Evidence map›Paper›PMID 36291328›Full record

ArticleBrain sciences2022

Embryonic Deletion of TXNIP in GABAergic Neurons Enhanced Oxidative Stress in PV+ Interneurons in Primary Somatosensory Cortex of Aging Mice: Relevance to Schizophrenia.

Ting Xue, Xiaodan Wang, Ying Hu, Ying Cheng, Han Li, Yuan Shi, Lijun Wang, Dongmin Yin, Donghong Cui

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 55% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
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

9 authors at 3 institutions in 1 country.

Ting XueShanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China.ORCID 0000-0002-3650-6308
Xiaodan WangShanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China.
Ying HuShenzhi Department of the Fourth Affiliated Hospital of Xinjiang Medical University, Urumqi 830000, China.
Ying ChengShanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China.
Han LiShanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China.
Yuan ShiShanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China.
Lijun WangShanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China.
Dongmin YinKey Laboratory of Brain Functional Genomics, Ministry of Education and Shanghai, School of Life Science, East China Normal University, Shanghai 200062, China.
Donghong CuiShanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China.
Shanghai Jiao Tong University · CNEast China Normal University · CNXinjiang Medical University · CN

Funding

National Natural Science Foundation of China 81671336National Natural Science Foundation of China 81801324Shanghai Natural Science Foundation 21ZR1455300Shanghai Sailing Program 17YF141630
6 · The paper itself

Abstract

The brain is susceptible to perturbations of redox balance, affecting neurogenesis and increasing the risks of psychiatric disorders. Thioredoxin-interacting protein (TXNIP) is an endogenous inhibitor of the thioredoxin antioxidant system. Its deletion or inhibition suggests protection for a brain with ischemic stroke or Alzheimer's disease. Combined with conditional knockout mice and schizophrenia samples, we aimed to investigate the function of TXNIP in healthy brain and psychiatric disorders, which are under-studied. We found TXNIP was remarkedly expressed in the prefrontal cortex (PFC) during healthy mice's prenatal and early postnatal periods, whereas it rapidly decreased throughout adulthood. During early life, TXNIP was primarily distributed in inhibitory and excitatory neurons. Contrary to the protective effect, the embryonic deletion of TXNIP in GABAergic (gamma-aminobutyric acid-ergic) neurons enhanced oxidative stress in PV

Indexed as

agingdeveloping brainGABAergicoxidative stressschizophreniathioredoxin-interacting protein (TXNIP)

Identifiers

PMID36291328
PMCPMC9599691
OpenAlexW4306362098

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.