Evidence map›Paper›PMID 26175842›Full record

ArticleOxidative medicine and cellular longevity2015

Octreotide Protects the Mouse Retina against Ischemic Reperfusion Injury through Regulation of Antioxidation and Activation of NF-κB.

Jun Wang, Ziqiang Sun, Junsheng Shen, Dongdong Wu, Fang Liu, Ruisheng Yang, Shaoping Ji, Ailing Ji, Yanzhang Li

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.7field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Neuroprotective Peptides in Retinal Disease.Journal of clinical medicine · 2019
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Occludin downregulation in high glucose is regulated by SSTRExperimental and therapeutic medicine · 2017
    Article
  17. Article
  18. Article
  19. 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

9 authors at 3 institutions in 1 country.

Jun WangMedical College of Henan University, Kaifeng 475004, China.
Ziqiang SunMedical College of Henan University, Kaifeng 475004, China.
Junsheng ShenMedical College, Henan Polytechnic University, Jiaozuo 454000, China.
Dongdong WuMedical College of Henan University, Kaifeng 475004, China.
Fang LiuThe First Affiliated Hospital of Henan University, Kaifeng 475001, China.
Ruisheng YangThe First Affiliated Hospital of Henan University, Kaifeng 475001, China.
Shaoping JiMedical College of Henan University, Kaifeng 475004, China.
Ailing JiMedical College of Henan University, Kaifeng 475004, China.
Yanzhang LiMedical College of Henan University, Kaifeng 475004, China.
Henan University · CNFirst Affiliated Hospital of Henan University · CNHenan Polytechnic University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatostatin (SST), an endogenous peptide, may exert anti-inflammatory and neuroprotective effects on retinal injury induced by ischemia. Retinal ischemic reperfusion (I/R) injury always produces many reactive oxygen species (ROS), which can aggravate the tissue damage. The effects of octreotide (OCT), a SST analogue, on retinal I/R injury and ROS formation, are not very clear. In this study, we observed the effects of OCT on morphological changes, oxidative stress, and cell death, induced by retinal I/R injury. The activation of nuclear factor κB (NF-κB) and intercellular adhesion molecule-1 (ICAM-1) were further evaluated in I/R retina treated with or without OCT. The retinal layer thickness was increased at 1 day after I/R and decreased at 7 days after I/R (P < 0.05). This effect was associated with increase in MDA and ROS levels (P < 0.05). The Tunel-positive cells increased and the number of ganglion cell layer (GCL) neurons decreased significantly after I/R injury. The expression of p-p65 and ICAM-1 increased significantly in I/R retinas (P < 0.05). Each effect was markedly attenuated by application of OCT. These data indicate that OCT protects the retina against retinal I/R damage, which could be through inhibition of oxidative stress and downregulation of NF-κB and ICAM-1 expression.

Indexed as

AnimalsAntioxidantsApoptosisCell SurvivalDisease Models, AnimalIntercellular Adhesion Molecule-1MalondialdehydeMiceMice, Inbred C57BLOctreotideOxidative StressProtective AgentsReactive Oxygen SpeciesReperfusion InjuryRetinaRetinal DiseasesAntioxidantsIntercellular Adhesion Molecule-1MalondialdehydeOctreotideProtective AgentsReactive Oxygen SpeciesTranscription Factor RelA

Identifiers

PMID26175842
PMCPMC4484568
OpenAlexW1497595749

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.