AI Article Synopsis

  • A study explored the effects of chikusetsusaponin IVa (CS) and its methyl ester (CS-ME) on inflammation in RAW264.7 macrophages exposed to lipopolysaccharide (LPS).
  • CS-ME was found to be more effective than CS in inhibiting the production of nitric oxide (NO) and prostaglandin E2 (PGE2), as well as key inflammatory cytokines like TNF-α, IL-6, and IL-1β.
  • The anti-inflammatory effects of CS-ME are likely due to its ability to decrease the expression of enzymes and proteins involved in inflammation (iNOS, COX-2) by downregulating transcription factors NF

Article Abstract

We investigated the effect of chikusetsusaponin IVa (CS) and chikusetsusaponin IVa methyl ester (CS-ME) from the roots of Achyranthes japonica NAKAI on lipopolysaccharide (LPS)-induced nitric oxide (NO) and prostaglandin E2 (PGE2) production in RAW264.7 macrophages. CS-ME more potently inhibited LPS-induced NO and PGE2 production than CS. CS-ME concentration-dependently inhibited LPS-induced tumor necrosis factor (TNF)-α and interleukin (IL)-6 and IL-1β production in RAW264.7 macrophages and mouse peritoneal macrophages. Consistent with these findings, CS-ME suppressed LPS-induced expression of inducible NO synthase (iNOS) and cyclooxygenase (COX)-2 at protein level as well as iNOS, COX-2, TNF-α, IL-6, and IL-1β at mRNA level. In addition, CS-ME suppressed LPS-induced transcriptional activity of nuclear factor (NF)-κB and activator protein (AP)-1. The anti-inflammatory properties of CS-ME might result from suppression of iNOS, COX-2, TNF-α, IL-6, and IL-1β expression through downregulation of NF-κB and AP-1 in macrophages.

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Source
http://dx.doi.org/10.1248/bpb.b15-00572DOI Listing

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