Evidence map›Paper›PMID 39895440›Full record

ArticleThe Journal of hand surgery2025

SARM1 Inhibition Maintains Axonal Integrity After Rat Sciatic Nerve Transection and Repair.

Ryan Sachar, Tony Y Lee, Aaron DiAntonio, Christopher J Dy, Jason Wever, Jeff Milbrandt, David M Brogan

Abstract read
In one paragraph

Article in The Journal of hand surgery, 2025. 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
–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

3 citing papers in PubMed.

  1. Review
  2. Advancing Peripheral Nerve Regeneration (Nerve SPACE 2025).Journal of hand surgery global online · 2026
    Article
  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

7 authors.

Ryan SacharDepartment of Orthopedic Surgery, Washington University in St. Louis, St. Louis, MO.
Tony Y LeeDepartment of Orthopedic Surgery, Washington University in St. Louis, St. Louis, MO.
Aaron DiAntonioDepartment of Genetics, Washington University in St. Louis, St. Louis, MO.
Christopher J DyDepartment of Orthopedic Surgery, Washington University in St. Louis, St. Louis, MO.
Jason WeverDepartment of Orthopedic Surgery, Washington University in St. Louis, St. Louis, MO.
Jeff MilbrandtDepartment of Genetics, Washington University in St. Louis, St. Louis, MO.
David M BroganDepartment of Orthopedic Surgery, Washington University in St. Louis, St. Louis, MO. Electronic address: brogand@wustl.edu.

Funding

DISSECTION OF SARM1-INDUCED AXON DEGENERATION AND CELL DEATHR01NS087632 · NINDS · WASHINGTON UNIVERSITY · PI Aaron Diantonio, JEFFREY D MILBRANDT · 2014 to 2026
$6.4M
Identification and Imaging of Skeletal Muscle Response to Graded Nerve CrushK08AR080260 · NIAMS · WASHINGTON UNIVERSITY · PI BROGAN, DAVID MICAH · 2022 to 2025
$624k
NIAMS NIH HHS K08 AR080260NINDS NIH HHS R01 NS087632
6 · The paper itself

Abstract

purposeSterile alpha and TlR motif containing-1 (SARM1) protein has been demonstrated to play a critical role in the initiation of Wallerian degeneration after nerve injury. The goal of this study was to assess whether blockade of SARM1 activity inhibits Wallerian degeneration following nerve transection, potentially promoting more rapid recovery of axonal function.

methodsAn adeno-associated virus plasmid encoded with a dominant-negative SARM1 protein fused with green fluorescent protein to impair SARM1 function, was injected into 24 juvenile rats to create a SARM1 dominant-negative (SARM1-DN) phenotype. Twenty-four control rats were injected with a control plasmid expressing only green fluorescent protein. Three weeks after transfection, the rats underwent unilateral sciatic nerve transection and repair. Walking track analysis and nonsurvival surgeries were performed at 2 days, 2 weeks, or 6 weeks to assess muscle strength and compound nerve action potential. Histomorphologic and electrodiagnostic studies were evaluated with mixed-effect analysis.

resultsHistomorphologic analysis showed maintenance of axons in the SARM1-DN animals at 2 weeks, with significantly improved compound nerve action potential amplitude. Muscle testing demonstrated greater gastrocnemius strength in SARM1 DN muscles at 2 days and 2 weeks compared to controls, although this was not maintained at 6 weeks.

conclusionInhibition of SARM1 resulted in early increases in number and myelination of axons and action potential after sciatic nerve transection and repair in SARM1-DN rats. CLINICAL RELEVANCE: SARM1 inhibition may offer the potential to delay Wallerian degeneration following nerve transection and enable earlier functional recovery of motor strength. .

Indexed as

Armadillo Domain ProteinsAxonsCytoskeletal ProteinsNerve RegenerationSciatic NerveWallerian DegenerationAnimalsDisease Models, AnimalMuscle StrengthRatsRats, Sprague-DawleyRecovery of FunctionArmadillo Domain ProteinsCytoskeletal ProteinsGene therapyperipheral nerveregenerationSARM1Wallerian degeneration

Identifiers

PMID39895440
PMCPMC12304245

What OpenQuestion holds

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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.