2023
DOI: 10.1093/infdis/jiad044
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Mitoquinone Mesylate and Mitochondrial DNA in End Organs in Humanized Mouse Model of Chronic Treated Human Immunodeficiency Virus Infection

Abstract: No treatment exists for mitochondrial dysfunction, a contributor to end-organ disease in human immunodeficiency virus (HIV). The mitochondrial antioxidant mitoquinone mesylate (MitoQ) attenuates mitochondrial dysfunction in preclinical mouse models of various diseases but has not been used in HIV. We used a humanized murine model of chronic HIV infection and polymerase chain reaction to show that HIV-1–infected mice treated with antiretroviral therapy and MitoQ for 90 days had higher ratios of human and murine… Show more

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Cited by 2 publications
(1 citation statement)
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“…Recently, mitochondrial antioxidant MitoQ (mitoquinone mesylate) has been shown to reduce ART and HIVassociated mitochondrial dysfunction in a humanized murine model. 236 Additionally, NAC, a potent antioxidant, reduced agents like coenzyme Q10, 237 which supports mitochondrial electron transport and reduces oxidative stress, or novel compounds that enhance mitochondrial biogenesis and function, could be integrated into HIV treatment regimens. New regimens should dualistically aim to reduce HIV-related inflammation and ART-induced toxicity with improved clinical outcomes.…”
Section: Antioxidants and Oxphosmentioning
confidence: 99%
“…Recently, mitochondrial antioxidant MitoQ (mitoquinone mesylate) has been shown to reduce ART and HIVassociated mitochondrial dysfunction in a humanized murine model. 236 Additionally, NAC, a potent antioxidant, reduced agents like coenzyme Q10, 237 which supports mitochondrial electron transport and reduces oxidative stress, or novel compounds that enhance mitochondrial biogenesis and function, could be integrated into HIV treatment regimens. New regimens should dualistically aim to reduce HIV-related inflammation and ART-induced toxicity with improved clinical outcomes.…”
Section: Antioxidants and Oxphosmentioning
confidence: 99%