Evidence map›Paper›PMID 22102982›Full record

ArticleDrug delivery letters2011

Brain-Delivery of Zinc-Ions as Potential Treatment for Neurological Diseases: Mini Review.

Andreas M Grabrucker, Magali Rowan, Craig C Garner

Abstract read
In one paragraph

Article in Drug delivery letters, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. Review
  3. Zinc in psychosis (Review).Molecular medicine reports · 2025
    Review
  4. Article
  5. Article
  6. Neurochemical Research of LOXBlock-1 and ZnSOBiological trace element research · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Magnesium and Zinc Oxide Nanoparticles fromMolecules (Basel, Switzerland) · 2022
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Crosstalk between zinc and free fatty acids in plasma.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Review
  18. Metal Ion Effects on Aβ and Tau Aggregation.International journal of molecular sciences · 2018
    Review
  19. Article
  20. Zinc Signal in Brain Diseases.International journal of molecular sciences · 2017
    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

3 authors at 1 institution in 1 country.

Andreas M GrabruckerDepartment of Psychiatry and Behavioral Sciences, Stanford School of Medicine, Stanford University, Stanford, CA, USA.
Magali Rowan
Craig C Garner
Stanford University · US

Funding

The Roles of Presynaptic Plasticity in Circuit Function and BehaviorP01NS053862 · NINDS · STANFORD UNIVERSITY · PI GARNER, CRAIG C · 2006 to 2010
$6.7M
Identification of Autism genes that regulate synaptic Nrx/Nlg signaling complexesR21MH091471 · NIMH · STANFORD UNIVERSITY · PI GARNER, CRAIG C · 2010 to 2011
$431k
Regulation of activity-dependent ProSAp2 synaptic dynamicsF31NS066786 · NINDS · STANFORD UNIVERSITY · PI ROWAN, MAGALI HOLT · 2009 to 2011
$116k
NIMH NIH HHS R21 MH091471NINDS NIH HHS F31 NS066786NINDS NIH HHS P01 NS053862
6 · The paper itself

Abstract

Homeostasis of metal ions such as Zn(2+) is essential for proper brain function. Moreover, the list of psychiatric and neurodegenerative disorders involving a dysregulation of brain Zn(2+)-levels is long and steadily growing, including Parkinson's and Alzheimer's disease as well as schizophrenia, attention deficit and hyperactivity disorder, depression, amyotrophic lateral sclerosis, Down's syndrome, multiple sclerosis, Wilson's disease and Pick's disease. Furthermore, alterations in Zn(2+)-levels are seen in transient forebrain ischemia, seizures, traumatic brain injury and alcoholism. Thus, the possibility of altering Zn(2+)-levels within the brain is emerging as a new target for the prevention and treatment of psychiatric and neurological diseases. Although the role of Zn(2+) in the brain has been extensively studied over the past decades, methods for controlled regulation and manipulation of Zn(2+) concentrations within the brain are still in their infancy. Since the use of dietary Zn(2+) supplementation and restriction has major limitations, new methods and alternative approaches are currently under investigation, such as the use of intracranial infusion of Zn(2+) chelators or nanoparticle technologies to elevate or decrease intracellular Zn(2+) levels. Therefore, this review briefly summarizes the role of Zn(2+) in psychiatric and neurodegenerative diseases and highlights key findings and impediments of brain Zn(2+)-level manipulation. Furthermore, some methods and compounds, such as metal ion chelation, redistribution and supplementation that are used to control brain Zn(2+)-levels in order to treat brain disorders are evaluated.

Identifiers

PMID22102982
PMCPMC3220161
OpenAlexW2062570429

What OpenQuestion holds

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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.