Atorvastatin Induces Bioenergetic Impairment and Oxidative Stress Through Reverse Electron Transport
Statins are the first-line therapy for managing elevated cholesterol levels that represent a risk of acute cardiovascular events. However, the use of statins is associated with several side effects, likely due to the depletion of Coenzyme Q<sub>10</sub> (CoQ<sub>10</sub>), a key component of the mitochondrial electron transport chain and a membrane antioxidant. In our study, we present evidence of the cytotoxic effects of Atorvastatin on human dermal fibroblasts in terms of oxidative stress and mitochondrial impairment. Interestingly, CoQ<sub>10</sub> supplementation in statin-treated cells significantly reduced ROS levels and restored mitochondrial oxygen consumption rate and the intracellular ATP/ADP ratio. Moreover, our data suggest that the mechanism for Atorvastatin off-target effects at high concentrations involves the inhibition of respiratory complexes I and III, leading to reverse electron transport and ROS production by Complex I. These findings highlight the potential benefits of CoQ<sub>10</sub> supplementation in mitigating statin-induced cytotoxicity and propose a mechanistic basis for the adverse effects associated with Atorvastatin therapy.
Authors
- Romana Fato (ORCID: https://orcid.org/0000-0002-8945-6826)
- Francesca Orsini
- Nicola Rizzardi (ORCID: https://orcid.org/0000-0002-9294-7116)
- Luca Pincigher (ORCID: https://orcid.org/0009-0002-9806-2789)
- Francesca Valenti (ORCID: https://orcid.org/0000-0002-7266-7352)
- Christian Bergamini (ORCID: https://orcid.org/0000-0003-4387-5117)
Institutions
- Indena (Italy) (IT)
- University of Bologna (IT)
Publication Details
- Journal
- Antioxidants
- Published
- 2025-09-23
- DOI
- https://doi.org/10.3390/antiox14101147
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- European Commission
- Università di Bologna