Evidence map›Paper›PMID 40993404›Full record

ArticleLab animal2025

A longitudinal rat forelimb model for assessing in vivo neuromuscular function following extremity reperfusion injury.

Omar A Selim, Aida Sarcon, Mehmet Tunaboylu, Chunfeng Zhao, Steven L Moran

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In one paragraph

Article in Lab animal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Omar A SelimDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA. selim.omar@mayo.edu.ORCID 0000-0002-4178-2227
Aida SarconDivision of Plastic Surgery, Mayo Clinic, Rochester, MN, USA.
Mehmet TunaboyluDivision of Plastic Surgery, Mayo Clinic, Rochester, MN, USA.ORCID 0009-0004-3859-5166
Chunfeng ZhaoDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA.
Steven L MoranDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA.

Funding

U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) T32 AR56950.
6 · The paper itself

Abstract

Rhabdomyolysis following revascularization of the ischemic upper extremity can lead to life- and limb-threatening sequelae. In the context of replantations and vascularized composite allografting, a reconstructive procedure usually reserved for upper limb amputees, prolonged tissue ischemia is detrimental to extremity functional recovery. Currently, validated survival small animal models of extremity reperfusion injury that permit longitudinal assessment of limb function are lacking. So far, studies that evaluated reperfusion injury-induced neuromuscular impairment have relied on terminal ex vivo procedures and did not provide clinically translatable measurements. Here we present a reliable rat model of extremity post-reperfusion syndrome (PRS) that comprehensively recapitulates the biochemical hallmarks of rhabdomyolysis secondary to upper-extremity reperfusion injury and allows the monitoring of in vivo upper limb function using clinically relevant electrodiagnostic and kinematic metrics. In addition to inducing severe metabolic derangements, our forelimb PRS model provided insights on gross motor and electrophysiological alterations following upper-extremity reperfusion injury. We identify gait coordination parameters-such as stride frequency and the forelimb-hindlimb coordination index-and electrophysiological metrics, including compound muscle action potential amplitude, as objective and noninvasive outcome measures for assessing limb function in small animal models of extremity PRS. This comprehensive, validated functional model can serve as an invaluable tool to evaluate therapeutics or preconditioning regimens to attenuate PRS and mitigate resulting neuromuscular dysfunction.

Indexed as

Disease Models, AnimalForelimbReperfusion InjuryRhabdomyolysisAnimalsMaleMuscle, SkeletalRats

Identifiers

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Registered trials

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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.