Beneficial Effects of Non-Encapsulated or Encapsulated Probiotic Supplementation on Microbiota Composition, Intestinal Barrier Functions, Inflammatory Profiles, and Glucose Tolerance in High Fat Fed Rats

Nutrients. 2019 Aug 22;11(9):1975. doi: 10.3390/nu11091975.

Abstract

Development of obesity-associated comorbidities is related to chronic inflammation, which has been linked to gut microbiota dysbiosis. Thus, modulating gut microbiota composition could have positive effects for metabolic disorders, supporting the use of probiotics as potential therapeutics in vivo, which may be enhanced by a microencapsulation technique. Here we investigated the effects of non-encapsulated or pectin-encapsulated probiotic supplementation (Lactobacillus paracasei subsp. paracasei L. casei W8®; L. casei W8) on gut microbiota composition and metabolic profile in high-fat (HF) diet-fed rats. Four male Wistar rat groups (n = 8/group) were fed 10% low-fat, 45% HF, or HF with non-encapsulated or encapsulated L. casei W8 (4 × 107 CFU/g diet) diet for seven weeks. Microbiota composition, intestinal integrity, inflammatory profiles, and glucose tolerance were assessed. Non-encapsulated and pectin-encapsulated probiotic supplementation positively modulated gut microbiota composition in HF-fed male rats. These changes were associated with improvements in gut barrier functions and local and systemic inflammation by non-encapsulated probiotics and improvement in glucose tolerance by encapsulated probiotic treatment. Thus, these findings suggest the potential of using oral non-encapsulated or encapsulated probiotic supplementation to ameliorate obesity-associated metabolic abnormalities.

Keywords: glucose tolerance; gut microbiota; inflammation; intestinal epithelial barrier; microencapsulation; probiotics.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Blood Glucose / metabolism*
  • Diet, High-Fat*
  • Disease Models, Animal
  • Dysbiosis
  • Energy Metabolism
  • Gastrointestinal Microbiome*
  • Glucose Intolerance / blood
  • Glucose Intolerance / etiology
  • Glucose Intolerance / microbiology
  • Glucose Intolerance / prevention & control*
  • Inflammation / blood
  • Inflammation / etiology
  • Inflammation / microbiology
  • Inflammation / prevention & control*
  • Inflammation Mediators / blood
  • Insulin / blood
  • Intestines / microbiology*
  • Lactobacillus / growth & development*
  • Male
  • Permeability
  • Probiotics / administration & dosage*
  • Rats, Wistar

Substances

  • Blood Glucose
  • Inflammation Mediators
  • Insulin

Supplementary concepts

  • Lactobacillus paracasei subsp. paracasei