Evidence map›Paper›PMID 35911169›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2022

Antidepressant Mechanism of Kaixinsan and Its Active Compounds Based on Upregulation of Antioxidant Thioredoxin.

Xia Li, Yuan-Bo Wang, Chao-Chen Wang, Rui Jing, Li-Hua Mu, Ping Liu, Yuan Hu

Open access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 62% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
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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

7 authors at 1 institution in 1 country.

Xia LiDepartment of Pharmacy, Medical Supplier Center of PLA General Hospital, Beijing 100853, China.ORCID https://orcid.org/0000-0002-3663-2208
Yuan-Bo WangDepartment of Pharmacy, Medical Supplier Center of PLA General Hospital, Beijing 100853, China.ORCID https://orcid.org/0000-0003-2407-1914
Chao-Chen WangDepartment of Pharmacy, Medical Supplier Center of PLA General Hospital, Beijing 100853, China.ORCID https://orcid.org/0000-0002-9639-095X
Rui JingDepartment of Pharmacy, Medical Supplier Center of PLA General Hospital, Beijing 100853, China.ORCID https://orcid.org/0000-0002-4175-0313
Li-Hua MuDepartment of Pharmacy, Medical Supplier Center of PLA General Hospital, Beijing 100853, China.ORCID https://orcid.org/0000-0001-9753-3775
Ping LiuDepartment of Pharmacy, Medical Supplier Center of PLA General Hospital, Beijing 100853, China.ORCID https://orcid.org/0000-0001-9408-8477
Yuan HuDepartment of Pharmacy, Medical Supplier Center of PLA General Hospital, Beijing 100853, China.ORCID https://orcid.org/0000-0002-5348-1974
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Kaixinsan (KXS), a traditional Chinese medicine formula, has been demonstrated to be effective in the treatment of depression. The present study applied a network pharmacology approach to dig out the new targets and mechanism of action of KXS and the active compounds in the treatment of depression. Methods: A network pharmacology approach based on public databases including ADME (absorption, distribution, metabolism, and excretion) evaluation, targets prediction, construction of networks, and molecule docking was used and validated the predicted new antioxidant targets and mechanisms in vitro. Based on an in vitro experiment, we verified the AKT1/Nrf2 pathway related to the thioredoxin (Trx) antioxidant mechanism. Results: The present study sorted 31 pharmacologically active components (kaempferol, ginsenoside rh2, ginsenoside rh4, stigmasterol, etc.) through the ADME algorithm from KXS. 136 potential molecular targets (AKT1, TNF, IL-1b, JUN, ESR1, NOS3, etc.) were predicted, of which there were 69 targets clearly related to depression. By compound-depression targets (C-DTs) network constructed, and protein-protein interaction networks (PPI) and KEGG pathway enrichment analyzed, we identified active compounds mediating depression-related targets to exert synergism on the predictive AKT1/Nrf2 pathway related to thioredoxin (Trx) antioxidant mechanism and other inflammation-related signaling pathways as well as neurotransmitter related signaling pathways. In the H Conclusions: Taken together, by comprehensive systems pharmacology approach analysis, we found that KXS and its active compounds might exhibit antioxidant effects by stimulating the AKT1/Nrf2 pathway in the treatment of depression, which might shed new light on innovative therapeutic tactics for the new aspects for depression in traditional Chinese medicine in future studies.

Identifiers

PMID35911169
PMCPMC9325646
OpenAlexW4286213809

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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.