Back to Search
Start Over
Reversal of visceral hypersensitivity in rat by Menthacarin®, a proprietary combination of essential oils from peppermint and caraway, coincides with mycobiome modulation
- Publication Year :
- 2018
-
Abstract
- Background: Irritable bowel syndrome (IBS) is a common gastrointestinal disorder associated with altered gastrointestinal microflora and increased nociception to colonic distension. This visceral hypersensitivity can be reversed in our rat maternal separation model by fungicides. Menthacarin® is a proprietary combination of essential oils from Mentha x piperita L. and Carum carvi. Because these oils exhibit antifungal and antibacterial properties, we investigated whether Menthacarin® can reverse existing visceral hypersensitivity in maternally separated rats. Methods: In non-handled and maternally separated rats, we used the visceromotor responses to colorectal distension as measure for visceral sensitivity. We evaluated this response before and 24 hours after water-avoidance stress and after 7 days treatment with Menthacarin® or control. The pre- and post-treatment mycobiome and microbiome were characterized by sequencing of fungal internal transcribed spacer 1 (ITS-1) and bacterial 16s rDNA regions. In vitro antifungal and antimicrobial properties of Menthacarin® were studied with radial diffusion assay. Key Results: Menthacarin® inhibited in vitro growth of yeast and bacteria. Water-avoidance caused visceral hypersensitivity in maternally separated rats, and this was reversed by treatment. Multivariate analyses of ITS-1 and 16S high throughput data showed that maternal separation, induced changes in the myco- and microbiome. Menthacarin® treatment of non-handled and maternally separated rats shifted the mycobiomes to more similar compositions. Conclusions & Inferences: The development of visceral hypersensitivity in maternally separated rats and the Menthacarin®-mediated reversal of hypersensitivity is associated with changes in the mycobiome. Therefore, Menthacarin® may be a safe and effective treatment option that should be tested for IBS. © 2018 The Authors. Neurogastroenterology & Motility Published by John Wiley & Sons Ltd. Chemicals / CAS: decanoic acid, 334-48-5, 3398-75-2; fluconazole, 86386-73-4; octanoic acid, 124-07-2, 1984-06-1, 74-81-7; peppermint oil, 8006-90-4; streptomycin, 57-92-1
- Subjects :
- Male
Unclassified drug
Visceral sensitivity
Assay
Digestive function
Treatment response
DNA 18S
Motor activity
Essential oil
Species composition
Candida albicans
High throughput sequencing
Decanoic acid
Antifungal activity
Radial diffusion assay
Fluconazole
Priority journal
Visceral hypersensitivity
Intestine flora
Antibiotic agent
Mentha piperita
Digestive tract agent
Penicillin derivative
Streptomycin
Caraway
Female
Antifungal agent
Drug mechanism
Bacillus subtilis
Physical sensitivity
Drug megadose
Abdominal pain
DNA 16S
Colorectal distension
Digestive system disease
Low drug dose
IBS
Octanoic acid
Dose response
Hypersensitivity
Animal model
Drug dose comparison
Animal experiment
Biology
Peppermint oil
Caraway oil
Menthacarin
Bacteria
Fungi
In vitro study
Bacterial DNA
Maternal deprivation
Nonhuman
Drug efficacy
Viscera
Fungal DNA
Growth inhibition
Dysbiosis
Rat
Microbiome
Antibacterial activity
Colorectal disease
Controlled study
Internal transcribed spacer 1
Mycobiome
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.dris...00893..b975c28bbc34261987a55518cf24118e