dl-Malic acid as a component of α-hydroxy acids: effect on 2,4-dinitrochlorobenzene-induced inflammation in atopic dermatitis-like skin lesionsin vitroandin vivo

哈卡特 趋化因子 化学 肿瘤坏死因子α 炎症 免疫学 分子生物学 体内 体外 医学 生物化学 生物 生物技术
作者
Bina Lee,Jun Heo,Sooyeon Hong,Eun‐Young Kim,Young Joo Sohn,Hyuk‐Sang Jung
出处
期刊:Immunopharmacology and Immunotoxicology [Taylor & Francis]
卷期号:41 (6): 614-621 被引量:24
标识
DOI:10.1080/08923973.2019.1680688
摘要

Background: dl-Malic acid (dl-M) is used widely in cosmetic formulations as a pH-adjuster or as a preservative. dl-M is used as an exfoliator in the form of α-hydroxy acids. However, the role of dl-M in skin diseases (including atopic dermatitis (AD)) has not been studied deeply. We wished to reveal the effect of dl-M on AD induced by 2,4-dinitrochlorobenzene (DNCB) in Balb/c mice.Methods: The thickness and immune-cell infiltration into the dermis and epidermis were evaluated. Moreover, serum levels of cytokines, as well as expression of mitogen-activated protein kinase (MAPK) and nuclear factor-kappa B (NF-κB) in tissue were measured in AD mice. We also studied the effect of dl-M on inflammatory mediators in a human keratinocyte (HaCaT) cell line. Results: The dl-M (high) group improved skin condition compared with the DNCB-treated group. The dl-M (high) group inhibited phosphorylation of MAPK and NF-κB in skin tissue. dl-M reduced serum levels of interleukin-4 and IgE. Finally, dl-M decreased the expression of thymus and activation-regulated chemokine, monocyte chemoattractant protein-1 and intercellular cell adhesion molecule induced by interferon-gamma/tumor necrosis factor-α in HaCaT cells. Discussion: These results suggest that dl-M can improve the skin conditions of AD mice.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
智慧完成签到,获得积分10
刚刚
刚刚
说不上好完成签到,获得积分10
刚刚
int0030完成签到,获得积分10
1秒前
YANG完成签到 ,获得积分10
1秒前
1秒前
1秒前
cijing完成签到,获得积分10
2秒前
问柳完成签到,获得积分10
2秒前
小圆子完成签到,获得积分10
2秒前
趁微风不躁完成签到,获得积分10
2秒前
大鹅莓烦恼完成签到,获得积分10
2秒前
11发布了新的文献求助10
3秒前
那一瞬的永恒完成签到,获得积分10
3秒前
霸气果汁完成签到,获得积分0
3秒前
颜凡桃完成签到,获得积分10
3秒前
xx完成签到 ,获得积分10
3秒前
3秒前
fu完成签到,获得积分10
3秒前
123完成签到,获得积分10
3秒前
tans0008完成签到,获得积分10
3秒前
龙凌音完成签到,获得积分10
3秒前
蓝桉完成签到,获得积分0
4秒前
充电宝应助东asdfghjkl采纳,获得10
4秒前
hahakeyan完成签到 ,获得积分10
4秒前
问水完成签到,获得积分10
4秒前
牧青应助daomaihu采纳,获得100
4秒前
牧青应助daomaihu采纳,获得100
4秒前
顺心囧完成签到 ,获得积分10
4秒前
壮观的谷冬完成签到,获得积分0
4秒前
柔弱毒娘完成签到,获得积分10
4秒前
图图完成签到,获得积分10
5秒前
entgegen完成签到,获得积分10
5秒前
jessie完成签到,获得积分10
6秒前
阿布与小佛完成签到 ,获得积分10
6秒前
sagitar发布了新的文献求助30
6秒前
6秒前
wuxu完成签到,获得积分10
6秒前
聪明小懒虫完成签到,获得积分20
6秒前
寒冷的咖啡豆完成签到,获得积分10
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
CLSI VET01S-2024 Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated From Animals (7th Ed) 500
DIPPR Project 801 - Full Version 380
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7766181
求助须知:如何正确求助?哪些是违规求助? 9310092
关于积分的说明 20315074
捐赠科研通 7351008
什么是DOI,文献DOI怎么找? 3315033
关于科研通互助平台的介绍 2464576
邀请新用户注册赠送积分活动 2329603