Evidence map›Paper›PMID 36375633›Full record

ArticleNeurochemistry international2023

Efficacy of novel SPAK inhibitor ZT-1a derivatives (1c, 1d, 1g & 1h) on improving post-stroke neurological outcome and brain lesion in mice.

Mohammad Iqbal H Bhuiyan, Sydney Fischer, Shivani M Patel, Helena Oft, Ting Zhang, Lesley M Foley, Jinwei Zhang, T Kevin Hitchens, Bradley J Molyneaux, Xianming Deng and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Neurochemistry international, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

11 authors at 5 institutions in 3 countries.

Mohammad Iqbal H BhuiyanDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, 15213, USA; Pittsburgh Institute for Neurodegenerative Disorders, University of Pittsburgh, Pittsburgh, PA, 15260, USA; Veterans Affairs Pittsburgh Health Care System, Geriatric Research, Educational and Clinical Center, Pittsburgh, PA, 15213, USA; Department of Pharmaceutical Sciences, School of Pharmacy, University of Texas at El Paso, El Paso, TX, 79968, USA.
Sydney FischerDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, 15213, USA; Pittsburgh Institute for Neurodegenerative Disorders, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
Shivani M PatelDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, 15213, USA; Pittsburgh Institute for Neurodegenerative Disorders, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
Helena OftDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, 15213, USA; Pittsburgh Institute for Neurodegenerative Disorders, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
Ting ZhangState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Xiamen University, Xiamen, Fujian, China.
Lesley M FoleyAnimal Imaging Center, University of Pittsburgh, Pittsburgh, PA, 15203, USA.
Jinwei ZhangInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, Hatherly Laboratory, Exeter, UK.
T Kevin HitchensAnimal Imaging Center, University of Pittsburgh, Pittsburgh, PA, 15203, USA; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, 15213, USA.
Bradley J MolyneauxDepartment of Neurology, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Xianming DengState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Xiamen University, Xiamen, Fujian, China.
Dandan SunDepartment of Neurology, University of Pittsburgh, Pittsburgh, PA, 15213, USA; Pittsburgh Institute for Neurodegenerative Disorders, University of Pittsburgh, Pittsburgh, PA, 15260, USA; Veterans Affairs Pittsburgh Health Care System, Geriatric Research, Educational and Clinical Center, Pittsburgh, PA, 15213, USA. Electronic address: sund@upmc.edu.
University of Pittsburgh · USInstitute for Neurodegenerative Disorders · USXiamen University · CNBrigham and Women's Hospital · USUniversity of Exeter · GB

Funding

Astrocytic WNK-SPAK-NKCC1 Cascade in White Matter Astrogliosis and InjuryR01NS119166 · NINDS · UNIVERSITY OF TEXAS EL PASO · PI Mohammad Iqbal Hossain Bhuiyan · 2022 to 2026
$2.3M
WNK as therapeutic targets for ischemic strokeI01BX002891 · VA · VETERANS HEALTH ADMINISTRATION · PI SUN, DANDAN · 2016 to 2025
–
BLRD Research Career Scientist Award ApplicationIK6BX005647 · VA · VETERANS HEALTH ADMINISTRATION · PI Dandan Sun · 2021 to 2026
–
BLRD VA I01 BX002891BLRD VA I01 BX006372BLRD VA IK6 BX005647NINDS NIH HHS R01 NS119166
6 · The paper itself

Abstract

SPAK inhibitor ZT-1a was previously shown to be neuroprotective in murine ischemic stroke models. In this study, we further examined the efficacy of four ZT-1a derivatives (ZT-1c, -1d, -1g and -1h) on reducing stroke-induced sensorimotor function impairment and brain lesions. Vehicle control (Veh) or ZT-1 derivatives were administered via osmotic pump to adult C57BL/6J mice during 3-21 h post-stroke. Neurological behavior of these mice was assessed at days 1, 3, 5, and 7 post-stroke and MRI T2WI and DTI analysis was subsequently conducted in ex vivo brains. Veh-treated stroke mice displayed sensorimotor function deficits compared to Sham mice. In contrast, mice receiving ZT-1a derivatives displayed significantly lower neurological deficits at days 3-7 post-stroke (p < 0.05), with ZT-1a, ZT-1c and ZT-1d showing greater impact than ZT-1h and ZT-1g. ZT-1a treatment was the most effective in reducing brain lesion volume on T2WI and in preserving NeuN + neurons (p < 0.01), followed by ZT-1d > -1c > -1g > -1h. The Veh-treated stroke mice displayed white matter tissue injury, reflected by reduced fractional anisotropy (FA) or axial diffusivity (AD) values in external capsule, internal capsule and hippocampus. In contrast, only ZT-1a-as well as ZT-1c-treated stroke mice exhibited significantly higher FA and AD values. These findings demonstrate that post-stroke administration of SPAK inhibitor ZT-1a and its derivatives (ZT-1c and ZT-1d) is effective in protecting gray and white matter tissues in ischemic brains, showing a potential for ischemic stroke therapy development.

Indexed as

Brain InjuriesIschemic StrokeNervous System DiseasesStrokeWhite MatterAnimalsBrainMiceMice, Inbred C57BLDTIIschemic strokeMRINeurodegenerationSPAK

Identifiers

PMID36375633
PMCPMC9839627
OpenAlexW4309095240

What OpenQuestion holds

Textmetadata
LicenceTDM
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.