Harmine and Imipramine Promote Antioxidant Activities in Prefrontal Cortex and Hippocampus
Open accessAbstract
A growing body of evidence has suggested that reactive oxygen species (ROS) may play an important role in the physiopathology of depression. Evidence has pointed to the β‐carboline harmine as a potential therapeutic target for the treatment of depression. The present study we evaluated the effects of acute and chronic administration of harmine (5, 10 and 15 mg/kg) and imipramine (10, 20 and 30 mg/kg) or saline in lipid and protein oxidation levels and superoxide dismutase (SOD) and catalase (CAT) activities in rat prefrontal cortex and hippocampus. Acute and chronic treatments with imipramine and harmine reduced lipid and protein oxidation, compared to control group in prefrontal cortex and hippocampus. The SOD and CAT activities increased with acute and chronic treatments with imipramine and harmine, compared to control group in prefrontal cortex and hippocampus. In conclusion, our results indicate positive effects of imipramine antidepressant and β‐carboline harmine of oxidative stress parameters, increasing SOD and CAT activities and decreasing lipid and protein oxidation.
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Imipramine treatment increases SOD and CAT activity and decreases lipid and protein damage in male rat prefrontal cortex and hippocampus after both acute and chronic treatment.
“Réus et al. (2010) reported increased SOD and CAT activity and decreased lipid and protein damage in male rat prefrontal cortex and hippocampus after both acute and chronic treatment with imipramine [17].”
From Preclinical and Clinical Evidence of Antioxidant Effects of Antidepressant Agents: Implications for the Pathophysiology of Major Depressive Disorder (2012) · cites this paper as [17]
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- Authors
- Réus, G. Z., Stringari, R. B., de Souza, B., Petronilho, F., Dal-Pizzol, F., Hallak, J. E., Zuardi, A. W., Crippa, J. A., & Quevedo, J.
- Affiliations
- Universidade de São Paulo (BR)
- Corresponding author
- Quevedo, João
- Venue
- Oxidative Medicine and Cellular Longevity
- Publisher
- Wiley
- Published
- 2010-01
- Volume
- 3
- Issue
- 5
- Pages
- 325-331
- ISSN
- 1942-0994 (ISSN-L)
- 1942-0900
- PMC
- PMC3154037
- OpenAlex
- W2058072416
- Cited by
- 110
- References
- 47
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 8 · 2023: 2 · 2022: 7 · 2021: 11 · 2020: 10 · 2019: 1 · 2018: 5 · 2017: 5 · 2016: 8 · 2015: 13 · 2014: 11 · 2013: 7 · 2012: 7
- FWCI
- 4.23
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Oxidative Medicine and Cellular Longevity (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Fundação de Amparo à Pesquisa do Estado de São Paulo
- Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina
- Topics
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Synthesis and bioactivity of alkaloids
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Keywords
- harmine, imipramine, depression, oxidative stress, reactive oxygen species, lipid peroxidation, protein oxidation, superoxide dismutase, catalase, prefrontal cortex, hippocampus, β-carbolines, antidepressant effects
- MeSH terms
- Animals, Antidepressive Agents, Catalase, Depression, Harmine, Hippocampus, Imipramine, Male, Superoxide Dismutase, Rats, Wistar, Prefrontal Cortex, Rats
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