Evidence map›Paper›PMID 28585890›Full record

ReviewExperimental biology and medicine (Maywood, N.J.)2017

Hypoxic conditioning and the central nervous system: A new therapeutic opportunity for brain and spinal cord injuries?

S Baillieul, S Chacaroun, S Doutreleau, O Detante, J L Pépin, S Verges

Registry-linked trialAbstract readReview
In one paragraph

Review in Experimental biology and medicine (Maywood, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05210088 (PLAsticity, Security and Tolerance to Intermittent Hypoxic Conditioning Following Stroke), which is not on this map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT05210088 phase1 / phase2withdrawnnot on this mapstarted 2024, after this paper: background citation

PLAsticity, Security and Tolerance to Intermittent Hypoxic Conditioning Following Stroke

TypeinterventionalSponsorUniversity Hospital, GrenobleRan2024 to 2024Enrolled0ConditionsStroke, Ischemic, Stroke SequelaeArmsHypoxia, intermittent, Normoxia
3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  11. Potential forBrain communications · 2024
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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.

S Baillieul1 CHU Grenoble Alpes, Physiology, Sleep and Exercise Department, Grenoble F-38042, France.
S Chacaroun2 INSERM, U1042, Grenoble F-38042, France.
S Doutreleau1 CHU Grenoble Alpes, Physiology, Sleep and Exercise Department, Grenoble F-38042, France.
O Detante4 CHU Grenoble Alpes, Pôle Psychiatrie Neurologie, Stroke Unit, Grenoble F-38042, France.
J L Pépin1 CHU Grenoble Alpes, Physiology, Sleep and Exercise Department, Grenoble F-38042, France.
S Verges2 INSERM, U1042, Grenoble F-38042, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Central nervous system diseases are among the most disabling in the world. Neuroprotection and brain recovery from either acute or chronic neurodegeneration still represent a challenge in neurology and neurorehabilitation as pharmacology treatments are often insufficiently effective. Conditioning the central nervous system has been proposed as a potential non-pharmacological neuro-therapeutic. Conditioning refers to a procedure by which a potentially deleterious stimulus is applied near to but below the threshold of damage to the organism to increase resistance to the same or even different noxious stimuli given above the threshold of damage. Hypoxic conditioning has been investigated in several cellular and preclinical models and is now recognized as inducing endogenous mechanisms of neuroprotection. Ischemic, traumatic, or chronic neurodegenerative diseases can benefit from hypoxic conditioning strategies aiming at preventing the deleterious consequences or reducing the severity of the pathological condition (preconditioning) or aiming at inducing neuroplasticity and recovery (postconditioning) following central nervous system injury. Hypoxic conditioning can consist in single (sustained) or cyclical (intermittent, interspersed by short period of normoxia) hypoxia stimuli which duration range from few minutes to several hours and that can be repeated over several days or weeks. This mini-review addresses the existing evidence regarding the use of hypoxic conditioning as a potential innovating neuro-therapeutic modality to induce neuroprotection, neuroplasticity and brain recovery. This mini-review also emphasizes issues which remain to be clarified and future researches to be performed in the field. Impact statement Neuroprotection and brain recovery from either acute or chronic neurodegeneration still represent a challenge in neurology and neurorehabilitation. Hypoxic conditioning may represent a harmless and efficient non-pharmacological new therapeutic modality in the field of neuroprotection and neuroplasticity, as supported by many preclinical data. Animal studies provide clear evidence for neuroprotection and neuroplasticity induced by hypoxic conditioning in several models of neurological disorders. These studies show improved functional outcomes when hypoxic conditioning is applied and provides important information to translate this intervention to clinical practice. Some studies in humans provide encouraging data regarding the tolerance and therapeutic effects of hypoxic conditioning strategies. The main issues to address in future research include the definition of the appropriate hypoxic dose and pattern of exposure, the determination of relevant physiological biomarkers to assess the effects of the treatment and the evaluation of combined strategies involving hypoxic conditioning and other pharmacological or non-pharmacological treatments.

Indexed as

HypoxiaAnimalsBrain InjuriesHumansIschemic PreconditioningSpinal Cord InjuriesCentral nervous systemconditioninghypoxianeurobiologyneuroprotectionphysiology

Identifiers

PMID28585890
PMCPMC5478009

What OpenQuestion holds

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Registered trials

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.