Evidence map›Paper›PMID 28785051›Full record

ArticleScientific reports2017

Phenothiazines Enhance Mild Hypothermia-induced Neuroprotection via PI3K/Akt Regulation in Experimental Stroke.

Hong An, Yunxia Duan, Di Wu, James Yip, Omar Elmadhoun, Joshua C Wright, Wenjuan Shi, Kaiyin Liu, Xiaoduo He, Jingfei Shi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

13 authors at 2 institutions in 2 countries.

Hong AnChina-America Institute of Neuroscience, Xuanwu Hospital, Capital Medical University, Beijing, China.
Yunxia DuanChina-America Institute of Neuroscience, Xuanwu Hospital, Capital Medical University, Beijing, China.
Di WuChina-America Institute of Neuroscience, Xuanwu Hospital, Capital Medical University, Beijing, China.
James YipDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI, USA.
Omar ElmadhounDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI, USA.
Joshua C WrightDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI, USA.
Wenjuan ShiCerebrovascular Diseases Research Institute, Xuanwu hospital, Capital Medical University, Beijing, China.
Kaiyin LiuDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI, USA.
Xiaoduo HeChina-America Institute of Neuroscience, Xuanwu Hospital, Capital Medical University, Beijing, China.
Jingfei ShiChina-America Institute of Neuroscience, Xuanwu Hospital, Capital Medical University, Beijing, China.
Fang JiangChina-America Institute of Neuroscience, Xuanwu Hospital, Capital Medical University, Beijing, China.
Xunming JiChina-America Institute of Neuroscience, Xuanwu Hospital, Capital Medical University, Beijing, China. jixm@ccmu.edu.cn.
Yuchuan DingChina-America Institute of Neuroscience, Xuanwu Hospital, Capital Medical University, Beijing, China.
Capital Medical University · CNWayne State University · US

Funding

Reducing Brain Hyperglycolysis: A Novel Strategy for Hyperglycemia after StrokeI01RX001964 · VA · JOHN D DINGELL VA MEDICAL CENTER · PI DING, YUCHUAN · 2016 to 2020
–
RRD VA I01 RX001964
6 · The paper itself

Abstract

Physical hypothermia has long been considered a promising neuroprotective treatment of ischemic stroke, but the treatment's various complications along with the impractical duration and depth of therapy significantly narrow its clinical scope. In the present study, the model of reversible right middle cerebral artery occlusion (MCAO) for 2 h was used. We combined hypothermia (33-35 °C for 1 h) with phenothiazine neuroleptics (chlorpromazine & promethazine) as additive neuroprotectants, with the aim of augmenting its efficacy while only using mild temperatures. We also investigated its therapeutic effects on the Phosphatidylinositol 3 kinase/Protein kinase B (PI3K/Akt) apoptotic pathway. The combination treatment achieved reduction in ischemic rat temperatures in the rectum, cortex and striatum significantly (P < 0.01) faster than hypothermia alone, accompanied by more obvious (P < 0.01) reduction of brain infarct volume and neurological deficits. The combination treatment remarkably (P < 0.05) increased expression of p-Akt and anti-apoptotic proteins (Bcl-2 and Bcl-xL), while reduced expression of pro-apoptotic proteins (AIF and Bax). Finally, the treatment's neuroprotective effects were blocked by a p-Akt inhibitor. By combining hypothermia with phenothiazines, we significantly enhanced the neuroprotective effects of mild hypothermia. This study also sheds light on the possible molecular mechanism for these effects which involves the PI3K/Akt signaling and apoptotic pathway.

Indexed as

AnimalsAntipsychotic AgentsChlorpromazineCombined Modality TherapyDisease Models, AnimalHypothermia, InducedMalePhenothiazinesPhosphatidylinositol 3-KinasesPhosphorylationPromethazineProto-Oncogene Proteins c-aktRatsRats, Sprague-DawleySignal TransductionStrokeAntipsychotic AgentsChlorpromazinePhenothiazinesPhosphatidylinositol 3-KinasesPromethazineProto-Oncogene Proteins c-akt

Identifiers

PMID28785051
PMCPMC5547051
OpenAlexW2741741696

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.