Aflatoxin B1-induced oxidative stress in canine small intestinal cells

• Published in: Journal of animal reproduction & biotechnology (Online) Vol. 39; no. 2; pp. 105 - 113
• Main Authors: Cho, Hyun-Woo, Seo, Kangmin, Lee, Min Young, Lee, Sang-Yeob, So, Kyoung Min, Kim, Ki Hyun, Chun, Ju Lan
• Format: Journal Article
• Language: English
• Published: 한국동물생명공학회(구 한국수정란이식학회) 30.06.2024; The Korean Society of Animal Reproduction and Biotechnology; 사단법인 한국동물생명공학회
• Subjects: aflatoxin b1; apoptosis; canine; intestinal epithelial barrier; small intestinal cell; 축산학; intestinal epithelial barrier; apoptosis; canine; aflatoxin B1; small intestinal cell
• ISSN: 2671-4639; 2671-4663
• DOI: 10.12750/JARB.39.2.105

Background: Aflatoxin B1 (AFB1) is a toxic metabolite generated by Aspergillus species and is commonly detected during the processing and storage of food; it is considered a group I carcinogen. The hepatotoxic effects, diseases, and mechanisms induced by AFB1 owing to chronic or acute exposure are well documented; however, there is a lack of research on its effects on the intestine, which is a crucial organ in the digestive process. Dogs are often susceptible to chronic AFB1 exposure owing to lack of variation in their diet, unlike humans, thereby rendering them prone to its effects. Therefore, we investigated the effects of AFB1 on canine small intestinal epithelial primary cells (CSIc). Methods: We treated CSIc with various concentrations of AFB1 (0, 1.25, 2.5, 5, 10, 20, 40, and 80 μM) for 24 h and analyzed cell viability and transepithelial-transendothelial electrical resistance (TEER) value. Additionally, we analyzed the mRNA expression of tight junction-related genes (OCLN, CLDN3, TJP1, and MUC2), antioxidant-related genes (CAT and GPX1), and apoptosis-related genes (BCL2, Bax, and TP53). Results: We found a significant decrease in CSIc viability and TEER values after treatment with AFB1 at concentrations of 20 μM or higher. Quantitative polymerase chain reaction analysis indicated a downregulation of OCLN, CLDN3, and TJP1 in CSIc treated with 20 μM or higher concentrations of AFB1. Additionally, AFB1 treatment downregulated CAT , GPX1, and BCL2. Conclusions: Acute exposure of CSIc to AFB1 induces toxicity, and exposure to AFB1 above a certain threshold compromises the barrier integrity of CSIc.