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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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 |
format |
Article |
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record_format |
scopus |
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Scopus |
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1818940564184236032 |