Transplacentally exposed human and monkey newborn infants show similar evidence of nucleoside reverse transcriptase inhibitor‐induced mitochondrial toxicity
- 19 March 2007
- journal article
- research article
- Published by Wiley in Environmental and Molecular Mutagenesis
- Vol. 48 (3-4) , 201-209
- https://doi.org/10.1002/em.20201
Abstract
Effective reduction in maternal‐fetal human immunodeficiency virus‐1 (HIV‐1) transmission has been achieved by administration of nucleoside reverse transcriptase inhibitors (NRTIs) during pregnancy, and although most exposed children are clinically normal at birth, mitochondrial dysfunction has been reported. To examine mitochondrial integrity on a molecular level, we evaluated mitochondrial morphology by electron microscopy (EM) and mitochondrial DNA (mtDNA) quantity in umbilical cords and cord blood from NRTI‐exposed and unexposed human and monkey newborns. Human subjects included infants born to HIV‐1‐infected mothers who received Combivir (Zidovudine [AZT] plus Lamivudine [3TC]) (n = 9) or AZT plus Didanosine [ddI] (n = 2) during pregnancy, and infants born to HIV‐1‐uninfected mothers (n = 7). NRTI‐exposed Erythrocebus patas monkey dams (n = 3 per treatment group) were given human‐equivalent dosing regimens containing 3TC, AZT/3TC, AZT/ddI, or Stavudine (d4T)/3TC during gestation. Four infants born to unexposed patas dams served as controls. Mitochondria in umbilical cord endothelial cells from NRTI‐exposed monkey and human infants showed substantial abnormal pathology by EM, the extent of which was quantified from coded photomicrographs and shown to be different (P < 0.05) from the unexposed monkey and human newborns. Significant (P < 0.05) mtDNA depletion was found in umbilical cords from both human and monkey NRTI‐exposed infants and in human, but not in monkey, cord blood leukocytes. For umbilical cords, an increase in mitochondrial morphological damage correlated with reduction in mtDNA quantity in fetal monkeys (r = 0.94). The treatment‐induced mitochondrial compromise in infant monkeys ranked as follows: d4T/3TC > AZT/ddI > AZT/3TC > 3TC. The study demonstrates that transplacental NRTI exposures induce similar mitochondrial damage in cord blood and umbilical cords taken from retroviral‐uninfected monkey infants and from human infants born to HIV‐1‐infected women. Environ. Mol. Mutagen., 2006.Keywords
This publication has 22 references indexed in Scilit:
- HIV neuromuscular disease and mitochondrial functionMitochondrion, 2004
- Cardiomyopathy, nucleoside reverse transcriptase inhibitors and mitochondria are linked through AIDS and its therapyMitochondrion, 2004
- Mitochondrial Damage Revealed by Morphometric and Semiquantitative Analysis of Mouse Pup Cardiomyocytes Following in Utero and Postnatal Exposure to Zidovudine and LamivudineToxicological Sciences, 2004
- Mitochondrial Toxicity in FetalErythrocebus patasMonkeys Exposed Transplacentally to Zidovudine Plus LamivudineAIDS Research and Human Retroviruses, 2004
- Mitochondrial toxicity of nrti antiviral drugs: an integrated cellular perspectiveNature Reviews Drug Discovery, 2003
- Persistent mitochondrial dysfunction in HIV-1-exposed but uninfected infantsAIDS, 2003
- Structural Determinants in Human DNA Polymerase γ Account for Mitochondrial Toxicity from Nucleoside AnalogsJournal of Molecular Biology, 2003
- The Sinusitis DebatePediatrics, 2002
- 3′-azido-3′-deoxythymidine (AZT) transplacental perfusion kinetics and DNA incorporation in normal human placentas perfused with AZTMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1999
- Persistence, gestation stage-dependent formation and interrelationship of benzo[a]pyrene-induced DNA adducts in mothers, placentae and fetuses of Erythrocebus patas monkeysCarcinogenesis: Integrative Cancer Research, 1993