The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats

The current study has been designed to examine the effect of multifunctional drug therapy on carbofuran induced acute (2.187mg/kg, s.c.) and sub-acute (0.2187mg/kg, s.c.) neurotoxicity in male wistar rats. Drug treatment which includes nimodipine (Ca2+ channel blocker), diazepam, ropinirole (dopamin...

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Published in:Environmental Toxicology and Pharmacology
Main Author: Chahal K.S.; Prakash A.; Majeed A.B.A.
Format: Article
Language:English
Published: Elsevier 2015
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84934755008&doi=10.1016%2fj.etap.2015.06.002&partnerID=40&md5=c2dccce19a06d8ab7767be959ff09238
id 2-s2.0-84934755008
spelling 2-s2.0-84934755008
Chahal K.S.; Prakash A.; Majeed A.B.A.
The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats
2015
Environmental Toxicology and Pharmacology
40
1
10.1016/j.etap.2015.06.002
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84934755008&doi=10.1016%2fj.etap.2015.06.002&partnerID=40&md5=c2dccce19a06d8ab7767be959ff09238
The current study has been designed to examine the effect of multifunctional drug therapy on carbofuran induced acute (2.187mg/kg, s.c.) and sub-acute (0.2187mg/kg, s.c.) neurotoxicity in male wistar rats. Drug treatment which includes nimodipine (Ca2+ channel blocker), diazepam, ropinirole (dopamine agonist) and GSPE (antioxidant) was started 2h after carbofuran administration. Morris water maze was employed for aiming spatial memory. Narrow beam walk and rotarod were employed for testing motor functions. Brain acetylcholinesterase activity, thiobarbituric acid reactive species, nitrite, reduced glutathione, catalase levels, and mitochondrial complexes were also estimated. Carbofuran treatment resulted in significant development of cognitive and motor functions manifested as impairment in learning and memory along with increased thiobarbituric acid reactive species, nitrite levels and decreased acetylcholinesterase activity, reduced glutathione, catalase levels, and mitochondrial complexes. The standard antidote therapy (atropine) was not able to provide neuroprotection but was able to provide symptomatic relief. The multifunctional drug therapy attenuated carbofuran induced cognitive and motor dysfunction, acetylcholinesterase activity and other biochemical parameters. The triple combination in sub-acute study may be avoided in future as two drug combinations provide adequate neuroprotection. Thus it can be concluded that standard antidotal therapy may not provide neuroprotection while the multifunctional drug therapy offers neuroprotection against carbofuran and may dramatically increase survival and life quality. © 2015 Elsevier B.V..
Elsevier
13826689
English
Article

author Chahal K.S.; Prakash A.; Majeed A.B.A.
spellingShingle Chahal K.S.; Prakash A.; Majeed A.B.A.
The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats
author_facet Chahal K.S.; Prakash A.; Majeed A.B.A.
author_sort Chahal K.S.; Prakash A.; Majeed A.B.A.
title The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats
title_short The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats
title_full The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats
title_fullStr The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats
title_full_unstemmed The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats
title_sort The role of multifunctional drug therapy against carbamate induced neuronal toxicity during acute and chronic phase in rats
publishDate 2015
container_title Environmental Toxicology and Pharmacology
container_volume 40
container_issue 1
doi_str_mv 10.1016/j.etap.2015.06.002
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-84934755008&doi=10.1016%2fj.etap.2015.06.002&partnerID=40&md5=c2dccce19a06d8ab7767be959ff09238
description The current study has been designed to examine the effect of multifunctional drug therapy on carbofuran induced acute (2.187mg/kg, s.c.) and sub-acute (0.2187mg/kg, s.c.) neurotoxicity in male wistar rats. Drug treatment which includes nimodipine (Ca2+ channel blocker), diazepam, ropinirole (dopamine agonist) and GSPE (antioxidant) was started 2h after carbofuran administration. Morris water maze was employed for aiming spatial memory. Narrow beam walk and rotarod were employed for testing motor functions. Brain acetylcholinesterase activity, thiobarbituric acid reactive species, nitrite, reduced glutathione, catalase levels, and mitochondrial complexes were also estimated. Carbofuran treatment resulted in significant development of cognitive and motor functions manifested as impairment in learning and memory along with increased thiobarbituric acid reactive species, nitrite levels and decreased acetylcholinesterase activity, reduced glutathione, catalase levels, and mitochondrial complexes. The standard antidote therapy (atropine) was not able to provide neuroprotection but was able to provide symptomatic relief. The multifunctional drug therapy attenuated carbofuran induced cognitive and motor dysfunction, acetylcholinesterase activity and other biochemical parameters. The triple combination in sub-acute study may be avoided in future as two drug combinations provide adequate neuroprotection. Thus it can be concluded that standard antidotal therapy may not provide neuroprotection while the multifunctional drug therapy offers neuroprotection against carbofuran and may dramatically increase survival and life quality. © 2015 Elsevier B.V..
publisher Elsevier
issn 13826689
language English
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