Please use this identifier to cite or link to this item: https://doi.org/10.1097/WNR.0000000000000179
Title: Andrographolide attenuates interleukin-1 beta-stimulated upregulation of chemokine CCL5 and glial fibrillary acidic protein in astrocytes
Authors: Wong, Siew-Ying 
Michelle G.K. Tan 
William A. Banks
Wong, WS Fred 
Wong, Peter T-H 
Lai, Mitchell KP 
Keywords: Science & Technology
Life Sciences & Biomedicine
Neurosciences
Neurosciences & Neurology
andrographolide
astrocyte
chemokines
cytokines
neuroinflammation
CENTRAL-NERVOUS-SYSTEM
TRANSGENIC INHIBITION
INFLAMMATION
ACTIVATION
INJURY
CELLS
RAT
Issue Date: 20-Aug-2014
Publisher: LIPPINCOTT WILLIAMS & WILKINS
Citation: Wong, Siew-Ying, Michelle G.K. Tan, William A. Banks, Wong, WS Fred, Wong, Peter T-H, Lai, Mitchell KP (2014-08-20). Andrographolide attenuates interleukin-1 beta-stimulated upregulation of chemokine CCL5 and glial fibrillary acidic protein in astrocytes. NEUROREPORT 25 (12) : 881-886. ScholarBank@NUS Repository. https://doi.org/10.1097/WNR.0000000000000179
Abstract: Andrographolide is a bioactive molecule isolated from Andrographis paniculata with anticancer and anti-inflammatory activities. In this study, we tested the effects of andrographolide on astrocyte-mediated neuroinflammatory responses. Cultured rat primary astrocytes were treated with proinflammatory cytokine interleukin 1β with or without pretreatment with andrographolide, and then processed for measurements of chemokine C-C motif ligand 5 (CCL5) and glial fibrillary acidic protein. The activation status of nuclear factor-κB activation that may underlie CCL5 upregulation was also measured. Andrographolide pretreatment was found to attenuate the upregulation of CCL5 and glial fibrillary basic protein as well as reduce the phosphorylation of nuclear factor-κB p65 and IκBα after interleukin 1β stimulation. These data suggest that andrographolide should be evaluated further as a therapeutic for central nervous system diseases characterized by astrocyte-mediated neuroinflammatory processes. © 2014 Wolters Kluwer Health Lippincott Williams & Wilkins.
Source Title: NEUROREPORT
URI: https://scholarbank.nus.edu.sg/handle/10635/188443
ISSN: 09594965
1473558X
DOI: 10.1097/WNR.0000000000000179
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