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Autophagy is a protective response to ethanol neurotoxicity

Overview of attention for article published in Autophagy, October 2014
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Article details
Title
Autophagy is a protective response to ethanol neurotoxicity
Published in
Autophagy, October 2014
DOI 10.4161/auto.21376
Pubmed ID
Authors
Abstract

Ethanol is a neuroteratogen and neurodegeneration is the most devastating consequence of developmental exposure to ethanol. The mechanisms underlying ethanol-induced neurodegeneration are complex. Ethanol exposure produces reactive oxygen species (ROS) which cause oxidative stress in the brain. We hypothesized that ethanol would activate autophagy to alleviate oxidative stress and neurotoxicity. Our results indicated that ethanol increased the level of the autophagic marker Map1lc3-II (LC3-II) and upregulated LC3 puncta in SH-SY5Y neuroblastoma cells. It also enhanced the levels of LC3-II and BECN1 in the developing brain; meanwhile, ethanol reduced SQSTM1 (p62) levels. Bafilomycin A(1), an inhibitor of autophagosome and lysosome fusion, increased p62 levels in the presence of ethanol. Bafilomycin A(1) and rapamycin potentiated ethanol-increased LC3 lipidation, whereas wortmannin and a BECN1-specific shRNA inhibited ethanol-promoted LC3 lipidation. Ethanol increased mitophagy, which was also modulated by BECN1 shRNA and rapamycin. The evidence suggested that ethanol promoted autophagic flux. Activation of autophagy by rapamycin reduced ethanol-induced ROS generation and ameliorated ethanol-induced neuronal death in vitro and in the developing brain, whereas inhibition of autophagy by wortmannin and BECN1-specific shRNA potentiated ethanol-induced ROS production and exacerbated ethanol neurotoxicity. Furthermore, ethanol inhibited the MTOR pathway and downregulation of MTOR offered neuroprotection. Taken together, the results suggest that autophagy activation is a neuroprotective response to alleviate ethanol toxicity. Ethanol modulation of autophagic activity may be mediated by the MTOR pathway.

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The data shown below were compiled from readership statistics for 72 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
Unknown 72 100%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Student > Master 13 18%
Student > Ph. D. Student 11 15%
Other 8 11%
Researcher 8 11%
Student > Bachelor 6 8%
Other 12 17%
Unknown 14 19%
Readers by discipline
Readers by discipline Count As %
Medicine and Dentistry 16 22%
Agricultural and Biological Sciences 15 21%
Biochemistry, Genetics and Molecular Biology 8 11%
Neuroscience 8 11%
Pharmacology, Toxicology and Pharmaceutical Science 4 6%
Other 7 10%
Unknown 14 19%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 19 August 2012.
All research outputs
#20,660,571
of 25,377,790 outputs
Outputs from Autophagy
#2,011
of 2,630 outputs
Outputs of similar age
#200,342
of 273,617 outputs
Outputs of similar age from Autophagy
#450
of 556 outputs
Altmetric has tracked 25,377,790 research outputs across all sources so far. This one is in the 10th percentile – i.e., 10% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,630 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.4. This one is in the 15th percentile – i.e., 15% of its peers scored the same or lower than it.
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