Notogisenoside Rg1 upregulates the thiol antioxidants and resists aging in rats
10.3969/j.issn.0529-1356.2010.02.005
- VernacularTitle:三七皂苷Rg1上调SD大鼠大脑皮质巯醇抗氧化物(酶)发挥抗衰老作用
- Author:
Tingting WANG
;
Xingguo LI
;
Shoumin LI
;
Xiyue FU
;
Wenmin WANG
;
Jun SUN
;
Qinglong AI
;
Di LU
- Publication Type:Journal Article
- Keywords:
Notoginsenoside Rg1;
Aβ_(1-42);
D-galactose;
Thiol antioxidant;
Pro-caspase-3;
Immunohistochemistry;
Western blotting;
Rat
- From:
Acta Anatomica Sinica
2010;41(2):191-196
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveIn order to investigate anti-ageing mechanisms of the notoginsenoside Rg1,we used Aβ_(1-42) and D-galactose to establish aging rat model. Methods Ninety rats were divided into three groups at random: sham group, model group, treatment group. Aging rat models were established by injecting peritoneally D-galactose (100 mg/kg) to the rats for 56 days and after 35 days aggregated Aβ_(1-42)(μg) was injected to the right lateral ventricle of rats. Meantime, rats were treated by intragastric administration the notoginsenoside Rg1. Then spatial memory of experimental rats was examined with the Morris water maze(MWM). The thiol antioxidants including glutathione reductase (GR) and glutathione peroxidase (GSH-Px) activities were examined by colorimetric method. The concentration of the pro-caspase-3 and Bcl-2 were examined by the immunohistochemistry and Western blotting method. Results In aging model rats escape latercies were significantly prolonged (P<0.05), while decreases were seen in the time of staying the third quadrants of platform, the number of crossing over a platform, the concentration of the GR, GSH-Px, and pro-caspase-3 as compared with the sham group(P<0.05). After treatment of the notoginsenoside Rg1, the aging model rats exhibited significant increases in the time of staying the third quadrants of platform, the number of crossing over a platform, the concentration of the GR, GSH-Px, and pro-caspase-3(P<0.05), while a decrease was observed in escape latercies as compared to control group(P<0.05). Moreover there was no significant difference in the expression of the Bcl-2(P>0.05). Conclusion The results from our study indicate that the notoginsenoside Rg1 could improve the oriented learning and memory capacity and prevent the neurodegeneration of central nervous systems in aging model rats by up-regulating the expression of the thiol antioxidants(including GR and GSH-Px) and resisting the cleavage of the pro-caspase-3.
