Evidence map›Paper›PMID 27517901›Full record

ArticleInternational journal of molecular sciences2016

Cytoprotection against Hypoxic and/or MPP⁺ Injury: Effect of δ-Opioid Receptor Activation on Caspase 3.

Yuan Xu, Feng Zhi, Naiyuan Shao, Rong Wang, Yilin Yang, Ying Xia

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Evidence-based complementary and alternative medicine : eCAM · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. The delta-opioid receptor and Parkinson's disease.CNS neuroscience & therapeutics · 2018
    Review
  16. 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 1 institution in 1 country.

Yuan XuModern Medical Research Center, The Third Affiliated Hospital of Soochow University, Changzhou 213000, Jiangsu, China. 13685262339@163.com.
Feng ZhiModern Medical Research Center, The Third Affiliated Hospital of Soochow University, Changzhou 213000, Jiangsu, China. danielzhif@163.com.
Naiyuan ShaoModern Medical Research Center, The Third Affiliated Hospital of Soochow University, Changzhou 213000, Jiangsu, China. naiyuanshao@126.com.
Rong WangModern Medical Research Center, The Third Affiliated Hospital of Soochow University, Changzhou 213000, Jiangsu, China. wangrong1949@163.com.
Yilin YangModern Medical Research Center, The Third Affiliated Hospital of Soochow University, Changzhou 213000, Jiangsu, China. bigyang@vip.sina.com.
Ying XiaDepartment of Neurosurgery, The University of Texas McGovern Medical School, Houston, TX 77030, USA. Y55738088@gmail.com.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pathological changes of Parkinson's disease (PD) are, at least partially, associated with the dysregulation of PTEN-induced putative kinase 1 (PINK1) and caspase 3. Since hypoxic and neurotoxic insults are underlying causes of PD, and since δ-opioid receptor (DOR) is neuroprotective against hypoxic/ischemic insults, we sought to determine whether DOR activation could protect the cells from damage induced by hypoxia and/or MPP⁺ by regulating PINK1 and caspase 3 expressions. We exposed PC12 cells to either severe hypoxia (0.5%-1% O₂) for 24-48 h or to MPP⁺ at different concentrations (0.5, 1, 2 mM) and then detected the levels of PINK1 and cleaved caspase 3. Both hypoxia and MPP⁺ reduced cell viability, progressively suppressed the expression of PINK1 and increased the cleaved caspase 3. DOR activation using UFP-512, effectively protected the cells from hypoxia and/or MPP⁺ induced injury, reversed the reduction in PINK1 protein and significantly attenuated the increase in the cleaved caspase 3. On the other hand, the application of DOR antagonist, naltrindole, greatly decreased cell viability and increased cleaved caspase 3. These findings suggest that DOR is cytoprotective against both hypoxia and MPP⁺ through the regulation of PINK1 and caspase 3 pathways.

Indexed as

1-Methyl-4-phenylpyridiniumAnimalsCaspase 3Cell HypoxiaCell SurvivalParkinson DiseasePC12 CellsProtein KinasesPTEN-Induced Putative KinaseRatsReceptors, Opioid, delta1-Methyl-4-phenylpyridiniumCaspase 3Protein KinasesPTEN-Induced Putative KinaseReceptors, Opioid, deltacaspase 3cytoprotectionhypoxiaMPP+Parkinson’s diseasePINK1δ-opioid receptor

Identifiers

PMID27517901
PMCPMC5000589
OpenAlexW2487697883

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.