Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Yonglin Wu has a total of 8 co-authors. Here are the top co-authors by number of shared publications:

  • Anqi Zhu

    Institute of Chinese Medicine Sciences, Guangdong Pharmaceutical University, Guangzhou 510006, China

    1 shared publication
  • Duosheng Luo

    Guangdong Metabolic Diseases Research Center of Integrated Chinese and Western Medicine, Key Laboratory of Glucolipid Metabolic Disorder, Ministry of Education of China, China; Institute of Chinese Medicine, Guangdong Pharmaceutical University, Guangdong TCM Key Laboratory for Metabolic Diseases, Guangzhou 510006, China

    1 shared publication
  • Kun-Ping Li

    School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China

    1 shared publication
  • Mengmeng Gao

    Institute of Chinese Medicine Sciences, Guangdong Pharmaceutical University, Guangzhou 510006, China

    1 shared publication
  • Xinyuan Kuai

    Institute of Chinese Medicine Sciences, Guangdong Pharmaceutical University, Guangzhou 510006, China

    1 shared publication
  • Yana Ye

    Zhanjiang Experimental Station, Chinese Academy of Tropical Agricultural Sciences, Zhanjiang 524013, China

    1 shared publication

Latest Publications

  • Open Access

    Purification Process and In Vitro and In Vivo Bioactivity Evaluation of Pectolinarin and Linarin from Cirsium japonicum

    by Yana Ye, Zhenlin Chen, Yonglin Wu, Mengmeng Gao, Anqi Zhu, Xinyuan Kuai, Duosheng Luo, Yanfen Chen, Kunping Li

    Pectolinarin and linarin are two major flavone O-glycosides of Cirsium japonicum, which has been used for thousands of years in traditional Chinese medicine. Pharmacological research on pectolinarin and linarin is meaningful and necessary. Here, a process for the purification of pectolinarin and linarin from C. japonicum was established using macroporous resin enrichment followed by prep-HPLC separation. The results show the purity of pectolinarin and linarin reached 97.39% and 96.65%, respectively. The in vitro bioactivities result shows the ORAC values of pectolinarin and linarin are 4543 and 1441 µmol TE/g, respectively, meanwhile their inhibition rate of BSA-MGO-derived AGEs is 63.58% and 19.31% at 2 mg/mL, which is 56.03% and 30.73% in the BSA-fructose system, respectively. The COX-2 inhibition rate at 50 µg/mL of linarin and pectolinarin reached 55.35% and 40.40%, respectively. Furthermore, the in vivo bioassay combining of histopathologic evaluation and biochemical analysis of liver glutamic oxaloacetic transaminase, serum creatinine and TNF-α show pectolinarin can alleviate lipopolysaccharide (LPS)-induced acute liver and kidney injury in mice. Metabolomics analysis shows that pectolinarin attenuates LPS-challenged liver and kidney stress through regulating the arachidonic acid metabolism and glutathione synthesis pathways. Collectively, our work presents a solid process for pectolinarin and linarin purification and has discovered a promising natural therapeutic agent—pectolinarin.