Involvement of Autophagy and Oxidative Stress-Mediated DNA Hypomethylation in Transgenerational Nephrotoxicity Induced in Rats by the Mycotoxin Fumonisin B1
Author:
Aldawood Nouf1, Almustafa Sarah2, Alwasel Saleh2, Aldahmash Waleed2, Ben Bacha Abir3ORCID, Alamri Abdullah4ORCID, Alanazi Mohammad4, Harrath Abdel Halim2ORCID
Affiliation:
1. Department of Biology, College of Science, Princess Nourah bint Abdulrahman University, Riyadh 11671, Saudi Arabia 2. Department of Zoology, College of Sciences, King Saud University, Riyadh 11451, Saudi Arabia 3. Department of Biochemistry, College of Sciences, King Saud University, Riyadh 11671, Saudi Arabia 4. Genome Research Chair, Department of Biochemistry, College of Sciences, King Saud University, Riyadh 11495, Saudi Arabia
Abstract
Fumonisin B1 (FB1), a mycotoxin produced by Fusarium verticillioides, is one of the most common pollutants in natural foods and agricultural crops. It can cause chronic and severe health issues in humans and animals. The aim of this study was to evaluate the transgenerational effects of FB1 exposure on the structure and function of the kidneys in offspring. Virgin female Wistar rats were randomly divided into three groups: group one (control) received sterile water, and groups two and three were intragastrically administered low (20 mg/kg) and high (50 mg/kg) doses of FB1, respectively, from day 6 of pregnancy until delivery. Our results showed that exposure to either dose of FB1 caused histopathological changes, such as atrophy, hypercellularity, hemorrhage, calcification, and a decrease in the glomerular diameter, in both the first and second generations. The levels of the antioxidant markers glutathione, glutathione S-transferase, and catalase significantly decreased, while malondialdehyde levels increased. Moreover, autophagy was induced, as immunofluorescence analysis revealed that LC-3 protein expression was significantly increased in both generations after exposure to either dose of FB1. However, a significant decrease in methyltransferase (DNMT3) protein expression was observed in the first generation in both treatment groups (20 mg/kg and 50 mg/kg), indicating a decrease in DNA methylation as a result of early-life exposure to FB1. Interestingly, global hypomethylation was also observed in the second generation in both treatment groups despite the fact that the mothers of these rats were not exposed to FB1. Thus, early-life exposure to FB1 induced nephrotoxicity in offspring of the first and second generations. The mechanisms of action underlying this transgenerational effect may include oxidative stress, autophagy, and DNA hypomethylation.
Funder
Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia
Subject
Health, Toxicology and Mutagenesis,Toxicology
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