Cited by 62Osteoarthritis Treatment and MechanismsAntioxidant Activity and Oxidative StressRedox biology and oxidative stress

Ascorbic Acid Provides Protection for Human Chondrocytes against Oxidative Stress

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CHANG, ZHIQIANG, HUO, LIFENG, LI, PENGFEI, WU, YIMIN, ZHANG, PEI·2015·Molecular Medicine Reports

Abstract

Oxidative stress is considered to be an important cause of dysfunction in chondrocytes and articular cartilage degradation, which leads to the pathogenesis of osteoarthritis (OA) and cartilage aging. The present study aimed to assess the effects of the widely applied antioxidant, ascorbic acid (AA), on human chondrocytes against hydrogen peroxide (H2O2) in vitro. Using annexin V‑fluorescein isothiocyanate, 3‑(4,5‑dimethylthiazol‑2‑yl)‑2,5‑diphenyl tetrazolium bromide and senescence‑associated β‑galactosidase assays, the present study identified that AA reduced apoptosis, reduced the loss of viability and markedly decreased H2O2‑mediated senescence in cells treated with H2O2. Furthermore, AA not only stimulated the expression levels of collagens and proteoglycans, but also inhibited the differentiation of chondrocytes under conditions of oxidative stress. In addition, reverse transcription‑quantitative polymerase chain reaction and western blotting demonstrated that AA decreased the activity of nrf2, NF‑κB, AP1 and matrix metalloproteinase‑3, which is stimulated by H2O2. In conclusion, AA efficiently protected human chondrocytes against damage induced by H2O2 by regulating multiple regulatory pathways.

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Crossref · 10.3892/mmr.2015.4231

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  • Ascorbic acid has a protective effect on human chondrocytes against OS by attenuating the increase of apoptosis, the loss of viability and the increase of senescence, and therefore hindering the development of osteoarthritis and aging of cartilage.

    “Moreover, AA was found to have a protective effect also on human chondrocytes against OS by attenuating the increase of apoptosis, the loss of viability and the increase of senescence, and therefore hindering the development of osteoarthritis and aging of cartilage [125,126].”

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References 45 · Cited by 62

Authors
CHANG, Z., HUO, L., LI, P., WU, Y., & ZHANG, P.
Affiliations
Second Affiliated Hospital of Inner Mongolia Medical University (CN)
Venue
Molecular Medicine Reports
Published
2015-08-20
Volume
12
Issue
5
Pages
7086-7092
ISSN
  • 1791-2997 (ISSN-L)
  • 1791-3004
OpenAlex
W1946894587
Cited by
62
References
45
Citations by year
2026: 8 · 2025: 5 · 2024: 7 · 2023: 3 · 2022: 7 · 2021: 7 · 2020: 5 · 2019: 5 · 2018: 5 · 2017: 4 · 2016: 6
FWCI
4.20
Type
journal article
Language
en
Open access
Locations
  • Molecular Medicine Reports (publishedVersion)
  • PubMed (publishedVersion)
Funders
Inner Mongolia Medical University
Topics
  • Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
  • Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
Keywords
vitamin C, chondrocytes, oxidative stress, hydrogen peroxide, osteoarthritis, cartilage degeneration, apoptosis, cellular senescence, collagen, proteoglycans, chondrogenic differentiation, Nrf2, NF-κB, AP-1, matrix metalloproteinase-3, antioxidants
MeSH terms
Antioxidants, Ascorbic Acid, Cell Line, Cell Survival, Collagen, Humans, Hydrogen Peroxide, Proteoglycans, Cellular Senescence, Apoptosis, Oxidative Stress, Chondrocytes

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