Literature DB >> 23679995

Telomerase inhibition may contribute to accelerated mitochondrial aging induced by anti-retroviral HIV treatment.

F M Bollmann1.   

Abstract

HIV-infected individuals undergoing long-term anti-retroviral treatment tend to show premature senescence. Accelerated mitochondrial aging induced by nucleoside reverse transcriptase inhibitors (NRTIs) has been implicated as a part of this phenomenon. Traditionally, this has been attributed to inhibition of mtDNA polymerase γ by these drugs, but alternative explanations have been proposed. It is known that NRTIs can not only inhibit viral reverse transcriptase, but also human telomerase. A number of extratelomeric roles of telomerase, including protection of mitochondrial DNA and function, have emerged recently. In this paper, I propose that inhibition of mitochondrial telomerase activity by NRTI drugs contributes to the mitochondrial toxicity and premature aging seen in treated HIV patients, and discuss objections and experimental testing of the hypothesis.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23679995     DOI: 10.1016/j.mehy.2013.04.028

Source DB:  PubMed          Journal:  Med Hypotheses        ISSN: 0306-9877            Impact factor:   1.538


  11 in total

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8.  Antiretroviral-Mediated Microglial Activation Involves Dysregulated Autophagy and Lysosomal Dysfunction.

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9.  Impact of HIV-1 tropism on the emergence of non-AIDS events in HIV-infected patients receiving fully suppressive antiretroviral therapy.

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10.  N-Acetylcysteine Reverses Antiretroviral-Mediated Microglial Activation by Attenuating Autophagy-Lysosomal Dysfunction.

Authors:  Ashutosh Tripathi; Annadurai Thangaraj; Ernest T Chivero; Palsamy Periyasamy; Maria E Burkovetskaya; Fang Niu; Ming-Lei Guo; Shilpa Buch
Journal:  Front Neurol       Date:  2020-09-04       Impact factor: 4.003

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