Cover image of the article: Identification of Intracellular Sources Responsible for Endogenous Reactive Oxygen Species Formation

Image Credit:Iran J Pharm Res

Identification of Intracellular Sources Responsible for Endogenous Reactive Oxygen Species Formation

Authors

Jalal Pourahmad1,*
1Department of Pharmacology and Toxicology, School of Pharmacy, Shaheed Beheshti University of Medical Sciences and health services, Tehran, Iran
*Corresponding Author: Department of Pharmacology and Toxicology, School of Pharmacy, Shaheed Beheshti University of Medical Sciences and health services, Tehran, Iran. Email:pourahmadj@sbmu.ac.ir

Iranian Journal of Pharmaceutical Research:Vol. 1, issue 1; 21-29
Published online:Nov 20, 2010
Article type:Research Article
Received:Feb 01, 2002
Accepted:Jul 01, 2002
How to Cite:Pourahmad J. Identification of Intracellular Sources Responsible for Endogenous Reactive Oxygen Species Formation. Iran J Pharm Res. 2002;1(1):e127580. doi: https://doi.org/10.22037/ijpr.2010.4

Abstract

The endogenous reactive oxygen species ("ROS") formation is associated with many pathologic states such as inflammatory diseases, neurodegenerative diseases, brain and heart ischemic injuries, cancer, and aging. The purpose of this study was to investigate the endogenous sources for "ROS" formation in intact isolated rat hepatocytes, in particular, peroxisomal oxidases, monoamine oxidase, xanthine oxidase, cytochrome P450, and mitochondria electron transport. The rat hepatocyte catalyzed oxidation of 2',7'-dichlorofluorescin to form the fluorescent 2,7'-dichlorofluorescein was used to measure endogenous and xenobiotic-induced reactive oxygen species ("ROS") formation by intact isolated rat hepatocytes. Various oxidase substrates and inhibitors were then used to identify the intracellular oxidases responsible. Endogenous "ROS" formation was markedly increased in catalase inhibited or GSH depleted hepatocytes, and was inhibited by "ROS" scavengers or desferoxamine. Endogenous "ROS" formation was also inhibited by cytochrome P450 inhibitors, but was not affected by oxypurinol, a xanthine oxidase inhibitor. Mitochondrial respiratory chain inhibitors or hypoxia, on the other hand, markedly increased "ROS" before cytotoxicity ensued. This suggests endogenous "ROS" formation can largely be attributed to oxygen reduction by reduced mitochondrial electron transport components and reduced cytochrome P450 isozymes. Addition of monoamine oxidase substrates increased antimycin A-resistant respiration and "ROS" formation before cytotoxicity ensued. On the other hand peroxisomal substrates readily induced "ROS" formation and were cytotoxic towards catalase inhibited hepatocytes, which suggests that peroxisomal catalase removes endogenous H2O2 formed in the peroxisomes. The consequences of upregulation of peroxisomal oxidases are discussed.

Highlights

Copyright

© 2002, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

Similar Articles

31
Jan
2012
Involvement of Four Different Intracellular Sites in Chloroacetaldehyde- Induced Oxidative Stress Cytotoxicity

Involvement of Four Different Intracellular Sites in Chloroacetaldehyde- Induced Oxidative Stress Cytotoxicity

Jalal Pourahmad,
Mir-Jamal Hosseini,
Mohammad Reza Eskandari,
Faezeh Rahmani

Pourahmad J, Hosseini M, Eskandari MR, Rahmani F. Involvement of Four Different Intracellular Sites in Chloroacetaldehyde- Induced Oxidative Stress Cytotoxicity. Iran J Pharm Res. 2012;11(1):e125796. doi: https://doi.org/10.22037/ijpr.2012.1082

20
Nov
2010
Iron Overload Induced Apoptotic Cell Death in Isolated Rat Hepatocytes Mediated by Reactive Oxygen Species

Iron Overload Induced Apoptotic Cell Death in Isolated Rat Hepatocytes Mediated by Reactive Oxygen Species

Abdolamir Allameh,
Asghar Amini-Harandi,
Farzaneh Osati-Ashtiani,
Peter J. O’Brien

Allameh A, Amini-Harandi A, Osati-Ashtiani F, O’Brien PJ. Iron Overload Induced Apoptotic Cell Death in Isolated Rat Hepatocytes Mediated by Reactive Oxygen Species. Iran J Pharm Res. 2022;7(2):e128579. doi: https://doi.org/10.22037/ijpr.2010.753

20
Nov
2010
Lysosomal Oxidative Stress Cytotoxicity Induced By Para-phenylenediamine Redox Cycling In Hepatocytes

Lysosomal Oxidative Stress Cytotoxicity Induced By Para-phenylenediamine Redox Cycling In Hepatocytes

Jalal Pourahmad,
Farzad Kobarfard,
Ataollah Shakoori

Pourahmad J, Kobarfard F, Shakoori A. Lysosomal Oxidative Stress Cytotoxicity Induced By Para-phenylenediamine Redox Cycling In Hepatocytes. Iran J Pharm Res. 2022;3(4):e128207. doi: https://doi.org/10.22037/ijpr.2010.601

31
Jan
2014
Propofol Attenuates Toxic Oxidative Stress by CCl4 in Liver Mitochondria and Blood in Rat

Propofol Attenuates Toxic Oxidative Stress by CCl4 in Liver Mitochondria and Blood in Rat

Akram Ranjbar,
Mohammad Sharifzadeh,
Jamshid Karimi,
Heidar Tavilani,
Maryam Baeeri,
Tavakol Heidary shayesteh
,et al.

Ranjbar A, Sharifzadeh M, Karimi J, Tavilani H, Baeeri M, et al. Propofol Attenuates Toxic Oxidative Stress by CCl4 in Liver Mitochondria and Blood in Rat. Iran J Pharm Res. 2014;13(1):e125446. doi: https://doi.org/10.22037/ijpr.2014.1421

31
Oct
2018
Mechanistic Approach for Thioridazine-Induced Hepatotoxicity and Potential Benefits of Melatonin and/or Coenzyme Q10 on Freshly Isolated Rat Hepatocytes

Mechanistic Approach for Thioridazine-Induced Hepatotoxicity and Potential Benefits of Melatonin and/or Coenzyme Q10 on Freshly Isolated Rat Hepatocytes

Aziz Eftekhari,
Elham Ahmadian,
Yadollah Azarmi,
Alireza Parvizpur,
Javad Khalili Fard,
Mohammad Ali Eghbal

Eftekhari A, Ahmadian E, Azarmi Y, Parvizpur A, Khalili Fard J, et al. Mechanistic Approach for Thioridazine-Induced Hepatotoxicity and Potential Benefits of Melatonin and/or Coenzyme Q10 on Freshly Isolated Rat Hepatocytes. Iran J Pharm Res. 2018;17(4):e124863. doi: https://doi.org/10.22037/ijpr.2018.2285

More by these authors

Jalal PourahmadPubMedScholar
Share
Cited by
Metrics