4.4 Article

Patchouli oil ameliorates acute colitis: A targeted metabolite analysis of 2,4,6-trinitrobenzenesulfonic acid-induced rats

期刊

EXPERIMENTAL AND THERAPEUTIC MEDICINE
卷 14, 期 2, 页码 1184-1192

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/etm.2017.4577

关键词

patchouli oil; 2,4,6-trinitrobenzenesulfonic acid; colitis; targeted metabolomics; tryptophan catabolites; gut microbial metabolites

资金

  1. National Natural Science Foundation of China [81303200, 21377106, 81173534]
  2. Guangdong Natural Science Foundation [S2013010016627, S2012010008893]
  3. Medical Scientific Research Foundation of Guangdong Province [A2013232]
  4. Administration of Traditional Chinese Medicine of Guangdong Province [20132142]
  5. Central Finance of China in Support of Development of Local Colleges and University [276]
  6. China state '12th Five year Plan' Scientific and Technological Support Scheme [2012BAI029B09]
  7. Hong Kong, Macao and Taiwan Science & Technology Cooperation Program of China [2014DFH30010]
  8. Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme

向作者/读者索取更多资源

The incidence of inflammatory bowel disease (IBD), characterized by chronic, relapsing intestinal inflammation, has continually increased in recent years. A previous study by our group identified five potential metabolic markers possibly associated with the pathology of 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced IBD in rats. The present study aimed to examine the potential therapeutic effects of the essential oil of Pogostemon cablin (also known as patchouli; PO) on TNBS-induced rats and investigate the concomitant metabolic changes by targeting the previously identified potential markers. Pogostemon cablin is widely used to treat gastrointestinal diseases, including IBD, in China. The results of the present study showed that PO (270 mg/kg, rectal instillation) significantly alleviated colonic damage and reduced disease activity indicators and colonic myeloperoxidase in TNBS-induced rats. In addition, a targeted metabolic profiling study identified that four metabolites were elevated in the urine of the animals in the TNBS group, which were significantly inhibited by treatment with PO: Two tryptophan metabolites [4-(2-aminophenyl)-2,4-dioxobutanoic acid and 4,6-cihydroxyquinoline] and two gut microbial metabolites (phenylacetylglycine and p-cresol glucuronide). Taken together, these findings suggested that PO ameliorated the symptoms of TNBS-induced IBD and reversed the metabolic changes potentially associated with TNBS-induced IBD in rats.

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