Evidence map›Paper›PMID 34606050›Full record

SynthesisMolecular neurobiology2021

Neuroprotective Role of Acidosis in Ischemia: Review of the Preclinical Evidence.

Jeff Ehresman, Ethan Cottrill, Justin M Caplan, Cameron G McDougall, Nicholas Theodore, Paul A Nyquist

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Molecular neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Delayed COCNS neuroscience & therapeutics · 2023
    Article
  4. Carbon dioxide and MAPK signalling: towards therapy for inflammation.Cell communication and signaling : CCS · 2023
    Review
  5. 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.

Jeff EhresmanDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Phipps 416, 600 N. Wolfe St., Baltimore, MD, 21287, USA.
Ethan CottrillDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Phipps 416, 600 N. Wolfe St., Baltimore, MD, 21287, USA.
Justin M CaplanDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Phipps 416, 600 N. Wolfe St., Baltimore, MD, 21287, USA.
Cameron G McDougallDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Phipps 416, 600 N. Wolfe St., Baltimore, MD, 21287, USA.
Nicholas TheodoreDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Phipps 416, 600 N. Wolfe St., Baltimore, MD, 21287, USA.
Paul A NyquistDepartment of Neurology, Johns Hopkins University School of Medicine, Phipps 416, 600 N. Wolfe St., Baltimore, MD, 21287, USA. pnyquis1@jhmi.edu.ORCID http://orcid.org/0000-0001-6078-3543
Johns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efforts to develop effective neuroprotective therapies for ischemic stroke have had little success to date. One promising approach to neuroprotection is ischemic postconditioning, which utilizes brief bouts of ischemia after acute ischemic stroke to elicit neuroprotection, although the mechanism is largely unknown. As the primary components of transient ischemia are local hypoxia and acidosis, and hypoxic postconditioning has had little success, it is possible that the acidosis component may be the primary driver. To address the evidence behind this, we performed a systematic review of preclinical studies focused on the neuroprotective role of transient acidosis after ischemia. Animal studies demonstrated that mild-to-moderate acidosis after ischemic events led to better functional neurologic outcomes with reduced infarct volumes, while severe acidosis often led to cerebral edema and worse functional outcomes. In vitro studies demonstrated that mild-to-moderate acidosis improves neuronal survival largely through two means: (1) inhibition of harmful superoxide formation in the excitotoxic pathway and (2) remodeling neuronal mitochondria to allow for efficient ATP production (i.e., oxidative phosphorylation), even in the absence of oxygen. Similar to the animal studies, acidotic postconditioning in humans would entail short cycles of carbon dioxide inhalation, which has already been demonstrated to be safe as part of a hypercapnic challenge when measuring cerebrovascular reactivity. Due to the preclinical efficacy of acidotic postconditioning, its relatively straightforward translation into humans, and the growing need for neuroprotective therapies, future preclinical studies should focus on filling the current knowledge gaps that are currently restricting the development of phase I/II clinical trials.

Indexed as

AcidosisAnimalsBrain IschemiaDisease Models, AnimalIschemic PostconditioningNeuroprotectionAcidosisAcidoticConditioningIschemicNeuroprotectionStroke

Identifiers

PMID34606050
OpenAlexW3203077941

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.