4.4 Article

Tetradecylthioacetic Acid Attenuates Inflammation and Has Antioxidative Potential During Experimental Colitis in Rats

Journal

DIGESTIVE DISEASES AND SCIENCES
Volume 58, Issue 1, Pages 97-106

Publisher

SPRINGER
DOI: 10.1007/s10620-012-2321-2

Keywords

Inflammatory bowel diseases; Dextran sulfate sodium; Oxidative stress; Inflammatory cytokines; Peroxisome proliferator-activated receptors

Funding

  1. Nordforsk [070010]
  2. Research Council of Norway [190287/110]
  3. Board of Nutrition Programmes (University of Bergen)
  4. Board of Nutrition Programmes (Western Norway Regional Health Authority)
  5. Spanish Ministry of Health [FI0800707, PI081843]
  6. Spanish Ministry of Science and Innovation [BFU2009-11879/BFI]
  7. Autonomous Government of Catalonia [2009SGR735]
  8. COST B-35 action

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The fatty acid analogue tetradecylthioacetic acid (TTA) is a moderate pan-activator of peroxisome proliferator-activated receptors (PPARs), and has in previous studies showed potential as an antioxidant and anti-inflammatory agent, both through PPAR and non-PPAR mediated mechanisms. This study aimed to determine whether TTA could alleviate dextran sulfate sodium (DSS)-induced colitis in rats. Male Wistar rats were fed a control diet (control- and DSS-group) or a diet supplemented with 0.4 % TTA (TTA + DSS-group) for 30 days, and DSS was added to the drinking water the last 7 days. Ultrasound measurements were performed at day 29. At day 30, rats were sacrificed and the distal colon was removed for histological evaluation and measurement of cytokine levels, oxidative damage, and gene expression. The disease activity index was not improved in the TTA + DSS-group compared to the DSS-group. However, ultrasound measurements showed a significantly reduced colonic wall thickening in the TTA + DSS-group. TNF-alpha, IL-1 beta, and IL-6 were reduced at the protein and mRNA level in the TTA + DSS-group. Moreover, TTA-treated rats demonstrated reduced colonic oxidative damage, while inducible nitric oxide synthase 2 mRNA expression was elevated in both the DSS- and TTA + DSS-groups. PPAR gamma signaling may be involved in the anti-inflammatory response to TTA, as Pparg mRNA expression was significantly upregulated in colon. This study demonstrated that the pan-PPAR agonist TTA reduced colonic oxidative damage and cytokine levels in a rat model of colitis, and its potential to ameliorate colitis should be further explored.

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