Evidence map›Paper›PMID 36189316›Full record

ArticleFrontiers in immunology2022

D-tagatose protects against oleic acid-induced acute respiratory distress syndrome in rats by activating PTEN/PI3K/AKT pathway.

Jian Huang, Bingjie Wang, Shaoyi Tao, Yuexia Hu, Ning Wang, Qiaoyun Zhang, Chunhui Wang, Chen Chen, Bingren Gao, Xingdong Cheng and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.7field-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

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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

11 authors at 5 institutions in 1 country.

Jian HuangDepartment of Cardiac Surgery, Lanzhou University Second Hospital, Lanzhou University, Lanzhou, China.
Bingjie WangDepartment of Anesthesiology, The Forth Affiliated Hospital of Anhui Medical University, Hefei, China.
Shaoyi TaoDepartment of Plastic Repair Burn Surgery Dermatology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Hefei, China.
Yuexia HuDepartment of Anesthesiology, The Forth Affiliated Hospital of Anhui Medical University, Hefei, China.
Ning WangDepartment of Anesthesiology, The Forth Affiliated Hospital of Anhui Medical University, Hefei, China.
Qiaoyun ZhangDepartment of Cardiac Surgery, Lanzhou University Second Hospital, Lanzhou University, Lanzhou, China.
Chunhui WangDepartment of Anesthesiology, The Forth Affiliated Hospital of Anhui Medical University, Hefei, China.
Chen ChenDepartment of Anesthesiology, The Forth Affiliated Hospital of Anhui Medical University, Hefei, China.
Bingren GaoDepartment of Cardiac Surgery, Lanzhou University Second Hospital, Lanzhou University, Lanzhou, China.
Xingdong ChengDepartment of Cardiac Surgery, Lanzhou University Second Hospital, Lanzhou University, Lanzhou, China.
Yongnan LiDepartment of Cardiac Surgery, Lanzhou University Second Hospital, Lanzhou University, Lanzhou, China.
First Affiliated Hospital of Anhui Medical University · CNLanzhou University Second Hospital · CNAnhui Medical University · CNLanzhou University · CNSecond Hospital of Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute respiratory distress syndrome (ARDS) is characterized by disruption of the alveolar-capillary barrier, resulting in severe alveolar edema and inflammation. D-tagatose (TAG) is a low-calorie fructose isomer with diverse biological activities whose role in ARDS has never been explored. We found that TAG protects lung tissues from injury in the oleic acid-induced rat model of ARDS. Seventeen male Sprague-Dawley rats were randomly assigned to 3 groups: Sham (n = 5), ARDS (n = 6), and TAG + ARDS (n = 6). The treatment groups were injected with oleic acid to induce ARDS, and the TAG + ARDS group was given TAG 3 days before the induction. After the treatments, the effect of TAG was evaluated by blood gas analysis and observing the gross and histological structure of the lung. The results showed that TAG significantly improved the oxygenation function, reduced the respiratory acidosis and the inflammatory response. TAG also improved the vascular permeability in ARDS rats and promoted the differentiation of alveolar type II cells, maintaining the stability of the alveolar structure. This protective effect of TAG on the lung may be achieved by activating the PTEN/PI3K/AKT pathway. Thus, TAG protects against oleic acid-induced ARDS in rats, suggesting a new clinical strategy for treating the condition.

Indexed as

Oleic AcidRespiratory Distress SyndromeAnimalsFructoseHexosesMalePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseRatsRats, Sprague-DawleyFructoseHexosesOleic AcidPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, rattagatoseacute respiratory distress syndromealveolarD-tagatoseoleic acidPTEN/PI3K/AKT pathway

Identifiers

PMID36189316
PMCPMC9520915
OpenAlexW4296095583

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.