Antiphotoaging and Skin-Protective Activities of Ardisia silvestris Ethanol Extract in Human Keratinocytes

is a traditional medicinal herb used in Vietnam and several other countries. However, the skin-protective properties of ethanol extract (As-EE) have not been evaluated. Human keratinocytes form the outermost barrier of the skin and are the main target of ultraviolet (UV) radiation. UV exposure cause...

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Published inPlants (Basel) Vol. 12; no. 5; p. 1167
Main Authors Huang, Lei, You, Long, Aziz, Nur, Yu, Seung Hui, Lee, Jong Sub, Choung, Eui Su, Luong, Van Dung, Jeon, Mi-Jeong, Hur, Moonsuk, Lee, Sarah, Lee, Byoung-Hee, Kim, Han Gyung, Cho, Jae Youl
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 01.03.2023
MDPI
Subjects
Activator protein 1
Aging (artificial)
anti-apoptosis
antioxidative capacity
AP-1
Apoptosis
Ardisia
Ardisia silvestris ethanol extract
Assaying
c-Jun protein
Care and treatment
Cell death
Cosmetics
Cytotoxicity
Dermatology
Ethanol
Genetic aspects
Herbal medicine
High performance liquid chromatography
Hyaluronic acid
Immunoblotting
JNK protein
Keratinocytes
Kinases
Liquid chromatography
MAP kinase
Materia medica, Vegetable
Medicinal plants
Mitogen-activated protein kinases
Oxidation
Physiological aspects
Plant extracts
Protected species
Proteins
Reactive oxygen species
Reporter gene
ROS
Rutin
Scavenging
Signal transduction
Signaling
Skin
Toxicity
Transcription factors
Ultraviolet radiation
UVB irradiation
South Korea
Vietnam
antioxidative capacity
anti-apoptosis
AP-1
Ardisia silvestris ethanol extract
ROS
UVB irradiation
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Abstract is a traditional medicinal herb used in Vietnam and several other countries. However, the skin-protective properties of ethanol extract (As-EE) have not been evaluated. Human keratinocytes form the outermost barrier of the skin and are the main target of ultraviolet (UV) radiation. UV exposure causes skin photoaging via the production of reactive oxygen species. Protection from photoaging is thus a key component of dermatological and cosmetic products. In this research, we found that As-EE can prevent UV-induced skin aging and cell death as well as enhance the barrier effect of the skin. First, the radical-scavenging ability of As-EE was checked using DPPH, ABTS, TPC, CUPRAC, and FRAP assays, and a 3-(4-5-dimethylthiazol-2-yl)-2-5-diphenyltetrazolium bromide assay was used to examine cytotoxicity. Reporter gene assays were used to determine the doses that affect skin-barrier-related genes. A luciferase assay was used to identify possible transcription factors. The anti-photoaging mechanism of As-EE was investigated by determining correlated signaling pathways using immunoblotting analyses. As-EE had no harmful effects on HaCaT cells, according to our findings, and As-EE revealed moderate radical-scavenging ability. With high-performance liquid chromatography (HPLC) analysis, rutin was found to be one of the major components. In addition, As-EE enhanced the expression levels of hyaluronic acid synthase-1 and occludin in HaCaT cells. Moreover, As-EE dose-dependently up-regulated the production of occludin and transglutaminase-1 after suppression caused by UVB blocking the activator protein-1 signaling pathway, in particular, the extracellular response kinase and c-Jun N-terminal kinase. Our findings suggest that As-EE may have anti-photoaging effects by regulating mitogen-activated protein kinase, which is good news for the cosmetics and dermatology sectors.
AbstractList Ardisia silvestris is a traditional medicinal herb used in Vietnam and several other countries. However, the skin-protective properties of A. silvestris ethanol extract (As-EE) have not been evaluated. Human keratinocytes form the outermost barrier of the skin and are the main target of ultraviolet (UV) radiation. UV exposure causes skin photoaging via the production of reactive oxygen species. Protection from photoaging is thus a key component of dermatological and cosmetic products. In this research, we found that As-EE can prevent UV-induced skin aging and cell death as well as enhance the barrier effect of the skin. First, the radical-scavenging ability of As-EE was checked using DPPH, ABTS, TPC, CUPRAC, and FRAP assays, and a 3-(4-5-dimethylthiazol-2-yl)-2-5-diphenyltetrazolium bromide assay was used to examine cytotoxicity. Reporter gene assays were used to determine the doses that affect skin-barrier-related genes. A luciferase assay was used to identify possible transcription factors. The anti-photoaging mechanism of As-EE was investigated by determining correlated signaling pathways using immunoblotting analyses. As-EE had no harmful effects on HaCaT cells, according to our findings, and As-EE revealed moderate radical-scavenging ability. With high-performance liquid chromatography (HPLC) analysis, rutin was found to be one of the major components. In addition, As-EE enhanced the expression levels of hyaluronic acid synthase-1 and occludin in HaCaT cells. Moreover, As-EE dose-dependently up-regulated the production of occludin and transglutaminase-1 after suppression caused by UVB blocking the activator protein-1 signaling pathway, in particular, the extracellular response kinase and c-Jun N-terminal kinase. Our findings suggest that As-EE may have anti-photoaging effects by regulating mitogen-activated protein kinase, which is good news for the cosmetics and dermatology sectors.
is a traditional medicinal herb used in Vietnam and several other countries. However, the skin-protective properties of ethanol extract (As-EE) have not been evaluated. Human keratinocytes form the outermost barrier of the skin and are the main target of ultraviolet (UV) radiation. UV exposure causes skin photoaging via the production of reactive oxygen species. Protection from photoaging is thus a key component of dermatological and cosmetic products. In this research, we found that As-EE can prevent UV-induced skin aging and cell death as well as enhance the barrier effect of the skin. First, the radical-scavenging ability of As-EE was checked using DPPH, ABTS, TPC, CUPRAC, and FRAP assays, and a 3-(4-5-dimethylthiazol-2-yl)-2-5-diphenyltetrazolium bromide assay was used to examine cytotoxicity. Reporter gene assays were used to determine the doses that affect skin-barrier-related genes. A luciferase assay was used to identify possible transcription factors. The anti-photoaging mechanism of As-EE was investigated by determining correlated signaling pathways using immunoblotting analyses. As-EE had no harmful effects on HaCaT cells, according to our findings, and As-EE revealed moderate radical-scavenging ability. With high-performance liquid chromatography (HPLC) analysis, rutin was found to be one of the major components. In addition, As-EE enhanced the expression levels of hyaluronic acid synthase-1 and occludin in HaCaT cells. Moreover, As-EE dose-dependently up-regulated the production of occludin and transglutaminase-1 after suppression caused by UVB blocking the activator protein-1 signaling pathway, in particular, the extracellular response kinase and c-Jun N-terminal kinase. Our findings suggest that As-EE may have anti-photoaging effects by regulating mitogen-activated protein kinase, which is good news for the cosmetics and dermatology sectors.
Ardisia silvestris is a traditional medicinal herb used in Vietnam and several other countries. However, the skin-protective properties of A. silvestris ethanol extract (As-EE) have not been evaluated. Human keratinocytes form the outermost barrier of the skin and are the main target of ultraviolet (UV) radiation. UV exposure causes skin photoaging via the production of reactive oxygen species. Protection from photoaging is thus a key component of dermatological and cosmetic products. In this research, we found that As-EE can prevent UV-induced skin aging and cell death as well as enhance the barrier effect of the skin. First, the radical-scavenging ability of As-EE was checked using DPPH, ABTS, TPC, CUPRAC, and FRAP assays, and a 3-(4-5-dimethylthiazol-2-yl)-2-5-diphenyltetrazolium bromide assay was used to examine cytotoxicity. Reporter gene assays were used to determine the doses that affect skin-barrier-related genes. A luciferase assay was used to identify possible transcription factors. The anti-photoaging mechanism of As-EE was investigated by determining correlated signaling pathways using immunoblotting analyses. As-EE had no harmful effects on HaCaT cells, according to our findings, and As-EE revealed moderate radical-scavenging ability. With high-performance liquid chromatography (HPLC) analysis, rutin was found to be one of the major components. In addition, As-EE enhanced the expression levels of hyaluronic acid synthase-1 and occludin in HaCaT cells. Moreover, As-EE dose-dependently up-regulated the production of occludin and transglutaminase-1 after suppression caused by UVB blocking the activator protein-1 signaling pathway, in particular, the extracellular response kinase and c-Jun N-terminal kinase. Our findings suggest that As-EE may have anti-photoaging effects by regulating mitogen-activated protein kinase, which is good news for the cosmetics and dermatology sectors.
Audience Academic
Author Lee, Jong Sub
Yu, Seung Hui
Huang, Lei
Aziz, Nur
Choung, Eui Su
Luong, Van Dung
You, Long
Jeon, Mi-Jeong
Lee, Sarah
Cho, Jae Youl
Lee, Byoung-Hee
Hur, Moonsuk
Kim, Han Gyung
AuthorAffiliation 1 Department of Biocosmetics, Sungkyunkwan University, Suwon 16419, Republic of Korea
4 DanjoungBio, Co., Ltd., Wonju 26303, Republic of Korea
2 Department of Integrative Biotechnology, Sungkyunkwan University, Suwon 16419, Republic of Korea
3 Pharmacy Program, Faculty of Science and Technology, Ma Chung University, Malang 65151, Indonesia
7 Research Institute of Biomolecule Control and Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon 16419, Republic of Korea
6 National Institute of Biological Resources, Environmental Research Complex, Incheon 222689, Republic of Korea
5 Department of Biology, Dalat University, 01 Phu Dong Thien Vuong, Dalat 66106, Vietnam
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Issue 5
Keywords antioxidative capacity
anti-apoptosis
AP-1
Ardisia silvestris ethanol extract
ROS
UVB irradiation
Language English
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gale_incontextgauss_ISR_A741844346
crossref_primary_10_3390_plants12051167
pubmed_primary_36904025
PublicationCentury 2000
PublicationDate 2023-03-01
PublicationDateYYYYMMDD 2023-03-01
PublicationDate_xml – month: 03
  year: 2023
  text: 2023-03-01
  day: 01
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
– name: Basel
PublicationTitle Plants (Basel)
PublicationTitleAlternate Plants (Basel)
PublicationYear 2023
Publisher MDPI AG
MDPI
Publisher_xml – name: MDPI AG
– name: MDPI
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Snippet is a traditional medicinal herb used in Vietnam and several other countries. However, the skin-protective properties of ethanol extract (As-EE) have not been...
Ardisia silvestris is a traditional medicinal herb used in Vietnam and several other countries. However, the skin-protective properties of A. silvestris...
Ardisia silvestris is a traditional medicinal herb used in Vietnam and several other countries. However, the skin-protective properties of A. silvestris...
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pubmed
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StartPage 1167
SubjectTerms Activator protein 1
Aging (artificial)
anti-apoptosis
antioxidative capacity
AP-1
Apoptosis
Ardisia
Ardisia silvestris ethanol extract
Assaying
c-Jun protein
Care and treatment
Cell death
Cosmetics
Cytotoxicity
Dermatology
Ethanol
Genetic aspects
Herbal medicine
High performance liquid chromatography
Hyaluronic acid
Immunoblotting
JNK protein
Keratinocytes
Kinases
Liquid chromatography
MAP kinase
Materia medica, Vegetable
Medicinal plants
Mitogen-activated protein kinases
Oxidation
Physiological aspects
Plant extracts
Protected species
Proteins
Reactive oxygen species
Reporter gene
ROS
Rutin
Scavenging
Signal transduction
Signaling
Skin
Toxicity
Transcription factors
Ultraviolet radiation
UVB irradiation
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Title Antiphotoaging and Skin-Protective Activities of Ardisia silvestris Ethanol Extract in Human Keratinocytes
URI https://www.ncbi.nlm.nih.gov/pubmed/36904025
https://www.proquest.com/docview/2785207726
https://search.proquest.com/docview/2786092986
https://pubmed.ncbi.nlm.nih.gov/PMC10007040
https://doaj.org/article/433fd93e88914916ace705a30f8fc7e4
Volume 12
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