Light-emitting diode irradiation at 590 nm combined with active substances modulates ultraviolet B radiation-induced keratinocyte inflammation

To evaluate the efficacy of yellow light-emitting diode (LED) irradiation at 590 nm, alone or in combination with anti-inflammatory active substances against ultraviolet (UV)-induced inflammation in keratinocytes. HaCaT keratinocytes were pretreated with LED yellow light (590 nm) alone or in combina...

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Veröffentlicht in:Lasers in medical science 2024-09, Vol.39 (1), p.231, Article 231
Hauptverfasser: Qin, Yumei, Jiang, Boyang, Yuan, Chunfen, Cui, Lei, Lu, Ming, Zheng, Xia, Yu, Minmin
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container_issue 1
container_start_page 231
container_title Lasers in medical science
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creator Qin, Yumei
Jiang, Boyang
Yuan, Chunfen
Cui, Lei
Lu, Ming
Zheng, Xia
Yu, Minmin
description To evaluate the efficacy of yellow light-emitting diode (LED) irradiation at 590 nm, alone or in combination with anti-inflammatory active substances against ultraviolet (UV)-induced inflammation in keratinocytes. HaCaT keratinocytes were pretreated with LED yellow light (590 nm) alone or in combination with an antiinflammatory active substance such as glycerophosphoinositol choline (GC), extract of grains of paradise (Aframomum melegueta Schum, AM), or a bisabolol and ginger root extract mixture (Bb-GE) before UVB irradiation. Following each treatment, we measured the levels of inflammatory mediators secreted by keratinocytes. HaCaT keratinocytes treated with UVB (300 mJ cm − ²) and then cultured for 24 h exhibited significantly upregulated expression of proinflammatory factors, including interleukin (IL)-1α, prostaglandin E2 (PGE2), and IL-8. After pretreatment with 590 nm LED, UVB-induced inflammatory responses were significantly inhibited. Co-pretreatment with 590 nm LED irradiation and GC further inhibited the expression of IL-1α and IL-8. IL-8 expression was inhibited by co-pretreatment with 590 nm LED irradiation and AM, whereas PGE2 expression was inhibited by co-pretreatment with 590 nm LED irradiation and Bb-GE. Co-treatment with 590 nm LED irradiation and various active substances modulated UVB-induced inflammation in keratinocytes, suggesting the potential application of this approach to prevent damage caused by voluntary sun exposure in daily life.
doi_str_mv 10.1007/s10103-024-04178-w
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HaCaT keratinocytes were pretreated with LED yellow light (590 nm) alone or in combination with an antiinflammatory active substance such as glycerophosphoinositol choline (GC), extract of grains of paradise (Aframomum melegueta Schum, AM), or a bisabolol and ginger root extract mixture (Bb-GE) before UVB irradiation. Following each treatment, we measured the levels of inflammatory mediators secreted by keratinocytes. HaCaT keratinocytes treated with UVB (300 mJ cm − ²) and then cultured for 24 h exhibited significantly upregulated expression of proinflammatory factors, including interleukin (IL)-1α, prostaglandin E2 (PGE2), and IL-8. After pretreatment with 590 nm LED, UVB-induced inflammatory responses were significantly inhibited. Co-pretreatment with 590 nm LED irradiation and GC further inhibited the expression of IL-1α and IL-8. IL-8 expression was inhibited by co-pretreatment with 590 nm LED irradiation and AM, whereas PGE2 expression was inhibited by co-pretreatment with 590 nm LED irradiation and Bb-GE. Co-treatment with 590 nm LED irradiation and various active substances modulated UVB-induced inflammation in keratinocytes, suggesting the potential application of this approach to prevent damage caused by voluntary sun exposure in daily life.</abstract><cop>London</cop><pub>Springer London</pub><pmid>39223344</pmid><doi>10.1007/s10103-024-04178-w</doi></addata></record>
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subjects Anti-Inflammatory Agents - pharmacology
Choline
Damage prevention
Dentistry
Dinoprostone - metabolism
Glycerophosphoinositol
HaCaT Cells
Humans
Inflammation
Interleukin 8
Interleukin-1alpha - metabolism
Interleukin-8 - metabolism
Irradiation
Keratinocytes
Keratinocytes - drug effects
Keratinocytes - metabolism
Keratinocytes - radiation effects
Lasers
Lasers, Semiconductor - therapeutic use
Light emitting diodes
Medicine
Medicine & Public Health
Monocyclic Sesquiterpenes - pharmacology
Optical Devices
Optics
Original Article
Photonics
Plant Extracts - pharmacology
Pretreatment
Prostaglandin E2
Quantum Optics
Radiation damage
Radiation effects
Sesquiterpenes - pharmacology
Ultraviolet radiation
Ultraviolet Rays - adverse effects
title Light-emitting diode irradiation at 590 nm combined with active substances modulates ultraviolet B radiation-induced keratinocyte inflammation
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