfusion group (IR group, n=50), high-dose NBP treatment group (high-dose group, n=50), middle-dose NBP treatment group (middle-dose group, n=25) and low-dose NBP treatment group (low-dose group, n=25). The later 4 groups were occluded the middle cerebral artery for 2 hours and reperfused. The sham group was sacrificed 24 hours after operation, and the other groups at 6, 12, 24, 48 and 72 hours after reperfusion, in which 5 of them were stained with TdT mediated dUTP Nick End Labeling (TUNEL) to observe the neuronal apoptosis, and immunohistochemistry to observe the expression of silent information regulation 2 homolog 1 (SIRT1) and peroxisome proliferator-activated receptorγcoactivator-1α(PGC-1α);the other 5 of sham group, IR group and high-dose group were observed with quantitative real-time PCR of SIRT1 and PGC-1α. Results Compared with the IR group, the number of apoptotic cells decreased and the SIRT1 and PGC-1αpositive cells increased in all NBP groups at each time (F>160.60, P<0.001), and it was the least of apoptotic cells and most of SIRT1 and PGC-1α positive cells in the high-dose group (P<0.05), while there was significant difference between the low-dose group and the middle-dose group, excluding 6 hours after reper-fusion (P<0.05). Compared with IR group, the expression of SIRT1 and PGC-1αmRNA increased in the high-dose group at each time (t>4.13, P<0.01). Conclusion NBP can protect brain from apoptosis in focal cerebral ischemia-reperfusion rats, which may relate to more ex-pression of SIRT1 and PGC-1α.
