Inhibitory effect of vitamin C on intrinsic aging in human dermal fibroblasts and hairless mice

Jae Hong Jeong, Mi Bo Kim, Changhee Kim, Jae Kwan Hwang

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

Vitamin C significantly reduced senescence-associated β-galactosidase (SA-β-gal) activity, with both the suppression of cell-cycle inhibitors (p53, p21, p16, and pRb) and stimulation of cell-cycle activators (E2F1 and E2F2). Vitamin C also effectively attenuated the hyperactivation of the phosphatidylinositol 3-kinase (PI3K)/protein kinase-B (AKT) signaling pathway. The expression of the longevity marker, the mammalian target of rapamycin (mTOR), was down-regulated by vitamin C while the expressions of forkhead box O3a (FoxO3a) and sirtuin1 (SIRT1) were up-regulated by vitamin C. In the middle-aged (MA) mice, oral administration of vitamin C significantly inhibited wrinkle formation, skin atrophy, and loss of elasticity through increasing collagen and elastic fiber. The increase in transepidermal water loss and the decrease in skin hydration were recovered by vitamin C treatment in the MA mice. Overall, vitamin C effectively prevents cellular senescence in vitro and in vivo suggesting it has protective potential against natural aging of the skin.

Original languageEnglish
Pages (from-to)555-564
Number of pages10
JournalFood Science and Biotechnology
Volume27
Issue number2
DOIs
Publication statusPublished - 2018 Apr 1

Bibliographical note

Funding Information:
Acknowledgements This work was supported by a Grant from the Kwang Dong Pharmaceutical Co., Ltd. (2013-8-1178).

Publisher Copyright:
© 2017, The Korean Society of Food Science and Technology and Springer Science+Business Media B.V.

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Food Science
  • Applied Microbiology and Biotechnology

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