Influence of GABA and GABA-producing Lactobacillus brevis DPC 6108 on the development of diabetes in a streptozotocin rat model

Benef Microbes. 2016 Jun;7(3):409-20. doi: 10.3920/BM2015.0154. Epub 2016 Mar 25.

Abstract

The aim of this study was to investigate if dietary administration of γ-aminobutyric acid (GABA)-producing Lactobacillus brevis DPC 6108 and pure GABA exert protective effects against the development of diabetes in streptozotocin (STZ)-induced diabetic Sprague Dawley rats. In a first experiment, healthy rats were divided in 3 groups (n=10/group) receiving placebo, 2.6 mg/kg body weight (bw) pure GABA or L. brevis DPC 6108 (~10(9)microorganisms). In a second experiment, rats (n=15/group) were randomised to five groups and four of these received an injection of STZ to induce type 1 diabetes. Diabetic and non-diabetic controls received placebo [4% (w/v) yeast extract in dH2O], while the other three diabetic groups received one of the following dietary supplements: 2.6 mg/kg bw GABA (low GABA), 200 mg/kg bw GABA (high GABA) or ~10(9) L. brevis DPC 6108. L. brevis DPC 6108 supplementation was associated with increased serum insulin levels (P<0.05), but did not alter other metabolic markers in healthy rats. Diabetes induced by STZ injection decreased body weight (P<0.05), increased intestinal length (P<0.05) and stimulated water and food intake. Insulin was decreased (P<0.05), whereas glucose was increased (P<0.001) in all diabetic groups, compared with non-diabetic controls. A decrease (P<0.01) in glucose levels was observed in diabetic rats receiving L. brevis DPC 6108, compared with diabetic-controls. Both the composition and diversity of the intestinal microbiota were affected by diabetes. Microbial diversity in diabetic rats supplemented with low GABA was not reduced (P>0.05), compared with non-diabetic controls while all other diabetic groups displayed reduced diversity (P<0.05). L. brevis DPC 6108 attenuated hyperglycaemia induced by diabetes but additional studies are needed to understand the mechanisms involved in this reduction.

Keywords: probiotic; streptozotocin; type-1 diabetes; γ-aminobutyric acid.

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic
  • Diabetes Mellitus, Experimental / prevention & control*
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / metabolism
  • Levilactobacillus brevis / metabolism
  • Placebos / administration & dosage
  • Probiotics / administration & dosage*
  • Rats, Sprague-Dawley
  • Treatment Outcome
  • gamma-Aminobutyric Acid / administration & dosage*
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • Antibiotics, Antineoplastic
  • Hypoglycemic Agents
  • Placebos
  • gamma-Aminobutyric Acid