Evidence map›Paper›PMID 38441012›Full record

ArticleCombinatorial chemistry & high throughput screening2025

Integrated Serum Pharmacochemistry and Network Pharmacological Analysis Used To Explore Possible Anti-Aging Mechanisms of the Ginsenosides.

Jing Li, Ruigang Li, Qing Yang, Xiaoran Liu, Xiaobo Qu, Na Li

Abstract read
PubMed Publisher
In one paragraph

Article in Combinatorial chemistry & high throughput screening, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

Jing LiJilin Ginseng Academy, Changchun University of Chinese Medicine, Changchun, 130117, China.
Ruigang LiPharmacy Department, The Third Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, 130021, China.
Qing YangJilin Ginseng Academy, Changchun University of Chinese Medicine, Changchun, 130117, China.
Xiaoran LiuJilin Ginseng Academy, Changchun University of Chinese Medicine, Changchun, 130117, China.
Xiaobo QuJilin Ginseng Academy, Changchun University of Chinese Medicine, Changchun, 130117, China.
Na LiJilin Ginseng Academy, Changchun University of Chinese Medicine, Changchun, 130117, China.
Changchun University of Chinese Medicine · CN

Funding

China Scholarship Council CSC[2023]43, 202308220116Science and Technology Research Project of the Education Department of Jilin Province JJKH20210989KJ
6 · The paper itself

Abstract

introductionAlthough constitutive ginsenosides are credited with ginseng's remarkable anti-aging efficacy, the mechanism of action and bioactive components of ginsenosides are unclear.

objectiveThe goal of the study was to examine the effect of ginsenosides on D-galactose (Dgal)- induced aging in rats and to figure out the underlying molecular mechanism using serum pharmacochemistry and network pharmacology.

methodsUsing behavioral, biochemical indexes, and histological analysis, ginsenosides were evaluated for their anti-aging effects in rats induced by D-gal, and effective ingredients absorbed in the blood were examined by ultra-performance liquid chromatography quadrupole time of flight coupled with mass spectrometry (UPLC-Q/TOF-MS) before being subjected to network pharmacology analysis.

resultsAs well as improving spatial learning and memory skills, Ginsenosides are known to regulate malondialdehyde (MDA), glutathione peroxidase (GSH-Px), total antioxidant capacity (T-AOC) and superoxide dismutase (SOD) activity. In addition, it improved the ultrastructure of neurons in D-gal-induced rats' hippocampus. Seventy-four absorption components and metabolites of ginsenosides were identified in aging rat serum. According to a network pharmacology study, ginsenosides have anti-aging properties by modulating the phosphatidylinositol 3-kinase/protein kinase B (PI3K/AKT) and mitogen-activated protein kinases (MAPK) signaling pathways.

conclusionThe potential mechanisms of the anti-aging effect of ginsenosides involve multiple components, targets, and pathways. These findings serve as a foundation for further research into the processes behind ginsenoside's anti-aging impact.

Indexed as

AgingGinsenosidesNetwork PharmacologyAnimalsGalactoseHippocampusMaleRatsRats, Sprague-DawleyGalactoseGinsenosidesAgingbioactive componentsginsenosidesmechanismnetwork pharmacologyserum pharmacochemistry.

Identifiers

PMID38441012
OpenAlexW4392471750

What Socratic 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 Socratic graph.