Evidence map›Paper›PMID 42771220›Full record

ReviewMolecular biology reports2026

Dysregulated polyamine metabolism in neurological disorders: molecular mechanisms and therapeutic opportunities.

Kehua Li, Qiongya Si, Chunxiang Zhang, Chaojie Zhang, Mengyao Wang, Jingnan Liu, Jianhua Zhao, Hongxia Xing, Junli Liu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kehua Li *Brain Hospital, Henan Medical Key Laboratory of Neurology, Henan Joint International Laboratory of Neurorestoratology for Senile Dementia, Henan Engineering Research Center for Neurorestoratology, Henan Engineering Technology Research Center for Neurorestoratology, Henan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China.ORCID http://orcid.org/0009-0006-9429-9438
Qiongya SiBrain Hospital, Henan Medical Key Laboratory of Neurology, Henan Joint International Laboratory of Neurorestoratology for Senile Dementia, Henan Engineering Research Center for Neurorestoratology, Henan Engineering Technology Research Center for Neurorestoratology, Henan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China.
Chunxiang ZhangBrain Hospital, Henan Medical Key Laboratory of Neurology, Henan Joint International Laboratory of Neurorestoratology for Senile Dementia, Henan Engineering Research Center for Neurorestoratology, Henan Engineering Technology Research Center for Neurorestoratology, Henan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China.
Chaojie ZhangBrain Hospital, Henan Medical Key Laboratory of Neurology, Henan Joint International Laboratory of Neurorestoratology for Senile Dementia, Henan Engineering Research Center for Neurorestoratology, Henan Engineering Technology Research Center for Neurorestoratology, Henan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China.
Mengyao WangBrain Hospital, Henan Medical Key Laboratory of Neurology, Henan Joint International Laboratory of Neurorestoratology for Senile Dementia, Henan Engineering Research Center for Neurorestoratology, Henan Engineering Technology Research Center for Neurorestoratology, Henan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China.
Jingnan LiuDivision of Breast Surgery, Department of General Surgery, The First Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China.
Jianhua ZhaoBrain Hospital, Henan Medical Key Laboratory of Neurology, Henan Joint International Laboratory of Neurorestoratology for Senile Dementia, Henan Engineering Research Center for Neurorestoratology, Henan Engineering Technology Research Center for Neurorestoratology, Henan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China.
Hongxia XingThe Third Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China. xhxwh02@163.com.
Junli Liu *Brain Hospital, Henan Medical Key Laboratory of Neurology, Henan Joint International Laboratory of Neurorestoratology for Senile Dementia, Henan Engineering Research Center for Neurorestoratology, Henan Engineering Technology Research Center for Neurorestoratology, Henan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, 453100, Henan, China. 1fy2018008@xxmu.edu.cn.ORCID http://orcid.org/0000-0001-7403-4383

Funding

The Graduate Research Innovation Support Program of Henan Medical University No. YJSCX202502Zthe Henan High-level Talent International Training Project No. GCC2026048the Henan Medical Researcher Overseas Training Program No. HNMOTO2025081the Henan Natural Science Foundation Project No. 262300420548the Henan Provincial Health Commission No. LHGJ20190457the Key Scientific Research Project Plan of Higher Education Institutions in Henan Province No. 25A320037
6 · The paper itself

Abstract

Polyamines (PAs), principally putrescine (Put), spermidine (Spd), and spermine (Spm), are ubiquitous aliphatic polycations that regulate nucleic-acid interactions, ion-channel activity, autophagy, redox balance, proteostasis, and immune signaling. Growing genetic, multi-omics, and experimental evidence indicates that disruption of PA biosynthesis, catabolism, acetylation, and transport contributes to neurological disease. In Alzheimer's disease (AD), altered PA flux intersects with Tau and amyloid-β (Aβ) pathology, methylation imbalance, oxidative stress, and impaired autophagic clearance. In Parkinson's disease (PD), PA transport and interconversion are linked to lysosomal dysfunction, mitochondrial stress, and α-synuclein toxicity; ATP13A2-associated Kufor-Rakeb syndrome further illustrates the neurological consequences of defective lysosomal PA transport. PA dysregulation is also implicated in amyotrophic lateral sclerosis (ALS), diabetic retinopathy, Snyder-Robinson syndrome, epilepsy, Bachmann-Bupp syndrome, and cerebral ischemia. This review integrates disease-specific evidence with four interconnected mechanisms-autophagy, oxidative stress, proteostasis, and neuroinflammation-and discusses therapeutic approaches including direct Spd administration, modulation of PA-metabolic enzymes and transporters, and combination strategies. Because PAs can exert both protective and toxic effects depending on concentration, cellular compartment, and disease context, translation will require CNS-relevant biomarkers, dose and route optimization, and explicit consideration of blood-brain barrier constraints.

Indexed as

Nervous System DiseasesPolyaminesAnimalsAutophagyHumansOxidative StressSpermidinePolyaminesSpermidineAutophagyNeurodegenerationOxidative stressPolyamine metabolismTauopathyTherapeutic targets

Identifiers

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.