Inhibitory effect of a tyrosine-fructose Maillard reaction product, 2,4-bis(p-hydroxyphenyl)-2-butenal on amyloid-β generation and inflammatory reactions via inhibition of NF-κB and STAT3 activation in cultured astrocytes and microglial BV-2 cells.

Abstract

BACKGROUND:

Amyloidogenesis is linked to neuroinflammation. The tyrosine-fructose Maillard reaction product, 2,4-bis(p-hydroxyphenyl)-2-butenal, possesses anti-inflammatory properties in cultured macrophages, and in an arthritis animal model. Because astrocytes and microglia are responsible for amyloidogenesis and inflammatory reactions in the brain, we investigated the anti-inflammatory and anti-amyloidogenic effects of 2,4-bis(p-hydroxyphenyl)-2-butenal in lipopolysaccharide (LPS)-stimulated astrocytes and microglial BV-2 cells.

METHODS:

Cultured astrocytes and microglial BV-2 cells were treated with LPS (1 μg/ml) for 24 h, in the presence (1, 2, 5 μM) or absence of 2,4-bis(p-hydroxyphenyl)-2-butenal, and harvested. We performed molecular biological analyses to determine the levels of inflammatory and amyloid-related proteins and molecules, cytokines, Aβ, and secretases activity. Nuclear factor-kappa B (NF-κB) DNA binding activity was determined using gel mobility shift assays.

RESULTS:

We found that 2,4-bis(p-hydroxyphenyl)-2-butenal (1, 2, 5 μM) suppresses the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) as well as the production of nitric oxide (NO), reactive oxygen species (ROS), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β) in LPS (1 μg/ml)-stimulated astrocytes and microglial BV-2 cells. Further, 2,4-bis(p-hydroxyphenyl)-2-butenal inhibited the transcriptional and DNA binding activity of NF-κB--a transcription factor that regulates genes involved in neuroinflammation and amyloidogenesis via inhibition of IκB degradation as well as nuclear translocation of p50 and p65. Consistent with the inhibitory effect on inflammatory reactions, 2,4-bis(p-hydroxyphenyl)-2-butenal inhibited LPS-elevated Aβ42 levels through attenuation of β- and γ-secretase activities. Moreover, studies using signal transducer and activator of transcription 3 (STAT3) siRNA and a pharmacological inhibitor showed that 2,4-bis(p-hydroxyphenyl)-2-butenal inhibits LPS-induced activation of STAT3.

CONCLUSIONS:

These results indicate that 2,4-bis(p-hydroxyphenyl)-2-butenal inhibits neuroinflammatory reactions and amyloidogenesis through inhibition of NF-κB and STAT3 activation, and suggest that 2,4-bis(p-hydroxyphenyl)-2-butenal may be useful for the treatment of neuroinflammatory diseases like Alzheimer's disease.

• Authors: Young-Jung Lee, Dong-Young Choi, Im Seup Choi, Jin-Yi Han, Heon-Sang Jeong, Sang Bae Han, Ki-Wan Oh, Jin Tae Hong
• Journal: Journal of neuroinflammation (J Neuroinflammation) Vol. 8 Pg. 132 (Oct 07 2011) ISSN: 1742-2094 [Electronic] England
• PMID: 21982455 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Aldehydes
• Amyloid beta-Peptides
• Interleukin-1beta
• Lipopolysaccharides
• NF-kappa B
• Reactive Oxygen Species
• STAT3 Transcription Factor
• Tumor Necrosis Factor-alpha
• Fructose
• Nitric Oxide
• Tyrosine
• 2-butenal
• Nitric Oxide Synthase Type II
• Nos2 protein, mouse
• Ptgs2 protein, mouse
• Cyclooxygenase 2

Topics

• Aldehydes (chemistry, pharmacology)
• Amyloid beta-Peptides (metabolism)
• Animals
• Astrocytes (cytology, drug effects, metabolism)
• Cell Line
• Cyclooxygenase 2 (genetics, metabolism)
• Fructose (metabolism)
• Humans
• Inflammation (metabolism)
• Interleukin-1beta (genetics, metabolism)
• Lipopolysaccharides (pharmacology)
• Maillard Reaction
• Mice
• Microglia (cytology, drug effects, metabolism)
• NF-kappa B (antagonists & inhibitors)
• Nitric Oxide (metabolism)
• Nitric Oxide Synthase Type II (genetics, metabolism)
• Reactive Oxygen Species (metabolism)
• STAT3 Transcription Factor (metabolism)
• Tumor Necrosis Factor-alpha (genetics, metabolism)
• Tyrosine (metabolism)