Evidence map›Paper›PMID 22467311›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2012

Functional role of astrocyte glutamate receptors and carbon monoxide in cerebral vasodilation response to glutamate.

Helena Parfenova, Dilyara Tcheranova, Shyamali Basuroy, Alexander L Fedinec, Jianxiong Liu, Charles W Leffler

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Control of astrocytic CaBiological research · 2024
    Article
  4. Article
  5. Observational
  6. Review
  7. Article
  8. The cold receptor TRPM8 activation leads to attenuation of endothelium-dependent cerebral vascular functions during head cooling.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  9. Article
  10. The role of gasotransmitters in neonatal physiology.Nitric oxide : biology and chemistry · 2020
    Review
  11. Article
  12. Pharmacologically increasing collateral perfusion during acute stroke using a carboxyhemoglobin gas transfer agent (Sanguinate™) in spontaneously hypertensive rats.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2018
    Article
  13. Article
  14. Article
  15. From unspecific to adjusted, how the BOLD response in the rat hippocampus develops during consecutive stimulations.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2017
    Article
  16. Review
  17. Review
  18. Carbon monoxide and the CNS: challenges and achievements.British journal of pharmacology · 2015
    Review
  19. Enteral supplements of a carbon monoxide donor CORM-A1 protect against cerebrovascular dysfunction caused by neonatal seizures.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2015
    Article
  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

6 authors at 1 institution in 1 country.

Helena ParfenovaDepartment of Physiology, University of Tennessee Health Science Center, Memphis, 38163, USA. hparfeno@uthsc.edu
Dilyara Tcheranova
Shyamali Basuroy
Alexander L Fedinec
Jianxiong Liu
Charles W Leffler
University of Tennessee Health Science Center · US

Funding

STUDIES OF THE CONTROL OF NEONATAL CIRCULATIONR01HL034059 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI PARFENOVA, HELENA · 1985 to 2016
$5.9M
CARBON MONOXIDE IN NEWBORN CEREBRAL CIRCULATIONR37HL042851 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI LEFFLER, CHARLES W. · 2000 to 2009
$3.5M
PERMISSIVE ROLE OF PGI-2 IN NEWBORN CEREBRAL CIRCULATIONR01HL042851 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI PARFENOVA, HELENA · 1991 to 2019
$3.4M
Cerebrovascular Stress and Circulating Endothelial CellsR01NS063936 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI PARFENOVA, HELENA · 2010 to 2014
$1.6M
Heme oxygenase and cerebral vascular injuryR01HL099655 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI PARFENOVA, HELENA · 2010 to 2013
$1.5M
Heme oxygenase and cerebral vascular injuryR01NS046385 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI PARFENOVA, HELENA · 2004 to 2008
$1.2M
NHLBI NIH HHS HL-34059NHLBI NIH HHS HL-42851NHLBI NIH HHS HL-99655NHLBI NIH HHS R01 HL042851NHLBI NIH HHS R01 HL099655NINDS NIH HHS NS-63936NINDS NIH HHS R01 NS046385NINDS NIH HHS R01 NS063936
6 · The paper itself

Abstract

In newborn pigs, vasodilation of pial arterioles in response to glutamate is mediated via carbon monoxide (CO), a gaseous messenger endogenously produced from heme degradation by a heme oxygenase (HO)-catalyzed reaction. We addressed the hypothesis that ionotropic glutamate receptors (iGluRs), including N-methyl-D-aspartic acid (NMDA)- and 2-amino-3-(5-methyl-3-oxo-1,2-oxazol-4-yl) propanoic acid (AMPA)/kainate-type receptors, expressed in cortical astrocytes mediate glutamate-induced astrocyte HO activation that leads to cerebral vasodilation. Acute vasoactive effects of topical iGluR agonists were determined by intravital microscopy using closed cranial windows in anesthetized newborn pigs. iGluR agonists, including NMDA, (±)1-aminocyclopentane-cis-1,3-dicarboxylic acid (cis-ACPD), AMPA, and kainate, produced pial arteriolar dilation. Topical L-2-aminoadipic acid, a gliotoxin that selectively disrupts glia limitans, reduced vasodilation caused by iGluR agonists, but not by hypercapnia, bradykinin, or sodium nitroprusside. In freshly isolated and cultured cortical astrocytes constitutively expressing HO-2, iGluR agonists NMDA, cis-ACPD, AMPA, and kainate rapidly increased CO production two- to threefold. Astrocytes overexpressing inducible HO-1 had high baseline CO but were less sensitive to glutamate stimulation of CO production when compared with HO-2-expressing astrocytes. Glutamate-induced astrocyte HO-2-mediated CO production was inhibited by either the NMDA receptor antagonist (R)-3C4HPG or the AMPA/kainate receptor antagonist DNQX. Accordingly, either antagonist abolished pial arteriolar dilation in response to glutamate, NMDA, and AMPA, indicating functional interaction among various subtypes of astrocytic iGluRs in response to glutamate stimulation. Overall, these data indicate that the astrocyte component of the neurovascular unit is responsible for the vasodilation response of pial arterioles to topically applied glutamate via iGluRs that are functionally linked to activation of constitutive HO in newborn piglets.

Indexed as

alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidAnimalsAnimals, NewbornArteriolesAstrocytesCarbon MonoxideCells, CulturedCerebrovascular CirculationFemaleGlutamatesHeme Oxygenase (Decyclizing)In Vitro TechniquesKainic AcidMaleModels, AnimalN-Methylaspartatealpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidCarbon MonoxideGlutamatesHeme Oxygenase (Decyclizing)Kainic AcidN-MethylaspartateReceptors, Glutamate

Identifiers

PMID22467311
PMCPMC3378289
OpenAlexW2096025654

What OpenQuestion holds

Textmetadata
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.