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China Journal of Chinese Materia Medica ; (24): 2511-2514, 2007.
Article in Chinese | WPRIM | ID: wpr-324338

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of C21 steroidal glycoside (CSG) from the root of Cynanchum auriculatum from Jiangsu on D-galactose (D-gal) induced aging model mice.</p><p><b>METHOD</b>D-gal aging mouse model was established by cervicodorsal region subcutaneous injection with D-gal once a day for eight successive weeks. The mice in the normal control group (NCG, non-modeled) and the model control group (MCG, modeled but untreated) were treated with 1% CMC-Na. The model mice in the low, middle and high-dose CSG and Vitamin E treated groups were treated with a dose of (10, 20, 40, 100 mg x kg(-1) per day, respectively. The SOD activity, MDA content and telomerase activity in serum, heart, liver and brain tissues of mice were measured.</p><p><b>RESULT</b>CSG could obviously increase the SOD activity and decrease the MDA level in serum, heart, liver and brain tissues in D-gal aging mice (P < 0.01). There was no significant difference between three CSG treated groups and Vitamin E treated groups. In comparison of telomerase activity between MCG and the treated groups, it was shown that there was a significant increase in serum in middle and high dose group, and in heart tissues in CSG and Vit E treated groups, but was not in liver and brain tissue.</p><p><b>CONCLUSION</b>This study demonstrates that CSG can antagonize free radical injury, increase the SOD activity and decrease the MDA content of serum, heart, liver and brain in D-gal aging mice, and increase the telomerase activity in serum and heart tissues but not in liver and brain tissue.</p>


Subject(s)
Animals , Female , Male , Mice , Aging , Metabolism , Brain , Metabolism , Cynanchum , Chemistry , Drugs, Chinese Herbal , Pharmacology , Galactose , Toxicity , Glycosides , Pharmacology , Liver , Metabolism , Malondialdehyde , Blood , Metabolism , Mice, Inbred ICR , Myocardium , Metabolism , Plant Roots , Chemistry , Plants, Medicinal , Chemistry , Random Allocation , Steroids , Pharmacology , Superoxide Dismutase , Blood , Metabolism , Telomerase , Metabolism
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