Cargando…
Attenuation of Cisplathin-Induced Toxic Oxidative Stress by Propofol
BACKGROUND: Antioxidant effects of propofol (2, 6-diisopropylphenol) were evaluated against cisplatin-induced oxidative stress in rat. OBJECTIVES: In this experimental study, 20 male rats were equally divided into 4 groups (5 rats each), and were treated by propofol (10 mg/kg/day, IP), or cisplatin...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286804/ https://www.ncbi.nlm.nih.gov/pubmed/25599022 http://dx.doi.org/10.5812/aapm.14221 |
_version_ | 1782351709278830592 |
---|---|
author | Taheri Moghadam, Ghazaleh Hosseini-Zijoud, Seyed-Mostafa Heidary Shayesteh, Tavakol Ghasemi, Hassan Ranjbar, Akram |
author_facet | Taheri Moghadam, Ghazaleh Hosseini-Zijoud, Seyed-Mostafa Heidary Shayesteh, Tavakol Ghasemi, Hassan Ranjbar, Akram |
author_sort | Taheri Moghadam, Ghazaleh |
collection | PubMed |
description | BACKGROUND: Antioxidant effects of propofol (2, 6-diisopropylphenol) were evaluated against cisplatin-induced oxidative stress in rat. OBJECTIVES: In this experimental study, 20 male rats were equally divided into 4 groups (5 rats each), and were treated by propofol (10 mg/kg/day, IP), or cisplatin (7 mg /kg/day, IP), or both. MATERIALS AND METHODS: Group one was control, while group 2 was given cisplatin (7 mg /kg/day, IP). Animals of the third group received only propofol (10 mg/kg/day, IP). Group 4 was given propofol with cisplatin once per day for 7 days. After treatment, blood urea nitrogen, creatinine levels, and oxidative stress markers such as total thiol groups (TTG), lipid peroxidation (LPO), and total antioxidant capacity (TAC) were measured. RESULTS: Oxidative stress induced by cisplatin, was evident by a significant increase in LPO and decrease in TTG and TAC. Propofol recovered cisplatin -induced changes in TAC, TTG and LPO in blood. CONCLUSIONS: It is concluded that oxidative damage is the mechanism of cisplatin toxicity, which can be recovered by propofol. |
format | Online Article Text |
id | pubmed-4286804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Kowsar |
record_format | MEDLINE/PubMed |
spelling | pubmed-42868042015-01-16 Attenuation of Cisplathin-Induced Toxic Oxidative Stress by Propofol Taheri Moghadam, Ghazaleh Hosseini-Zijoud, Seyed-Mostafa Heidary Shayesteh, Tavakol Ghasemi, Hassan Ranjbar, Akram Anesth Pain Med Research Article BACKGROUND: Antioxidant effects of propofol (2, 6-diisopropylphenol) were evaluated against cisplatin-induced oxidative stress in rat. OBJECTIVES: In this experimental study, 20 male rats were equally divided into 4 groups (5 rats each), and were treated by propofol (10 mg/kg/day, IP), or cisplatin (7 mg /kg/day, IP), or both. MATERIALS AND METHODS: Group one was control, while group 2 was given cisplatin (7 mg /kg/day, IP). Animals of the third group received only propofol (10 mg/kg/day, IP). Group 4 was given propofol with cisplatin once per day for 7 days. After treatment, blood urea nitrogen, creatinine levels, and oxidative stress markers such as total thiol groups (TTG), lipid peroxidation (LPO), and total antioxidant capacity (TAC) were measured. RESULTS: Oxidative stress induced by cisplatin, was evident by a significant increase in LPO and decrease in TTG and TAC. Propofol recovered cisplatin -induced changes in TAC, TTG and LPO in blood. CONCLUSIONS: It is concluded that oxidative damage is the mechanism of cisplatin toxicity, which can be recovered by propofol. Kowsar 2014-09-09 /pmc/articles/PMC4286804/ /pubmed/25599022 http://dx.doi.org/10.5812/aapm.14221 Text en Copyright © 2014, Iranian Society of Regional Anesthesia and Pain Medicine (ISRAPM); Published by Kowsar. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited. |
spellingShingle | Research Article Taheri Moghadam, Ghazaleh Hosseini-Zijoud, Seyed-Mostafa Heidary Shayesteh, Tavakol Ghasemi, Hassan Ranjbar, Akram Attenuation of Cisplathin-Induced Toxic Oxidative Stress by Propofol |
title | Attenuation of Cisplathin-Induced Toxic Oxidative Stress by Propofol |
title_full | Attenuation of Cisplathin-Induced Toxic Oxidative Stress by Propofol |
title_fullStr | Attenuation of Cisplathin-Induced Toxic Oxidative Stress by Propofol |
title_full_unstemmed | Attenuation of Cisplathin-Induced Toxic Oxidative Stress by Propofol |
title_short | Attenuation of Cisplathin-Induced Toxic Oxidative Stress by Propofol |
title_sort | attenuation of cisplathin-induced toxic oxidative stress by propofol |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286804/ https://www.ncbi.nlm.nih.gov/pubmed/25599022 http://dx.doi.org/10.5812/aapm.14221 |
work_keys_str_mv | AT taherimoghadamghazaleh attenuationofcisplathininducedtoxicoxidativestressbypropofol AT hosseinizijoudseyedmostafa attenuationofcisplathininducedtoxicoxidativestressbypropofol AT heidaryshayestehtavakol attenuationofcisplathininducedtoxicoxidativestressbypropofol AT ghasemihassan attenuationofcisplathininducedtoxicoxidativestressbypropofol AT ranjbarakram attenuationofcisplathininducedtoxicoxidativestressbypropofol |