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Effect of Lichong Decoction on expression of IGF-I and proliferating cell nuclear antigen mRNA in rat model of uterine leiomyoma

OBJECTIVE: To study the effect of Lichong Decoc- tion (Lichong Decoction for strengthening an- ti-pathogenic Qi and eliminating blood stasis) on the expression of insulin-like growth factor-I (IGF-I) and proliferating cell nuclear antigen (PCNA) mRNA in a rat model of uterine leiomyoma. METHODS: Fif...

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Published in:Journal of traditional Chinese medicine 2012-12, Vol.32 (4), p.636-640
Main Authors: Li, Donghua, Zhang, Yalan, Han, Hongjuan, Geng, Jianguo, Xie, Xiaolei, Zheng, Jiubo, Wang, Yasong, Zou, Xiaoli
Format: Article
Language:English
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Summary:OBJECTIVE: To study the effect of Lichong Decoc- tion (Lichong Decoction for strengthening an- ti-pathogenic Qi and eliminating blood stasis) on the expression of insulin-like growth factor-I (IGF-I) and proliferating cell nuclear antigen (PCNA) mRNA in a rat model of uterine leiomyoma. METHODS: Fifty female Wistar rats were random- ized into a normal control group, model group, Li- chong Decoction group, Guizhifuling Capsule (Cap- sule containing Cassia Twig and Poria) group, and Mifepristone group. The uterine leiomyoma model was established by peritoneal injections of exoge- nous estrogen and progesterone hormone. The ul- trastructural changes in cells of rat uterine tissues were observed with transmission electron micros- copy, and the expression of IGF-I and PCNA mRNAwas detected by real-time fluorescent quantitative PCR. RESULTS: Following treatment, cells in the Lichong Decoction group appeared to be arranged normal- ly, the cellular morphology were almost in a normal state, hyperplasia and hypertrophy of the chondrio- some was reduced, collagen fibers were arranged in a regular manner, without obvious hyperplasia, and the expression of IGF-I and PCNA mRNA was significantly decreased compared with the model group (P〈0.01). CONCLUSIONS: The effect of Lichong Decoction on uterine leiomyoma is related to its function in re- ducing the expression of IGF-I and PCNA mRNA.
ISSN:0255-2922
DOI:10.1016/S0254-6272(13)60084-9