The effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues

The toxicities of two widely used organophosphate insecticides, malathion and parathion, and their oxygen analogues were investigated in rats fed different levels of dietary protein. Male weanling rats were pair-fed either 5 or 20% casein diets for 10 days and control animals received a 20% casein d...

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Main Author: Bloomer, Catherine Carico
Other Authors: Biochemistry and Nutrition
Format: Others
Language:en
Published: Virginia Polytechnic Institute and State University 2016
Subjects:
Online Access:http://hdl.handle.net/10919/71068
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spelling ndltd-VTETD-oai-vtechworks.lib.vt.edu-10919-710682021-05-05T05:40:17Z The effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues Bloomer, Catherine Carico Biochemistry and Nutrition LD5655.V855 1971.B48 The toxicities of two widely used organophosphate insecticides, malathion and parathion, and their oxygen analogues were investigated in rats fed different levels of dietary protein. Male weanling rats were pair-fed either 5 or 20% casein diets for 10 days and control animals received a 20% casein diet ad libitum. Toxicity studies showed that rats which received 5% casein diets were more susceptible to malathion and malaoxon (LD₅₀ = 151.1 mg/kg and 7.75 mg/kg) when compared with rats pair-fed 20% casein (LD₅₀ = 273.6 mg/kg and 14.33 mg/kg) or with rats fed 20% casein ad libitum (LD₅₀ = 418.6 mg/kg and 15.23 mg/kg). Rats which received 5% casein diets were similarly more susceptible to parathion and paraoxon (LD₅₀ = 1.24 mg/kg and 0.385 mg/kg) when compared with rats pair-fed 20% casein (LD₅₀ = 1.65 mg/kg and 0.537 mg/kg) or with rats fed 20% casein ad libitum (LD₅₀ = 2.04 mg/kg and 0.666 mg/kg). Toxicities of both the inactive parent co~pounds and their active analogues were affected by dietary protein intake. Metabolism studies· based on excretion of p-nitrophenol, a metabolite of parathion and paraoxon, were largely inconclusive. It is concluded from these studies that dietary protein intake is of major importance in determining the toxicities of malathion and parathion and their oxygen analogues and that the major effect of dietary protein is probably on the degradation and not the activation of the parent compounds. It is further concluded that populations on low protein intake may be in greater danger than their well-fed counterparts when exposed to acute levels of these organophosphates and possibly other similar compounds. Master of Science 2016-05-23T14:57:40Z 2016-05-23T14:57:40Z 1971 Thesis Text http://hdl.handle.net/10919/71068 en OCLC# 33892741 In Copyright http://rightsstatements.org/vocab/InC/1.0/ v, 63 leaves application/pdf application/pdf Virginia Polytechnic Institute and State University
collection NDLTD
language en
format Others
sources NDLTD
topic LD5655.V855 1971.B48
spellingShingle LD5655.V855 1971.B48
Bloomer, Catherine Carico
The effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues
description The toxicities of two widely used organophosphate insecticides, malathion and parathion, and their oxygen analogues were investigated in rats fed different levels of dietary protein. Male weanling rats were pair-fed either 5 or 20% casein diets for 10 days and control animals received a 20% casein diet ad libitum. Toxicity studies showed that rats which received 5% casein diets were more susceptible to malathion and malaoxon (LD₅₀ = 151.1 mg/kg and 7.75 mg/kg) when compared with rats pair-fed 20% casein (LD₅₀ = 273.6 mg/kg and 14.33 mg/kg) or with rats fed 20% casein ad libitum (LD₅₀ = 418.6 mg/kg and 15.23 mg/kg). Rats which received 5% casein diets were similarly more susceptible to parathion and paraoxon (LD₅₀ = 1.24 mg/kg and 0.385 mg/kg) when compared with rats pair-fed 20% casein (LD₅₀ = 1.65 mg/kg and 0.537 mg/kg) or with rats fed 20% casein ad libitum (LD₅₀ = 2.04 mg/kg and 0.666 mg/kg). Toxicities of both the inactive parent co~pounds and their active analogues were affected by dietary protein intake. Metabolism studies· based on excretion of p-nitrophenol, a metabolite of parathion and paraoxon, were largely inconclusive. It is concluded from these studies that dietary protein intake is of major importance in determining the toxicities of malathion and parathion and their oxygen analogues and that the major effect of dietary protein is probably on the degradation and not the activation of the parent compounds. It is further concluded that populations on low protein intake may be in greater danger than their well-fed counterparts when exposed to acute levels of these organophosphates and possibly other similar compounds. === Master of Science
author2 Biochemistry and Nutrition
author_facet Biochemistry and Nutrition
Bloomer, Catherine Carico
author Bloomer, Catherine Carico
author_sort Bloomer, Catherine Carico
title The effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues
title_short The effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues
title_full The effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues
title_fullStr The effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues
title_full_unstemmed The effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues
title_sort effects of different levels of dietary protein on the toxicity and metabolism of malathion and parathion and their oxygen analogues
publisher Virginia Polytechnic Institute and State University
publishDate 2016
url http://hdl.handle.net/10919/71068
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