Evidence map›Paper›PMID 36065974›Full record

ReviewHistology and histopathology2022

Roles of glutamate in brain injuries after subarachnoid hemorrhage.

Fumihiro Kawakita, Hideki Kanamaru, Reona Asada, Yume Suzuki, Mai Nampei, Hideki Nakajima, Hiroki Oinaka, Hidenori Suzuki

Abstract readReview
PubMed Publisher
In one paragraph

Review in Histology and histopathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Article
  4. Article
  5. Review
  6. Article
  7. Role of microglia after subarachnoid hemorrhage.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Review
  8. Article
  9. Review
  10. Review
  11. 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

8 authors at 1 institution in 1 country.

Fumihiro KawakitaDepartment of Neurosurgery, Mie University Graduate School of Medicine, Tsu, Japan.
Hideki KanamaruDepartment of Neurosurgery, Mie University Graduate School of Medicine, Tsu, Japan.
Reona AsadaDepartment of Neurosurgery, Mie University Graduate School of Medicine, Tsu, Japan.
Yume SuzukiDepartment of Neurosurgery, Mie University Graduate School of Medicine, Tsu, Japan.
Mai NampeiDepartment of Neurosurgery, Mie University Graduate School of Medicine, Tsu, Japan.
Hideki NakajimaDepartment of Neurosurgery, Mie University Graduate School of Medicine, Tsu, Japan.
Hiroki OinakaDepartment of Neurosurgery, Mie University Graduate School of Medicine, Tsu, Japan.
Hidenori SuzukiDepartment of Neurosurgery, Mie University Graduate School of Medicine, Tsu, Japan. suzuki02@med.mie-u.ac.jp.
Mie University · JP

Funding

JSPS KAKENHI JP20K09346JSPS KAKENHI JP20K17963JSPS KAKENHI JP22K16684
6 · The paper itself

Abstract

Aneurysmal subarachnoid hemorrhage (SAH) is a stroke type with a high rate of mortality and morbidity. Post-SAH brain injury as a determinant of poor outcome is classified into the following two types: early brain injury (EBI) and delayed cerebral ischemia (DCI). EBI consists of various acute brain pathophysiologies that occur within the first 72 hours of SAH in a clinical setting. The underlying mechanisms of DCI are considered to be cerebral vasospasm or microcirculatory disturbance, which develops mostly 4 to 14 days after clinical SAH. Glutamate is the principal neurotransmitter in the central nervous system, but excessive glutamate is known to induce neurotoxicity. Experimental and clinical studies have revealed that excessive glutamates are released after SAH. In addition, many studies have reported the relationships between excessive glutamate release or overactivation of glutamate receptors and excitotoxicity, cortical spreading depolarization, seizure, increased blood-brain barrier permeability, neuroinflammation, microthrombosis formation, microvasospasm, cerebral vasospasm, impairments of brain metabolic supply and demand, impaired neurovascular coupling, and so on, all of which potentially contribute to the development of EBI or DCI. As glutamates always exert their functions through one or more of 4 major receptors of glutamates, it would be valuable to know the mechanisms as to how glutamates cause these pathologies, and the possibility that a glutamate receptor antagonist may block the pathologies. To prevent the mechanistic steps leading to glutamate-mediated neurotoxicity may ameliorate SAH-induced brain injuries and improve the outcomes. This review addresses the current knowledge of glutamate-mediated neurotoxicity, focusing on EBI and DCI after SAH.

Indexed as

Brain InjuriesSubarachnoid HemorrhageVasospasm, IntracranialGlutamic AcidHumansMicrocirculationGlutamic Acid

Identifiers

PMID36065974
OpenAlexW4297580845

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.