| Frontiers in Pharmacology | |
| Dietary geraniol by oral or enema administration strongly reduces dysbiosis and systemic inflammation in dextran sulphate sodium-treated mice. | |
| Massimo eCampieri1  Fernando eRizzello1  Elena eCavazza1  Luigia eDe Fazio1  Manuela eCentanni1  Maria Chiara Valerii1  Antonio eStrillacci1  Enzo eSpisni1  Marco eCandela1  Chiara eRicci2  | |
| [1] University of Bologna;University of Brescia; | |
| 关键词: Inflammation; Geraniol; Cyclooxygenase-2 (COX-2); Inflammatory bowel disease (IBD); Dextran sulphate sodium (DSS)-induced colitis; Dysbiosis.; | |
| DOI : 10.3389/fphar.2016.00038 | |
| 来源: DOAJ | |
【 摘 要 】
(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 sulphate sodium (DSS)-induced colitis mouse model. Ge-OH was orally administered to C57BL/6 mice at daily doses of 30 and 120mg kg(-1) body weight, starting six 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.
【 授权许可】
Unknown