We found a match
Your institution may have rights to this item. Sign in to continue.
- Title
Naringin acts as a TRPV1 antagonist to attenuate UVB‐induced senescence and damage in HaCaT cells.
- Authors
Zhu, Ying‐jie; Chen, Hu‐lin; Cai, Xin‐jie; Zhan, Bang‐le; Liu, Xiao‐ming
- Abstract
This study aimed to explore the mechanism of naringin (Nar) in alleviating ultraviolet B (UVB)‐induced HaCaT cell senescence and damage. Human keratinocytes (HaCaT cells) were divided into control, UVB, UVB + Nar, UVB + Cap, and UVB + Nar + Cap groups. Analysis was performed using the MTT assay to assess cell viability, flow cytometry to measure the apoptosis level, SA‐β‐Gal staining to observe cellular senescence, and Western blot to assess protein levels of TRPV1, p16, p53, p21, matrix metalloproteinase (MMP)‐1, and MMP‐9. Both UVB irradiation and capsaicin (Cap) treatment upregulated the expression of TRPV1 in HaCaT cells, inhibited cell proliferation, promoted apoptosis, and increased the expression of p16, p53, p21, MMP‐1, and MMP‐9. Nar treatment reversed the above effects via inhibition of TRPV1 expression, thereby relieving senescence and cell damage induced by UVB irradiation. Taken together, these findings suggest that Nar can reduce UVB‐induced senescence and damage in HaCaT cells by acting as an antagonist of TRPV1.
- Subjects
TRPV cation channels; NARINGIN; P16 gene; AGING; CELLULAR aging; MATRIX metalloproteinases
- Publication
Chemical Biology & Drug Design, 2024, Vol 103, Issue 1, p1
- ISSN
1747-0277
- Publication type
Article
- DOI
10.1111/cbdd.14390