Effect of ligustrazine on nNOS expression and neuranagenesis in adult rats after cerebral ischemia-reperfusion injury.
- Author:
Cun-fang QI
1
;
Yong LIU
;
Jian-shui ZHANG
;
Yu-mei TIAN
;
Xin-lin CHEN
;
Peng-bo ZHANG
;
Xin-li XIAO
;
Jun-feng ZHANG
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Anti-Inflammatory Agents, Non-Steroidal; pharmacology; Blotting, Western; Brain; blood supply; drug effects; enzymology; Brain Ischemia; complications; Cell Proliferation; drug effects; Cerebral Ventricles; blood supply; drug effects; pathology; Dentate Gyrus; blood supply; drug effects; pathology; Immunohistochemistry; Male; Nerve Regeneration; drug effects; Nitric Oxide Synthase Type I; biosynthesis; Pyrazines; pharmacology; Random Allocation; Rats; Rats, Sprague-Dawley; Reperfusion Injury; etiology; physiopathology
- From: Journal of Southern Medical University 2007;27(6):771-774
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo observe the effect of ligustrazine on cell proliferation in the subventricular zone (SVZ) and dentate gyrus (DG) and nNOS expression in rat brain after cerebral ischemia-reperfusion injury.
METHODSMale SD rats were randomly divided into normal control group, sham operation group, model group and ligustrazine treatment group. The latter two groups were further divided into 5 subgroups for observation at 1, 3, 7, 14 and 21 days after reperfusion following a 2-hour middle cerebral artery occlusion (MCAO). The cells in S phase were labeled with BrdU, and immunohistochemistry was employed to detect BrdU- and nNOS-positive cells. The numbers of BrdU-positive cells in the SVZ and DG were measured. The expression of nNOS was detected by Western blotting.
RESULTSnNOS expression increased significantly in the model group as compared to the sham operation group (P<0.05), and ligustrazine treatment significantly lowered the expression level in comparison with the model group (P<0.05). Compared with the model group, a significant increase in BrdU-positive cells occurred in the SVZ of rats 1 and 3 days after igustrazine treatment (P<0.05), along with an increase of DG BrdU-positive cells.
CONCLUSIONLigustrazine significantly restrains ischemia-reperfusion injury-induced nNOS activity enhancement and promotes cell proliferation in the SVZ and DG of adult rats after ischemia-reperfusion injury.
