Gastrodin attenuates perfluorooctanoic acid-induced liver injury by regulating gut microbiota composition in mice

Bioengineered. 2021 Dec;12(2):11546-11556. doi: 10.1080/21655979.2021.2009966.

Abstract

Perfluorooctanoic acid (PFOA) can accumulate in the livers of humans and animals via the food chain, resulting into liver injury, which is closely related to intestinal flora dysbiosis. Gastrodin has been reported to have hepatoprotective effect. However, whether gastrodin can alleviate PFOA-induced liver injury via modulating gut microbiota remains unclear. Herein, a PFOA-induced liver injury model was established by gavage of PFOA (5 mg/kg body weight) in 2% Tween 80 solution once daily for 6 weeks in mice, and then gastrodin in saline (20 mg/kg body weight) was used once daily for 8 weeks to treat liver damage. The biochemical indexes associated with liver function, oxidative stress, and inflammatory factors were examined. Hematoxylin-eosin staining was used to determine the liver histopathological changes. Besides, 16S rRNA sequencing was used to analyze the difference of gut microbiota between the model and treatment groups. The results showed that gastrodin significantly improved the oxidative stress caused by PFOA. Intestinal flora analysis showed that gastrodin treatment significantly increased the relative abundance of probiotics, such as Lactobacillus, Bifidobacterium, and Bacteroides, while the harmful bacteria, including Desulfovibrio were decreased. Gastrodin treatment also significantly increased the level of short-chain fatty acids (SCFAs), such as butyric acid and isobutyric acid. Spearman correlation analysis showed that the composition changes of gut microbiota and SCFAs increase were both beneficial to alleviate the liver injury caused by PFOA. To sum up, gastrodin can effectively alleviate PFOA-induced liver injury through regulating gut microbiota composition.

Keywords: Perfluorooctanoic acid; gastrodin; gut microbiota; liver injury; short-chain fatty acids.

MeSH terms

  • Animals
  • Benzyl Alcohols / pharmacology*
  • Benzyl Alcohols / toxicity*
  • Caprylates
  • Cecum / metabolism
  • Cytokines / blood
  • Disease Models, Animal
  • Fatty Acids, Volatile / metabolism
  • Fluorocarbons
  • Gastrointestinal Microbiome* / drug effects
  • Glucosides / pharmacology*
  • Glucosides / toxicity*
  • Hepatomegaly / blood
  • Hepatomegaly / pathology
  • Inflammation Mediators / blood
  • Liver / drug effects
  • Liver / injuries*
  • Liver / microbiology*
  • Liver / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Oxidative Stress / drug effects
  • Phylogeny
  • Protective Agents / pharmacology

Substances

  • Benzyl Alcohols
  • Caprylates
  • Cytokines
  • Fatty Acids, Volatile
  • Fluorocarbons
  • Glucosides
  • Inflammation Mediators
  • Protective Agents
  • gastrodin
  • perfluorooctanoic acid

Grants and funding

The authors reported there is no funding associated with the work featured in this article.