Background: (Trans)-3,7-Dimethyl-2,6-octadien-1-ol, commonly called geraniol (Ge-OH), is an acyclic monoterpene alcohol with well-known anti-inflammatory and antimicrobial properties. Ge-OH is a non-toxic compound classified as Generally Recognized As Safe (GRAS) by the US Food and Drug Administration and the European Food Security Agency. Methods: Ge-OH was orally administered at a maximum daily dose of 8 mg kg (- 1) body weight for four weeks in a delayed release formulation capable of reaching the colon. Fecal microbiota and blood cytokines were analyzed before and after Ge-OH treatment, as well as IBS symptomatology by using Visual Analogue Scale (VAS-IBS). Results: The results show that orally administered Ge-OH is a powerful modulator of the intestinal microbial ecosystem, capable of leading to increased relative abundances of Collinsella and especially Faecalibacterium, a well-known health-promoting butyrate producer consistently found to be decreased in IBS patients. Moreover, Ge-OH strongly improved the clinical symptoms of colitis by significantly reducing the score recorded by the VAS-IBS questionnaire. Clinical improvement was associated with a significant reduction in the circulating MIP-1β, a chemokine found to be increased in several IBS patients. Conclusion: Ge-OH could be a powerful component for food supplement targeted to the treatment of IBS patients. Trial registration: ISRCTN47041881, retrospectively registered on 19th July 2018.

Dietary geraniol ameliorates intestinal dysbiosis and relieves symptoms in irritable bowel syndrome patients: A pilot study

Ricci C.;
2018-01-01

Abstract

Background: (Trans)-3,7-Dimethyl-2,6-octadien-1-ol, commonly called geraniol (Ge-OH), is an acyclic monoterpene alcohol with well-known anti-inflammatory and antimicrobial properties. Ge-OH is a non-toxic compound classified as Generally Recognized As Safe (GRAS) by the US Food and Drug Administration and the European Food Security Agency. Methods: Ge-OH was orally administered at a maximum daily dose of 8 mg kg (- 1) body weight for four weeks in a delayed release formulation capable of reaching the colon. Fecal microbiota and blood cytokines were analyzed before and after Ge-OH treatment, as well as IBS symptomatology by using Visual Analogue Scale (VAS-IBS). Results: The results show that orally administered Ge-OH is a powerful modulator of the intestinal microbial ecosystem, capable of leading to increased relative abundances of Collinsella and especially Faecalibacterium, a well-known health-promoting butyrate producer consistently found to be decreased in IBS patients. Moreover, Ge-OH strongly improved the clinical symptoms of colitis by significantly reducing the score recorded by the VAS-IBS questionnaire. Clinical improvement was associated with a significant reduction in the circulating MIP-1β, a chemokine found to be increased in several IBS patients. Conclusion: Ge-OH could be a powerful component for food supplement targeted to the treatment of IBS patients. Trial registration: ISRCTN47041881, retrospectively registered on 19th July 2018.
2018
2017
Altra università italiana
LS7_3 Pharmacology, pharmacogenomics, drug discovery and design, drug therapy
Esperti anonimi
Inglese
Internazionale
18
1
338
Dysbiosis; Geraniol; Inflammation; Irritable bowel syndrome (IBS); Microbiota; Acyclic Monoterpenes; Adult; Bacteria; Dietary Supplements; Dysbiosis; Female; Gastrointestinal Microbiome; Humans; Intestines; Irritable Bowel Syndrome; Male; Middle Aged; Pilot Projects; Retrospective Studies; Terpenes; Young Adult
Nessuno
no
12
info:eu-repo/semantics/article
262
Rizzello, F.; Ricci, C.; Scandella, M.; Cavazza, E.; Giovanardi, E.; Valerii, M. C.; Campieri, M.; Comparone, A.; De Fazio, L.; Candela, M.; Turroni, ...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11379/529573
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