High-dose Glycerol Monolaurate Up-Regulated Beneficial Indigenous Microbiota without Inducing Metabolic Dysfunction and Systemic Inflammation: New Insights into Its Antimicrobial Potential

Nutrients. 2019 Aug 22;11(9):1981. doi: 10.3390/nu11091981.

Abstract

Glycerol monolaurate (GML) has potent antimicrobial and anti-inflammatory activities. The present study aimed to assess the dose-dependent antimicrobial-effects of GML on the gut microbiota, glucose and lipid metabolism and inflammatory response in C57BL/6 mice. Mice were fed on diets supplemented with GML at dose of 400, 800 and 1600 mg kg-1 for 4 months, respectively. Results showed that supplementation of GML, regardless of the dosages, induced modest body weight gain without affecting epididymal/brown fat pad, lipid profiles and glycemic markers. A high dose of GML (1600 mg kg-1) showed positive impacts on the anti-inflammatory TGF-β1 and IL-22. GML modulated the indigenous microbiota in a dose-dependent manner. It was found that 400 and 800 mg kg-1 GML improved the richness of Barnesiella, whereas a high dosage of GML (1600 mg kg-1) significantly increased the relative abundances of Clostridium XIVa, Oscillibacter and Parasutterella. The present work indicated that GML could upregulate the favorable microbial taxa without inducing systemic inflammation and dysfunction of glucose and lipid metabolism.

Keywords: anti-inflammation; barrier function; glycerol monolaurate; gut microbiota; metabolic dysfunction.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology*
  • Anti-Inflammatory Agents / pharmacology*
  • Bacteria / drug effects*
  • Bacteria / growth & development
  • Bacteria / metabolism
  • Biomarkers / blood
  • Blood Glucose / drug effects
  • Blood Glucose / metabolism
  • Dose-Response Relationship, Drug
  • Energy Metabolism / drug effects*
  • Feces / microbiology
  • Gastrointestinal Microbiome / drug effects*
  • Inflammation / blood
  • Inflammation / immunology
  • Inflammation / prevention & control*
  • Inflammation Mediators / blood
  • Interleukin-22
  • Interleukins / blood
  • Intestines / drug effects*
  • Intestines / microbiology
  • Laurates / pharmacology*
  • Lipids / blood
  • Male
  • Mice, Inbred C57BL
  • Monoglycerides / pharmacology*
  • Transforming Growth Factor beta1 / blood

Substances

  • Anti-Bacterial Agents
  • Anti-Inflammatory Agents
  • Biomarkers
  • Blood Glucose
  • Inflammation Mediators
  • Interleukins
  • Laurates
  • Lipids
  • Monoglycerides
  • Tgfb1 protein, mouse
  • Transforming Growth Factor beta1
  • monolaurin