Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 May;94(5):1417-1441.
doi: 10.1007/s00204-020-02721-6. Epub 2020 Apr 4.

Redox metabolism modulation as a mechanism in SSRI toxicity and pharmacological effects

Affiliations
Review

Redox metabolism modulation as a mechanism in SSRI toxicity and pharmacological effects

Maria-Georgia Ștefan et al. Arch Toxicol. 2020 May.

Abstract

Depressive disorders are amongst the greatest mental health challenges, with an increasing number of patients being diagnosed each year. Though it has not yet been fully elucidated, redox metabolism imbalances and oxidative stress seem to play a major role in the pathogenesis of depressive disorders. Selective serotonin reuptake inhibitors (SSRIs) are the most prescribed antidepressants, considered to have a better tolerability. However, several adverse effects have been reported and the mechanisms involved in their pharmacological activity are not entirely understood. SSRIs have been shown to influence the redox metabolism, which could be involved in their toxicity and pharmacological effects. A comparative analysis of published in vivo and in vitro data regarding the activity of SSRIs on the redox metabolism pathways has been performed in this paper, with an emphasis on mechanistical aspects. Furthermore, a comparison between oxidative stress biomarker levels reported by different studies was attempted. The reviewed data point towards both pro- and antioxidant effects of SSRIs, dependent on tissue/cell type and dose/concentration, suggest a redox modulating potential of these compounds. In hepatic and testicular tissue, the majority of reviewed studies reported pro-oxidant effects, with possible implications towards the hepatotoxicity and sexual dysfunction that were reported following SSRI treatment; while in brain, the most common findings were antioxidant effects that could partially explain their antidepressant activity. However, given the heterogeneity of the reviewed data, further research is needed to fully understand the impact of SSRIs on redox metabolism and its implications.

Keywords: Biomarkers; Hepatotoxicity; Oxidative stress; Redox signaling; Selective serotonin reuptake inhibitors; Sexual dysfunction.

PubMed Disclaimer

References

    1. Abdel-Salam OMEE, Youness ER, Khadrawy YA, Sleem AA (2013) Brain and liver oxidative stress after sertraline and haloperidol treatment in mice. J Basic Clin Physiol Pharmacol 24:115–123. https://doi.org/10.1515/jbcpp-2012-0022 - DOI - PubMed
    1. Abdel-Sater KA, Abdel-Daiem WM, Sayyed Bakheet M (2012) The gender difference of selective serotonin reuptake inhibitor, fluoxetine in adult rats with stress-induced gastric ulcer. Eur J Pharmacol 688:42–48. https://doi.org/10.1016/j.ejphar.2012.04.019 - DOI - PubMed
    1. Aksu U, Guner I, Yaman OM et al (2014) Fluoxetine ameliorates imbalance of redox homeostasis and inflammation in an acute kidney injury model. J Physiol Biochem 70:925–934. https://doi.org/10.1007/s13105-014-0361-0 - DOI - PubMed
    1. Assasa MF, Mohammed ES, Moustafa OM, Abo Alfotoh AMA (2019) Histopathological study of the chronic toxic effects of dapoxetine administration on testes of male albino rats. Egypt J Hosp Med 74(8):1698–1701
    1. Banay-Schwartz M, Kenessey A, DeGuzman T et al (1992) Protein content of various regions of rat brain and adult and aging human brain. Age (Omaha) 15:51–54. https://doi.org/10.1007/BF02435024 - DOI

MeSH terms

Substances

LinkOut - more resources