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Sub-chronic effect of neem based pesticide (Vepacide) on acetylcholinesterase and ATPases in rat

Acetylcholinesterases (AChE), Na + -K + , Mg 2+ and Ca 2+ -ATPases were monitored in rat brain when treated orally with 80, 160 and 320 mg/kg of Vepacide, an active ingredient from neem seed oil, daily for 90 days. Brain AChE, Na + -K + and Ca 2+ -ATPases were inhibited whereas Mg 2+ -ATPase levels...

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Published in:Journal of environmental science and health. Part B, Pesticides, food contaminants, and agricultural wastes Pesticides, food contaminants, and agricultural wastes, 1999-09, Vol.34 (5), p.873-884
Main Authors: Rahman, M.F, Siddiqui, M.K.J, Jamil, K
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container_title Journal of environmental science and health. Part B, Pesticides, food contaminants, and agricultural wastes
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creator Rahman, M.F
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description Acetylcholinesterases (AChE), Na + -K + , Mg 2+ and Ca 2+ -ATPases were monitored in rat brain when treated orally with 80, 160 and 320 mg/kg of Vepacide, an active ingredient from neem seed oil, daily for 90 days. Brain AChE, Na + -K + and Ca 2+ -ATPases were inhibited whereas Mg 2+ -ATPase levels were enhanced in both the sexes after 45 and 90 days of treatment. The relative sensitivities of these ATPases to Vepacide indicated that Ca 2+ -ATPase being more sensitive than Na + -K + -ATPase in both the sexes. The magnitude of Ca 2+ -ATPase inhibited by this compound was higher than that of brain AChE. It appears to be sexual dimorphism in the alterations of brain AChE, Na + -K + and Mg 2+ -ATPases by Vepacide with females being significant when compared with males. After 28 days of post treatment the alterations observed were approached to those of controls both in male and female rats showing reversal of the toxicity. These results indicated that the ATPases were potently inhibited by Vepacide and seemed to be its precise target among the enzyme studied. This can be used as biochemical marker of exposure to this neem derived product.
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Brain AChE, Na + -K + and Ca 2+ -ATPases were inhibited whereas Mg 2+ -ATPase levels were enhanced in both the sexes after 45 and 90 days of treatment. The relative sensitivities of these ATPases to Vepacide indicated that Ca 2+ -ATPase being more sensitive than Na + -K + -ATPase in both the sexes. The magnitude of Ca 2+ -ATPase inhibited by this compound was higher than that of brain AChE. It appears to be sexual dimorphism in the alterations of brain AChE, Na + -K + and Mg 2+ -ATPases by Vepacide with females being significant when compared with males. After 28 days of post treatment the alterations observed were approached to those of controls both in male and female rats showing reversal of the toxicity. These results indicated that the ATPases were potently inhibited by Vepacide and seemed to be its precise target among the enzyme studied. 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Part B, Pesticides, food contaminants, and agricultural wastes</title><addtitle>J Environ Sci Health B</addtitle><description>Acetylcholinesterases (AChE), Na + -K + , Mg 2+ and Ca 2+ -ATPases were monitored in rat brain when treated orally with 80, 160 and 320 mg/kg of Vepacide, an active ingredient from neem seed oil, daily for 90 days. Brain AChE, Na + -K + and Ca 2+ -ATPases were inhibited whereas Mg 2+ -ATPase levels were enhanced in both the sexes after 45 and 90 days of treatment. The relative sensitivities of these ATPases to Vepacide indicated that Ca 2+ -ATPase being more sensitive than Na + -K + -ATPase in both the sexes. The magnitude of Ca 2+ -ATPase inhibited by this compound was higher than that of brain AChE. It appears to be sexual dimorphism in the alterations of brain AChE, Na + -K + and Mg 2+ -ATPases by Vepacide with females being significant when compared with males. After 28 days of post treatment the alterations observed were approached to those of controls both in male and female rats showing reversal of the toxicity. These results indicated that the ATPases were potently inhibited by Vepacide and seemed to be its precise target among the enzyme studied. 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Psychology</subject><subject>inhibition</subject><subject>Insecticides - administration &amp; dosage</subject><subject>Insecticides - toxicity</subject><subject>Male</subject><subject>Mammalia</subject><subject>Medical sciences</subject><subject>neem</subject><subject>neem compound</subject><subject>oral administration</subject><subject>Pesticides, fertilizers and other agrochemicals toxicology</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Sex Characteristics</subject><subject>Toxicology</subject><subject>Triterpenes - administration &amp; dosage</subject><subject>Triterpenes - toxicity</subject><subject>Vepacide</subject><issn>0360-1234</issn><issn>1532-4109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkF1rFTEQhoNY7LH6A7zRXIjoxepMsl8Bb0pptVBQ6NHbdZJN7Mpuckz2oOffN4c9olCoVzMwzzO8vIw9Q3iL0MI7kDWgkEqBko0UUjxgK6ykKEoE9ZCt9vciA-Uxe5zSDwBsJdaP2DFCWdcIzYp9u97qwtzE4AfDrXPWzDw47q2duKZke76xaR7M0Fv--qvd0H57w4PnZOy8G81NGAefERszzcn3_HT9Oa-JD55Hmp-wI0djsk8P84StL87XZx-Lq08fLs9OrwpTtmIuiHRtSWMphdKy1gYMVDl-VUvRkGpsg7p0LVSVQNs73QupS0TMinYZOmGvlrebGH5uc55uGpKx40jehm3qsJGqhqbNIC6giSGlaF23icNEcdchdPtWuzutZuf54flWT7b_x1hqzMDLA0DJ0OgieTOkv5xCpVrI2PsFG7wLcaJfIY59N9NuDPGPI--L0fxXv2N18-85my8W01Ho6HvM4JdrAShBKFkrgfIW0Busdg</recordid><startdate>199909</startdate><enddate>199909</enddate><creator>Rahman, M.F</creator><creator>Siddiqui, M.K.J</creator><creator>Jamil, K</creator><general>Taylor &amp; Francis Group</general><general>Taylor &amp; Francis</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>199909</creationdate><title>Sub-chronic effect of neem based pesticide (Vepacide) on acetylcholinesterase and ATPases in rat</title><author>Rahman, M.F ; Siddiqui, M.K.J ; Jamil, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-aab6eab14329b36bc0c0536056327a97e71b4f805521edfbd23b4111ab1bf563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Acetylcholinesterase</topic><topic>Acetylcholinesterase - metabolism</topic><topic>Adenosine Triphosphatases - metabolism</topic><topic>adenosinetriphosphatase</topic><topic>Administration, Oral</topic><topic>and Ca</topic><topic>Animal, plant and microbial ecology</topic><topic>Animals</topic><topic>application rate</topic><topic>Applied ecology</topic><topic>ATPases</topic><topic>Azadirachta indica</topic><topic>Biological and medical sciences</topic><topic>brain</topic><topic>Brain - drug effects</topic><topic>Brain - enzymology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Ecotoxicology, biological effects of pollution</topic><topic>Effects of pollution and side effects of pesticides on vertebrates</topic><topic>enzyme activity</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>inhibition</topic><topic>Insecticides - administration &amp; dosage</topic><topic>Insecticides - toxicity</topic><topic>Male</topic><topic>Mammalia</topic><topic>Medical sciences</topic><topic>neem</topic><topic>neem compound</topic><topic>oral administration</topic><topic>Pesticides, fertilizers and other agrochemicals toxicology</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Sex Characteristics</topic><topic>Toxicology</topic><topic>Triterpenes - administration &amp; dosage</topic><topic>Triterpenes - toxicity</topic><topic>Vepacide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rahman, M.F</creatorcontrib><creatorcontrib>Siddiqui, M.K.J</creatorcontrib><creatorcontrib>Jamil, K</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of environmental science and health. 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Part B, Pesticides, food contaminants, and agricultural wastes</jtitle><addtitle>J Environ Sci Health B</addtitle><date>1999-09</date><risdate>1999</risdate><volume>34</volume><issue>5</issue><spage>873</spage><epage>884</epage><pages>873-884</pages><issn>0360-1234</issn><eissn>1532-4109</eissn><coden>JPFCD2</coden><abstract>Acetylcholinesterases (AChE), Na + -K + , Mg 2+ and Ca 2+ -ATPases were monitored in rat brain when treated orally with 80, 160 and 320 mg/kg of Vepacide, an active ingredient from neem seed oil, daily for 90 days. Brain AChE, Na + -K + and Ca 2+ -ATPases were inhibited whereas Mg 2+ -ATPase levels were enhanced in both the sexes after 45 and 90 days of treatment. The relative sensitivities of these ATPases to Vepacide indicated that Ca 2+ -ATPase being more sensitive than Na + -K + -ATPase in both the sexes. The magnitude of Ca 2+ -ATPase inhibited by this compound was higher than that of brain AChE. It appears to be sexual dimorphism in the alterations of brain AChE, Na + -K + and Mg 2+ -ATPases by Vepacide with females being significant when compared with males. After 28 days of post treatment the alterations observed were approached to those of controls both in male and female rats showing reversal of the toxicity. These results indicated that the ATPases were potently inhibited by Vepacide and seemed to be its precise target among the enzyme studied. This can be used as biochemical marker of exposure to this neem derived product.</abstract><cop>Philadelphia, PA</cop><pub>Taylor &amp; Francis Group</pub><pmid>10466107</pmid><doi>10.1080/03601239909373232</doi><tpages>12</tpages></addata></record>
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identifier ISSN: 0360-1234
ispartof Journal of environmental science and health. Part B, Pesticides, food contaminants, and agricultural wastes, 1999-09, Vol.34 (5), p.873-884
issn 0360-1234
1532-4109
language eng
recordid cdi_pubmed_primary_10466107
source Taylor and Francis Science and Technology Collection
subjects Acetylcholinesterase
Acetylcholinesterase - metabolism
Adenosine Triphosphatases - metabolism
adenosinetriphosphatase
Administration, Oral
and Ca
Animal, plant and microbial ecology
Animals
application rate
Applied ecology
ATPases
Azadirachta indica
Biological and medical sciences
brain
Brain - drug effects
Brain - enzymology
Dose-Response Relationship, Drug
Ecotoxicology, biological effects of pollution
Effects of pollution and side effects of pesticides on vertebrates
enzyme activity
Female
Fundamental and applied biological sciences. Psychology
inhibition
Insecticides - administration & dosage
Insecticides - toxicity
Male
Mammalia
Medical sciences
neem
neem compound
oral administration
Pesticides, fertilizers and other agrochemicals toxicology
rat
Rats
Rats, Wistar
Sex Characteristics
Toxicology
Triterpenes - administration & dosage
Triterpenes - toxicity
Vepacide
title Sub-chronic effect of neem based pesticide (Vepacide) on acetylcholinesterase and ATPases in rat
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