Gene interactions and pathways from curated databases and text-mining
PloS one 2012, PMID: 22363816

Resveratrol inhibits inflammatory responses via the mammalian target of rapamycin signaling pathway in cultured LPS-stimulated microglial cells.

Zhong, Lian-Mei; Zong, Yi; Sun, Lin; Guo, Jia-Zhi; Zhang, Wei; He, Ying; Song, Rui; Wang, Wen-Min; Xiao, Chun-Jie; Lu, Di

BACKGROUND

Resveratrol have been known to possess many pharmacological properties including antioxidant, cardioprotective and anticancer effects. Although current studies indicate that resveratrol produces neuroprotection against neurological disorders, the precise mechanisms for its beneficial effects are still not fully understood. We investigate the effect of anti-inflammatory and mechamisms of resveratrol by using lipopolysaccharide (LPS)-stimulated murine microglial BV-2 cells.

RESULTS

BV-2 cells were treated with resveratrol (25, 50, and 100 µM) and/or LPS (1 µg/ml). Nitric oxide (NO) and prostaglandin E2 (PGE2) were measured by Griess reagent and ELISA. The mRNA and protein levels of proinflammatory proteins and cytokines were analysed by RT-PCR and double immunofluorescence labeling, respectively. Phosphorylation levels of PTEN (phosphatase and tensin homolog deleted on chromosome 10), Akt, mammalian target of rapamycin (mTOR), mitogen-activated protein kinases (MAPKs) cascades, inhibitor κB-α (IκB-α) and cyclic AMP-responsive element-binding protein (CREB) were measured by western blot. Resveratrol significantly attenuated the LPS-induced expression of NO, PGE2, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β) and nuclear factor-κB (NF-κB) in BV-2 cells. Resveratrol increased PTEN, Akt and mTOR phosphorylation in a dose-dependent manner or a time-dependent manner. Rapamycin (10 nM), a specific mTOR inhibitor, blocked the effects of resveratrol on LPS-induced microglial activation. In addition, mTOR inhibition partially abolished the inhibitory effect of resveratrol on the phosphorylation of IκB-α, CREB, extracellular signal-regulated kinase 1/2 (ERK1/2), c-Jun N-terminal protein kinase (JNK), and p38 mitogen-activated protein kinase (p38 MAPK).

CONCLUSIONS

This study indicates that resveratrol inhibited LPS-induced proinflammatory enzymes and proinflammatory cytokines via down-regulation phosphorylation of NF-κB, CREB and MAPKs family in a mTOR-dependent manner. These findings reveal, in part, the molecular basis underlying the anti-inflammatory properties of resveratrol.

Diseases/Pathways annotated by Medline MESH: Inflammation, MAP Kinase Signaling System
Document information provided by NCBI PubMed

Text Mining Data

tumor necrosis factor-a (TNF-a) → LPS: " Resveratrol significantly attenuated the LPS induced expression of NO, PGE2, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), tumor necrosis factor-a (TNF-a) , interleukin-1ß (IL-1ß) and nuclear factor-?B ( NF-?B ) in BV-2 cells "

interleukin-1ß (IL-1ß) → LPS: " Resveratrol significantly attenuated the LPS induced expression of NO, PGE2, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), tumor necrosis factor-a (TNF-a), interleukin-1ß (IL-1ß) and nuclear factor-?B ( NF-?B ) in BV-2 cells "

inducible nitric oxide synthase (iNOS) → LPS: " Resveratrol significantly attenuated the LPS induced expression of NO, PGE2, inducible nitric oxide synthase (iNOS) , cyclooxygenase-2 (COX-2), tumor necrosis factor-a (TNF-a), interleukin-1ß (IL-1ß) and nuclear factor-?B ( NF-?B ) in BV-2 cells "

cyclooxygenase-2 (COX-2) → LPS: " Resveratrol significantly attenuated the LPS induced expression of NO, PGE2, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2) , tumor necrosis factor-a (TNF-a), interleukin-1ß (IL-1ß) and nuclear factor-?B ( NF-?B ) in BV-2 cells "

CREB — mTOR: " This study indicates that resveratrol inhibited LPS induced proinflammatory enzymes and proinflammatory cytokines via down-regulation phosphorylation of NF-?B, CREB and MAPKs family in a mTOR dependent manner "

Manually curated Databases

No curated data.