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Downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon
Diazinon (DZN) is an organophosphate insecticide which exerts its effect through the inhibition of acetylcholinesterase enzyme (AChE). In this work, we studied the development of tolerance to subchronic p.o. administration of DZN in rats, under both in vivo and in vitro conditions. A group of 20 rat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615940/ https://www.ncbi.nlm.nih.gov/pubmed/28959576 http://dx.doi.org/10.1016/j.toxrep.2016.06.002 |
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author | Ivanović, Saša R. Dimitrijević, Blagoje Ćupić, Vitomir Jezdimirović, Milanka Borozan, Sunčica Savić, Mila Savić, Djordje |
author_facet | Ivanović, Saša R. Dimitrijević, Blagoje Ćupić, Vitomir Jezdimirović, Milanka Borozan, Sunčica Savić, Mila Savić, Djordje |
author_sort | Ivanović, Saša R. |
collection | PubMed |
description | Diazinon (DZN) is an organophosphate insecticide which exerts its effect through the inhibition of acetylcholinesterase enzyme (AChE). In this work, we studied the development of tolerance to subchronic p.o. administration of DZN in rats, under both in vivo and in vitro conditions. A group of 20 rats (2 groups, n = 10) was administered p.o. the 1/10 of established LD(50) DZN (namely 55.87 mg/kg bw) for 28 days. On the 14th and 28th day of study with isolated diaphragm and ileum, we examined the downregulation of nicotinic and muscarinic receptor function through Electrical Field Stimulation (EFS). Maximum contractility of the diaphragm was recorded on the 14th day of the study (25% higher compared to the non-treated rats), while on the 28th day the contractions almost did not differ from the values found in non-treated rats. EFS of isolated ileum on the 14th day of study caused significantly higher contractions compared to the non-treated rats, but after 28 days, ileum contractions decreased approximately to the level of contractions in non-treated rats. On the 14th study day, we also recorded increased amplitude of spontaneous ileum contractions, compared to non-treated rats. The application of increasing ACh concentrations caused dose-dependent ileum contractions, without statistically significant differences of median effective concentration (EC(50)) values in non-treated and treated rats. Tolerance to subchronic DZN administration develops due to various adaptation mechanisms, including the most important one—downregulation of nicotinic and muscarinic receptor function. |
format | Online Article Text |
id | pubmed-5615940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56159402017-09-28 Downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon Ivanović, Saša R. Dimitrijević, Blagoje Ćupić, Vitomir Jezdimirović, Milanka Borozan, Sunčica Savić, Mila Savić, Djordje Toxicol Rep Article Diazinon (DZN) is an organophosphate insecticide which exerts its effect through the inhibition of acetylcholinesterase enzyme (AChE). In this work, we studied the development of tolerance to subchronic p.o. administration of DZN in rats, under both in vivo and in vitro conditions. A group of 20 rats (2 groups, n = 10) was administered p.o. the 1/10 of established LD(50) DZN (namely 55.87 mg/kg bw) for 28 days. On the 14th and 28th day of study with isolated diaphragm and ileum, we examined the downregulation of nicotinic and muscarinic receptor function through Electrical Field Stimulation (EFS). Maximum contractility of the diaphragm was recorded on the 14th day of the study (25% higher compared to the non-treated rats), while on the 28th day the contractions almost did not differ from the values found in non-treated rats. EFS of isolated ileum on the 14th day of study caused significantly higher contractions compared to the non-treated rats, but after 28 days, ileum contractions decreased approximately to the level of contractions in non-treated rats. On the 14th study day, we also recorded increased amplitude of spontaneous ileum contractions, compared to non-treated rats. The application of increasing ACh concentrations caused dose-dependent ileum contractions, without statistically significant differences of median effective concentration (EC(50)) values in non-treated and treated rats. Tolerance to subchronic DZN administration develops due to various adaptation mechanisms, including the most important one—downregulation of nicotinic and muscarinic receptor function. Elsevier 2016-06-07 /pmc/articles/PMC5615940/ /pubmed/28959576 http://dx.doi.org/10.1016/j.toxrep.2016.06.002 Text en © 2016 Published by Elsevier Ireland Ltd. 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 Ivanović, Saša R. Dimitrijević, Blagoje Ćupić, Vitomir Jezdimirović, Milanka Borozan, Sunčica Savić, Mila Savić, Djordje Downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon |
title | Downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon |
title_full | Downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon |
title_fullStr | Downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon |
title_full_unstemmed | Downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon |
title_short | Downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon |
title_sort | downregulation of nicotinic and muscarinic receptor function in rats after subchronic exposure to diazinon |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615940/ https://www.ncbi.nlm.nih.gov/pubmed/28959576 http://dx.doi.org/10.1016/j.toxrep.2016.06.002 |
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