Evidence map›Paper›PMID 26973525›Full record

ArticleFrontiers in pharmacology2016

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

Luigia De Fazio, Enzo Spisni, Elena Cavazza, Antonio Strillacci, Marco Candela, Manuela Centanni, Chiara Ricci, Fernando Rizzello, Massimo Campieri, Maria C Valerii

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
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  14. Therapeutic potential ofFrontiers in microbiology · 2023
    Article
  15. Frontiers in nutrition · 2023
    Article
  16. Review
  17. Antifungal Activity of Natural Compounds vs.Antibiotics (Basel, Switzerland) · 2022
    Article
  18. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Luigia De FazioBiology Unit, Department of Biological, Geological and Environmental Sciences, University of Bologna Bologna, Italy.
Enzo SpisniBiology Unit, Department of Biological, Geological and Environmental Sciences, University of Bologna Bologna, Italy.
Elena CavazzaBiology Unit, Department of Biological, Geological and Environmental Sciences, University of Bologna Bologna, Italy.
Antonio StrillacciBiology Unit, Department of Biological, Geological and Environmental Sciences, University of Bologna Bologna, Italy.
Marco CandelaDepartment of Pharmacy and Biotechnology, University of Bologna Bologna, Italy.
Manuela CentanniDepartment of Pharmacy and Biotechnology, University of Bologna Bologna, Italy.
Chiara RicciDepartment of Clinical and Experimental Sciences, University of Brescia Brescia, Italy.
Fernando RizzelloDepartment of Medical and Surgical Sciences, University of Bologna Bologna, Italy.
Massimo CampieriDepartment of Medical and Surgical Sciences, University of Bologna Bologna, Italy.
Maria C ValeriiBiology Unit, Department of Biological, Geological and Environmental Sciences, University of Bologna Bologna, Italy.
University of Bologna · ITUniversity of Brescia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

cyclooxygenase-2 (COX-2)dextran sulfate sodium (DSS)-induced colitisdysbiosisgeraniolinflammationinflammatory bowel disease (IBD)

Identifiers

PMID26973525
PMCPMC4776160
OpenAlexW2297722296

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.