Panax notoginseng alleviates oxidative stress through miRNA regulations based on systems biology approach

被引:0
作者
Tang, Yun [1 ,2 ]
Chen, Yi-Gang [1 ,2 ]
Huang, Hsi-Yuan [1 ,2 ]
Li, Shang-Fu [1 ,2 ]
Zuo, Hua-Li [1 ,2 ]
Chen, Ji-Hang [1 ]
Li, Li-Ping [2 ]
Mao, Run-Bo [1 ]
Lin, Yang-Chi-Dung [1 ,2 ]
Huang, Hsien-Da [1 ,2 ]
机构
[1] Chinese Univ Hong Kong, Sch Med, Shenzhen 518172, Guangdong, Peoples R China
[2] Chinese Univ Hong Kong, Warshel Inst Computat Biol, Shenzhen 518172, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Panax notoginseng (PNS or Sanqi); Anti-oxidant; Metabolic disorder; MicroRNA; Systems biology; PANCREATIC BETA-CELLS; GLUTAMATE CYSTEINE LIGASE; INSULIN-RESISTANCE; TRANSCRIPTOME; EXPRESSION; ISLETS; OVEREXPRESSION; MICRORNAS; MECHANISM; PROTECTS;
D O I
10.1186/s13020-023-00768-y
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
BackgroundHerbal medicine Sanqi (SQ), the dried root or stem of Panax notoginseng (PNS), has been reported to have anti-diabetic and anti-obesity effects and is usually administered as a decoction for Chinese medicine. Alternative to utilizing PNS pure compound for treatment, we are motivated to propose an unconventional scheme to investigate the functions of PNS mixture. However, studies providing a detailed overview of the transcriptomics-based signaling network in response to PNS are seldom available.MethodsTo explore the reasoning of PNS in treating metabolic disorders such as insulin resistance, we implemented a systems biology-based approach with RNA sequencing (RNA-seq) and miRNA sequencing data to elucidate key pathways, genes and miRNAs involved.ResultsFunctional enrichment analysis revealed PNS up-regulating oxidative stress-related pathways and down-regulating insulin and fatty acid metabolism. Superoxide dismutase 1 (SOD1), peroxiredoxin 1 (PRDX1), heme oxygenase-1 (Hmox1) and glutamate cysteine ligase (GCLc) mRNA and protein levels, as well as related miRNA levels, were measured in PNS treated rat pancreatic beta cells (INS-1). PNS treatment up-regulated Hmox1, SOD1 and GCLc expression while down-regulating miR-24-3p and miR-139-5p to suppress oxidative stress. Furthermore, we verified the novel interactions between miR-139-5p and miR-24-3p with GCLc and SOD1.ConclusionThis work has demonstrated the mechanism of how PNS regulates cellular molecules in metabolic disorders. Therefore, combining omics data with a systems biology strategy could be a practical means to explore the potential function and molecular mechanisms of Chinese herbal medicine in the treatment of metabolic disorders.
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页数:19
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