Anti-Photoaging Effect of Hydrolysates from Pacific Whiting Skin via MAPK/AP-1, NF-κB, TGF-β/Smad, and Nrf-2/HO-1 Signaling Pathway in UVB-Induced Human Dermal Fibroblasts

Mar Drugs. 2022 Apr 30;20(5):308. doi: 10.3390/md20050308.

Abstract

Chronic exposure to ultraviolet (UV) light promotes the breakdown of collagen in the skin and disrupts the extracellular matrix (ECM) structure, leading to skin wrinkling. Pacific whiting (Merluccius productus) is a fish abundant on the Pacific coast. In the current study, we investigated the anti-wrinkle effect of hydrolysate from Pacific whiting skin gelatin (PWG) in UVB-irradiated human dermal fibroblasts and the molecular mechanisms involved. PWG effectively restored type 1 procollagen synthesis reduced by UVB-irradiation. Also, we found that PWG inhibited collagen degradation by inhibiting MMP1 expression. Furthermore, PWG decreased cytokines TNF-α, IL-6, and IL-1β associated with inflammatory responses and increased antioxidant enzymes, HO-1, SOD, GPx, CAT, and GSH content, a defense system against oxidative stress. In terms of molecular mechanisms, PWG increased collagen synthesis through activating the transforming growth factor β (TGF-β)/Smad pathway and decreased collagen degradation through inhibiting the mitogen-activated protein kinases/activator protein 1 (MAPK/AP-1) pathway. It also suppressed the inflammatory response through suppressing the nuclear factor-κB (NF-κB) pathway and increased antioxidant enzyme activity through activating the nuclear factor erythroid 2/heme oxygenase 1 (Nrf-2/HO-1) pathway. These multi-target mechanisms suggest that PWG may serve as an effective anti-photoaging material.

Keywords: MAPK/AP-1; Matrix metalloproteinase; Merluccius productus; NF-κB; Nrf-2/HO-1; TGF-β/Smad; type I procollagen.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Antioxidants / pharmacology
  • Collagen Type I / metabolism
  • Fibroblasts* / physiology
  • Fibroblasts* / radiation effects
  • GATA1 Transcription Factor / metabolism
  • GATA1 Transcription Factor / pharmacology
  • Gadiformes*
  • Heme Oxygenase (Decyclizing) / metabolism
  • Heme Oxygenase (Decyclizing) / pharmacology
  • Humans
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Protein Hydrolysates / pharmacology
  • Signal Transduction
  • Skin
  • Skin Aging / physiology
  • Tissue Extracts / therapeutic use
  • Transcription Factor AP-1 / metabolism
  • Transforming Growth Factor beta / metabolism
  • Ultraviolet Rays / adverse effects

Substances

  • Antioxidants
  • Collagen Type I
  • GATA1 Transcription Factor
  • NF-kappa B
  • Protein Hydrolysates
  • Tissue Extracts
  • Transcription Factor AP-1
  • Transforming Growth Factor beta
  • Heme Oxygenase (Decyclizing)
  • Mitogen-Activated Protein Kinases

Grants and funding