Bisphenol A Exposure Induces Small Intestine Damage Through Oxidative Stress, Inflammation, and Microbiota Alteration in Rats

Bisphenol A (BPA), a widespread environmental contaminant used in plastics and resins, poses significant health risks due to its endocrine-disrupting properties and potential for inducing intestinal toxicity. This study explored the toxicological effects of BPA on the small intestine of rats, focusi...

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Main Authors: Kai Wang, Juan Tang, Dan Shen, Yansen Li, Kentaro Nagaoka, Chunmei Li
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Toxics
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Online Access:https://www.mdpi.com/2305-6304/13/5/331
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author Kai Wang
Juan Tang
Dan Shen
Yansen Li
Kentaro Nagaoka
Chunmei Li
author_facet Kai Wang
Juan Tang
Dan Shen
Yansen Li
Kentaro Nagaoka
Chunmei Li
author_sort Kai Wang
collection DOAJ
description Bisphenol A (BPA), a widespread environmental contaminant used in plastics and resins, poses significant health risks due to its endocrine-disrupting properties and potential for inducing intestinal toxicity. This study explored the toxicological effects of BPA on the small intestine of rats, focusing on the duodenum, jejunum, and ileum. Histopathological evaluation revealed that the duodenum experienced the most severe structural damage, including villous atrophy, epithelial shedding, and mitochondrial degeneration. BPA exposure disrupted oxidative stress homeostasis by reducing superoxide dismutase activity and increasing malondialdehyde levels, along with upregulating antioxidant-related genes like <i>GPX2</i> and <i>HO-1</i> upregulated, indicating lipid peroxidation and oxidative damage. Inflammatory markers such as <i>IL-1</i> and <i>NFκB</i> were significantly upregulated, highlighting an active inflammatory response and epithelial cell apoptosis. BPA also altered lipid metabolism, with increased expression of lipogenic genes such as <i>SREBP-1c</i> and <i>FAS</i>, indicating metabolic dysregulation. Fecal microbiota analysis revealed reduced α-diversity, enrichment of pathogenic taxa like <i>Escherichia-Shigella</i>, and depletion of beneficial genera such as <i>Lachnospiraceae NK4A136 group</i>, exacerbating gut inflammation and barrier dysfunction. These findings suggest that BPA-induced small intestinal damage is driven by oxidative stress, inflammation, and gut dysbiosis, with the duodenum and jejunum being the more vulnerable segments.
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spelling doaj-art-c4e7c1f8529845a0bb9505c87d3dc6752025-08-20T03:12:15ZengMDPI AGToxics2305-63042025-04-0113533110.3390/toxics13050331Bisphenol A Exposure Induces Small Intestine Damage Through Oxidative Stress, Inflammation, and Microbiota Alteration in RatsKai Wang0Juan Tang1Dan Shen2Yansen Li3Kentaro Nagaoka4Chunmei Li5College of Animal Science and Technology, Nanjing Agriculture University, Nanjing 210095, ChinaCollege of Animal Science and Technology, Nanjing Agriculture University, Nanjing 210095, ChinaCollege of Animal Science and Technology, Nanjing Agriculture University, Nanjing 210095, ChinaCollege of Animal Science and Technology, Nanjing Agriculture University, Nanjing 210095, ChinaCooperative Department of Veterinary Medicine, Tokyo University of Agriculture and Technology, Tokyo 183-8538, JapanCollege of Animal Science and Technology, Nanjing Agriculture University, Nanjing 210095, ChinaBisphenol A (BPA), a widespread environmental contaminant used in plastics and resins, poses significant health risks due to its endocrine-disrupting properties and potential for inducing intestinal toxicity. This study explored the toxicological effects of BPA on the small intestine of rats, focusing on the duodenum, jejunum, and ileum. Histopathological evaluation revealed that the duodenum experienced the most severe structural damage, including villous atrophy, epithelial shedding, and mitochondrial degeneration. BPA exposure disrupted oxidative stress homeostasis by reducing superoxide dismutase activity and increasing malondialdehyde levels, along with upregulating antioxidant-related genes like <i>GPX2</i> and <i>HO-1</i> upregulated, indicating lipid peroxidation and oxidative damage. Inflammatory markers such as <i>IL-1</i> and <i>NFκB</i> were significantly upregulated, highlighting an active inflammatory response and epithelial cell apoptosis. BPA also altered lipid metabolism, with increased expression of lipogenic genes such as <i>SREBP-1c</i> and <i>FAS</i>, indicating metabolic dysregulation. Fecal microbiota analysis revealed reduced α-diversity, enrichment of pathogenic taxa like <i>Escherichia-Shigella</i>, and depletion of beneficial genera such as <i>Lachnospiraceae NK4A136 group</i>, exacerbating gut inflammation and barrier dysfunction. These findings suggest that BPA-induced small intestinal damage is driven by oxidative stress, inflammation, and gut dysbiosis, with the duodenum and jejunum being the more vulnerable segments.https://www.mdpi.com/2305-6304/13/5/331bisphenol Aintestinal barrieroxidative stressgut microbiotatoxicological impact
spellingShingle Kai Wang
Juan Tang
Dan Shen
Yansen Li
Kentaro Nagaoka
Chunmei Li
Bisphenol A Exposure Induces Small Intestine Damage Through Oxidative Stress, Inflammation, and Microbiota Alteration in Rats
Toxics
bisphenol A
intestinal barrier
oxidative stress
gut microbiota
toxicological impact
title Bisphenol A Exposure Induces Small Intestine Damage Through Oxidative Stress, Inflammation, and Microbiota Alteration in Rats
title_full Bisphenol A Exposure Induces Small Intestine Damage Through Oxidative Stress, Inflammation, and Microbiota Alteration in Rats
title_fullStr Bisphenol A Exposure Induces Small Intestine Damage Through Oxidative Stress, Inflammation, and Microbiota Alteration in Rats
title_full_unstemmed Bisphenol A Exposure Induces Small Intestine Damage Through Oxidative Stress, Inflammation, and Microbiota Alteration in Rats
title_short Bisphenol A Exposure Induces Small Intestine Damage Through Oxidative Stress, Inflammation, and Microbiota Alteration in Rats
title_sort bisphenol a exposure induces small intestine damage through oxidative stress inflammation and microbiota alteration in rats
topic bisphenol A
intestinal barrier
oxidative stress
gut microbiota
toxicological impact
url https://www.mdpi.com/2305-6304/13/5/331
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