Lactobacillus plantarum YS-3 Prevents Activated Carbon-Induced Constipation in Mice

J Med Food. 2018 Jun;21(6):575-584. doi: 10.1089/jmf.2017.4109. Epub 2018 May 14.

Abstract

The aim of this study was to determine the effects of Lactobacillus plantarum YS-3 (LP-YS3) on activated carbon-induced constipation in Kunming mice. The results of the experiment show that the antigastric acid activity and bile salt tolerance of LP-YS3 were stronger than those of Lactobacillus bulgaricus (LB). LP-YS3 inhibited loss of body weight caused by constipation and further reductions in fecal weight, particle number, and water content in mice. Moreover, LP-YS3 elevated the gastrointestinal transit rate and reduced the time required for initial black stool defecation. LP-YS3 also elevated motilin (MTL), endothelin (ET), acetylcholinesterase (AChE), substance P (SP), and VIP serum levels and reduced somatostatin (SS) levels in constipated mice. Hematoxylin-eosin (H&E) staining revealed that high concentration of LP-YS3 reduced the incidence of injuries to small intestine villi and the intestinal wall compared to carbon-induced constipation groups. Reverse transcription-polymerase chain reaction and western blot experiments demonstrated that LP-YS3 upregulated c-Kit, stem cell factor, and glial cell line-derived neurotrophic factor mRNA and protein expression and downregulated transient receptor potential vanilloid 1 and nitric oxide synthase expression in small intestine tissue from constipated mice. In conclusion, high concentrations of LP-YS3 had stronger and more beneficial effects than LB. Based on these results, we conclude that LP-YS3 can effectively inhibit constipation.

Keywords: Lactobacillus bulgaricus; Lactobacillus plantarum YS-3; constipation; gene expression.

MeSH terms

  • Animals
  • Carbon / adverse effects*
  • Carbon / chemistry
  • Constipation / drug therapy*
  • Constipation / genetics
  • Constipation / microbiology
  • Constipation / physiopathology
  • Defecation / drug effects
  • Female
  • Humans
  • Intestine, Small / drug effects
  • Intestine, Small / metabolism
  • Intestine, Small / microbiology
  • Intestine, Small / physiopathology
  • Lactobacillus plantarum / physiology*
  • Mice
  • Nitric Oxide Synthase / genetics
  • Nitric Oxide Synthase / metabolism
  • Probiotics / administration & dosage*
  • TRPV Cation Channels / genetics
  • TRPV Cation Channels / metabolism

Substances

  • TRPV Cation Channels
  • Carbon
  • Nitric Oxide Synthase