Related Experiment Video
Updated: Jun 21, 2026

A Pre-clinical Rat Model for the Study of Ischemia-reperfusion Injury in Reconstructive Microsurgery
Published on: November 8, 2019
Effect of intrauterine ischaemia-reperfusion injury on rat skin
A F Kaptanoglu1, A Solaroglu, E Okutan
1Department of Dermatology, Bayindir Hospital Ankara, Ankara, Turkey. asliozol@superonline.com
Introduction:
It was previously demonstrated that decreased maternal blood flow might create impairment in skin development. The aim of this study was to show by means of lipid peroxidation the effect of intrauterine ischaemia-reperfusion injury on fetal rat skin.
Methods:
In total, 24 female Spraque-Dawley rats, 19 days pregnant, were used. They were separated into three groups (n = 8): a control group, a sham-operated group and an experimental group. Laparotomy was performed on all three groups. In the sham-operated and experimental groups, utero-ovarian artery dissection was performed in addition. In the experimental group, fetal ischaemia was induced by clamping the utero-ovarian artery bilaterally for 30 min, and reperfusion was achieved by removing the clamps for 60 min. At the end of the experiment, the fetuses were removed by caesarean section and skin specimens were taken from the fetuses. Lipid peroxidation in the skin tissues was determined as thiobarbituric acid reactive substance (TBARS) concentration for each fetal rat. One-way ANOVA and post hoc tests were used for statistical analysis.
Results:
The level of TBARS was significantly increased in the fetal rat skin after ischaemia-reperfusion injury compared with the control group.
Conclusion:
Lipid peroxidation has an important role in intrauterine ischaemia-reperfusion-induced fetal skin damage in rats.
More Related Videos
10:24Ischemic Tissue Injury in the Dorsal Skinfold Chamber of the Mouse: A Skin Flap Model to Investigate Acute Persistent Ischemia
Published on: November 17, 2014
06:29Inducing Ischemia-reperfusion Injury in the Mouse Ear Skin for Intravital Multiphoton Imaging of Immune Responses
Published on: December 22, 2016