Evidence map›Paper›PMID 22820296›Full record

ArticleBrain research2012

Decreased VEGF expression and microvascular density, but increased HIF-1 and 2α accumulation and EPO expression in chronic moderate hyperoxia in the mouse brain.

Girriso F Benderro, Xiaoyan Sun, Youzhi Kuang, Joseph C Lamanna

Open access · greenAbstract read
In one paragraph

Article in Brain research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

38 citing papers in PubMed, 63 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Astrocytic responses to high glucose impair barrier formation in cerebral microvessel endothelial cells.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  14. Review
  15. Impaired Cognitive Performance in Mice Exposed to Prolonged Hyperoxia.Advances in experimental medicine and biology · 2022
    Article
  16. Article
  17. Article
  18. Review
  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

4 authors at 2 institutions in 1 country.

Girriso F BenderroDepartment of Anatomy, Case Western Reserve University, Cleveland, OH, USA.
Xiaoyan Sun
Youzhi Kuang
Joseph C Lamanna
Case Western Reserve University · USUniversity School · US

Funding

BRAIN VASCULAR AND METABOLIC ADAPTATION TO HYPOXIAR01NS038632 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI LAMANNA, JOSEPH CHARLES · 2000 to 2014
$4.7M
NINDS NIH HHS NS-38632NINDS NIH HHS R01 NS038632
6 · The paper itself

Abstract

Normal brain function is dependent on continuous and controlled oxygen delivery. Chronic moderate hypoxia leads to angiogenesis, suggesting a modulatory role for oxygen in determining capillary density. The objective of this study was to determine physiologic and brain angiogenic adaptational changes during chronic moderate normobaric hyperoxia in mice. Four-month old C56BL/6J mice were kept in a normobaric chamber at 50% O(2) for up to 3 weeks. Normoxic littermates were kept in the same room outside the chamber. Freshly collected or fixed brain specimens were analyzed by RT-PCR, Western blot analysis and immunohistochemistry. Results show accumulation of hypoxia inducible factors 1 and 2α (HIF-1 and 2α), and increased expression of erythropoietin (EPO), cyclooxygenase-2 (COX-2) and angiopoietin-2 (Ang-2). Conversely, vascular endothelial growth factor (VEGF), and VEGF receptor-2 (KDR/Flk-1), Peroxisome proliferator-activated receptor gamma coactivator 1-α (PGC-1α) and prolylhydroxylase-2 (PHD-2) expressions were decreased. VEGF mRNA level was diminished but there was no change in HIF-1α mRNA and von Hippel Lindau E3 ubiquitin ligase (VHL) protein expression. Microvascular density was significantly diminished by the end of the 3rd week of hyperoxia. Overall, our results are: (1) increased expression of the potent neuroprotective molecule, EPO; (2) diminished expression of the potent angiogenic factor, VEGF; and (3) decreased microvascular density. We can, therefore, conclude that brain microvascular density can be controlled by HIF-independent mechanisms, and that brain capillary density is a continuously adjusted variable with tissue oxygen availability as one of the controlling modulators.

Indexed as

Angiopoietin-2AnimalsBasic Helix-Loop-Helix ProteinsBody WeightCerebral CortexCyclooxygenase 2Disease Models, AnimalEndothelial PAS Domain-Containing Protein 1ErythropoietinGene Expression RegulationHematocritHyperoxiaHypoxia-Inducible Factor 1MaleMiceMice, Inbred C57BLAngiopoietin-2Basic Helix-Loop-Helix ProteinsCyclooxygenase 2Endothelial PAS Domain-Containing Protein 1ErythropoietinHypoxia-Inducible Factor 1OxygenRNA, MessengerVascular Endothelial Growth Factor A

Identifiers

PMID22820296
PMCPMC3454487
OpenAlexW2059345537

What OpenQuestion holds

Textmetadata
LicenceTDM
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.