Evidence map›Paper›PMID 40260983›Full record

ArticleVeterinary medicine and science2025

Ethyl Pyruvate Injection Enhances the Ischaemic Zone Viability in Burn Wounds in Rats.

Hossein Khoori Babalhakam, Mohsen Maleki, Mohammad Foad Noorbakhsh, Khosro Safari Nikroo, Farzad Hayati

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Article in Veterinary medicine and science, 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
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hossein Khoori BabalhakamDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.
Mohsen MalekiDepartment of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.ORCID 0000-0001-7064-8193
Mohammad Foad NoorbakhshDepartment of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Khosro Safari NikrooDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.
Farzad HayatiDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveBurn injuries are a significant clinical challenge due to excessive oxidative stress, inflammation and progressive tissue necrosis, leading to delayed healing and functional impairment. Ethyl pyruvate (EP) has been shown to possess potent anti-inflammatory, antioxidant, anti-apoptotic and anti-fibrotic properties, making it a promising therapeutic agent for burn wound treatment. This study aimed to evaluate the efficacy of EP in promoting burn wound healing and preventing tissue necrosis.

methodFollowing the induction of thermal damage, 30 male Wistar rats were randomly allocated to one of three distinct groups. The Test 1 group received EP 30 min, 12, 24, 36, 48, 60 and 72 h post-injury, and the Test 2 group was treated with a single dose of EP 30 min post-thermal injury. The control group received a single intraperitoneal (IP) injection of an equivalent volume of normal saline solution (0.9%). On the 3rd and 21st days after the injury, five rats from each group were euthanized. Macroscopic, histopathological and immunohistochemical assessments were performed along with biochemical evaluations that included malondialdehyde (MDA), total antioxidant capacity (TAC) and HP measurements.

resultsThe positive effects of EP on reducing and controlling oxidative stress, inflammation and death were achieved. Generally, inflammation control further preservation of the stasis zone and accelerated healing in the coagulation area were also proven.

conclusionThis study revealed that administering EP through injection can effectively halt the ongoing tissue necrosis in the stasis zone and significantly promote wound healing, primarily due to its anti-inflammatory and antioxidant properties.

Indexed as

BurnsPyruvatesWound HealingAnimalsAntioxidantsMaleOxidative StressRandom AllocationRatsRats, WistarAntioxidantsethyl pyruvatePyruvatesburnethyl pyruvatehealingratskinwound

Identifiers

PMID40260983
PMCPMC12012845

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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.