Mitochondrial dysfunctions in HIV infection and antiviral drug treatment

被引:12
|
作者
Ganta, Krishna Kumar [1 ]
Chaubey, Binay [1 ]
机构
[1] Univ Calcutta, Ctr Adv Study, Dept Bot, Funct Genom Lab, 35 Ballygunge Circular Rd, Kolkata 700019, India
关键词
HIV; antiretroviral therapy; mitochondrial dysfunction; mtDNA depletion; intrinsic apoptosis; REVERSE-TRANSCRIPTASE INHIBITORS; ENDOPLASMIC-RETICULUM STRESS; PROTEASE INHIBITORS; IN-VITRO; MEMBRANE PERMEABILIZATION; INTEGRASE INHIBITORS; NUCLEOSIDE ANALOGS; OXIDATIVE STRESS; T-CELLS; EFAVIRENZ;
D O I
10.1080/17425255.2019.1692814
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: With the introduction of highly active anti-retroviral therapy (HAART), treatment of HIV infection has improved radically, shifting the concept of HIV disease from a highly mortal epidemic to a chronic illness which needs systematic management. However, HAART does not target the integrated proviral DNA. Hence, prolonged use of antiviral drugs is needed for sustaining life. As a consequence, severe side effects emerge. Several parameters involve in causing these adverse effects. Mitochondrial dysfunctions were pointed as common factor among them. It is, therefore, necessary to critically examine mitochondrial dysfunction in order to understand the side effects. Areas covered: There are many events involved in causing drug-induced side-effects; in this review, we only highlight mitochondrial dysfunctions as one of the events. We present up-to-date findings on mitochondrial dysfunction caused by HIV infection and antiviral drug treatment. Both in vivo and in vitro studies on mitochondrial dysfunction like change in morphology, membrane depolarization, mitophagy, mitochondrial DNA depletion, and intrinsic apoptosis have been discussed. Expert opinion: Mitochondrial dysfunction is associated with severe complications that often lead to discontinuation or change in treatment regimen. Prior knowledge of side effects of antiviral drugs would help in better management and future research should focus to avoid mitochondrial targeting of antiviral drugs while maintaining their antiviral properties.
引用
收藏
页码:1043 / 1052
页数:10
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