Anti-inflammatory effects of daidzein on primary astroglial cell culture
Journal
Nutritional Neuroscience
Journal Volume
12
Journal Issue
3
Pages
123-134
Date Issued
2009
Author(s)
Abstract
Introduction: Alzheimer's disease is the common cause of dementia in old people. The pathological hallmarks of Alzheimer's disease include neuronal loss, deposition of amyloid-β, andInstitute of presence of neurofibrillary tangles. The endogenous steroid estrogen has been shown to affect neuronal growth, differentiation and survival, while isoflavones also have a neuroprotective effect on human cortical neurons. Daidzein, however, has a superior neuron-protective effect to other isoflavones. The present study is to determine whether daidzein is able to inhibit the production of pro-inflammatory mediators under amyloid-β and lipopolysaccharide stimulation. Materials and methods: Astrocyte cells were stimulated with amyloid-β or lipopolysaccharide in the absence and presence of diadzein. Nitric oxide released into the culture media was determined using the Griess reaction, and concentrations of IL-1, IL-6, TNF-α and estrogen receptor gene expression were measured by semi-quantitative real-time polymerase chain reaction assay. Results: Diadzein-treatment increases astrocyte cell counts and attains its maximal effect at the 10 -12M concentration. The addition of 20 μM amyloid-β or 10 -6 g/ml LPS can significantly decrease the viability of astrocytes, up-regulated IL-1, IL-6, TNF-α mRNA and estrogen receptor expression; in addition, 1-h daidzein pre-treatment can restore the decreased viability of astrocytes induced by amyloid-β or lipopolysaccharide as well as down-regulate their mRNA expression. Conclusions: It seems that this response is estrogen receptor-mediated. These results further increase the possibility that daidzein may have potential to ameliorate the inflammatory process and also alleviate the risk of Alzheimer's disease progression. ? 2009 W. S. Maney & Son Ltd.
SDGs
Other Subjects
amyloid beta protein; cytokine; daidzein; estradiol; estrogen receptor; interleukin 1; interleukin 6; lipopolysaccharide; messenger RNA; nitric oxide; reactive oxygen metabolite; tumor necrosis factor alpha; amyloid beta protein; antiinflammatory agent; cytokine; daidzein; estrogen receptor; interleukin 1; interleukin 6; isoflavone derivative; lipopolysaccharide; messenger RNA; nitric oxide; tumor necrosis factor alpha; Alzheimer disease; animal cell; antiinflammatory activity; article; astrocyte; cell count; cell culture; cell proliferation; cell stimulation; cell viability; concentration response; controlled study; cytotoxicity; down regulation; gene expression; inflammation; mouse; nonhuman; nucleotide sequence; priority journal; quantitative analysis; real time polymerase chain reaction; upregulation; animal; biosynthesis; cell division; cell survival; cytology; drug effect; genetics; Institute for Cancer Research mouse; metabolism; Alzheimer Disease; Amyloid beta-Protein; Animals; Anti-Inflammatory Agents; Astrocytes; Cell Division; Cell Survival; Cells, Cultured; Cytokines; Gene Expression; Interleukin-1; Interleukin-6; Isoflavones; Lipopolysaccharides; Mice; Mice, Inbred ICR; Nitric Oxide; Receptors, Estrogen; RNA, Messenger; Tumor Necrosis Factor-alpha
Type
journal article