Evidence map›Paper›PMID 36139149›Full record

ReviewBiomolecules2022

Ginsenoside and Its Therapeutic Potential for Cognitive Impairment.

Hui Feng, Mei Xue, Hao Deng, Shiqi Cheng, Yue Hu, Chunxiang Zhou

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

  1. Efficacy and Safety ofNutrients · 2024
    Trial
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Brain plasticity and ginseng.Journal of ginseng research · 2024
    Review
  12. Anti-leukemia effects of ginsenoside monomer: A narrative review of pharmacodynamics study.Current therapeutic research, clinical and experimental · 2024
    Review
  13. Article
  14. Review
  15. Cognitive Impairment in Multiple Sclerosis.Bioengineering (Basel, Switzerland) · 2023
    Review
  16. Review
  17. Article
  18. Review
  19. Article
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 3 institutions in 1 country.

Hui FengSchool of Chinese Medicine, Nanjing University of Chinese Medicine, Nanjing 210024, China.
Mei XueSchool of Chinese Medicine, Nanjing University of Chinese Medicine, Nanjing 210024, China.
Hao DengTianjin Key Laboratory of Translational Research of TCM Prescription and Syndrome, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300073, China.
Shiqi ChengDepartment of Neurology, The Second Affiliated Hospital of Nanchang University, Nanchang 330008, China.
Yue HuSchool of Chinese Medicine, Nanjing University of Chinese Medicine, Nanjing 210024, China.ORCID 0000-0002-8966-1934
Chunxiang ZhouSchool of Chinese Medicine, Nanjing University of Chinese Medicine, Nanjing 210024, China.
Nanjing University of Chinese Medicine · CNFirst Teaching Hospital of Tianjin University of Traditional Chinese Medicine · CNNanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cognitive impairment (CI) is one of the major clinical features of many neurodegenerative diseases. It can be aging-related or even appear in non-central nerve system (CNS) diseases. CI has a wide spectrum that ranges from the cognitive complaint with normal screening tests to mild CI and, at its end, dementia. Ginsenosides, agents extracted from a key Chinese herbal medicine (ginseng), show great promise as a new therapeutic option for treating CI. This review covered both clinical trials and preclinical studies to summarize the possible mechanisms of how ginsenosides affect CI in different diseases. It shows that ginsenosides can modulate signaling pathways associated with oxidative stress, apoptosis, inflammation, synaptic plasticity, and neurogenesis. The involved signaling pathways mainly include the PI3K/Akt, CREB/BDNF, Keap1/Nrf2 signaling, and NF-κB/NLRP3 inflammasome pathways. We hope to provide a theoretical basis for the treatment of CI for related diseases by ginsenosides.

Indexed as

Cognitive DysfunctionDrugs, Chinese HerbalGinsenosidesBrain-Derived Neurotrophic FactorHumansInflammasomesKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2NF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktBrain-Derived Neurotrophic FactorDrugs, Chinese HerbalGinsenosidesInflammasomesKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2NF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktapoptosiscognitive impairmentginsenosidesinflammationpharmacological properties

Identifiers

PMID36139149
PMCPMC9496100
OpenAlexW4296252605

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.