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Antioxidant Effects of Some Drugs on Immobilization Stress Combined with Cold Restraint Stress

The aim of this work was to investigate the effect on antioxidant potential of some commonly used drugs (morphine, tramadol, bromocriptine, haloperidol and azithromycin) on immobilization stress (IS) combined with cold restraint stress (CRS) in the rat. After the drug treatment the animals were kept...

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Autores principales: Popovic, Mira, Janicijevic-Hudomal, Snezana, Kaurinovic, Biljana, Rasic, Julijana, Trivic, Svetlana, Vojnović, Matilda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254731/
https://www.ncbi.nlm.nih.gov/pubmed/19924083
http://dx.doi.org/10.3390/molecules14114505
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author Popovic, Mira
Janicijevic-Hudomal, Snezana
Kaurinovic, Biljana
Rasic, Julijana
Trivic, Svetlana
Vojnović, Matilda
author_facet Popovic, Mira
Janicijevic-Hudomal, Snezana
Kaurinovic, Biljana
Rasic, Julijana
Trivic, Svetlana
Vojnović, Matilda
author_sort Popovic, Mira
collection PubMed
description The aim of this work was to investigate the effect on antioxidant potential of some commonly used drugs (morphine, tramadol, bromocriptine, haloperidol and azithromycin) on immobilization stress (IS) combined with cold restraint stress (CRS) in the rat. After the drug treatment the animals were kept immobilized in the cold chamber at 4±0.3ºC for 3 hours and then decapitaed and the livers were extracted. The following parameters were determined in the liver homogenate: content of reduced glutathione, activities of catalase, xanthine oxidase, glutathione reductase, glutathione peroxidase, peroxidase, and lipid peroxidation intensity. A battery of biochemical assays was used and the resulting data were statistically analyzed. Combined stress exhibited a prooxidative action (increased catalase activity, lowered content of reduced glutathione). Significantly enhanced catalase activity that was observed in all groups compared to the control indicates that the primary reactive oxygen species (ROS) metabolite is hydrogen peroxide, which decomposes very rapidly (very high catalase activity), thus hindering formation of OH radicals as the most toxic ROS. None of the tested drugs showed a protective effect on combined IS and CRS. The intensity of lipid peroxidation did not change either in the combined stress or under additional influence of the drugs. Probably, under our experimental conditions, the time was not sufficiently long to observe damage of lipid membrane by ROS.
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spelling pubmed-62547312018-11-30 Antioxidant Effects of Some Drugs on Immobilization Stress Combined with Cold Restraint Stress Popovic, Mira Janicijevic-Hudomal, Snezana Kaurinovic, Biljana Rasic, Julijana Trivic, Svetlana Vojnović, Matilda Molecules Article The aim of this work was to investigate the effect on antioxidant potential of some commonly used drugs (morphine, tramadol, bromocriptine, haloperidol and azithromycin) on immobilization stress (IS) combined with cold restraint stress (CRS) in the rat. After the drug treatment the animals were kept immobilized in the cold chamber at 4±0.3ºC for 3 hours and then decapitaed and the livers were extracted. The following parameters were determined in the liver homogenate: content of reduced glutathione, activities of catalase, xanthine oxidase, glutathione reductase, glutathione peroxidase, peroxidase, and lipid peroxidation intensity. A battery of biochemical assays was used and the resulting data were statistically analyzed. Combined stress exhibited a prooxidative action (increased catalase activity, lowered content of reduced glutathione). Significantly enhanced catalase activity that was observed in all groups compared to the control indicates that the primary reactive oxygen species (ROS) metabolite is hydrogen peroxide, which decomposes very rapidly (very high catalase activity), thus hindering formation of OH radicals as the most toxic ROS. None of the tested drugs showed a protective effect on combined IS and CRS. The intensity of lipid peroxidation did not change either in the combined stress or under additional influence of the drugs. Probably, under our experimental conditions, the time was not sufficiently long to observe damage of lipid membrane by ROS. Molecular Diversity Preservation International 2009-11-10 /pmc/articles/PMC6254731/ /pubmed/19924083 http://dx.doi.org/10.3390/molecules14114505 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Popovic, Mira
Janicijevic-Hudomal, Snezana
Kaurinovic, Biljana
Rasic, Julijana
Trivic, Svetlana
Vojnović, Matilda
Antioxidant Effects of Some Drugs on Immobilization Stress Combined with Cold Restraint Stress
title Antioxidant Effects of Some Drugs on Immobilization Stress Combined with Cold Restraint Stress
title_full Antioxidant Effects of Some Drugs on Immobilization Stress Combined with Cold Restraint Stress
title_fullStr Antioxidant Effects of Some Drugs on Immobilization Stress Combined with Cold Restraint Stress
title_full_unstemmed Antioxidant Effects of Some Drugs on Immobilization Stress Combined with Cold Restraint Stress
title_short Antioxidant Effects of Some Drugs on Immobilization Stress Combined with Cold Restraint Stress
title_sort antioxidant effects of some drugs on immobilization stress combined with cold restraint stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254731/
https://www.ncbi.nlm.nih.gov/pubmed/19924083
http://dx.doi.org/10.3390/molecules14114505
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