Evidence map›Paper›PMID 41964710›Full record

ReviewCellular and molecular neurobiology2026

Metabolic Symbiosis and Vulnerability in the CNS Axon-Myelin Unit.

Kun Miao, Meng Meng, Liangjing Liu, Meiyu Li, Yuanyuan Bai, Ying Guo, Guohui Zhang, Jiming Kong, Jiao Mu

Abstract readReview
In one paragraph

Review in Cellular and molecular neurobiology, 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.

Kun Miao *Department of Pathology, Hebei North University, No. 11 Zuanshinan Road, Zhangjiakou, 075000, Hebei, PR China.ORCID http://orcid.org/0009-0000-3953-776X
Meng Meng *Department of Forensic Medicine, Hebei North University, No. 11 Zuanshinan Road, Zhangjiakou, 075000, Hebei, PR China.ORCID http://orcid.org/0009-0009-8922-7087
Liangjing LiuDepartment of Pharmacy, Hebei North University, Hebei Key Laboratory of Neuropharmacology, No. 11 Zuanshinan Road, Zhangjiakou, 075000, Hebei, PR China.
Meiyu LiDepartment of Pathology, Hebei North University, No. 11 Zuanshinan Road, Zhangjiakou, 075000, Hebei, PR China.
Yuanyuan BaiDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China.
Ying GuoDepartment of Pathology, Hebei North University, No. 11 Zuanshinan Road, Zhangjiakou, 075000, Hebei, PR China.
Guohui ZhangDepartment of Pathology, Hebei North University, No. 11 Zuanshinan Road, Zhangjiakou, 075000, Hebei, PR China. 18931316008@163.com.
Jiming KongDepartment of Human Anatomy and Cell Science, Rady Faculty of Health Sciences, Faculty of Medicine, Max Rady College of Medicine, University of Manitoba, 745 Bannatyne, Winnipeg, MB, R3E 0J9, Canada. jiming.kong@umanitoba.ca.ORCID http://orcid.org/0000-0002-2859-9831
Jiao MuDepartment of Pathology, Hebei North University, No. 11 Zuanshinan Road, Zhangjiakou, 075000, Hebei, PR China. m18931315882_1@163.com.ORCID http://orcid.org/0000-0002-3488-0056

Funding

Hebei North University Doctoral Start-up Funding Project BSJJ202512the Natural Science Foundation of Hebei Province C2024405023
6 · The paper itself

Abstract

Axonal degeneration and demyelination are common pathological phenotypes in central nervous system (CNS) injury and degenerative diseases. Axonal and myelin diseases have generally been considered distinct phenomena, although our knowledge of why the axon-myelin unit (AMU), as a highly interconnected structure, serves as a common point of vulnerability to damage remains inadequate. In this review, we first reaffirm that the tight biological interconnections between axons and myelin should be recognized as a "symbiotic" unit across development, metabolism, and disease progression. Second, we systematically delineate the fundamental structural architecture and metabolic coupling of AMU. Third, we analyze how the impairment of one component of AMU influences the survival and functional integrity of others. In conclusion, we present a unique conceptual framework indicating that therapeutic methods targeting bioenergetic support in the CNS should concentrate on the energy coupling pathways and damage-crossover mechanisms of the AMU.

Indexed as

AxonsCentral Nervous SystemMyelin SheathAnimalsDemyelinating DiseasesEnergy MetabolismHomeostasisHumansNeurodegenerative DiseasesAxonal degenerationAxon-myelin unitDemyelination.Lactate shuttleMCT1Metabolic coupling

Identifiers

PMID41964710
PMCPMC13184064

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.