Evidence map›Paper›PMID 36307999›Full record

ArticlePharmaceutical biology2022

Mechanism of Huangqi-Honghua combination regulating the gut microbiota to affect bile acid metabolism towards preventing cerebral ischaemia-reperfusion injury in rats.

Kai Wang, Yue Chen, Jinyi Cao, Ruimin Liang, Yi Qiao, Likun Ding, Xiaojuan Yang, Zhifu Yang

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

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  10. Histology and histopathology · 2024
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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.

Kai WangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yue ChenDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Jinyi CaoDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Ruimin LiangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yi QiaoDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Likun DingDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xiaojuan YangPharmacy Department, Xi'an Daxing Hospital, Xi'an, China.
Zhifu YangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Air Force Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextEffective treatment of ischaemic stroke is required to combat its high prevalence and incidence. Although the combination of

objectiveThe objective of this study is to elucidate the mechanism underlying Huangqi-Honghua (HQ-HH) for the treatment of ischaemic stroke by gut microbiota analysis and metabonomics. MATERIALS AND

methodsSprague-Dawley rats were randomly assigned to the sham, model, HQ-HH, and Naoxintong (NXT) groups. The middle cerebral artery occlusion-reperfusion model was established after 7 days of intragastric administration in the HQ-HH (4.5 g/kg, qd) and NXT (1.0 g/kg, qd) groups. The neurological examination, infarct volume, gut microbiota, bile acids, and inflammation markers were assessed after 72 h of reperfusion.

resultsCompared with the model group, HQ-HH significantly reduced the neurological deficit scores of the model rats (2.0 ± 0.2 vs. 3.16 ± 0.56), and reduced the cerebral infarct volume (27.83 ± 3.95 vs. 45.17 ± 2.75), and reduced the rate of necrotic neurons (26.35 ± 4.37 vs. 53.50 ± 9.61). HQ-HH regulating gut microbiota, activating the bile acid receptor FXR, maintaining the homeostasis of bile acid, reducing Th17 cells and increasing Treg cells in the rat brain, reducing the inflammatory response, and improving cerebral ischaemia-reperfusion injury.

conclusionsThese data indicate that HQ-HH combination can improve ischaemic stroke by regulating the gut microbiota to affect bile acid metabolism, providing experimental evidence for the wide application of HQ-HH in clinical practice of ischaemic stroke.

Indexed as

Brain IschemiaCarthamus tinctoriusGastrointestinal MicrobiomeIschemic StrokeReperfusion InjuryStrokeAnimalsBile Acids and SaltsDrugs, Chinese HerbalInfarction, Middle Cerebral ArteryRatsRats, Sprague-DawleyReperfusionBile Acids and SaltsDrugs, Chinese HerbalHonghua extract, Carthamus tinctoriusinflammationischaemic strokeTraditional Chinese Medicine

Identifiers

PMID36307999
PMCPMC9621259
OpenAlexW4307812556

What OpenQuestion holds

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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.