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Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure
We have earlier demonstrated the potential of monocrotophos (MCP), a highly toxic organophosphorus insecticide (OPI), to elicit insulin resistance in rats after chronic exposure. Given the understanding of role of paraoxonase1 (PON1) in OPI toxicity and diabetes pathology, this study was envisaged t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Slovak Toxicology Society SETOX
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085301/ https://www.ncbi.nlm.nih.gov/pubmed/32210701 http://dx.doi.org/10.2478/intox-2019-0015 |
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author | NAGARAJU, Raju JOSHI, Apurva Kumar R. VAMADEVA, Sowmya Giriyapura SHARDA, Rajini Padmanabhan |
author_facet | NAGARAJU, Raju JOSHI, Apurva Kumar R. VAMADEVA, Sowmya Giriyapura SHARDA, Rajini Padmanabhan |
author_sort | NAGARAJU, Raju |
collection | PubMed |
description | We have earlier demonstrated the potential of monocrotophos (MCP), a highly toxic organophosphorus insecticide (OPI), to elicit insulin resistance in rats after chronic exposure. Given the understanding of role of paraoxonase1 (PON1) in OPI toxicity and diabetes pathology, this study was envisaged to understand the effect of duration of exposure to MCP on plasma PON1 activity in rats. Rats were administered MCP per os at 1/20 and 1/10(th) LD(50) as daily doses for 180 days. Interim blood samples were collected at 15, 30, 45, 90 and 180 d for analysis of plasma parameters. Exposure to MCP for 45 resulted in persistent trend of hyperinsulinemia, while significant increase in fasting glucose levels was observed after 180 days. MCP caused suppression of plasma cholinesterase activity though the study period, albeit extent of inhibition was more severe during the early phase of the study. Exposure to MCP for 180 d resulted in hypertriglyceridemia and marginal decrease in HDL-C levels. MCP failed to modulate PON1 activity in plasma during the early phase of the study (up to 45 d). However, prolonged exposure resulted in significant increase in the plasma PON1 activity. This suggests that manifestation of insulin resistance in rats subjected to chronic exposure to MCP is associated with increase in PON1 activity. Our work provides rationale for studying whether the increase in PON1 activity observed in the present study serves to counter the deleterious effect of long term exposure to organophosphorus insecticides on metabolic homeostasis. |
format | Online Article Text |
id | pubmed-7085301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Slovak Toxicology Society SETOX |
record_format | MEDLINE/PubMed |
spelling | pubmed-70853012020-03-24 Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure NAGARAJU, Raju JOSHI, Apurva Kumar R. VAMADEVA, Sowmya Giriyapura SHARDA, Rajini Padmanabhan Interdiscip Toxicol Original Article We have earlier demonstrated the potential of monocrotophos (MCP), a highly toxic organophosphorus insecticide (OPI), to elicit insulin resistance in rats after chronic exposure. Given the understanding of role of paraoxonase1 (PON1) in OPI toxicity and diabetes pathology, this study was envisaged to understand the effect of duration of exposure to MCP on plasma PON1 activity in rats. Rats were administered MCP per os at 1/20 and 1/10(th) LD(50) as daily doses for 180 days. Interim blood samples were collected at 15, 30, 45, 90 and 180 d for analysis of plasma parameters. Exposure to MCP for 45 resulted in persistent trend of hyperinsulinemia, while significant increase in fasting glucose levels was observed after 180 days. MCP caused suppression of plasma cholinesterase activity though the study period, albeit extent of inhibition was more severe during the early phase of the study. Exposure to MCP for 180 d resulted in hypertriglyceridemia and marginal decrease in HDL-C levels. MCP failed to modulate PON1 activity in plasma during the early phase of the study (up to 45 d). However, prolonged exposure resulted in significant increase in the plasma PON1 activity. This suggests that manifestation of insulin resistance in rats subjected to chronic exposure to MCP is associated with increase in PON1 activity. Our work provides rationale for studying whether the increase in PON1 activity observed in the present study serves to counter the deleterious effect of long term exposure to organophosphorus insecticides on metabolic homeostasis. Slovak Toxicology Society SETOX 2019-11 2020-02-20 /pmc/articles/PMC7085301/ /pubmed/32210701 http://dx.doi.org/10.2478/intox-2019-0015 Text en Copyright © 2019 SETOX & Institute of Experimental Pharmacology and Toxicology, SASc. https://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License. (CC BY-NC-ND 4.0) |
spellingShingle | Original Article NAGARAJU, Raju JOSHI, Apurva Kumar R. VAMADEVA, Sowmya Giriyapura SHARDA, Rajini Padmanabhan Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure |
title | Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure |
title_full | Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure |
title_fullStr | Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure |
title_full_unstemmed | Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure |
title_short | Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure |
title_sort | plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085301/ https://www.ncbi.nlm.nih.gov/pubmed/32210701 http://dx.doi.org/10.2478/intox-2019-0015 |
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