Anti-inflammatory effect of sargachromanol G isolated from Sargassum siliquastrum in RAW 264.7 cells

Weon Jong Yoon; Soo Jin Heo; Sang Chul Han; Hye Ja Lee; Gyeoung Jin Kang; Hee Kyoung Kang; Jin Won Hyun; Young Sang Koh; Eun Sook Yoo

doi:10.1007/s12272-012-0812-5

Anti-inflammatory effect of sargachromanol G isolated from Sargassum siliquastrum in RAW 264.7 cells

Weon Jong Yoon, Soo Jin Heo, Sang Chul Han, Hye Ja Lee, Gyeoung Jin Kang, Hee Kyoung Kang, Jin Won Hyun, Young Sang Koh, Eun Sook Yoo

Medicine - Cardiology Division

Research output: Contribution to journal › Article › peer-review

65 Scopus citations

Abstract

A study on the anti-inflammatory activity of brown alga Sargassum siliquastrum led to the isolation of sargachromanol G (SG). In this study, the anti-inflammatory effect and the action mechanism of SG have been investigated in murine macrophage cell line RAW 264.7. SG dosedependently inhibited the production of inflammatory markers [nitric oxide (NO), inducible nitric oxide synthase (iNOS), prostaglandin E₂ (PGE₂), and cyclooxygenase-2 (COX-2)] and pro-inflammatory cytokines [tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6] induced by LPS treatment. To further elucidate the mechanism of this inhibitory effect of SG, we studied LPSinduced nuclear factor-κB (NF-κB) activation and mitogen-activated protein kinases (MAPKs) phosphorylation. SG inhibited the phosphorylation IκB-α and NF-κB (p65 and p50) and MAPK (ERK1/2, JNK, and p38) in a dose dependent manner. These results suggest that the anti-inflammatory activity of SG results from its modulation of pro-inflammatory cytokines and mediators via the suppression of NF-κB activation and MAPK phosphorylation.

Original language	English (US)
Pages (from-to)	1421-1430
Number of pages	10
Journal	Archives of Pharmacal Research
Volume	35
Issue number	8
DOIs	https://doi.org/10.1007/s12272-012-0812-5
State	Published - Aug 2012

Bibliographical note

Funding Information:
This work was supported by the National Research Foundation of Korea Grant funded by the Korean Government (MEST) (NRF-C1-2011-0021039)

Keywords

Inflammatory markers
MAPK
NF-κB
Pro-inflammatory cytokines
Sargachromanol G
Sargassum siliquastrum

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10.1007/s12272-012-0812-5

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title = "Anti-inflammatory effect of sargachromanol G isolated from Sargassum siliquastrum in RAW 264.7 cells",

abstract = "A study on the anti-inflammatory activity of brown alga Sargassum siliquastrum led to the isolation of sargachromanol G (SG). In this study, the anti-inflammatory effect and the action mechanism of SG have been investigated in murine macrophage cell line RAW 264.7. SG dosedependently inhibited the production of inflammatory markers [nitric oxide (NO), inducible nitric oxide synthase (iNOS), prostaglandin E2 (PGE2), and cyclooxygenase-2 (COX-2)] and pro-inflammatory cytokines [tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6] induced by LPS treatment. To further elucidate the mechanism of this inhibitory effect of SG, we studied LPSinduced nuclear factor-κB (NF-κB) activation and mitogen-activated protein kinases (MAPKs) phosphorylation. SG inhibited the phosphorylation IκB-α and NF-κB (p65 and p50) and MAPK (ERK1/2, JNK, and p38) in a dose dependent manner. These results suggest that the anti-inflammatory activity of SG results from its modulation of pro-inflammatory cytokines and mediators via the suppression of NF-κB activation and MAPK phosphorylation.",

keywords = "Inflammatory markers, MAPK, NF-κB, Pro-inflammatory cytokines, Sargachromanol G, Sargassum siliquastrum",

author = "Yoon, {Weon Jong} and Heo, {Soo Jin} and Han, {Sang Chul} and Lee, {Hye Ja} and Kang, {Gyeoung Jin} and Kang, {Hee Kyoung} and Hyun, {Jin Won} and Koh, {Young Sang} and Yoo, {Eun Sook}",

note = "Funding Information: This work was supported by the National Research Foundation of Korea Grant funded by the Korean Government (MEST) (NRF-C1-2011-0021039)",

year = "2012",

month = aug,

doi = "10.1007/s12272-012-0812-5",

language = "English (US)",

volume = "35",

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journal = "Archives of Pharmacal Research",

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TY - JOUR

T1 - Anti-inflammatory effect of sargachromanol G isolated from Sargassum siliquastrum in RAW 264.7 cells

AU - Yoon, Weon Jong

AU - Heo, Soo Jin

AU - Han, Sang Chul

AU - Lee, Hye Ja

AU - Kang, Gyeoung Jin

AU - Kang, Hee Kyoung

AU - Hyun, Jin Won

AU - Koh, Young Sang

AU - Yoo, Eun Sook

N1 - Funding Information: This work was supported by the National Research Foundation of Korea Grant funded by the Korean Government (MEST) (NRF-C1-2011-0021039)

PY - 2012/8

Y1 - 2012/8

N2 - A study on the anti-inflammatory activity of brown alga Sargassum siliquastrum led to the isolation of sargachromanol G (SG). In this study, the anti-inflammatory effect and the action mechanism of SG have been investigated in murine macrophage cell line RAW 264.7. SG dosedependently inhibited the production of inflammatory markers [nitric oxide (NO), inducible nitric oxide synthase (iNOS), prostaglandin E2 (PGE2), and cyclooxygenase-2 (COX-2)] and pro-inflammatory cytokines [tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6] induced by LPS treatment. To further elucidate the mechanism of this inhibitory effect of SG, we studied LPSinduced nuclear factor-κB (NF-κB) activation and mitogen-activated protein kinases (MAPKs) phosphorylation. SG inhibited the phosphorylation IκB-α and NF-κB (p65 and p50) and MAPK (ERK1/2, JNK, and p38) in a dose dependent manner. These results suggest that the anti-inflammatory activity of SG results from its modulation of pro-inflammatory cytokines and mediators via the suppression of NF-κB activation and MAPK phosphorylation.

AB - A study on the anti-inflammatory activity of brown alga Sargassum siliquastrum led to the isolation of sargachromanol G (SG). In this study, the anti-inflammatory effect and the action mechanism of SG have been investigated in murine macrophage cell line RAW 264.7. SG dosedependently inhibited the production of inflammatory markers [nitric oxide (NO), inducible nitric oxide synthase (iNOS), prostaglandin E2 (PGE2), and cyclooxygenase-2 (COX-2)] and pro-inflammatory cytokines [tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6] induced by LPS treatment. To further elucidate the mechanism of this inhibitory effect of SG, we studied LPSinduced nuclear factor-κB (NF-κB) activation and mitogen-activated protein kinases (MAPKs) phosphorylation. SG inhibited the phosphorylation IκB-α and NF-κB (p65 and p50) and MAPK (ERK1/2, JNK, and p38) in a dose dependent manner. These results suggest that the anti-inflammatory activity of SG results from its modulation of pro-inflammatory cytokines and mediators via the suppression of NF-κB activation and MAPK phosphorylation.

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KW - MAPK

KW - NF-κB

KW - Pro-inflammatory cytokines

KW - Sargachromanol G

KW - Sargassum siliquastrum

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Anti-inflammatory effect of sargachromanol G isolated from Sargassum siliquastrum in RAW 264.7 cells

Abstract

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