Objective： To investigate the effects of Zhizi Chuanxiong Capsule（ZCC, 栀子川芎胶囊） on abnormal DNA methylation in a rabbit model of atherosclerosis（AS）. Methods： After 1 week of adaptive feeding, 48 New Zealan...Objective： To investigate the effects of Zhizi Chuanxiong Capsule（ZCC, 栀子川芎胶囊） on abnormal DNA methylation in a rabbit model of atherosclerosis（AS）. Methods： After 1 week of adaptive feeding, 48 New Zealand white rabbits were randomly divided into 4 groups： a control group（n=12） fed with normal diet for 22 weeks; a model group（n=12） fed with high fat diet for 14 weeks followed by 8 weeks of normal diet feeding; a low-dose ZCC group（n=12） fed with high fat diet and low-dose ZCC for 14 weeks, followed by 8 weeks of normal diet and low-dose drug; a high-dose ZCC group（n=12） fed with high fat diet and high-dose drug for 14 weeks, followed by 8 weeks of normal diet and high-dose drug. After 22 weeks of feeding, blood samples were taken from the rabbit ear vein, and the genomic DNA was extracted for methylation immunoprecipitation sequencing（Medip-seq）. The aorta tissues were collected for hematoxylin-eosin（HE） staining. Results： Eight rabbits died during the feeding process. HE staining showed that the size of the lipid deposition on vessel wall and atherosclerotic plaque formation were reduced in both low-and high-dose group. The Medip-seq results showed that there were 146 abnormally methylated genes（including both hypermethylated gene and hypomethylated genes） in the model group, compared with the control group. Gene Ontology（GO） and Pathway analysis showed that these abnormally methylated genes were found to be involved in multiple AS-related functions and pathways, such as protein kinase C activity, cholesterol transport, mitogen-activated protein kinase（MAPK） signaling pathway, peroxisome proliferater-activated receptor signaling pathway, vascular smooth muscle contraction, inflammation and so on. The abnormal methylated genes in AS model group were altered in both low-and high-dose groups： low-dose ZCC could change 72 of the 146 abnormally methylated genes, highdose ZCC could change 71. Through GO and Pathway analysis, these altered methylated genes were involved in protein kinase C activity, inflammatory pathway, MAPK signaling pathway, vascular endothelial growth factor signaling pathway, etc. Conclusion： ZCC could treat AS through regulating the abnormal hypermethylated and hypomethylated genes in AS rabbit model.展开更多
基金Supported by National Natural Science Foundation of China(No.81603490)China Post Doctoral Science Foundation(No.2016M590187)
文摘Objective： To investigate the effects of Zhizi Chuanxiong Capsule（ZCC, 栀子川芎胶囊） on abnormal DNA methylation in a rabbit model of atherosclerosis（AS）. Methods： After 1 week of adaptive feeding, 48 New Zealand white rabbits were randomly divided into 4 groups： a control group（n=12） fed with normal diet for 22 weeks; a model group（n=12） fed with high fat diet for 14 weeks followed by 8 weeks of normal diet feeding; a low-dose ZCC group（n=12） fed with high fat diet and low-dose ZCC for 14 weeks, followed by 8 weeks of normal diet and low-dose drug; a high-dose ZCC group（n=12） fed with high fat diet and high-dose drug for 14 weeks, followed by 8 weeks of normal diet and high-dose drug. After 22 weeks of feeding, blood samples were taken from the rabbit ear vein, and the genomic DNA was extracted for methylation immunoprecipitation sequencing（Medip-seq）. The aorta tissues were collected for hematoxylin-eosin（HE） staining. Results： Eight rabbits died during the feeding process. HE staining showed that the size of the lipid deposition on vessel wall and atherosclerotic plaque formation were reduced in both low-and high-dose group. The Medip-seq results showed that there were 146 abnormally methylated genes（including both hypermethylated gene and hypomethylated genes） in the model group, compared with the control group. Gene Ontology（GO） and Pathway analysis showed that these abnormally methylated genes were found to be involved in multiple AS-related functions and pathways, such as protein kinase C activity, cholesterol transport, mitogen-activated protein kinase（MAPK） signaling pathway, peroxisome proliferater-activated receptor signaling pathway, vascular smooth muscle contraction, inflammation and so on. The abnormal methylated genes in AS model group were altered in both low-and high-dose groups： low-dose ZCC could change 72 of the 146 abnormally methylated genes, highdose ZCC could change 71. Through GO and Pathway analysis, these altered methylated genes were involved in protein kinase C activity, inflammatory pathway, MAPK signaling pathway, vascular endothelial growth factor signaling pathway, etc. Conclusion： ZCC could treat AS through regulating the abnormal hypermethylated and hypomethylated genes in AS rabbit model.
