2024-03-29T15:23:54Zhttps://repositori.uji.es/oai/requestoai:repositori.uji.es:10234/1269702021-06-10T18:09:30Zcom_10234_36080com_10234_9col_10234_36082
Repositori UJI
author
Funes, Haryes A.
author
Apostolova, Nadezda
author
Alegre, Fernando
author
Blas García, Ana
author
Álvarez, Ángeles
author
Martí Cabrera, Miguel
author
Esplugues Mota, Juan V.
2015-07-09T09:16:47Z
2015-07-09T09:16:47Z
2014-05
FUNES, Haryes A., et al. Neuronal bioenergetics and acute mitochondrial dysfunction: a clue to understanding the central nervous system side effects of Efavirenz. Journal of Infectious Diseases, 2014, 210.9: 1385-1395.
http://hdl.handle.net/10234/126970
http://dx.doi.org/10.1093/infdis/jiu273
Background. Neurological pathogenesis is associated with mitochondrial dysfunction and differences in neuronal/glial handling of oxygen and glucose. The main side effects attributed to efavirenz involve the CNS, but the underlying mechanisms are unclear.
Methods. Human cell lines and rat primary cultures of neurons and astrocytes were treated with clinically relevant efavirenz concentration.
Results. Efavirenz alters mitochondrial respiration, enhances reactive oxygen species generation, undermines mitochondrial membrane potential, and reduces adenosine triphosphate (ATP) levels in a concentration-dependent fashion in both neurons and glial cells. However, it activates adenosine monophosphate–activated protein kinase only in glial cells, upregulating glycolysis and increasing intracellular ATP levels, which do not occur in neurons. To reproduce the conditions that often exist in human immunodeficiency virus–related neuroinflammatory disorders, the effects of efavirenz were evaluated in the presence of exogenous nitric oxide, an inflammatory mediator and mitochondrial inhibitor. The combination potentiated the effects on mitochondrial parameters in both neurons and glial cells, but ATP generation and lactate production were enhanced only in glial cells.
Conclusions. Efavirenz affects the bioenergetics of neurons through a mechanism involving acute mitochondrial inhibition, an action exacerbated in neuroinflammatory conditions. A similar scenario of glial cells survival and degeneration of neurons with signs of mitochondrial dysfunction and oxidative stress has been associated with neurocognitive disorders.
eng
© The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved.
mitochondria
HIV
neurotoxicity
central nervous system
efavirenz
nitric oxide
HIV-associated neurocognitive disorders
Neuronal Bioenergetics and Acute Mitochondrial Dysfunction: A Clue to Understanding the Central Nervous System Side Effects of Efavirenz
info:eu-repo/semantics/article
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