Evidence map›Paper›PMID 22847190›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2012

Ginkgolic acid inhibits HIV protease activity and HIV infection in vitro.

Jian-Ming Lü, Shaoyu Yan, Saha Jamaluddin, Sarah M Weakley, Zhengdong Liang, Edward B Siwak, Qizhi Yao, Changyi Chen

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

35 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Ginkgolic acid inhibits CD8Journal of pharmaceutical analysis · 2025
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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

8 authors at 2 institutions in 1 country.

Jian-Ming LüMichael E. DeBakey Department of Surgery, Molecular Surgeon Research Center, Baylor College of Medicine, Houston, TX, USA.
Shaoyu Yan
Saha Jamaluddin
Sarah M Weakley
Zhengdong Liang
Edward B Siwak
Qizhi Yao
Changyi Chen
Michael E. DeBakey VA Medical Center · USBaylor College of Medicine · US

Funding

Virology CoreP30AI036211 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI BUTEL, JANET S · 1994 to 2015
$21.7M
HIV PROTEASE INHIBITORS EFFECT--NENDOTHELIAL DYSFUNCTIONR01HL065916 · NHLBI · EMORY UNIVERSITY · PI CHEN, CHANGYI · 2000 to 2004
$1.8M
Effects of HAART drugs on endothelial dysfunction of pu*R01HL083471 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI CHEN, CHANGYI · 2005 to 2009
$1.8M
Molecular Surgeon Research Training on Vascular DiseaseT32HL083774 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI CHEN, CHANGYI · 2008 to 2012
$970k
NHLBI NIH HHS R01 HL065916NHLBI NIH HHS R01 HL083471NHLBI NIH HHS T32 HL083774NHLBI NIH HHS T32HL083774NIAID NIH HHS P30 AI036211
6 · The paper itself

Abstract

backgroundSeveral HIV protease mutations, which are resistant to clinical HIV protease inhibitors (PIs), have been identified. There is a great need for second-generation PIs with different chemical structures and/or with an alternative mode of inhibition. Ginkgolic acid is a natural herbal substance and a major component of the lipid fraction in the nutshells of the Ginkgo biloba tree. The objective of this study was to determine whether ginkgolic acid could inhibit HIV protease activity in a cell free system and HIV infection in human cells. MATERIAL/

methodsPurified ginkgolic acid and recombinant HIV-1 HXB2 KIIA protease were used for the HIV protease activity assay. Human peripheral blood mononuclear cells (PBMCs) were used for HIV infection (HIV-1SF162 virus), determined by a p24gag ELISA. Cytotoxicity was also determined.

resultsGinkgolic acid (31.2 µg/ml) inhibited HIV protease activity by 60%, compared with the negative control, and the effect was concentration-dependent. In addition, ginkgolic acid treatment (50 and 100 µg/ml) effectively inhibited the HIV infection at day 7 in a concentration-dependent manner. Ginkgolic acid at a concentration of up to 150 µg/ml demonstrated very limited cytotoxicity.

conclusionsGinkgolic acid effectively inhibits HIV protease activity in a cell free system and HIV infection in PBMCs without significant cytotoxicity. Ginkgolic acid may inhibit HIV protease through different mechanisms than current FDA-approved HIV PI drugs. These properties of ginkgolic acid make it a promising therapy for HIV infection, especially as the clinical problem of viral resistance to HIV PIs continues to grow.

Indexed as

Cell DeathCell-Free SystemDose-Response Relationship, DrugGinkgolidesHIV InfectionsHIV ProteaseHIV Protease InhibitorsHumansJurkat CellsLactonesSalicylatesginkgolic acidginkgolide Aginkgolide BGinkgolidesHIV ProteaseHIV Protease InhibitorsLactonesSalicylates

Identifiers

PMID22847190
PMCPMC3560711
OpenAlexW1988255276

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.