Evidence map›Paper›PMID 21402058›Full record

ArticleBrain research2011

Hypoxia-induced angiogenesis is delayed in aging mouse brain.

Girriso F Benderro, Joseph C Lamanna

Abstract read
In one paragraph

Article in Brain research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
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  11. Astrocytic responses to high glucose impair barrier formation in cerebral microvessel endothelial cells.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. A Rationale for Hypoxic and Chemical Conditioning in Huntington's Disease.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. Microvascular Alterations in Alzheimer's Disease.Frontiers in cellular neuroscience · 2020
    Review
  20. 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

2 authors at 1 institution in 1 country.

Girriso F BenderroDepartment of Anatomy, Case Western Reserve University, Cleveland, OH 44106, USA.
Joseph C Lamanna
Case Western Reserve University · US

Funding

BRAIN VASCULAR AND METABOLIC ADAPTATION TO HYPOXIAR01NS038632 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI LAMANNA, JOSEPH CHARLES · 2000 to 2014
$4.7M
Angiogenic Response to Hypoxia and Ketosis in Rat BrainR01HL092933 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI LAMANNA, JOSEPH CHARLES · 2009 to 2012
$1.6M
NHLBI NIH HHS R01 HL092933NINDS NIH HHS NS-38632NINDS NIH HHS R01 NS038632
6 · The paper itself

Abstract

Chronic moderate hypoxia results in systemic and central nervous system adaptations that allow acclimatization. Long-term responses to hypoxia involve systemic physiological changes, metabolic regulation, and vascular remodeling. To investigate whether aging affects systemic and cerebral angiogenic adaptational changes in response to prolonged hypoxia, the present study assessed the responses of 4month old ("young") C57BL/6 mice and 24month old ("aged") C57BL/6 mice to chronic hypobaric hypoxia of 0.4atm (290torr). Compared to young mice, delayed body weight-loss recovery and a lag in polycythemic response were observed in aged mice. As previously shown, hypoxia inducible factor-1α (HIF-1α) accumulation was attenuated and vascular endothelial growth factor (VEGF) expression was decreased in the cerebral cortex of aged mice. Conversely, cyclooxygenase-2 (COX-2), angiopoietin-2 (Ang-2), and peroxisome proliferator-activated receptor gamma coactivator 1-α (PGC-1α) protein upregulation were not affected in the aged mice. Despite an initial delay in cerebral angiogenic response in aged mice in the first week of hypoxia, no significant differences were observed in microvascular density between young and aged mice in normoxia and at 2 and 3weeks of hypoxia. Taken together, these observations indicate that, even though the HIF-1 response to hypoxia is greatly attenuated, HIF-1 independent compensatory pathways are eventually able to maintain baseline and cerebral angiogenic adaptational changes to chronic hypoxia in aged mice. The delayed adaptive response, however, may result in decreased survival in the aged cohort.

Indexed as

AgingAngiopoietin-2AnimalsBrainCyclooxygenase 2Hypoxia, BrainHypoxia-Inducible Factor 1, alpha SubunitImmunohistochemistryMiceMice, Inbred C57BLNeovascularization, PhysiologicPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaTrans-ActivatorsTranscription FactorsVascular Endothelial Growth Factor AAngiopoietin-2Cyclooxygenase 2Hif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mouseTrans-ActivatorsTranscription FactorsVascular Endothelial Growth Factor A

Identifiers

PMID21402058
PMCPMC3082052
OpenAlexW2041100617

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Registered trials

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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.