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
相关论文
共 50 条
  • [21] Influence of mitochondrial control of apoptosis on the pathogenesis, complications and treatment of HIV infection
    Phenix, BN
    Badley, AD
    BIOCHIMIE, 2002, 84 (2-3) : 251 - 264
  • [22] HIV-INFECTION, RACE, AND DRUG-TREATMENT HISTORY
    WATTERS, JK
    LEWIS, DK
    AIDS, 1990, 4 (07) : 697 - 697
  • [23] Antiretroviral drug treatment of CNS HIV-1 infection
    Yilmaz, Aylin
    Price, Richard W.
    Gisslen, Magnus
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2012, 67 (02) : 299 - 311
  • [24] AIDS AND HIV INFECTION - IMPLICATIONS FOR DRUG-ABUSE TREATMENT
    BROWN, BS
    BESCHNER, GM
    JOURNAL OF DRUG ISSUES, 1989, 19 (01) : 141 - 162
  • [25] A NOVEL ANTIVIRAL STRATEGY FOR HIV-INFECTION
    MAY, BA
    MEDICAL HYPOTHESES, 1993, 40 (02) : 93 - 94
  • [26] ANTIVIRAL THERAPY AGAINST HIV-INFECTION
    MITSUYA, H
    YARCHOAN, R
    HAYASHI, S
    BRODER, S
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1990, 22 (06) : 1282 - 1294
  • [27] Optimal timing of antiviral therapy in HIV infection
    Berman, S. M.
    Journal of Applied Probability, 1994, 31//A
  • [28] HIV antiviral drug resistance: patient comprehension
    Racey, C. Sarai
    Zhang, Wendy
    Brandson, Eirikka K.
    Fernandes, Kimberly A.
    Tzemis, Despina
    Harrigan, P. Richard
    Montaner, Julio S. G.
    Barrios, Rolando
    Toy, Junine
    Hogg, Robert S.
    AIDS CARE-PSYCHOLOGICAL AND SOCIO-MEDICAL ASPECTS OF AIDS/HIV, 2010, 22 (07): : 816 - 826
  • [29] Treatment of primary effusion lymphoma with highly active antiviral therapy in the setting of HIV infection
    Ripamonti, Diego
    Marini, Basilio
    Rambaldi, Alessandro
    Suter, Fredy
    AIDS, 2008, 22 (10) : 1236 - 1237
  • [30] Extrahepatic Complications of Hepatitis C Virus Infection in HIV and the Impact of Successful Antiviral Treatment
    Lo Re, Vincent, III
    CLINICAL INFECTIOUS DISEASES, 2017, 64 (04) : 498 - 500