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Juglans mandshurica leaf extract protects skin fibroblasts from damage by regulating the oxidative defense system

Gunhyuk Park1, Dae Sik Jang, Myung Sook Oh

  • 1Department of Life and Nanopharmaceutical Science, and Kyung Hee East-West Pharmaceutical Research Institute, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea.

Insights

The leaf extract of Manchurian walnut (Juglans mandshurica MAX.) protects human skin cells from oxidative damage. This extract regulates antioxidant systems, preventing collagen breakdown and skin aging.

Area of Science:

  • Dermatology
  • Biochemistry
  • Pharmacology

Background:

  • Skin aging results from genetic and environmental factors, often involving reactive oxygen species (ROS) that degrade collagen.
  • Metalloproteinase-1 (MMP-1) activation by ROS breaks down type I collagen (COL1A1), leading to wrinkles.
  • Manchurian walnut (Juglans mandshurica MAX.) exhibits known anti-tumor, anti-oxidative, and anti-bacterial properties.

Purpose of the Study:

  • To investigate the protective effects of Manchurian walnut leaf extract (JME) against oxidative stress in human skin fibroblasts.
  • To determine if JME can mitigate damage induced by hydrogen peroxide (H₂O₂).

Main Methods:

  • HS68 human skin fibroblasts were exposed to H₂O₂ with and without JME.
  • Cell viability was assessed using MTT and LDH assays.
  • ROS production, glutathione levels, and antioxidant enzyme activity (heme oxygenase-1, Nrf2) were measured.
  • MMP-1 and COL1A1 levels were quantified.
  • MAPK signaling pathways (ERK, p38, JNK) were analyzed via phosphorylation assays.

Main Results:

  • JME significantly protected HS68 cells from H₂O₂-induced damage in a dose-dependent manner.
  • JME regulated ROS production and enhanced cellular antioxidant defenses by increasing glutathione and heme oxygenase-1 levels via Nrf2 activation.
  • JME prevented H₂O₂-induced MMP-1 elevation and COL1A1 reduction.
  • JME inhibited the phosphorylation of ERK, p38, and JNK signaling pathways.

Conclusions:

  • JME demonstrates significant protective effects against oxidative stress in human skin fibroblasts.
  • The extract functions by modulating the cellular oxidative defense system and inhibiting pro-aging signaling pathways.
  • JME holds potential for preventing skin aging caused by oxidative damage.

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