Evidence map›Paper›PMID 35415192›Full record

ArticleBurns & trauma2022

Betulinic acid accelerates diabetic wound healing by modulating hyperglycemia-induced oxidative stress, inflammation and glucose intolerance.

Weiguo Xie, Weigang Hu, Zhuo Huang, Min Li, Hongyu Zhang, Xiaodong Huang, Paul Yao

Open access · diamondAbstract read
In one paragraph

Article in Burns & trauma, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

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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 2 institutions in 1 country.

Weiguo XieInstitute of Burns, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, 430060 P.R. China.
Weigang HuInstitute of Burns, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, 430060 P.R. China.
Zhuo HuangInstitute of Burns, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, 430060 P.R. China.
Min LiInstitute of Burns, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, 430060 P.R. China.
Hongyu ZhangDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, 518036, P.R. China.
Xiaodong HuangInstitute of Burns, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, 430060 P.R. China.
Paul YaoInstitute of Burns, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, 430060 P.R. China.ORCID https://orcid.org/0000-0001-9407-0779
Tongren Hospital · CNPeking University Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Diabetes significantly delays wound healing through oxidative stress, inflammation and impaired re-epithelialization that lead to defective regulation of the healing process, although the related mechanism remains unclear. Here, we aim to investigate the potential role and mechanism for the beneficial effect of betulinic acid (BA) on diabetic wound healing. Methods: The molecular effect of BA on hyperglycemia-mediated gene expression, oxidative stress, inflammation and glucose uptake was evaluated in endothelial, fibroblast and muscle cells. Burn injury was introduced to streptozotocin-induced diabetic rats and BA administration through either an intraperitoneal (IP) or topical (TOP) technique was used for wound treatment. Glucose tolerance was evaluated in both muscle tissue and fibroblasts, while oxidative stress and inflammation were determined in both the circulatory system and in wound tissues. The effect of BA on the wound healing process was also evaluated. Results: BA treatment reversed hyperglycemia-induced glucose transporter type 4 (GLUT4) suppression in both muscle and fibroblast cells. This treatment also partly reversed hyperglycemia-mediated suppression of endothelial nitric oxide synthase (eNOS), nuclear factor erythroid 2-related factor 2 (Nrf2) signaling and nuclear factor NFκB p65 subunit (NFκB p65) activation in endothelial cells. An Conclusions: BA treatment ameliorates hyperglycemia-mediated glucose intolerance, endothelial dysfunction, oxidative stress and inflammation. Administration of BA by both IP and TOP techniques was found to significantly accelerate diabetic wound healing, indicating that BA could be a potential therapeutic candidate for diabetic wound healing.

Indexed as

Betulinic acidDiabetesGlucoseHyperglycemiaInflammationNuclear factor κBOxidative stressWound healing

Identifiers

PMID35415192
PMCPMC8993492
OpenAlexW4210777429

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.