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Neurorestoration of Sustained Attention in a Model of HIV-1 Associated Neurocognitive Disorders

Due to the sustained prevalence of human immunodeficiency virus (HIV)-1 associated neurocognitive disorders (HAND) in the post-combination antiretroviral therapy (cART) era, as well as the increased prevalence of older HIV-1 seropositive individuals, there is a critical need to develop adjunctive th...

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Autores principales: Moran, Landhing M., McLaurin, Kristen A., Booze, Rosemarie M., Mactutus, Charles F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691343/
https://www.ncbi.nlm.nih.gov/pubmed/31447657
http://dx.doi.org/10.3389/fnbeh.2019.00169
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author Moran, Landhing M.
McLaurin, Kristen A.
Booze, Rosemarie M.
Mactutus, Charles F.
author_facet Moran, Landhing M.
McLaurin, Kristen A.
Booze, Rosemarie M.
Mactutus, Charles F.
author_sort Moran, Landhing M.
collection PubMed
description Due to the sustained prevalence of human immunodeficiency virus (HIV)-1 associated neurocognitive disorders (HAND) in the post-combination antiretroviral therapy (cART) era, as well as the increased prevalence of older HIV-1 seropositive individuals, there is a critical need to develop adjunctive therapeutics targeted at preserving and/or restoring neurocognitive function. To address this knowledge gap, the present study examined the utility of S-Equol (SE), a phytoestrogen produced by gut microbiota, as an innovative therapeutic strategy. A signal detection operant task with varying signal durations (1,000, 500, 100 ms) was utilized to assess sustained attention in HIV-1 transgenic (Tg) and control animals. During the signal detection pretest assessment, HIV-1 Tg animals displayed profound deficits in stimulus-response learning and sustained attention relative to control animals. Subsequently, between 6 and 8 months of age, HIV-1 Tg and control animals were treated with a daily oral dose of either placebo or SE (0.05, 0.1, 0.2 mg) and a posttest assessment was conducted in the signal detection operant task with varying signal durations. In HIV-1 Tg animals, a linear decrease in the number of misses at 100 ms was observed as SE dose increased, suggesting a dose response with the most effective dose at 0.2 mg SE, approximating controls. Comparison of the number of misses across signal durations at the pretest and posttest revealed a preservation of neurocognitive function in HIV-1 Tg animals treated with 0.2 mg SE; an effect that was in sharp contrast to the neurocognitive decline observed in HIV-1 Tg animals treated with placebo. The results support the utility of 0.2 mg SE as a potential efficacious neuroprotective and/or neurorestorative therapeutic for sustained attention, in the absence of any adverse peripheral effects, in the HIV-1 Tg rat. Thus, the present study highlights the critical need for further in vivo studies to elucidate the full potential and generalizability of phytoestrogen treatment for HAND.
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spelling pubmed-66913432019-08-23 Neurorestoration of Sustained Attention in a Model of HIV-1 Associated Neurocognitive Disorders Moran, Landhing M. McLaurin, Kristen A. Booze, Rosemarie M. Mactutus, Charles F. Front Behav Neurosci Neuroscience Due to the sustained prevalence of human immunodeficiency virus (HIV)-1 associated neurocognitive disorders (HAND) in the post-combination antiretroviral therapy (cART) era, as well as the increased prevalence of older HIV-1 seropositive individuals, there is a critical need to develop adjunctive therapeutics targeted at preserving and/or restoring neurocognitive function. To address this knowledge gap, the present study examined the utility of S-Equol (SE), a phytoestrogen produced by gut microbiota, as an innovative therapeutic strategy. A signal detection operant task with varying signal durations (1,000, 500, 100 ms) was utilized to assess sustained attention in HIV-1 transgenic (Tg) and control animals. During the signal detection pretest assessment, HIV-1 Tg animals displayed profound deficits in stimulus-response learning and sustained attention relative to control animals. Subsequently, between 6 and 8 months of age, HIV-1 Tg and control animals were treated with a daily oral dose of either placebo or SE (0.05, 0.1, 0.2 mg) and a posttest assessment was conducted in the signal detection operant task with varying signal durations. In HIV-1 Tg animals, a linear decrease in the number of misses at 100 ms was observed as SE dose increased, suggesting a dose response with the most effective dose at 0.2 mg SE, approximating controls. Comparison of the number of misses across signal durations at the pretest and posttest revealed a preservation of neurocognitive function in HIV-1 Tg animals treated with 0.2 mg SE; an effect that was in sharp contrast to the neurocognitive decline observed in HIV-1 Tg animals treated with placebo. The results support the utility of 0.2 mg SE as a potential efficacious neuroprotective and/or neurorestorative therapeutic for sustained attention, in the absence of any adverse peripheral effects, in the HIV-1 Tg rat. Thus, the present study highlights the critical need for further in vivo studies to elucidate the full potential and generalizability of phytoestrogen treatment for HAND. Frontiers Media S.A. 2019-08-06 /pmc/articles/PMC6691343/ /pubmed/31447657 http://dx.doi.org/10.3389/fnbeh.2019.00169 Text en Copyright © 2019 Moran, McLaurin, Booze and Mactutus. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Moran, Landhing M.
McLaurin, Kristen A.
Booze, Rosemarie M.
Mactutus, Charles F.
Neurorestoration of Sustained Attention in a Model of HIV-1 Associated Neurocognitive Disorders
title Neurorestoration of Sustained Attention in a Model of HIV-1 Associated Neurocognitive Disorders
title_full Neurorestoration of Sustained Attention in a Model of HIV-1 Associated Neurocognitive Disorders
title_fullStr Neurorestoration of Sustained Attention in a Model of HIV-1 Associated Neurocognitive Disorders
title_full_unstemmed Neurorestoration of Sustained Attention in a Model of HIV-1 Associated Neurocognitive Disorders
title_short Neurorestoration of Sustained Attention in a Model of HIV-1 Associated Neurocognitive Disorders
title_sort neurorestoration of sustained attention in a model of hiv-1 associated neurocognitive disorders
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691343/
https://www.ncbi.nlm.nih.gov/pubmed/31447657
http://dx.doi.org/10.3389/fnbeh.2019.00169
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