Evidence map›Paper›PMID 36769273›Full record

ReviewInternational journal of molecular sciences2023

The Protective Role of Glutathione on Zinc-Induced Neuron Death after Brain Injuries.

Min Kyu Park, Bo Young Choi, A Ra Kho, Song Hee Lee, Dae Ki Hong, Beom Seok Kang, Si Hyun Lee, Sang Won Suh

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing 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.

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

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

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Natural Compounds and Glutathione: Beyond Mere Antioxidants.Antioxidants (Basel, Switzerland) · 2023
    Review
  13. 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.

Min Kyu ParkDepartment of Physiology, College of Medicine, Hallym University, Chuncheon 24252, Republic of Korea.
Bo Young ChoiInstitute of Sport Science, Hallym University, Chuncheon 24252, Republic of Korea.ORCID 0000-0002-9579-3503
A Ra KhoNeuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Song Hee LeeDepartment of Physiology, College of Medicine, Hallym University, Chuncheon 24252, Republic of Korea.
Dae Ki HongDepartment of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA.
Beom Seok KangDepartment of Physiology, College of Medicine, Hallym University, Chuncheon 24252, Republic of Korea.
Si Hyun LeeDepartment of Physiology, College of Medicine, Hallym University, Chuncheon 24252, Republic of Korea.
Sang Won SuhDepartment of Physiology, College of Medicine, Hallym University, Chuncheon 24252, Republic of Korea.

Funding

Hallym University Research Fund 202204-009National Research Foundation of Korea 2020R1A2C2008480
6 · The paper itself

Abstract

Glutathione (GSH) is necessary for maintaining physiological antioxidant function, which is responsible for maintaining free radicals derived from reactive oxygen species at low levels and is associated with improved cognitive performance after brain injury. GSH is produced by the linkage of tripeptides that consist of glutamic acid, cysteine, and glycine. The adequate supplementation of GSH has neuroprotective effects in several brain injuries such as cerebral ischemia, hypoglycemia, and traumatic brain injury. Brain injuries produce an excess of reactive oxygen species through complex biochemical cascades, which exacerbates primary neuronal damage. GSH concentrations are known to be closely correlated with the activities of certain genes such as excitatory amino acid carrier 1 (EAAC1), glutamate transporter-associated protein 3-18 (Gtrap3-18), and zinc transporter 3 (ZnT3). Following brain-injury-induced oxidative stress, EAAC1 function is negatively impacted, which then reduces cysteine absorption and impairs neuronal GSH synthesis. In these circumstances, vesicular zinc is also released into the synaptic cleft and then translocated into postsynaptic neurons. The excessive influx of zinc inhibits glutathione reductase, which inhibits GSH's antioxidant functions in neurons, resulting in neuronal damage and ultimately in the impairment of cognitive function. Therefore, in this review, we explore the overall relationship between zinc and GSH in terms of oxidative stress and neuronal cell death. Furthermore, we seek to understand how the modulation of zinc can rescue brain-insult-induced neuronal death after ischemia, hypoglycemia, and traumatic brain injury.

Indexed as

AntioxidantsBrain Injuries, TraumaticCell DeathCysteineExcitatory Amino Acid Transporter 3GlutathioneHumansNeuronsOxidative StressReactive Oxygen SpeciesZincAntioxidantsCysteineExcitatory Amino Acid Transporter 3GlutathioneReactive Oxygen SpeciesZincexcitatory amino acid carrier 1glutathioneneuronal deathoxidative stresszinczinc transporter 3

Identifiers

PMID36769273
PMCPMC9917832

What OpenQuestion holds

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LicenceCC BY
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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.