Andrographolide derivative AL-1 ameliorates TNBS-induced colitis in mice: involvement of NF-кB and PPAR-γ signaling pathways

Sci Rep. 2016 Jul 20:6:29716. doi: 10.1038/srep29716.

Abstract

Andrographolide is a traditional herb medicine, widely used in Asia for conditions involving inflammation. The andrographlide-lipoic acid conjugate, AL-1, has been found being able to alleviate inflammation in our previous reports. Although the anti-inflammatory activity of AL-1 contributes to its cytoprotective effects, whether AL-1 can improve inflammatory bowel disease (IBD) and the underlying mechanisms of its action remain largely unknown. In this study, we investigated the anti-inflammatory effects of AL-1 in C57BL/6 mice with trinitrobenzenesulfonic acid (TNBS)-induced colitis. The body weight loss and length change of colon after TNBS instillation were more severe than those in normal mice. AL-1 treatment led to significant reductions in disease activity index (DAI), macroscopic score and colon mucosa damage index (CMDI) associated with TNBS administration. AL-1 inhibited the inflammatory response via lowering the level of inflammatory cytokines and myeloperoxidase (MPO) activity. AL-1 attenuated the expression of p-p65, p-IκBα and COX-2 in the colitis mice. The alleviation of colon injury by AL-1 treatment was also evidenced by the increased expression of PPAR-γ. These results indicated that AL-1 could protect intestinal tract from the injury induced by TNBS in mice, suggesting that AL-1 may have potential in treatment for IBD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology*
  • Colitis / chemically induced
  • Colitis / metabolism
  • Colitis / prevention & control*
  • Colon / drug effects
  • Colon / metabolism
  • Colon / pathology
  • Cytokines / metabolism
  • Diterpenes / chemistry
  • Inflammation Mediators / metabolism
  • Mice, Inbred C57BL
  • NF-kappa B / metabolism*
  • PPAR gamma / metabolism*
  • Peroxidase / metabolism
  • Signal Transduction / drug effects*
  • Thioctic Acid / chemistry
  • Trinitrobenzenesulfonic Acid

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Diterpenes
  • Inflammation Mediators
  • NF-kappa B
  • PPAR gamma
  • andrographolide
  • Thioctic Acid
  • Trinitrobenzenesulfonic Acid
  • Peroxidase