Theragra chalcogramma Hydrolysates, Rich in Gly-Leu-Pro-Ser-Tyr-Thr, Exerts Anti-Photoaging Potential via Targeting MAPK and NF-κB Pathways in SD Rats

Previous studies have revealed that excessive exposure to UV irradiation is the main cause of skin photoaging and the signaling pathways of MAPK and NF-κB are involved in this progression. The present study aims to investigate the anti-photoaging effects of low molecular weight hydrolysates from The...

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Published in:Marine Drugs
Main Authors: Defeng Xu, Mouming Zhao, Haisheng Lin, Caihong Li
Format: Article in Journal/Newspaper
Language:English
Published: MDPI AG 2022
Subjects:
Online Access:https://doi.org/10.3390/md20050286
https://doaj.org/article/f34e8cb081b64776bd87e4efd6a91876
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spelling ftdoajarticles:oai:doaj.org/article:f34e8cb081b64776bd87e4efd6a91876 2023-05-15T18:32:50+02:00 Theragra chalcogramma Hydrolysates, Rich in Gly-Leu-Pro-Ser-Tyr-Thr, Exerts Anti-Photoaging Potential via Targeting MAPK and NF-κB Pathways in SD Rats Defeng Xu Mouming Zhao Haisheng Lin Caihong Li 2022-04-01T00:00:00Z https://doi.org/10.3390/md20050286 https://doaj.org/article/f34e8cb081b64776bd87e4efd6a91876 EN eng MDPI AG https://www.mdpi.com/1660-3397/20/5/286 https://doaj.org/toc/1660-3397 doi:10.3390/md20050286 1660-3397 https://doaj.org/article/f34e8cb081b64776bd87e4efd6a91876 Marine Drugs, Vol 20, Iss 286, p 286 (2022) skin photoaging Theragra chalcogramma oxidative stress inflammation cascading signaling Biology (General) QH301-705.5 article 2022 ftdoajarticles https://doi.org/10.3390/md20050286 2022-12-30T22:30:17Z Previous studies have revealed that excessive exposure to UV irradiation is the main cause of skin photoaging and the signaling pathways of MAPK and NF-κB are involved in this progression. The present study aims to investigate the anti-photoaging effects of low molecular weight hydrolysates from Theragra chalcogramma (TCH) and to clarify the underlying mechanism. The degradation of mechanical barrier functions in photoaged skin was substantially ameliorated after TCH administration; meanwhile, TCH significantly elevated the antioxidant capacity and suppressed the over-production of inflammatory cytokine IL-1β. Moreover, the histopathological deteriorations such as epidermal hyperplasia and dermal loss were significantly alleviated, along with the increase in procollagen type I content and decrease in MMP-1 activity ( p < 0.05). Furthermore, TCH effectively blocked the MAPK and NF-κB signaling pathways through inhibition of the phosphorylation of p38, JNK, ERK, iκB, and p65 proteins. Collectively, these data indicate that TCH has potential as a novel ingredient for the development of anti-photoaging foods. Article in Journal/Newspaper Theragra chalcogramma Directory of Open Access Journals: DOAJ Articles Marine Drugs 20 5 286
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic skin photoaging
Theragra chalcogramma
oxidative stress
inflammation
cascading signaling
Biology (General)
QH301-705.5
spellingShingle skin photoaging
Theragra chalcogramma
oxidative stress
inflammation
cascading signaling
Biology (General)
QH301-705.5
Defeng Xu
Mouming Zhao
Haisheng Lin
Caihong Li
Theragra chalcogramma Hydrolysates, Rich in Gly-Leu-Pro-Ser-Tyr-Thr, Exerts Anti-Photoaging Potential via Targeting MAPK and NF-κB Pathways in SD Rats
topic_facet skin photoaging
Theragra chalcogramma
oxidative stress
inflammation
cascading signaling
Biology (General)
QH301-705.5
description Previous studies have revealed that excessive exposure to UV irradiation is the main cause of skin photoaging and the signaling pathways of MAPK and NF-κB are involved in this progression. The present study aims to investigate the anti-photoaging effects of low molecular weight hydrolysates from Theragra chalcogramma (TCH) and to clarify the underlying mechanism. The degradation of mechanical barrier functions in photoaged skin was substantially ameliorated after TCH administration; meanwhile, TCH significantly elevated the antioxidant capacity and suppressed the over-production of inflammatory cytokine IL-1β. Moreover, the histopathological deteriorations such as epidermal hyperplasia and dermal loss were significantly alleviated, along with the increase in procollagen type I content and decrease in MMP-1 activity ( p < 0.05). Furthermore, TCH effectively blocked the MAPK and NF-κB signaling pathways through inhibition of the phosphorylation of p38, JNK, ERK, iκB, and p65 proteins. Collectively, these data indicate that TCH has potential as a novel ingredient for the development of anti-photoaging foods.
format Article in Journal/Newspaper
author Defeng Xu
Mouming Zhao
Haisheng Lin
Caihong Li
author_facet Defeng Xu
Mouming Zhao
Haisheng Lin
Caihong Li
author_sort Defeng Xu
title Theragra chalcogramma Hydrolysates, Rich in Gly-Leu-Pro-Ser-Tyr-Thr, Exerts Anti-Photoaging Potential via Targeting MAPK and NF-κB Pathways in SD Rats
title_short Theragra chalcogramma Hydrolysates, Rich in Gly-Leu-Pro-Ser-Tyr-Thr, Exerts Anti-Photoaging Potential via Targeting MAPK and NF-κB Pathways in SD Rats
title_full Theragra chalcogramma Hydrolysates, Rich in Gly-Leu-Pro-Ser-Tyr-Thr, Exerts Anti-Photoaging Potential via Targeting MAPK and NF-κB Pathways in SD Rats
title_fullStr Theragra chalcogramma Hydrolysates, Rich in Gly-Leu-Pro-Ser-Tyr-Thr, Exerts Anti-Photoaging Potential via Targeting MAPK and NF-κB Pathways in SD Rats
title_full_unstemmed Theragra chalcogramma Hydrolysates, Rich in Gly-Leu-Pro-Ser-Tyr-Thr, Exerts Anti-Photoaging Potential via Targeting MAPK and NF-κB Pathways in SD Rats
title_sort theragra chalcogramma hydrolysates, rich in gly-leu-pro-ser-tyr-thr, exerts anti-photoaging potential via targeting mapk and nf-κb pathways in sd rats
publisher MDPI AG
publishDate 2022
url https://doi.org/10.3390/md20050286
https://doaj.org/article/f34e8cb081b64776bd87e4efd6a91876
genre Theragra chalcogramma
genre_facet Theragra chalcogramma
op_source Marine Drugs, Vol 20, Iss 286, p 286 (2022)
op_relation https://www.mdpi.com/1660-3397/20/5/286
https://doaj.org/toc/1660-3397
doi:10.3390/md20050286
1660-3397
https://doaj.org/article/f34e8cb081b64776bd87e4efd6a91876
op_doi https://doi.org/10.3390/md20050286
container_title Marine Drugs
container_volume 20
container_issue 5
container_start_page 286
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