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Alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats

Acrylamide is a vinyl monomer that is widely used for the synthesis of polyacrylamides, the treatment of drinking water, and as an additive in cosmetics. Acrylamide is also produced during the thermal processing of carbohydrate-rich foods. Although the potential toxic effects of acrylamide have been...

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Autores principales: Rivadeneyra-Domínguez, Eduardo, Becerra-Contreras, Yesenia, Vázquez-Luna, Alma, Díaz-Sobac, Rafaél, Rodríguez-Landa, Juan Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258226/
https://www.ncbi.nlm.nih.gov/pubmed/30510905
http://dx.doi.org/10.1016/j.toxrep.2018.11.006
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author Rivadeneyra-Domínguez, Eduardo
Becerra-Contreras, Yesenia
Vázquez-Luna, Alma
Díaz-Sobac, Rafaél
Rodríguez-Landa, Juan Francisco
author_facet Rivadeneyra-Domínguez, Eduardo
Becerra-Contreras, Yesenia
Vázquez-Luna, Alma
Díaz-Sobac, Rafaél
Rodríguez-Landa, Juan Francisco
author_sort Rivadeneyra-Domínguez, Eduardo
collection PubMed
description Acrylamide is a vinyl monomer that is widely used for the synthesis of polyacrylamides, the treatment of drinking water, and as an additive in cosmetics. Acrylamide is also produced during the thermal processing of carbohydrate-rich foods. Although the potential toxic effects of acrylamide have been reported, few studies have evaluated biochemical parameters in blood. The present study investigated alterations of blood chemistry, hepatic function, and blood cytometry in acrylamide-treated rats. Thirty-two male Wistar rats were assigned to four experimental groups (n = 8/group): one control group received 0.3 ml of vehicle (saline solution), and the other three groups received acrylamide (25, 50, and 75 mg/kg, i.p., for 14 days). At the end of treatment, blood samples were collected to obtain serum, which was then processed using a Vitros250 device. For blood cytometry, the samples were processed in a Sysmex analyzer. The blood chemistry results showed that urea nitrogen, urea, and creatinine were elevated in the acrylamide-treated groups. Tests of hepatic function showed that total and direct bilirubins, transaminases, and alkaline phosphatase were also elevated compared with vehicle, whereas the levels of total proteins and albumin decreased. Blood cytometry showed that the levels of erythrocytes, hemoglobin, hematocrit, leukocytes, and platelets and mean cell volume decreased in the acrylamide-treated groups compared with vehicle. Overall, the present findings indicate that acrylamide causes deleterious effects on renal and hepatic physiology, producing dose-dependent alterations of blood chemistry and cytometry parameters in male Wistar rats.
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spelling pubmed-62582262018-12-03 Alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats Rivadeneyra-Domínguez, Eduardo Becerra-Contreras, Yesenia Vázquez-Luna, Alma Díaz-Sobac, Rafaél Rodríguez-Landa, Juan Francisco Toxicol Rep Article Acrylamide is a vinyl monomer that is widely used for the synthesis of polyacrylamides, the treatment of drinking water, and as an additive in cosmetics. Acrylamide is also produced during the thermal processing of carbohydrate-rich foods. Although the potential toxic effects of acrylamide have been reported, few studies have evaluated biochemical parameters in blood. The present study investigated alterations of blood chemistry, hepatic function, and blood cytometry in acrylamide-treated rats. Thirty-two male Wistar rats were assigned to four experimental groups (n = 8/group): one control group received 0.3 ml of vehicle (saline solution), and the other three groups received acrylamide (25, 50, and 75 mg/kg, i.p., for 14 days). At the end of treatment, blood samples were collected to obtain serum, which was then processed using a Vitros250 device. For blood cytometry, the samples were processed in a Sysmex analyzer. The blood chemistry results showed that urea nitrogen, urea, and creatinine were elevated in the acrylamide-treated groups. Tests of hepatic function showed that total and direct bilirubins, transaminases, and alkaline phosphatase were also elevated compared with vehicle, whereas the levels of total proteins and albumin decreased. Blood cytometry showed that the levels of erythrocytes, hemoglobin, hematocrit, leukocytes, and platelets and mean cell volume decreased in the acrylamide-treated groups compared with vehicle. Overall, the present findings indicate that acrylamide causes deleterious effects on renal and hepatic physiology, producing dose-dependent alterations of blood chemistry and cytometry parameters in male Wistar rats. Elsevier 2018-11-06 /pmc/articles/PMC6258226/ /pubmed/30510905 http://dx.doi.org/10.1016/j.toxrep.2018.11.006 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Rivadeneyra-Domínguez, Eduardo
Becerra-Contreras, Yesenia
Vázquez-Luna, Alma
Díaz-Sobac, Rafaél
Rodríguez-Landa, Juan Francisco
Alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats
title Alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats
title_full Alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats
title_fullStr Alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats
title_full_unstemmed Alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats
title_short Alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats
title_sort alterations of blood chemistry, hepatic and renal function, and blood cytometry in acrylamide-treated rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258226/
https://www.ncbi.nlm.nih.gov/pubmed/30510905
http://dx.doi.org/10.1016/j.toxrep.2018.11.006
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