Evidence map›Paper›PMID 27596007›Full record

ArticleInflammation2016

Inhibiting HMGB1 Reduces Cerebral Ischemia Reperfusion Injury in Diabetic Mice.

Chong Wang, Jie Jiang, Xiuping Zhang, Linjie Song, Kai Sun, Ruxiang Xu

Open access · hybridAbstract read
In one paragraph

Article in Inflammation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.8field-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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Design of an Anti-HMGB1 Synthetic Antibody forJournal of the American Chemical Society · 2023
    Article
  7. Article
  8. Review
  9. Increased high-mobility group box 1 levels are associated with depression after acute ischemic stroke.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Ability of Post-treatment Glycyrrhizic Acid to Mitigate Cerebral Ischemia/Reperfusion Injury in Diabetic Mice.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  15. Review
  16. Review
  17. The Role of High Mobility Group Box 1 in Ischemic Stroke.Frontiers in cellular neuroscience · 2019
    Review
  18. Article
  19. Article
  20. 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

6 authors at 4 institutions in 1 country.

Chong WangThe Military General Hospital of Beijing, PLA, Beijing, 100700, People's Republic of China.
Jie JiangJining First People Hospital, Jining, 272011, People's Republic of China.
Xiuping ZhangJinan Central Hospital, Jinan, 250012, People's Republic of China.
Linjie SongJinan Central Hospital, Jinan, 250012, People's Republic of China.
Kai SunGraduate School, Weifang Medical University, Weifang, 261053, People's Republic of China.
Ruxiang XuThe Military General Hospital of Beijing, PLA, Beijing, 100700, People's Republic of China. ruxiang_xu@163.com.
Jinan Central Hospital · CNThe Military General Hospital of Beijing PLA · CNJining First People's Hospital · CNWeifang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High mobility group box1 (HMGB1) promotes inflammatory injury, and accumulating evidence suggests that it plays a key role in brain ischemia reperfusion (I/R), as well as the development of diabetes mellitus (DM). The purpose of this study was to investigate whether HMGB1 plays a role in brain I/R in a DM mouse model. Diabetes mellitus was induced by a high-calorie diet and streptozotocin treatment, and cerebral ischemia was induced by middle cerebral artery occlusion. We examined HMGB1 levels following cerebral I/R injury in DM and non-DM mice and evaluated the influence of altered HMGB1 levels on the severity of cerebral injury. Serum HMGB1 levels and the inflammatory factors IL-1β, IL-6, and inflammation-related enzyme iNOS were significantly elevated in DM mice with brain I/R compared with non-DM mice with brain I/R. Blocking HMGB1 function by intraperitoneal injection of anti-HMGB1 neutralizing antibodies reversed the inflammatory response and the extent of brain damage, suggesting that HMGB1 plays an important role in cerebral ischemic stroke in diabetic mice.

Indexed as

AnimalsAntibodiesBrain IschemiaDiabetes Mellitus, ExperimentalHMGB1 ProteinInfarction, Middle Cerebral ArteryInflammationMiceReperfusion InjuryAntibodiesHMGB1 Proteinbrain ischemia reperfusiondiabetes mellitusHMGB1

Identifiers

PMID27596007
PMCPMC5112296
OpenAlexW2508123333

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.