Time-dependent oxidative stress caused by benznidazole
- PMID: 11642718
- DOI: 10.1179/135100001101536328
Time-dependent oxidative stress caused by benznidazole
Abstract
Benznidazole (BZN) is a nitroimidazole derivative which has a notable trypanocide activity, and it is the only drug used in Brazil and Argentina for the treatment of Chagas' disease. The drug in current use is thought to act, at least in part, by inducing oxidative stress within the parasite. Imidazolic compounds are involved in the production of reactive oxygen species (ROS). In order to evaluate the effect of BZN on ROS production and on the antioxidant status of the host, male rats were treated for different periods of time (2, 4, 6, 10 and 30 days) with 40 mg BZN/kg body weight. After treatment, biomarkers of oxidative stress such as the activities of catalase (CAT), superoxide dismutase (SOD), glutathione-S-transferase (GST) and glutathione reductase (GR), and also thiobarbituric acid reactive species (TBARS), reduced glutathione (GSH), total glutathione (TG) and oxidized glutathione (GSSG) concentrations, were measured in crude hepatic homogenates. Our results revealed that BZN is able to cause tissue damage as shown by increased TBARS content, inhibition of some antioxidants and induction of other antioxidants in a concentration- and time-dependent manner. The tissue damage measured as TBARS increased up to the 10th day of treatment. GST activity was inhibited during the BZN treatment. On the other hand, CAT and GR showed similar increased activities at the beginning, followed by decreased activities at the end of the treatment. After 30 days of treatment, GR activity remained low while CAT activity was high, compared to controls. The SOD activities remained unchanged throughout the experimental period. GSH showed lower values at the beginning of BZN treatment but the hepatic concentrations were enhanced at the end of the experimental period. Total glutathione showed a similar profile, and oxidized glutathione showed higher values in rats treated with BZN. In conclusion, these results indicate that, at therapeutic doses, BZN treatment elicits an oxidative stress in rat hepatocytes.
Similar articles
-
Antioxidant therapy attenuates oxidative insult caused by benzonidazole in chronic Chagas' heart disease.Int J Cardiol. 2010 Nov 5;145(1):27-33. doi: 10.1016/j.ijcard.2009.06.033. Epub 2009 Jul 21. Int J Cardiol. 2010. PMID: 19625091
-
Age-related changes of antioxidant enzyme activities, glutathione status and lipid peroxidation in rat erythrocytes after heat stress.Life Sci. 2004 Aug 13;75(13):1551-65. doi: 10.1016/j.lfs.2004.03.020. Life Sci. 2004. PMID: 15261761
-
Effects of exposure to BDE-99 on oxidative status of liver and kidney in adult rats.Toxicology. 2010 Apr 30;271(1-2):51-6. doi: 10.1016/j.tox.2010.03.006. Epub 2010 Mar 17. Toxicology. 2010. PMID: 20223270
-
Protective role of Vitamin E pre-treatment on N-nitrosodiethylamine induced oxidative stress in rat liver.Chem Biol Interact. 2005 Oct 20;156(2-3):101-11. doi: 10.1016/j.cbi.2005.08.001. Chem Biol Interact. 2005. PMID: 16144695
-
Lead-induced oxidative damage in rats/mice: A meta-analysis.J Trace Elem Med Biol. 2020 Mar;58:126443. doi: 10.1016/j.jtemb.2019.126443. Epub 2019 Dec 4. J Trace Elem Med Biol. 2020. PMID: 31841831 Review.
Cited by
-
Phylobioactive hotspots in plant resources used to treat Chagas disease.iScience. 2021 Mar 15;24(4):102310. doi: 10.1016/j.isci.2021.102310. eCollection 2021 Apr 23. iScience. 2021. PMID: 33870129 Free PMC article.
-
Purinergic Antagonist Suramin Aggravates Myocarditis and Increases Mortality by Enhancing Parasitism, Inflammation, and Reactive Tissue Damage in Trypanosoma cruzi-Infected Mice.Oxid Med Cell Longev. 2018 Sep 30;2018:7385639. doi: 10.1155/2018/7385639. eCollection 2018. Oxid Med Cell Longev. 2018. PMID: 30364017 Free PMC article.
-
Benefits of Ascorbic Acid in Association with Low-Dose Benznidazole in Treatment of Chagas Disease.Antimicrob Agents Chemother. 2018 Aug 27;62(9):e00514-18. doi: 10.1128/AAC.00514-18. Print 2018 Sep. Antimicrob Agents Chemother. 2018. PMID: 29987143 Free PMC article.
-
Memory impairment in chronic experimental Chagas disease: Benznidazole therapy reversed cognitive deficit in association with reduction of parasite load and oxidative stress in the nervous tissue.PLoS One. 2021 Jan 5;16(1):e0244710. doi: 10.1371/journal.pone.0244710. eCollection 2021. PLoS One. 2021. PMID: 33400707 Free PMC article.
-
Insights of potential trypanocidal effect of the synthetic derivative (2E)-1-(4-aminophenyl)-3-(2,4-dichlorophenyl)prop-2-en-1-one: in vitro assay, MEV analysis, quantum study, molecular docking, molecular dynamics, MPO analysis, and predictive ADMET.Naunyn Schmiedebergs Arch Pharmacol. 2024 Oct;397(10):7797-7818. doi: 10.1007/s00210-024-03138-z. Epub 2024 May 9. Naunyn Schmiedebergs Arch Pharmacol. 2024. PMID: 38722342
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous