Increased Cadmium Excretion Due to Oral Administration of Lactobacillus plantarum Strains by Regulating Enterohepatic Circulation in Mice

J Agric Food Chem. 2019 Apr 10;67(14):3956-3965. doi: 10.1021/acs.jafc.9b01004. Epub 2019 Apr 1.

Abstract

The heavy metal cadmium (Cd) is a contaminant widely distributed in the food chain. In the present study, 8-week oral administration of a probiotic strain, Lactobacillus plantarum CCFM8610, markedly decreased blood Cd levels in volunteers. Further animal study showed that three L. plantarum strains administered orally exhibited significantly different effects on the regulation of bile acid (BA) metabolism and Cd excretion in mice. Among the strains, L. plantarum CCFM8610 showed the most significant effects on enhancing hepatic BA synthesis, biliary glutathione output, and fecal BA excretion. Biliary Cd output and fecal Cd excretion were markedly increased after L. plantarum CCFM8610 administration, resulting in a marked reduction in tissue Cd levels. The regulation of BA homeostasis and Cd excretion was due to the suppression of the enterohepatic farnesoid X receptor-fibroblast growth factor 15 (FXR-FGF15) axis by L. plantarum CCFM8610 and could be abolished by treatment with the FXR agonist GW4064. The regulatory effects were also related to the gut microbiota, as antibiotic pretreatment reversed L. plantarum CCFM8610-induced effects in BA and Cd metabolism.

Keywords: Lactobacillus plantarum; bile acid; cadmium; enterohepatic circulation; gut microbiota.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Animals
  • Bile Acids and Salts / metabolism
  • Cadmium / blood
  • Cadmium / metabolism*
  • Enterohepatic Circulation / drug effects*
  • Feces / chemistry
  • Female
  • Fibroblast Growth Factors / genetics
  • Fibroblast Growth Factors / metabolism
  • Gastrointestinal Microbiome / drug effects
  • Humans
  • Lactobacillus plantarum / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Probiotics / administration & dosage*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism

Substances

  • Bile Acids and Salts
  • Fxr1h protein, mouse
  • RNA-Binding Proteins
  • fibroblast growth factor 15, mouse
  • Cadmium
  • Fibroblast Growth Factors