Detoxification of Oral Exposure to Benzo(a)pyrene by Lactobacillus plantarum CICC 23121 in Mice

Mol Nutr Food Res. 2021 Jun;65(12):e2001149. doi: 10.1002/mnfr.202001149. Epub 2021 May 10.

Abstract

This study's previous work showed that the carcinogen and mutagen benzo(a)pyrene (BaP) can be adsorbed by Lactobacillus cells in vitro. However, in vivo BaP detoxification by lactic acid bacteria has not yet been investigated. The present study evaluates the effects of orally administered Lactobacillus plantarum CICC 23121 in BaP-treated mice. Oral administration of 50 mg kg-1 BaP perturbed the intestinal microflora, caused Proteobacteria to predominate, and severely damaged DNA. However, oral administration of 5 × 1010 CFU mL-1 CICC 23121 in BaP-treated mice enhances fecal BaP excretion from 181.70 ± 1.04 µg/(g∙h) to 271.47 ± 11.71 µg/(g∙h) after 6 h. Fecal BaP excretion reaches up to 280.66 ± 22.97 µg/(g∙h) after the first 4 days of orally administered CICC 23121 and decreased to 94.31 ± 2.64 µg/(g∙h) by day 11. Intestinal microbiota are restored and Firmicutes predominates. CICC 23121 alleviates BaP-induced DNA damage and reduces tail length from 56.37 ± 5.31 to 39.69 ± 4.27 µm. Therefore, oral CICC23121 consumption is a promising strategy for reducing BaP toxicity in mice. To the best of our knowledge, this report is the first report to demonstrate in vivo that Lactobacillus cells can detoxify BaP.

Keywords: Lactobacillus plantarum; benzo(a)pyrene; detoxification; mouse model; toxicology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Benzo(a)pyrene / administration & dosage*
  • Benzo(a)pyrene / pharmacokinetics*
  • Cytochrome P-450 CYP1A1 / genetics
  • Cytochrome P-450 CYP1A1 / metabolism
  • DNA Damage
  • Fatty Acids, Volatile / metabolism
  • Feces
  • Female
  • Gastrointestinal Microbiome / drug effects
  • Gastrointestinal Microbiome / genetics
  • Inactivation, Metabolic / drug effects*
  • Lactobacillus plantarum*
  • Liver / drug effects
  • Mice
  • Oxidative Stress / drug effects
  • Probiotics / pharmacology
  • Weight Gain / drug effects

Substances

  • Fatty Acids, Volatile
  • Benzo(a)pyrene
  • Cyp1a1 protein, mouse
  • Cytochrome P-450 CYP1A1