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Abstract: SA-PO448

Toxicodendron vernicifluum Extract Ameliorates Renal Injury in Unilateral Ureteral Obstruction Mice

Session Information

Category: Development, Stem Cells, and Regenerative Medicine

  • 500 Development, Stem Cells, and Regenerative Medicine

Authors

  • Choi, Dae Eun, Chungnam National University, Daejeon, Korea (the Republic of)
  • Choi, Wonjung, Chungnam National University, Daejeon, Korea (the Republic of)
  • Kim, Da bi, Chungnam national university, Daejeon, Korea (the Republic of)
  • Kim, Eunji, Chungnam national university, Daejeon, Korea (the Republic of)
  • Hwang, Tae Woong, Chungnam National University, Daejeon, Korea (the Republic of)
  • Kim, Jwajin, Chungnam National University, Daejeon, Korea (the Republic of)
  • Na, Ki Ryang, Chungnam National University, Daejeon, Korea (the Republic of)
  • Lee, Kang Wook, Chungnam National University, Daejeon, Korea (the Republic of)
  • Jeong, Jin young, Chungnam national university, Daejeon, Korea (the Republic of)
  • Chang, Yoon-Kyung, The Catholic University of Korea, Daejeon, Korea (the Republic of)
Background

Toxicodendron†vernicifluumis used as a traditional herbal medicine in Asia. The physiological properties and antioxidative effects of Toxicodendron vernicifluum extract (TV) have been demonstrated in several experimental studies. The physiological properties and antioxidative effects of Toxicodendron vernicifluum extract (TV) have been demonstrated in several experimental studies. This study evaluated the possible renoprotective effects of TV on UUO induced tubular damage, as well as the mechanism through which it exerts antioxidative and antiapoptotic effects against UUO induced cell death.

Methods

Male Sprague–Dawley rats weighing 180–200 g each were assigned to one of two groups. The first group (UUO+TV) of rats drank TV for 2 weeks before surgery. The second group (UUO) of rats drank water for 2 weeks. Three days later, a morphologic evaluation of renal injury was conducted using hematoxylin and eosin and TUNEL staining. The renal protein expression of PCNA, caspase3,
Nrf2, catalase, and phosphorylated p38 as markers of autophagy was determined by immunoblotting.

Results

Obstruction injury caused marked apoptosis and oxidative stress in the UUO group. It also increased the level of phosphorylated p38 and decreased the level of PCNA, suggesting delayed recovery from damage. The number of TUNEL positive cells, which were detected based on DNA fragmentation, was increased in the UUO group. Notably, there was a significant relationship with increased expression of cleaved caspase3, which was counteracted by TV treatment. Moreover, a comparison with the UUO group revealed that TV significantly enhanced the regulation of autophagy and autophagic flux.

Conclusion

Taken together, our findings suggest that the induction of autophagy protects against UUO induced apoptotic damage via ROS and a p38 regulated pathway in this in vivo model.

Funding

  • Clinical Revenue Support