Evidence map›Paper›PMID 19525894›Full record

ArticleJournal of neuropathology and experimental neurology2009

A rat model of human immunodeficiency virus 1 encephalopathy using envelope glycoprotein gp120 expression delivered by SV40 vectors.

Jean-Pierre Louboutin, Lokesh Agrawal, Beverly A S Reyes, Elisabeth J Van Bockstaele, David S Strayer

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In one paragraph

Article in Journal of neuropathology and experimental neurology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  4. Interaction of paroxetine with mitochondrial proteins mediates neuroprotection.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2015
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  5. Review
  6. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jean-Pierre LouboutinDepartment of Pathology, Thomas Jefferson University, Philadelphia, PA 19107, USA. jplouboutin@hotmail.com
Lokesh Agrawal
Beverly A S Reyes
Elisabeth J Van Bockstaele
David S Strayer
Thomas Jefferson University · US

Funding

Use of SV40 derived vectors to inhibit HIV 1 infectionP01AI048244 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI STRAYER, DAVID S · 2000 to 2003
$3.3M
Targeting HIV infection of the cns using gene deliveryR01MH070287 · NIMH · THOMAS JEFFERSON UNIVERSITY · PI STRAYER, DAVID S · 2004 to 2008
$1.9M
Opioids, Stress and Noradrenergic NeuronsK02DA015395 · NIDA · THOMAS JEFFERSON UNIVERSITY · PI VAN BOCKSTAELE, ELISABETH J · 2002 to 2006
$611k
PROTECTING CNS CELLS FROM HIV AND HIV-INDUCED INJURYR21MH069122 · NIMH · THOMAS JEFFERSON UNIVERSITY · PI STRAYER, DAVID S · 2003 to 2004
$314k
NIAID NIH HHS AI48244NIAID NIH HHS P01 AI048244NIDA NIH HHS K02 DA015395NIMH NIH HHS MH69122NIMH NIH HHS MH70287NIMH NIH HHS R01 MH070287NIMH NIH HHS R21 MH069122
6 · The paper itself

Abstract

Human immunodeficiency virus 1 (HIV-1) encephalopathy is thought to result in part from the toxicity of HIV-1 envelope glycoprotein gp120 for neurons. Experimental systems for studying the effects of gp120 and other HIV proteins on the brain have been limited to the acute effects of recombinant proteins in vitro or in vivo in simian immunodeficiency virus-infected monkeys. We describe an experimental rodent model of ongoing gp120-induced neurotoxicity in which HIV-1 envelope is expressed in the brain using an SV40-derived gene delivery vector, SV(gp120). When it is inoculated stereotaxically into the rat caudate putamen, SV(gp120) caused a partly hemorrhagic lesion in which neuron and other cell apoptosis continues for at least 12 weeks. Human immunodeficiency virus gp120 is expressed throughout this time, and some apoptotic cells are gp120 positive. Malondialdehyde and 4-hydroxynonenal assays indicated that there was lipid peroxidation in these lesions. Prior administration of recombinant SV40 vectors carrying antioxidant enzymes, copper/ zinc superoxide dismutase or glutathione peroxidase, was protective against SV(gp120)-induced oxidative injury and apoptosis. Thus, in vivo inoculation of SV(gp120) into the rat caudate putamen causes ongoing oxidative stress and apoptosis in neurons and may therefore represent a useful animal model for studying the pathogenesis and treatment of HIV-1 envelope-related brain damage.

Indexed as

Disease Models, AnimalAdenoviruses, SimianAIDS Dementia ComplexAldehydesAnimalsCalcium-Binding ProteinsCell DeathDNA-Binding ProteinsFemaleGene Expression Regulation, ViralGenetic VectorsGlial Fibrillary Acidic ProteinGlutathione PeroxidaseHIV-1HIV Envelope Protein gp120Humans4-hydroxy-2-nonenalAIF1 protein, humanAldehydesCalcium-Binding ProteinsDAPIDNA-Binding ProteinsGlial Fibrillary Acidic ProteinGlutathione PeroxidaseHIV Envelope Protein gp120IndolesMicrofilament ProteinsPhosphopyruvate Hydratase

Identifiers

PMID19525894
PMCPMC4711345
OpenAlexW2086389996

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.