4‐Hexyl‐1, 3‐phenylenediol, a nuclear factor‐κB inhibitor, improves photodamaged skin and clinical signs of ageing in a double‐blinded, randomized controlled trial. (11th June 2015)
- Record Type:
- Journal Article
- Title:
- 4‐Hexyl‐1, 3‐phenylenediol, a nuclear factor‐κB inhibitor, improves photodamaged skin and clinical signs of ageing in a double‐blinded, randomized controlled trial. (11th June 2015)
- Main Title:
- 4‐Hexyl‐1, 3‐phenylenediol, a nuclear factor‐κB inhibitor, improves photodamaged skin and clinical signs of ageing in a double‐blinded, randomized controlled trial
- Authors:
- Kaur, S.
Kizoulis, M.
Fantasia, J.
Oddos, T.
Bigot, N.
Galera, P.
Tucker‐Samaras, S.
Leyden, J.J.
Southall, M.D. - Abstract:
- <abstract abstract-type="main" id="bjd13747-abs-0001"> <title>Summary</title> <sec id="bjd13747-sec-0001" sec-type="section"> <title>Background</title> <p>The nuclear factor‐κB (NF‐κB) pathway is a key mediator of inflammation; however, few studies have examined the direct effects of NF‐κB inhibition on the skin.</p> </sec> <sec id="bjd13747-sec-0002" sec-type="section"> <title>Objectives</title> <p>To investigate NF‐κB activity in cultured human fibroblasts and to investigate the effects of 4‐hexyl‐1, 3‐phenylenediol (an NF‐κB inhibitor) on elastin and collagen gene expression <italic>in vitro</italic> and on the clinical appearance of photodamaged skin.</p> </sec> <sec id="bjd13747-sec-0003" sec-type="section"> <title>Methods</title> <p>The amount and activity of NF‐κB in human fibroblasts obtained from donors (17–78 years old) was measured after transfection with a NF‐κB reporter and a luciferase promoter system. The expression of extracellular matrix (ECM) genes was determined using quantitative polymerase chain reaction. Women with moderate skin photodamage were randomized to daily treatment with a topical lotion containing 4‐hexyl‐1, 3‐phenylenediol (<italic>n </italic>=<italic> </italic>30) or vehicle (<italic>n </italic>=<italic> </italic>29) for 8 weeks, with clinical assessments at baseline and weeks 2, 4 and 8.</p> </sec> <sec id="bjd13747-sec-0004" sec-type="section"> <title>Results</title> <p>Fibroblasts obtained from donors older than 50 years had higher NF‐κB<abstract abstract-type="main" id="bjd13747-abs-0001"> <title>Summary</title> <sec id="bjd13747-sec-0001" sec-type="section"> <title>Background</title> <p>The nuclear factor‐κB (NF‐κB) pathway is a key mediator of inflammation; however, few studies have examined the direct effects of NF‐κB inhibition on the skin.</p> </sec> <sec id="bjd13747-sec-0002" sec-type="section"> <title>Objectives</title> <p>To investigate NF‐κB activity in cultured human fibroblasts and to investigate the effects of 4‐hexyl‐1, 3‐phenylenediol (an NF‐κB inhibitor) on elastin and collagen gene expression <italic>in vitro</italic> and on the clinical appearance of photodamaged skin.</p> </sec> <sec id="bjd13747-sec-0003" sec-type="section"> <title>Methods</title> <p>The amount and activity of NF‐κB in human fibroblasts obtained from donors (17–78 years old) was measured after transfection with a NF‐κB reporter and a luciferase promoter system. The expression of extracellular matrix (ECM) genes was determined using quantitative polymerase chain reaction. Women with moderate skin photodamage were randomized to daily treatment with a topical lotion containing 4‐hexyl‐1, 3‐phenylenediol (<italic>n </italic>=<italic> </italic>30) or vehicle (<italic>n </italic>=<italic> </italic>29) for 8 weeks, with clinical assessments at baseline and weeks 2, 4 and 8.</p> </sec> <sec id="bjd13747-sec-0004" sec-type="section"> <title>Results</title> <p>Fibroblasts obtained from donors older than 50 years had higher NF‐κB activity compared with cells from younger donors; inhibition of the NF‐κB pathway with 4‐hexyl‐1, 3‐phenylenediol enhanced the expression of ECM genes. In women, treatment for 8 weeks with 4‐hexyl‐1, 3‐phenylenediol significantly improved crow's feet fine lines, cheek wrinkles, age spots, mottled pigmentation and radiance compared with both the vehicle and baseline. Furthermore, treatment with 4‐hexyl‐1, 3‐phenylenediol resulted in a twofold greater clinical improvement in overall photodamage compared with the vehicle group.</p> </sec> <sec id="bjd13747-sec-0005" sec-type="section"> <title>Conclusions</title> <p>Inhibition of the proinflammatory NF‐κB pathway resulted in increased expression of ECM proteins <italic>in vitro</italic> and significant clinical improvement in photodamaged skin.</p> </sec> </abstract> … (more)
- Is Part Of:
- British journal of dermatology. Volume 173:Number 1(2015:Jul.)
- Journal:
- British journal of dermatology
- Issue:
- Volume 173:Number 1(2015:Jul.)
- Issue Display:
- Volume 173, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 173
- Issue:
- 1
- Issue Sort Value:
- 2015-0173-0001-0000
- Page Start:
- 218
- Page End:
- 226
- Publication Date:
- 2015-06-11
- Subjects:
- Dermatology -- Periodicals
Skin -- Diseases -- Periodicals
616.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2133 ↗
https://academic.oup.com/bjd ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bjd.13747 ↗
- Languages:
- English
- ISSNs:
- 0007-0963
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2307.400000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3797.xml