THE EXPRESSION OF NOS IN THE APOPTOSIS OF NEURONS FOLLOWING HYPOXIA/REOXYGENATION AND THE PROTECTIVE EFFECT OF EGB
- VernacularTitle:一氧化氮合酶与缺氧复氧所致神经细胞凋亡及银杏叶提取物的保护作用
- Author:
Fengqing JI
;
Xu YUE
;
Haimei SUN
;
Yanru GUO
;
Chongjie GUO
;
Tiande ZHAO
- Publication Type:Journal Article
- Keywords:
Hypoxia/reoxygenation;
Primary culture;
Neurons;
NOS;
EGB
- From:
Acta Anatomica Sinica
1955;0(03):-
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the dynamic expression of nitric oxide synthase(NOS) in the apoptosis of primary cultured rat cortical neruons following hypoxia/reoxygenation(H/R) and the protective role of extract of ginkgo biloba(EGB). Methods The cortical neurons of E16-17 days fetal rat were primarily cultured.The apoptosis model of primary cultured cortical nurons following H/R was established by using W-G staning,electromicroscopy,TUNEL staining.The dynamic expression of NOS different H/R times was investigated with NADPH-diaphorase histochemical method. Results H/R can cause apoptosis of primary cultured rat cortical neurons.In the experiment of H-2R-0,H-4R-0, H-6R-0,H-8R-0 and H-2R 18,H-4R 18,H-6R 18 H-8R 18,the apoptosis cells occurred after 4 hour hypoxia.The increasing of apoptosis cell acted as time-dependence and the peak value was at H-8R 18.The expression of NOS increased both after 2 hour hypoxia and reoxygenation 18 hour after 8 hour hypoxia compared with the normal control group.EGB could inhibit the increasing and decrease the percentage of apoptosis.Conclusion The apoptosis of primary cultured rat cortical neurons could be induced by H/R.The increasing of NO might be one of the mechannisms of apoptosis.EGB could singnificantly inhibit the apoptosis by means of inhibiting the expression of NOS and reducing the production of NO.;
