Evidence map›Paper›PMID 22573102›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2012

Protective effects of isothiocyanates on blood-CSF barrier disruption induced by oxidative stress.

Jianming Xiang, Gina N Alesi, Ningna Zhou, Richard F Keep

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. The HAntioxidants (Basel, Switzerland) · 2021
    Article
  6. Isothiocyanates: cholinesterase inhibiting, antioxidant, and anti-inflammatory activity.Journal of enzyme inhibition and medicinal chemistry · 2018
    Article
  7. Review
  8. The Phenolic Components ofOxidative medicine and cellular longevity · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Stress-induced stimulation of choline transport in cultured choroid plexus epithelium exposed to low concentrations of cadmium.American journal of physiology. Regulatory, integrative and comparative physiology · 2014
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. 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

4 authors at 1 institution in 1 country.

Jianming XiangDepartment of Neurosurgery, Medical School, University of Michigan, Ann Arbor, MI 48109, USA. jmxxdrnx@umich.edu
Gina N Alesi
Ningna Zhou
Richard F Keep
University of Michigan–Ann Arbor · US

Funding

Endothelial Preconditioning and Ischemic Brain InjuryR01NS034709 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KEEP, RICHARD F · 1996 to 2013
$3.6M
NINDS NIH HHS NS-034709NINDS NIH HHS R01 NS034709
6 · The paper itself

Abstract

The choroid plexuses (CPs) form the blood-cerebrospinal fluid (CSF) barrier (BCSFB) and play an important role in maintaining brain normal function and the brain response to injury. Many neurological disorders are associated with oxidative stress that can impact CP function. This study examined the effects of isothiocyanates, an abundant component in cruciferous vegetables, on H(2)O(2)-induced BCSFB disruption and CP cell death in vitro. It further examined the potential role of a transcription factor, nuclear factor erythroid 2-related factor 2 (Nrf2), in isothiocyanate-induced protection. Sulforaphane (SF) significantly reduced H(2)O(2)-induced BCSFB disruption as assessed by transepithelial electrical resistance (29 ± 7% reduction vs. 92 ± 2% decrease in controls) and [(3)H]mannitol permeability. Allyl-isothiocyanate (AITC) had a similar protective effect. H(2)O(2)-induced epithelial cell death was also reduced by these isothiocyanates. In primary CP cells, SF and AITC reduced cell death by 42 ± 3% and 53 ± 10%, respectively. Similar protection was found in a CP cell line Z310. Protection was only found with pretreatment for 12-48 h and not with acute exposure (1 h). The protective effects of SF and AITC were associated with Nrf2 nuclear translocation and upregulated expression of antioxidative systems regulated by Nrf2, including heme oxygenase-1, NAD(P)H quinine oxidoreductase, and cysteine/glutamate exchange transporter. Thus isothiocyanates, as diet or medicine, may be a method for protecting BCSFB in neurological disorders.

Indexed as

AnimalsAntioxidantsApoptosisBlood-Brain BarrierCell LineCells, CulturedChoroid PlexusHydrogen PeroxideIn Vitro TechniquesIsothiocyanatesModels, AnimalNF-E2-Related Factor 2Oxidative StressRatsRats, Sprague-DawleySulfoxides2,3,4-tri-O-acetylarabinopyranosyl isothiocyanateAntioxidantsHydrogen PeroxideIsothiocyanatesNF-E2-Related Factor 2sulforaphaneSulfoxidesThiocyanates

Identifiers

PMID22573102
PMCPMC3404638
OpenAlexW2023414434

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.