Cynandione A from <i>Cynanchum wilfordii</i> Attenuates the Production of Inflammatory Mediators in LPS-Induced BV-2 Microglial Cells <i>via</i> NF-κB Inactivation

Biological and Pharmaceutical Bulletin
2014.0

Abstract

Cynanchum wilfordii is one of most widely used medicinal plants in Oriental medicine for the treatment of various conditions. In the present study, we isolated cynandione A (CA) from an extract of Cynanchum wilfordii roots (CWE) and investigated the effects of CA on the expression of inducible nitric oxide synthase (iNOS) and pro-inflammatory cytokines in lipopolysaccharide (LPS)-induced BV-2 microglial cells. CWE and CA significantly decreased LPS-induced nitric oxide production and the expression of iNOS in a concentration-dependent manner, while they (CWE up to 500 microg/mL and CA up to 80 microM) did not exhibit cytotoxic activity. Results from reverse transcription-polymerase chain reaction (RT-PCR) analysis and enzyme-linked immunosorbent assay (ELISA) showed that CA significantly attenuated the expression of tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), and IL-1beta in LPS-stimulated BV-2 cells. Furthermore, CA inhibited the phosphorylation of inhibitor kappa B-alpha (IkappaB-alpha) and translocation of nuclear factor-kappa B (NF-kappaB) to the BV-2 cell nucleus, indicating that CWE and CA may have effective anti-inflammatory activities via NF-kappaB inactivation in stimulated microglial cells.

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