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.

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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

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article

Atorvastatin Induces Bioenergetic Impairment and Oxidative Stress Through Reverse Electron Transport

Romana Fato, Francesca Orsini, Nicola Rizzardi, Luca Pincigher et al.
Antioxidants
Computational Drug Discovery Methods
article

Atorvastatin Induces Bioenergetic Impairment and Oxidative Stress Through Reverse Electron Transport

Romana Fato, Francesca Orsini, Nicola Rizzardi, Luca Pincigher, Francesca Valenti, Christian Bergamini
article en

Abstract

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.

AntioxidantsVol. 14(10)
Indena (Italy) (IT), University of Bologna (IT)
European Commission, Università di Bologna
Openalex Percentile: Top 73%
Computational Drug Discovery Methods
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