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Immunotoxicity evaluation by subchronic oral administration of clothianidin in Sprague-Dawley rats
Neonicotinoid pesticides (NNs) act as agonists on nicotinic acetylcholine receptors (nAChRs) of insects, and there have been concerns about the effects of NNs on the health of mammals. Since nAChRs are expressed in immune cells, it is possible that NNs disturb the immune system. However, few reports...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118483/ https://www.ncbi.nlm.nih.gov/pubmed/31983703 http://dx.doi.org/10.1292/jvms.19-0689 |
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author | ONARU, Kanoko OHNO, Shuji KUBO, Shizuka NAKANISHI, Satoki HIRANO, Tetsushi MANTANI, Youhei YOKOYAMA, Toshifumi HOSHI, Nobuhiko |
author_facet | ONARU, Kanoko OHNO, Shuji KUBO, Shizuka NAKANISHI, Satoki HIRANO, Tetsushi MANTANI, Youhei YOKOYAMA, Toshifumi HOSHI, Nobuhiko |
author_sort | ONARU, Kanoko |
collection | PubMed |
description | Neonicotinoid pesticides (NNs) act as agonists on nicotinic acetylcholine receptors (nAChRs) of insects, and there have been concerns about the effects of NNs on the health of mammals. Since nAChRs are expressed in immune cells, it is possible that NNs disturb the immune system. However, few reports have examined the immunotoxicity of clothianidin (CLO), a widely-used NN. Here, we report the effects of CLO on immune organs and type IV allergic reactions in ear auricles. We orally administered CLO at 0, 30 and 300 mg/kg/day (CLO-0, 30 and 300) to Sprague-Dawley rats for 28 days. The effects were evaluated by organ and body weights, histopathology, and immunohistochemistry (TCRαβ, CD4, CD8, CD11b, CD68, CD103). In addition, some cecal contents were subjected to preliminary gut microbiota analysis, because microbiota contribute to host homeostasis, including the immunity. Our results showed loose stool, suppression of body weight gain, significant changes in organ weights (thymus: decreased; liver: increased) and changes of the gut microbiota in the CLO-300 group. There were no obvious histopathological changes in immune organs. Granulomas of the ear auricles were found in one rat of each of the CLO-30 and 300 groups, but CLO had no apparent effect on the thickness or immunohistochemistry in the ear auricles. We present new evidence that CLO affects the thymus and intestine, and might enhance the local inflammatory response. These findings should contribute to the appropriate evaluation of the safety of NNs in the future. |
format | Online Article Text |
id | pubmed-7118483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71184832020-04-08 Immunotoxicity evaluation by subchronic oral administration of clothianidin in Sprague-Dawley rats ONARU, Kanoko OHNO, Shuji KUBO, Shizuka NAKANISHI, Satoki HIRANO, Tetsushi MANTANI, Youhei YOKOYAMA, Toshifumi HOSHI, Nobuhiko J Vet Med Sci Toxicology Neonicotinoid pesticides (NNs) act as agonists on nicotinic acetylcholine receptors (nAChRs) of insects, and there have been concerns about the effects of NNs on the health of mammals. Since nAChRs are expressed in immune cells, it is possible that NNs disturb the immune system. However, few reports have examined the immunotoxicity of clothianidin (CLO), a widely-used NN. Here, we report the effects of CLO on immune organs and type IV allergic reactions in ear auricles. We orally administered CLO at 0, 30 and 300 mg/kg/day (CLO-0, 30 and 300) to Sprague-Dawley rats for 28 days. The effects were evaluated by organ and body weights, histopathology, and immunohistochemistry (TCRαβ, CD4, CD8, CD11b, CD68, CD103). In addition, some cecal contents were subjected to preliminary gut microbiota analysis, because microbiota contribute to host homeostasis, including the immunity. Our results showed loose stool, suppression of body weight gain, significant changes in organ weights (thymus: decreased; liver: increased) and changes of the gut microbiota in the CLO-300 group. There were no obvious histopathological changes in immune organs. Granulomas of the ear auricles were found in one rat of each of the CLO-30 and 300 groups, but CLO had no apparent effect on the thickness or immunohistochemistry in the ear auricles. We present new evidence that CLO affects the thymus and intestine, and might enhance the local inflammatory response. These findings should contribute to the appropriate evaluation of the safety of NNs in the future. The Japanese Society of Veterinary Science 2020-01-27 2020-03 /pmc/articles/PMC7118483/ /pubmed/31983703 http://dx.doi.org/10.1292/jvms.19-0689 Text en ©2020 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Toxicology ONARU, Kanoko OHNO, Shuji KUBO, Shizuka NAKANISHI, Satoki HIRANO, Tetsushi MANTANI, Youhei YOKOYAMA, Toshifumi HOSHI, Nobuhiko Immunotoxicity evaluation by subchronic oral administration of clothianidin in Sprague-Dawley rats |
title | Immunotoxicity evaluation by subchronic oral administration of clothianidin in Sprague-Dawley rats |
title_full | Immunotoxicity evaluation by subchronic oral administration of clothianidin in Sprague-Dawley rats |
title_fullStr | Immunotoxicity evaluation by subchronic oral administration of clothianidin in Sprague-Dawley rats |
title_full_unstemmed | Immunotoxicity evaluation by subchronic oral administration of clothianidin in Sprague-Dawley rats |
title_short | Immunotoxicity evaluation by subchronic oral administration of clothianidin in Sprague-Dawley rats |
title_sort | immunotoxicity evaluation by subchronic oral administration of clothianidin in sprague-dawley rats |
topic | Toxicology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118483/ https://www.ncbi.nlm.nih.gov/pubmed/31983703 http://dx.doi.org/10.1292/jvms.19-0689 |
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