Evidence map›Paper›PMID 41050974›Full record

ArticlePlastic and reconstructive surgery. Global open2025

Efficacy of Batroxobin on Ischemia-Reperfusion Injury in Epigastric Artery Island Flaps in Rats.

Kotaro Imagawa, Haruchika Masuda, Daiki Morita, Shizuka Otsuka, Tadashi Akamatsu

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Article in Plastic and reconstructive surgery. Global open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kotaro ImagawaFrom the Department of Plastic Surgery, Tokai University Hachioji Hospital, Hachioji, Tokyo, Japan.
Haruchika MasudaRegenerative Medicine Research Division, Shonan Research Institute of Innovative Medicine of Shonan Kamakura General Hospital, Kamakura, Kanagawa, Japan.
Daiki MoritaDepartment of Plastic Surgery, Tokai University, Hiratsuka, Kanagawa, Japan.
Shizuka OtsukaDepartment of Plastic Surgery, Tokai University, Hiratsuka, Kanagawa, Japan.
Tadashi AkamatsuDepartment of Plastic Surgery, Tokai University, Hiratsuka, Kanagawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Batroxobin is a thrombin-like enzyme derived from snake venom that exhibits not only antithrombotic effects due to its fibrinogen-degrading effects, but also inflammatory and tissue-protective effects by inhibiting neutrophil extracellular traps (NETs). This study aimed to investigate the effects of batroxobin on NET suppression and flap necrosis reduction in a rat island flap ischemia-reperfusion injury (IRI) model. Methods: An island flap was created on the abdominal wall of a rat. The vascular pedicle was clamped for 6 hours and then released to establish the IRI model. Batroxobin (10 BU/kg) was administered intraperitoneally at the time of clamp release in the experimental group, whereas the control group received normal saline. The extent of blood perfusion within the flap was assessed using laser Doppler imaging, and NET expression was evaluated via S100A9 staining. Results: Laser Doppler imaging exhibited the accelerated reperfusion area in batroxobin-treated rats compared with controls; 7 days postreperfusion, the rate of recovered area was 78.1% in the batroxobin group versus 44.6% in the control group. Histological analysis at 48 hours postreperfusion by S100A9 staining showed significantly reduced NETs in the batroxobin group; the S100A9-positive cells were 199.4 ± 63.7 per low power field in the batroxobin group versus 352.0 ± 76.4 per low power field in the control group. These findings indicate that batroxobin effectively preserved blood perfusion with a protective effect against tissue injury in the flap IRI model. Conclusions: These findings suggest that batroxobin may serve as a promising therapeutic agent for mitigating inflammatory tissue damage caused by IRI.

Identifiers

PMID41050974
PMCPMC12494047

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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.