Evidence map›Paper›PMID 37491673›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2024

Puerarin attenuates valproate-induced features of ASD in male mice via regulating Slc7a11-dependent ferroptosis.

Peiyan Jiang, Lianyu Zhou, Linyang Zhao, Xinghang Fei, Zhifei Wang, Tianyao Liu, Yexi Tang, Dabing Li, Hong Gong, Yi Luo and 4 more

Open access · greenAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
9.1field-weighted citation impact, top 2% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

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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

14 authors at 2 institutions in 1 country.

Peiyan Jiang *Department of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.
Lianyu Zhou *Department of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.ORCID 0000-0002-6094-683X
Linyang ZhaoDepartment of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.
Xinghang FeiDepartment of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.
Zhifei WangDepartment of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.
Tianyao LiuDepartment of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.
Yexi TangDepartment of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.
Dabing LiSchool of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Hong GongDepartment of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.
Yi LuoDepartment of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China.
Song LiThe Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Hui YangThe Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Huiling LiaoThe Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan, China. 157776358@qq.com.
Xiaotang FanDepartment of Military Cognitive Psychology, School of Psychology, Army Medical University, 400038, Chongqing, China. fanxiaotang2005@163.com.ORCID 0000-0001-5694-1828
Army Medical University · CNSouthwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a complicated, neurodevelopmental disorder characterized by social deficits and stereotyped behaviors. Accumulating evidence suggests that ferroptosis is involved in the development of ASD, but the underlying mechanism remains elusive. Puerarin has an anti-ferroptosis function. Here, we found that the administration of puerarin from P12 to P15 ameliorated the autism-associated behaviors in the VPA-exposed male mouse model of autism by inhibiting ferroptosis in neural stem cells of the hippocampus. We highlight the role of ferroptosis in the hippocampus neurogenesis and confirm that puerarin treatment inhibited iron overload, lipid peroxidation accumulation, and mitochondrial dysfunction, as well as enhanced the expression of ferroptosis inhibitory proteins, including Nrf2, GPX4, Slc7a11, and FTH1 in the hippocampus of VPA mouse model of autism. In addition, we confirmed that inhibition of xCT/Slc7a11-mediated ferroptosis occurring in the hippocampus is closely related to puerarin-exerted therapeutic effects. In conclusion, our study suggests that puerarin targets core symptoms and hippocampal neurogenesis reduction through ferroptosis inhibition, which might be a potential drug for autism intervention.

Indexed as

Autism Spectrum DisorderAutistic DisorderFerroptosisIsoflavonesAnimalsDisease Models, AnimalMaleMiceValproic AcidIsoflavonespuerarinValproic Acid

Identifiers

PMID37491673
PMCPMC10789763
OpenAlexW4385259322

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.