Effects of borneol and thymoquinone on TNBS-induced colitis in mice
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18226358
PII: file/6086/fb2008a0001.pdf
Knihovny.cz E-resources
- MeSH
- Benzoquinones pharmacology MeSH
- Cytokines genetics metabolism MeSH
- DNA metabolism MeSH
- Camphanes pharmacology MeSH
- Colitis chemically induced pathology MeSH
- Colon drug effects pathology MeSH
- Trinitrobenzenesulfonic Acid pharmacology MeSH
- RNA, Messenger genetics metabolism MeSH
- Mice MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Gene Expression Regulation drug effects MeSH
- DNA Restriction Enzymes metabolism MeSH
- Body Weight drug effects MeSH
- Organ Size drug effects MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Benzoquinones MeSH
- Cytokines MeSH
- DNA MeSH
- isoborneol MeSH Browser
- Camphanes MeSH
- Trinitrobenzenesulfonic Acid MeSH
- RNA, Messenger MeSH
- DNA Restriction Enzymes MeSH
- thymoquinone MeSH Browser
Components of plant essential oils have been reported to have health benefit properties, including antioxidative, anti-tumour, antimicrobial, anti-stress, and immunomodulative activities. We examined the anti-inflammatory effects of thymoquinone, the active ingredient in the volatile oil of Nigella sativa seeds, and borneol, the active component of Salvia officinalis essential oil, on TNBS-induced colitis in mice. Thymoquinone was added to the commercial diet at a concentration of 0.05 % and borneol at two concentrations (0.09% and 0.18%) and fed to ICR mice 5 days before induction of TNBS colitis. Seven days after TNBS administration the mice were killed and macroscopic and histological scores were evaluated. Cytokine mRNA expression in colonic tissue was assessed using quantitative realtime RT-PCR. We did not detect any significant changes in macroscopic and histological scores between experimental and control groups, but we observed a significant decrease in proinflammatory cytokine (IL-1beta and IL-6) mRNA expression in colon tissue in the 0.09% and 0.18% borneol-treated groups of mice in comparison to the control group. Surprisingly, we were not able to confirm anti-inflammatory effects of thymoquinone in TNBS colitis. In conclusion, our data show that borneol is able to significantly suppress proinflammatory cytokine mRNA expression in colonic inflammation, although no significant morphological changes are visible.
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