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Dietary Geraniol by Oral or Enema Administration Strongly Reduces Dysbiosis and Systemic Inflammation in Dextran Sulfate Sodium-Treated Mice. | LitMetric

AI Article Synopsis

  • Geraniol (Ge-OH) is a monoterpene alcohol with anti-inflammatory, antitumoral, and antimicrobial properties, commonly used in food preservation and animal farming.
  • A study tested Ge-OH's effectiveness against colitis in mice, administering it orally and via enema, focusing on its impact on inflammation and gut microbiome health.
  • Results showed that Ge-OH significantly alleviated colitis symptoms, reduced inflammatory markers like COX-2, and could be a promising treatment for intestinal inflammation and dysbiosis.

Article Abstract

(Trans)-3,7-Dimethyl-2,6-octadien-1-ol, commonly called geraniol (Ge-OH), is an acyclic monoterpene alcohol with well-known anti-inflammatory, antitumoral, and antimicrobial properties. It is widely used as a preservative in the food industry and as an antimicrobial agent in animal farming. The present study investigated the role of Ge-OH as an anti-inflammatory and anti-dysbiotic agent in the dextran sulfate sodium (DSS)-induced colitis mouse model. Ge-OH was orally administered to C57BL/6 mice at daily doses of 30 and 120 mg kg((-1)) body weight, starting 6 days before DSS treatment and ending the day after DSS removal. Furthermore, Ge-OH 120 mg kg((-1)) dose body weight was administered via enema during the acute phase of colitis to facilitate its on-site action. The results show that orally or enema-administered Ge-OH is a powerful antimicrobial agent able to prevent colitis-associated dysbiosis and decrease the inflammatory systemic profile of colitic mice. As a whole, Ge-OH strongly improved the clinical signs of colitis and significantly reduced cyclooxygenase-2 (COX-2) expression in colonocytes and in the gut wall. Ge-OH could be a powerful drug for the treatment of intestinal inflammation and dysbiosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776160PMC
http://dx.doi.org/10.3389/fphar.2016.00038DOI Listing

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