Wang Hongliang, Xing Wei, Tang Shijie, Wang Zhenglin, Lv Tiantian, Wu Yan, Guo Shuzhen, Li Chun, Han Jing, Zhu Ruixin, Wang Wei
College of Basic Medicine, Key Laboratory of Ministry of Education (Syndromes and Formulas), Key Laboratory of Beijing (Syndromes and Formulas), Beijing University of Chinese medicine, Beijing 100029, China.
School of Public Health, Capital Medical University, Beijing 100069, China.
Int J Genomics. 2017;2017:4832125. doi: 10.1155/2017/4832125. Epub 2017 Nov 29.
HuoXueJieDu (HXJD) formula exerts protective effects against diabetic retinopathy (DR) in rats, but its underlying mechanism remains unknown. In the present study, the diabetic rats were established using streptozocin. The administration of HXJD was initiated at 20 weeks after diabetes induction and continued for 12 weeks. Whole genome expression profiles in rat retinas were examined using microarray technology. Differential gene expression and pathway enrichment analysis were conducted on the microarray data, with validation through real-time PCR and immunohistochemical staining. The results showed that 170 genes and several IPA canonical pathways related to inflammation, matrix metabolism, and phototransduction were regulated by HXJD. PCR validation of selected genes, including SOCS3, STAT3, TIMP1, and A2M, confirmed the gene expression changes influenced by HXJD. In addition, the immunohistochemical staining results suggested that critical members of the SOCS3-STAT3 pathway were also affected by HXJD. Taken together, these results indicated that SOCS3-STAT3 and TIMP1-A2M pathways might mediate the alleviation of HXJD activities in rats with diabetic retinopathy.
活血解毒(HXJD)方剂对大鼠糖尿病视网膜病变(DR)具有保护作用,但其潜在机制尚不清楚。在本研究中,使用链脲佐菌素建立糖尿病大鼠模型。在糖尿病诱导后20周开始给予HXJD,并持续给药12周。使用微阵列技术检测大鼠视网膜中的全基因组表达谱。对微阵列数据进行差异基因表达和通路富集分析,并通过实时PCR和免疫组织化学染色进行验证。结果表明,HXJD调节了170个基因以及与炎症、基质代谢和光转导相关的几个IPA经典通路。对包括SOCS3、STAT3、TIMP1和A2M在内的选定基因进行PCR验证,证实了受HXJD影响的基因表达变化。此外,免疫组织化学染色结果表明,SOCS3-STAT3通路的关键成员也受到HXJD的影响。综上所述,这些结果表明,SOCS3-STAT3和TIMP1-A2M通路可能介导了HXJD对糖尿病视网膜病变大鼠作用的减轻。