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Oxidative Stress and Mitochondrial Impairment After Treatment with Anti-HIV Drugs: Clinical Implications
被引:42
|作者:
Blas-Garcia, Ana
[1
,2
]
Apostolova, Nadezda
[1
,2
]
Esplugues, Juan V.
[1
,2
,3
]
机构:
[1] Univ Valencia, Fac Med, Dept Farmacol, Valencia 46010, Spain
[2] CIBERehd, Valencia, Spain
[3] Hosp Univ Dr Peset, Valencia, Spain
关键词:
Antiretroviral therapy;
ROS;
mitochondria;
HIV;
cardiovascular disease;
lipodystrophy;
adverse effects;
NRTI;
PI;
NNRTI;
diabetes;
REVERSE-TRANSCRIPTASE INHIBITORS;
ACTIVE ANTIRETROVIRAL THERAPY;
PROTEASE INHIBITORS;
HEPATITIS-C;
INSULIN-RESISTANCE;
MOLECULAR-MECHANISMS;
GENE-EXPRESSION;
POTENTIAL ROLE;
NEURODEGENERATIVE DISEASES;
MYOCARDIAL-INFARCTION;
D O I:
10.2174/138161211798764951
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Thirty years after the discovery of HIV infection, there are numerous antiretroviral drugs that control the disease when administered in a potent combination referred to as Highly Active Antiretroviral Therapy (HAART). This therapy reduces the viral load and improves immune system reconstitution, leading to a significant reduction of HIV-related morbidity and mortality. However, HAART does not completely eliminate HIV, so treatment must continue throughout the patient's life. Prolonged use of HAART has been related to long-term adverse events that can compromise patient health. These deleterious effects have been reported for the majority of antiretroviral drugs and are the most common causes for therapy discontinuation. In most of these adverse events, such as diabetes, cardiovascular diseases, neurological disorders and metabolic alterations, oxidative stress and mitochondrial impairment play important roles. This review covers the implication of antiretroviral drugs in the overproduction of reactive oxygen species and the reduction of antioxidant defences, and in the consequent mitochondrial dysfunction, focusing on the molecular mechanisms involved and the clinical implications for HIV-infected patients.
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页码:4076 / 4086
页数:11
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