Evidence map›Paper›PMID 18055541›Full record

ArticleThe American journal of pathology2007

Protection against human immunodeficiency virus type 1 Tat neurotoxicity by Ginkgo biloba extract EGb 761 involving glial fibrillary acidic protein.

Wei Zou, Byung Oh Kim, Betty Y Zhou, Ying Liu, Albee Messing, Johnny J He

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
8.9field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 53 citations in OpenAlex.

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  11. [The Journal of pharmacology and experimental therapeutics · 2020
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  15. HIV Tat Impairs Neurogenesis through Functioning As a Notch Ligand and Activation of Notch Signaling Pathway.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  16. Article
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  18. Brain Invasion by CD4(+) T Cells Infected with a Transmitted/Founder HIV-1BJZS7 During Acute Stage in Humanized Mice.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2016
    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

6 authors at 4 institutions in 2 countries.

Wei ZouDepartment of Microbiology and Immunology, Indiana University School of Medicine, R2 302, 950 W. Walnut St., Indianapolis, IN 46202, USA.
Byung Oh Kim
Betty Y Zhou
Ying Liu
Albee Messing
Johnny J He
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineSangji University · KRUniversity of Wisconsin–Madison · US

Funding

The impact of GFAP mutations upon filament networksP01NS042803 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI GOLDMAN, JAMES · 2002 to 2012
$11.1M
MECHANISMS OF HIV-1 ENTRY AND PATHOGENESIS IN ASTROCYTESR01NS039804 · NINDS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI HE, JOHNNY J · 2000 to 2008
$2.3M
Tat Interaction with LRP and Its Role in AIDS DementiaR01MH065158 · NIMH · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI HE, JOHNNY J · 2002 to 2006
$1.5M
Use a novel Tat transgenic model to develop neuroAIDS therapeuticsR21DA022986 · NIDA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI HE, JOHNNY J · 2006 to 2007
$391k
ROBOTICS FOR REHABILITATION THERAPY-27533352-275033352N01HD033352 · NICHD · REGENTS OF THE UNIVERSITY OF C · PI REINKENSMEYER, DAVID J. · 2004 to 2006
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NICHD NIH HHS N01 HD033352NICHD NIH HHS P30HD033352NIDA NIH HHS R21 DA022986NIDA NIH HHS R21DA022986NIMH NIH HHS R01 MH065158NIMH NIH HHS R01MH065158NINDS NIH HHS P01 NS042803NINDS NIH HHS P01NS42803NINDS NIH HHS R01 NS039804NINDS NIH HHS R01NS039804
6 · The paper itself

Abstract

Human immunodeficiency virus (HIV)-1 Tat protein is an important pathogenic factor in HIV-associated neuropathogenesis. Despite recent progress, the molecular mechanisms underlying Tat neurotoxicity are still not completely understood. However, few therapeutics have been developed to specifically target HIV infection in the brain. Recent development of an inducible brain-specific Tat transgenic mouse model has made it possible to define the mechanisms of Tat neurotoxicity and evaluate anti-neuroAIDS therapeutic candidates in the context of a whole organism. Herein, we demonstrate that administration of EGb 761, a standardized formulation of Ginkgo biloba extract, markedly protected Tat transgenic mice from Tat-induced developmental retardation, inflammation, death, astrocytosis, and neuron loss. EGb 761 directly down-regulated glial fibrillary acidic protein (GFAP) expression at both protein and mRNA levels. This down-regulation was, at least in part, attributable to direct effects of EGb 761 on the interactions of the AP1 and NF-kappaB transcription factors with the GFAP promoter. Most strikingly, Tat-induced neuropathological phenotypes including macrophage/microglia activation, central nervous system infiltration of T lymphocytes, and oxidative stress were significantly alleviated in GFAP-null/Tat transgenic mice. Taken together, these results provide the first evidence to support the potential for clinical use of EGb 761 to treat HIV-associated neurological diseases. Moreover, these findings suggest for the first time that GFAP activation is directly involved in Tat neurotoxicity, supporting the notion that astrocyte activation or astrocytosis may directly contribute to HIV-associated neurological disorders.

Indexed as

HIV-1AnimalsApoptosisAstrocytesCell Line, TumorGinkgo bilobaGinkgo ExtractGlial Fibrillary Acidic ProteinHumansMiceMice, TransgenicNeurotoxicity SyndromesPlant Extractstat Gene Products, Human Immunodeficiency VirusTranscription, GeneticGinkgo biloba extractGinkgo ExtractGlial Fibrillary Acidic ProteinPlant Extractstat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID18055541
PMCPMC2111115
OpenAlexW2168144334

What OpenQuestion holds

Textmetadata
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.