Loliolide, isolated from Sargassum horneri; abate LPS-induced inflammation via TLR mediated NF-KB, MAPK pathways in macrophages

被引:23
作者
Jayawardena, Thilina U. [1 ]
Kim, Hyun-Soo [2 ]
Sanjeewa, K. K. Asanka [1 ]
Han, Eui Joeng [3 ]
Jee, Youngheun [4 ,5 ]
Ahn, Ginnae [3 ]
Rho, Jung-Rae [6 ]
Jeon, You-Jin [1 ,7 ]
机构
[1] Jeju Natl Univ, Dept Marine Life Sci, Jeju 690756, South Korea
[2] Natl Marine Biodivers Inst Korea, 75,Jangsan Ro 101 Gil, Janghang Eup, Seocheon, South Korea
[3] Chonnam Natl Univ, Dept Food Technol & Nutr, Yeosu 59626, South Korea
[4] Jeju Natl Univ, Dept Vet Med, Jeju 690756, South Korea
[5] Jeju Natl Univ, Vet Med Res Inst, Jeju 690756, South Korea
[6] Kunsan Natl Univ, Dept Oceanog, Jeonbuk 573701, South Korea
[7] Jeju Natl Univ, Inst Marine Sci, Jeju 63333, South Korea
来源
ALGAL RESEARCH-BIOMASS BIOFUELS AND BIOPRODUCTS | 2021年 / 56卷
关键词
Sargassum horneri; TLR2; 4; NF-KB; MAPK; pro-inflammatory mediators; terpene lactone; TUMOR-NECROSIS-FACTOR; NITRIC-OXIDE; KAPPA-B; SULFATED POLYSACCHARIDE; GENE-EXPRESSION; INNATE IMMUNITY; STRESS; P38; RECOGNITION; ACTIVATION;
D O I
10.1016/j.algal.2021.102297
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The secondary metabolite terpene lactone; 6-hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)one; (Loliolide) from Sargassum horneri which is abundant on the shores of South Korea was investigated for its anti-inflammatory properties in RAW 264.7 macrophages under LPS stimulation. Isolation and identification were assisted by HPCPC, HPLC-MS, GC-MS, and NMR. Initial assessments of NO production downregulation influenced further studies of inflammatory mediators such that; iNOS, COX-2, and pro-inflammatory cytokines including PGE2 which were significantly declined with loliolide treatment. Inflammation is initiated via the identification of alien matter from the cell membrane; the toll-like receptor modulated NF-KB was investigated combined with MAPK signaling. Experimental outputs manifested the potential of loliolide to abate the inflammation in macrophages which were confronted by LPS. Hence, this provides insight to the mediation of inflammatory disorders through the sustainable use of abundant natural source marine algae and utilizing its secondary metabolites.
引用
收藏
页数:8
相关论文
共 47 条
[1]   Tumor necrosis factor as a therapeutic target of rheumatologic disease [J].
Ackermann, Christoph ;
Kavanaugh, Arthur .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2007, 11 (11) :1369-1384
[2]   Role of redox potential and reactive oxygen species in stress signaling [J].
Adler, V ;
Yin, ZM ;
Tew, KD ;
Ronai, Z .
ONCOGENE, 1999, 18 (45) :6104-6111
[3]   iNOS-mediated nitric oxide production and its regulation [J].
Aktan, F .
LIFE SCIENCES, 2004, 75 (06) :639-653
[4]   Antifouling chromanols isolated from brown alga Sargassum horneri [J].
Cho, Ji Young .
JOURNAL OF APPLIED PHYCOLOGY, 2013, 25 (01) :299-309
[5]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867
[6]   Mechanisms and functions of p38 MAPK signalling [J].
Cuadrado, Ana ;
Nebreda, Angel R. .
BIOCHEMICAL JOURNAL, 2010, 429 :403-417
[7]   3β-Hydroxy-Δ5-steroidal congeners from a column fraction of Dendronephthya puetteri attenuate LPS-induced inflammatory responses in RAW 264.7 macrophages and zebrafish embryo model [J].
Fernando, I. P. Shanura ;
Lee, Won Woo ;
Jayawardena, Thilina U. ;
Kang, Min-Cheol ;
Ann, Yong-Seok ;
Ko, Chang-ik ;
Park, Young Jin ;
Jeon, You-Jin .
RSC ADVANCES, 2018, 8 (33) :18626-18634
[8]   Anti-inflammatory potential of alginic acid from Sargassum horneri against urban aerosol-induced inflammatory responses in keratinocytes and macrophages [J].
Fernando, I. P. Shanura ;
Jayawardena, Thilina U. ;
Sanjeewa, K. K. Asanka ;
Wang, Lei ;
Jeon, You-Jin ;
Lee, Won Woo .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2018, 160 :24-31
[9]   DROSOPHILA TOLL AND IL-1 RECEPTOR [J].
GAY, NJ ;
KEITH, FJ .
NATURE, 1991, 351 (6325) :355-356
[10]   In vivo ethanol exposure down-regulates TLR2-, TLR4-, and TLR9-mediated macrophage inflammatory response by limiting p38 and ERK1/2 activation [J].
Goral, J ;
Kovacs, EJ .
JOURNAL OF IMMUNOLOGY, 2005, 174 (01) :456-463