Cargando…

Clinical evaluation of the safety and efficacy of a timosaponin A‐III‐based antiwrinkle agent against skin aging

BACKGROUND: Timosaponin A‐III (TA‐III) is known to exist in the medicinal herb of Anemarrhena asphodeloides as one of major chemical components. AIMS: The photoprotective properties of TA‐III on UVB‐exposed HaCaT cells were evaluated on the antiwrinkle effects and skin safety in terms of clinical tr...

Descripción completa

Detalles Bibliográficos
Autores principales: Im, A‐Rang, Seo, Young Kyoung, Cho, Se Hee, O, Kyeong Hee, Kim, Ki Mo, Chae, Sungwook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003920/
https://www.ncbi.nlm.nih.gov/pubmed/31215156
http://dx.doi.org/10.1111/jocd.13035
_version_ 1783494624097075200
author Im, A‐Rang
Seo, Young Kyoung
Cho, Se Hee
O, Kyeong Hee
Kim, Ki Mo
Chae, Sungwook
author_facet Im, A‐Rang
Seo, Young Kyoung
Cho, Se Hee
O, Kyeong Hee
Kim, Ki Mo
Chae, Sungwook
author_sort Im, A‐Rang
collection PubMed
description BACKGROUND: Timosaponin A‐III (TA‐III) is known to exist in the medicinal herb of Anemarrhena asphodeloides as one of major chemical components. AIMS: The photoprotective properties of TA‐III on UVB‐exposed HaCaT cells were evaluated on the antiwrinkle effects and skin safety in terms of clinical trial. METHODS: The level of matrix metalloproteinase (MMP)‐1, tissue inhibitor of metalloproteinases (TIMPs), and pro‐inflammatory cytokines were measured in HaCaT cells following UVB irradiation. To evaluate the clinical safety of an agent containing 0.25% of TA‐III for use on human skin. Female subjects (n = 21) between the ages of 43 and 55 who met the criteria for subject selection were selected. They were beginning to form or had already formed wrinkles. RESULTS: UVB irradiation increased MMP‐1 expression and pro‐inflammatory cytokines. These increases were attenuated by TA‐III pretreatment of UVB‐exposed HaCaT cells. We found that the agent containing 0.25% of TA‐III ameliorated skin wrinkling. A comparison between groups showed that wrinkle parameters were significantly reduced after 12 weeks of product use (P < 0.05). According to skin safety result, TA‐III showed no dermatological toxicity was found in participants. CONCLUSIONS: In conclusion, TA‐III could provide protection against photoaging and daily application of TA‐III for 12 weeks significantly reduced signs of facial aging by limiting wrinkle formation.
format Online
Article
Text
id pubmed-7003920
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-70039202020-02-11 Clinical evaluation of the safety and efficacy of a timosaponin A‐III‐based antiwrinkle agent against skin aging Im, A‐Rang Seo, Young Kyoung Cho, Se Hee O, Kyeong Hee Kim, Ki Mo Chae, Sungwook J Cosmet Dermatol Skin Care Articles BACKGROUND: Timosaponin A‐III (TA‐III) is known to exist in the medicinal herb of Anemarrhena asphodeloides as one of major chemical components. AIMS: The photoprotective properties of TA‐III on UVB‐exposed HaCaT cells were evaluated on the antiwrinkle effects and skin safety in terms of clinical trial. METHODS: The level of matrix metalloproteinase (MMP)‐1, tissue inhibitor of metalloproteinases (TIMPs), and pro‐inflammatory cytokines were measured in HaCaT cells following UVB irradiation. To evaluate the clinical safety of an agent containing 0.25% of TA‐III for use on human skin. Female subjects (n = 21) between the ages of 43 and 55 who met the criteria for subject selection were selected. They were beginning to form or had already formed wrinkles. RESULTS: UVB irradiation increased MMP‐1 expression and pro‐inflammatory cytokines. These increases were attenuated by TA‐III pretreatment of UVB‐exposed HaCaT cells. We found that the agent containing 0.25% of TA‐III ameliorated skin wrinkling. A comparison between groups showed that wrinkle parameters were significantly reduced after 12 weeks of product use (P < 0.05). According to skin safety result, TA‐III showed no dermatological toxicity was found in participants. CONCLUSIONS: In conclusion, TA‐III could provide protection against photoaging and daily application of TA‐III for 12 weeks significantly reduced signs of facial aging by limiting wrinkle formation. John Wiley and Sons Inc. 2019-06-18 2020-02 /pmc/articles/PMC7003920/ /pubmed/31215156 http://dx.doi.org/10.1111/jocd.13035 Text en © 2019 The Authors. Journal of Cosmetic Dermatology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Skin Care Articles
Im, A‐Rang
Seo, Young Kyoung
Cho, Se Hee
O, Kyeong Hee
Kim, Ki Mo
Chae, Sungwook
Clinical evaluation of the safety and efficacy of a timosaponin A‐III‐based antiwrinkle agent against skin aging
title Clinical evaluation of the safety and efficacy of a timosaponin A‐III‐based antiwrinkle agent against skin aging
title_full Clinical evaluation of the safety and efficacy of a timosaponin A‐III‐based antiwrinkle agent against skin aging
title_fullStr Clinical evaluation of the safety and efficacy of a timosaponin A‐III‐based antiwrinkle agent against skin aging
title_full_unstemmed Clinical evaluation of the safety and efficacy of a timosaponin A‐III‐based antiwrinkle agent against skin aging
title_short Clinical evaluation of the safety and efficacy of a timosaponin A‐III‐based antiwrinkle agent against skin aging
title_sort clinical evaluation of the safety and efficacy of a timosaponin a‐iii‐based antiwrinkle agent against skin aging
topic Skin Care Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003920/
https://www.ncbi.nlm.nih.gov/pubmed/31215156
http://dx.doi.org/10.1111/jocd.13035
work_keys_str_mv AT imarang clinicalevaluationofthesafetyandefficacyofatimosaponinaiiibasedantiwrinkleagentagainstskinaging
AT seoyoungkyoung clinicalevaluationofthesafetyandefficacyofatimosaponinaiiibasedantiwrinkleagentagainstskinaging
AT chosehee clinicalevaluationofthesafetyandefficacyofatimosaponinaiiibasedantiwrinkleagentagainstskinaging
AT okyeonghee clinicalevaluationofthesafetyandefficacyofatimosaponinaiiibasedantiwrinkleagentagainstskinaging
AT kimkimo clinicalevaluationofthesafetyandefficacyofatimosaponinaiiibasedantiwrinkleagentagainstskinaging
AT chaesungwook clinicalevaluationofthesafetyandefficacyofatimosaponinaiiibasedantiwrinkleagentagainstskinaging