Premium
Does gender influence cardiovascular remodeling in C57 BL /6J mice fed a high‐fat, high‐sucrose and high‐salt diet?
Author(s) -
PereiraSilva Debora Cristina,
MachadoSilva Rayane Paula,
CastroPinheiro Camila,
FernandesSantos Caroline
Publication year - 2019
Publication title -
international journal of experimental pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.671
H-Index - 72
eISSN - 1365-2613
pISSN - 0959-9673
DOI - 10.1111/iep.12318
Subject(s) - medicine , endocrinology , muscle hypertrophy , aorta
Summary Animal models are widely used to study the physiopathology of human diseases. However, the influence of gender on modern society diet style‐induced cardiovascular disease has not thus far been explored in these models. Thus, this study investigated cardiovascular remodelling in C57 BL /6J mice fed a diet rich in saturated fat, sucrose and salt, evaluating gender effect on this process. Male and female C57 BL /6J mice were fed AIN 93M diet or a modified AIN 93M rich in fat, sucrose and salt ( HFSS ) for 12 weeks. Body mass, water and food intake and cardiovascular remodelling were assessed. The HFSS diet did not lead to body mass gain or glucose metabolism disturbance as assessed by serum glucose, insulin and oral glucose tolerance test. However, female mice on a HFSS diet had increased visceral and subcutaneous adiposity. Only male mice displayed heart hypertrophy. The left ventricle was not hypertrophied in either male or female mice, but its lumen was dilated. Intramyocardial arteries and the thoracic aorta showed media thickening in male mice, but in the female it was only observed in the thoracic aorta. Finally, intramyocardial artery dilation was present in both genders, but not in the aorta. Therefore changes in LV dimensions and arterial remodelling were influenced by both gender and the HFSS diet. In conclusion, male and female C57 BL /6J mice suffered cardiovascular remodelling after 12 weeks of HFSS feeding, although they did not develop obesity or diabetes. Sexual dimorphism occurred in response to diet for body adiposity, heart hypertrophy and intramyocardial artery remodelling.