Evidence map›Paper›PMID 25275487›Full record

ArticlePloS one2014

Triptolide preserves cognitive function and reduces neuropathology in a mouse model of Alzheimer's disease.

Shaowu Cheng, Kyle J LeBlanc, Ling Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Neurotrophic Natural Products.Progress in the chemistry of organic natural products · 2024
    Article
  4. Research progress of natural products and their derivatives against Alzheimer's disease.Journal of enzyme inhibition and medicinal chemistry · 2023
    Review
  5. Article
  6. Review
  7. Review
  8. A worldwide bibliometric analysis of triptolide research from 1997 to 2021.American journal of translational research · 2022
    Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Therapeutic applications and delivery systems for triptolide.Drug delivery and translational research · 2020
    Review
  15. Article
  16. Article
  17. Article
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  19. Article
  20. Review
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

3 authors at 1 institution in 1 country.

Shaowu ChengDepartment of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota, United States of America.
Kyle J LeBlancDepartment of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota, United States of America.
Ling LiDepartment of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota, United States of America.
University of Minnesota · US

Funding

Protective Mechanisms of Statins in Alzheimer's DiseaseR01AG031846 · NIA · UNIVERSITY OF MINNESOTA · PI LI, LING · 2008 to 2012
$1.5M
NIA NIH HHS AG031846NIA NIH HHS R01 AG031846
6 · The paper itself

Abstract

Triptolide, a major bioactive ingredient of a widely used herbal medicine, has been shown to possess multiple pharmacological functions, including potential neuroprotective effects pertinent to Alzheimer's disease (AD) in vitro. However, the therapeutic potential of triptolide for AD in vivo has not been thoroughly evaluated. In the present study, we investigated the impact of peripherally administered triptolide on AD-related behavior and neuropathology in APPswe/PS1ΔE9 (APP/PS1) mice, an established model of AD. Our results showed that two-month treatment with triptolide rescued cognitive function in APP/PS1 mice. Immunohistochemical analyses indicated that triptolide treatment led to a significant decrease in amyloid-β (Aβ) deposition and neuroinflammation in treated mice. In contrast to previous findings in vitro, biochemical analyses showed that triptolide treatment did not significantly affect the production pathway of Aβ in vivo. Intriguingly, further analyses revealed that triptolide treatment upregulated the level of insulin-degrading enzyme, a major Aβ-degrading enzyme in the brain, indicating that triptolide treatment reduced Aβ pathology by enhancing the proteolytic degradation of Aβ. Our findings demonstrate that triptolide treatment ameliorates key behavioral and neuropathological changes found in AD, suggesting that triptolide may serve as a potential therapeutic agent for AD.

Indexed as

Alzheimer DiseaseAmyloid beta-Protein PrecursorAnimalsAnxietyBrainCognitionDisease Models, AnimalDiterpenesEpoxy CompoundsHabituation, PsychophysiologicInflammationMemory DisordersMiceMice, TransgenicPhenanthrenesPresenilin-1Amyloid beta-Protein PrecursorDiterpenesEpoxy CompoundsPhenanthrenesPresenilin-1triptolide

Identifiers

PMID25275487
PMCPMC4183525
OpenAlexW2058346173

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.