BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways

Our preliminary screening has shown that curcumin derivative BDMC33 [2,6-bis(2,5-dimethoxybenzylidene)cyclohexanone] exerted promising nitric oxide inhibitory activity in activated macrophages. However, the molecular basis and mechanism for its pharmacological action is yet to be elucidated. The aim...

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Main Authors: Lee, Ka Heng, Chow, Yuh Lit, Vidyadaran, Sharmili, Abas, Faridah, Mohammed Alitheen, Noorjahan Banu, Shaari, Khozirah, Israf Ali, Daud Ahmad, Lajis, Nordin, Ahmad, Syahida
Format: Article
Language:English
Published: MDPI 2012
Online Access:http://psasir.upm.edu.my/id/eprint/78007/1/78007.pdf
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author Lee, Ka Heng
Chow, Yuh Lit
Vidyadaran, Sharmili
Abas, Faridah
Mohammed Alitheen, Noorjahan Banu
Shaari, Khozirah
Israf Ali, Daud Ahmad
Lajis, Nordin
Ahmad, Syahida
author_facet Lee, Ka Heng
Chow, Yuh Lit
Vidyadaran, Sharmili
Abas, Faridah
Mohammed Alitheen, Noorjahan Banu
Shaari, Khozirah
Israf Ali, Daud Ahmad
Lajis, Nordin
Ahmad, Syahida
author_sort Lee, Ka Heng
collection UPM
description Our preliminary screening has shown that curcumin derivative BDMC33 [2,6-bis(2,5-dimethoxybenzylidene)cyclohexanone] exerted promising nitric oxide inhibitory activity in activated macrophages. However, the molecular basis and mechanism for its pharmacological action is yet to be elucidated. The aim of this study was to investigate the anti-inflammatory properties of BDMC33 and elucidate its underlying mechanism action in macrophage cells. Our current study demonstrated that BDMC33 inhibits the secretion of major pro-inflammatory mediators in stimulated macrophages, and includes NO, TNF-α and IL-1β through interference in both nuclear factor kappaB (NF-κB) and mitogen activator protein kinase (MAPK) signaling cascade in IFN-γ/LPS-stimulated macrophages. Moreover, BDMC33 also interrupted LPS signaling through inhibiting the surface expression of CD-14 accessory molecules. In addition, the inhibitory action of BDMC33 not only restricted the macrophages cell (RAW264.7), but also inhibited the secretion of NO and TNF-α in IFN-γ/LPS-challenged microglial cells (BV-2). The experimental data suggests the inflammatory action of BDMC33 on activated macrophage-like cellular systems, which could be used as a future therapeutic agent in the management of chronic inflammatory diseases.
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spelling upm.eprints-780072020-06-01T09:04:26Z http://psasir.upm.edu.my/id/eprint/78007/ BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways Lee, Ka Heng Chow, Yuh Lit Vidyadaran, Sharmili Abas, Faridah Mohammed Alitheen, Noorjahan Banu Shaari, Khozirah Israf Ali, Daud Ahmad Lajis, Nordin Ahmad, Syahida Our preliminary screening has shown that curcumin derivative BDMC33 [2,6-bis(2,5-dimethoxybenzylidene)cyclohexanone] exerted promising nitric oxide inhibitory activity in activated macrophages. However, the molecular basis and mechanism for its pharmacological action is yet to be elucidated. The aim of this study was to investigate the anti-inflammatory properties of BDMC33 and elucidate its underlying mechanism action in macrophage cells. Our current study demonstrated that BDMC33 inhibits the secretion of major pro-inflammatory mediators in stimulated macrophages, and includes NO, TNF-α and IL-1β through interference in both nuclear factor kappaB (NF-κB) and mitogen activator protein kinase (MAPK) signaling cascade in IFN-γ/LPS-stimulated macrophages. Moreover, BDMC33 also interrupted LPS signaling through inhibiting the surface expression of CD-14 accessory molecules. In addition, the inhibitory action of BDMC33 not only restricted the macrophages cell (RAW264.7), but also inhibited the secretion of NO and TNF-α in IFN-γ/LPS-challenged microglial cells (BV-2). The experimental data suggests the inflammatory action of BDMC33 on activated macrophage-like cellular systems, which could be used as a future therapeutic agent in the management of chronic inflammatory diseases. MDPI 2012 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/78007/1/78007.pdf Lee, Ka Heng and Chow, Yuh Lit and Vidyadaran, Sharmili and Abas, Faridah and Mohammed Alitheen, Noorjahan Banu and Shaari, Khozirah and Israf Ali, Daud Ahmad and Lajis, Nordin and Ahmad, Syahida (2012) BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways. International Journal of Molecular Sciences, 13 (3). pp. 2985-3008. ISSN 1661-6596; ESSN: 1422-0067 https://www.mdpi.com/1422-0067/13/3/2985 10.3390/ijms13032985
spellingShingle Lee, Ka Heng
Chow, Yuh Lit
Vidyadaran, Sharmili
Abas, Faridah
Mohammed Alitheen, Noorjahan Banu
Shaari, Khozirah
Israf Ali, Daud Ahmad
Lajis, Nordin
Ahmad, Syahida
BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways
title BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways
title_full BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways
title_fullStr BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways
title_full_unstemmed BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways
title_short BDMC33, a curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways
title_sort bdmc33 a curcumin derivative suppresses inflammatory responses in macrophage like cellular system role of inhibition in nf κb and mapk signaling pathways
url http://psasir.upm.edu.my/id/eprint/78007/1/78007.pdf
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