Therapeutic effect of activated carbon-induced constipation mice with Lactobacillus fermentum Suo on treatment

Int J Mol Sci. 2014 Nov 28;15(12):21875-95. doi: 10.3390/ijms151221875.

Abstract

The aim of this study was to investigate the effects of Lactobacillus fermentum Suo (LF-Suo) on activated carbon-induced constipation in ICR (Institute of Cancer Research) mice. ICR mice were orally administered with lactic acid bacteria for 9 days. Body weight, diet intake, drinking amount, defecation status, gastrointestinal transit and defecation time, and the serum levels of MTL (motilin), Gas (gastrin), ET (endothelin), SS (somatostatin), AChE (acetylcholinesterase), SP (substance P), VIP (vasoactive intestinal peptide) were used to evaluate the preventive effects of LF-Suo on constipation. Bisacodyl, a laxative drug, was used as a positive control. The normal, control, 100 mg/kg bisacodyl treatment, LB (Lactobacillus bulgaricus)-, LF-Suo (L)- and LF-Suo (H)-treated mice showed the time to the first black stool defecation at 90, 218, 117, 180, 155 and 137 min, respectively. By the oral administration of LB-, LF-Suo (L), LF-Suo (H) or bisacodyl (100 mg/kg), the gastrointestinal transit was reduced to 55.2%, 72.3%, 85.5% and 94.6%, respectively, of the transit in normal mice, respectively. In contrast to the control mice, the serum levels of MTL, Gas, ET, AChE, SP and VIP were significantly increased and the serum levels of SS were reduced in the mice treated with LF-Suo (p < 0.05). By the RT-PCR (reverse transcription-polymerase chain reaction) and western blot assays, LF-Suo increased the c-Kit, SCF (stem cell factor), GDNF (glial cell line-derived neurotrophic factor) and decreased TRPV1 (transient receptor potential vanilloid 1), NOS (nitric oxide synthase) expressions of small intestine tissue in mice. These results demonstrate that lactic acid bacteria has preventive effects on mouse constipation and LF-Suo demonstrated the best functional activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Weight
  • Charcoal
  • Constipation / genetics
  • Constipation / physiopathology
  • Constipation / therapy*
  • Defecation
  • Diet
  • Disease Models, Animal
  • Drinking Behavior
  • Female
  • Gastrointestinal Transit
  • Gene Expression Regulation
  • Glial Cell Line-Derived Neurotrophic Factor / genetics
  • Glial Cell Line-Derived Neurotrophic Factor / metabolism
  • Hydrophobic and Hydrophilic Interactions
  • Intestine, Small / pathology
  • Intestine, Small / physiopathology
  • Limosilactobacillus fermentum / physiology*
  • Mice
  • Mice, Inbred ICR
  • Nitric Oxide Synthase / genetics
  • Nitric Oxide Synthase / metabolism
  • Proto-Oncogene Proteins c-kit / genetics
  • Proto-Oncogene Proteins c-kit / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Stem Cell Factor / genetics
  • Stem Cell Factor / metabolism
  • TRPV Cation Channels / genetics
  • TRPV Cation Channels / metabolism
  • Time Factors

Substances

  • Glial Cell Line-Derived Neurotrophic Factor
  • RNA, Messenger
  • Stem Cell Factor
  • TRPV Cation Channels
  • TRPV1 protein, mouse
  • Charcoal
  • Nitric Oxide Synthase
  • Proto-Oncogene Proteins c-kit