Volume 19 Supplement 2

Eighth International Symposium on Intensive Care and Emergency Medicine for Latin America

Open Access

Brain death and changes in solid organ characteristics due to acute lack of female sex hormones

  • Roberto Armstrong Junior1,
  • Ana Cristina B Faloppa1,
  • Guilherme K Kudo1,
  • Luiz Felipe P Moreira1,
  • Paulina Sannomiya1,
  • Raif R Simão1 and
  • Sueli G Ferreira1
Critical Care201519(Suppl 2):P50


Published: 28 September 2015


Previous studies have suggested that female sex hormones have a protective action, because they contribute to reduce the inflammatory degree in females after trauma.


This study aimed to investigate sex differences in the course of the inflammatory process in rats subjected to brain death (BD).


Wistar rats were randomized into three groups (male rats, n = 5; female rats, n = 10; and ovariectomized rats, n = 5) and subjected to BD by rapid inflation of a catheter Fogarty® 4F. The liver, kidneys, lungs and the heart were collected after 6 hours and samples (4 µm) were stained with H&E for histological analyses. Leukocyte infiltration, edema and hemorrhage were measured and data were compared using GraphPad Prism v.6.10, and p values lower than 0.05 were considered significant.


Female rats exhibited increased leukocyte infiltration into the lungs and the heart when compared with male rats (p = 0.009 in the lungs and p = 0.022 in the heart) and presented also a sudden decrease in estradiol levels 6 hours after BD (p = 0.01). The intensity of hemorrhage was greater in ovariectomized rats compared with the other groups (p = 0.001) in the lungs. All groups presented slight to moderate leukocyte infiltration and absence to slight hemorrhage in the liver. Leukocyte infiltration had a wide distribution in female rat kidneys, and in male and ovariectomized rat kidneys infiltration varied from absent to slight.


The increased inflammation in the lungs and heart of female rats might be a result of the lack of female sex hormones. Therefore, the idea of introducing a therapeutic use of female sex hormones on female BD donors could be considered.



Financial support: FAPESP 2013/20282-0.

Authors’ Affiliations

Heart Institute (INCOR), University of São Paulo Medical School


© Junior et al.; 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.