(-)-Loliolide Isolated fromSargassum horneriProtects against Fine Dust-Induced Oxidative Stress in Human Keratinocytes

被引:26
|
作者
Dias, Mawalle Kankanamge Hasitha Madhawa [1 ]
Madusanka, Dissanayaka Mudiyanselage Dinesh [1 ]
Han, Eui Jeong [1 ]
Kim, Min Ju [1 ]
Jeon, You-Jin [2 ,3 ]
Kim, Hyun-Soo [2 ,4 ]
Fernando, Ilekuttige Priyan Shanura [5 ]
Ahn, Ginnae [1 ,5 ]
机构
[1] Chonnam Natl Univ, Dept Food Technol & Nutr, Yeosu 59626, South Korea
[2] Jeju Natl Univ, Sch Marine Biomed Sci, Dept Marine Life Sci, Jeju 63243, South Korea
[3] Jeju Natl Univ, Marine Sci Inst, Jeju 63333, Self Governing, South Korea
[4] Natl Marine Biodivers Inst Korea, 75,Jangsan Ro 101 Gil, Janghang Eup 33662, Seocheon, South Korea
[5] Chonnam Natl Univ, Dept Marine Biofood Sci, Yeosu 59626, South Korea
基金
新加坡国家研究基金会;
关键词
Sargassum horneri; (-)-loliolide; fine dust; oxidative stress; HaCaT; apoptosis; SARGASSUM-HORNERI; ASIAN DUST; APOPTOSIS; FRAGMENTATION; PARTICLES; ISLAND; ACID; DNA;
D O I
10.3390/antiox9060474
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The emergence of fine dust (FD) among air pollutants has taken a toll during the past few decades, and it has provided both controversy and a platform for open conversation amongst world powers for finding sustainable solutions and effective treatments for health issues. The present study emphasizes the protective effects of (-)-loliolide (HTT) isolated fromSargassum horneriagainst FD-induced oxidative stress in human HaCaT keratinocytes. The purification of (-)-loliolide was carried out by centrifugal partition chromatography. HTT did not show any cytotoxicity, and it further illustrated the potential to increase cell viability by reducing the reactive oxygen species (ROS) production in FD-stimulated keratinocytes. Furthermore, HTT suppressed FD-stimulated DNA damage and the formation of apoptotic bodies, and it reduced the population of cells in the sub-G(1)apoptosis phase. FD-induced apoptosis was advancing through the mitochondria-mediated apoptosis pathway. The cytoprotective effects of the HTT against FD-stimulated oxidative damage is mediated through squaring the nuclear factor E2-related factor 2 (Nrf2)-mediated heme oxygenase-1 (HO-1) pathway, dose-dependently increasing HO-1 and NAD(P)H dehydrogenase (quinone) 1 (NQO1) levels in the cytosol while concomitantly improving the nuclear translocation of Nrf2. Future studies could implement the protective functionality of HTT in producing pharmaceuticals that utilize natural products and benefit the diseased.
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页数:12
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