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[白首乌C21甾体苷对D-半乳糖致衰老模型小鼠的影响]

[Effect of C21 steroidal glycoside from root of Cynanchum auriculatum on D-galactose induced aging model mice].

作者信息

Zhang Shi-Xia, Li Xin, Yin Jia-Le, Chen Li-Li, Zhang Hong-Quan

机构信息

The Medical and Pharmaceutical Academy of Yangzhou University, Yangzhou 225001, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2007 Dec;32(23):2511-4.

Abstract

OBJECTIVE

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.

METHOD

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.

RESULT

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.

CONCLUSION

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.

摘要

目的

研究江苏产白首乌根中C21甾体糖苷(CSG)对D-半乳糖(D-gal)诱导的衰老模型小鼠的影响。

方法

通过颈背部皮下注射D-半乳糖,连续8周每天1次,建立D-半乳糖衰老小鼠模型。正常对照组(NCG,未造模)和模型对照组(MCG,造模但未处理)小鼠给予1%羧甲基纤维素钠(CMC-Na)。低、中、高剂量CSG组及维生素E组的模型小鼠分别给予剂量为(10、20、40、100 mg·kg⁻¹)的药物,每日1次。检测小鼠血清、心脏、肝脏和脑组织中的超氧化物歧化酶(SOD)活性、丙二醛(MDA)含量和端粒酶活性。

结果

CSG可明显提高D-半乳糖衰老小鼠血清、心脏、肝脏和脑组织中的SOD活性,降低MDA水平(P < 0.01)。三个CSG处理组与维生素E处理组之间无显著差异。比较MCG与各处理组之间的端粒酶活性,结果显示中、高剂量组血清中端粒酶活性显著升高,CSG组和维生素E组心脏组织中端粒酶活性升高,但肝脏和脑组织中无变化。

结论

本研究表明,CSG可拮抗自由基损伤,提高D-半乳糖衰老小鼠血清、心脏、肝脏和脑组织中的SOD活性,降低MDA含量,并提高血清和心脏组织中的端粒酶活性,但对肝脏和脑组织无此作用。

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