Heart and Vascular Centre, Semmelweis University, Budapest, Hungary.
Faculty of Medicine, Institute of Surgical Pathology, University of Freiburg Medical Center, Freiburg, Germany.
Am J Physiol Heart Circ Physiol. 2022 Jul 1;323(1):H204-H222. doi: 10.1152/ajpheart.00654.2021. Epub 2022 Jun 10.
Investigating the effect of sex on pressure unloading therapy in a clinical scenario is limited by several nonstandardized factors. Hence, we sought to study sex-related similarities and differences under laboratory conditions. Pressure overload was induced in male and female rats by aortic banding (AB) for 6 and 12 wk. Age-matched sham-operated animals served as controls. Pressure unloading was performed by aortic debanding at . Different aspects of myocardial remodeling were characterized by echocardiography, pressure-volume analysis, histology, qRT-PCR, and explorative proteomics. Hypertrophy, increased fetal gene expression, interstitial fibrosis, and prolonged active relaxation were noted in the AB groups at in both sexes. However, decompensation of systolic function and further deterioration of diastolic function only occurred in male AB rats at . AB induced similar proteomic alterations in both sexes at , whereas characteristic differences were found at . After debanding, regression of hypertrophy and recovery of diastolic function took place to a similar extent in both sexes. Nevertheless, fibrosis, transcription of β-myosin-to-α-myosin heavy chain ratio, and myocardial proteomic alterations were reduced to a greater degree in females than in males. Debanding exposed anti-remodeling properties in both sexes and prevented the functional decline in males. Female sex is associated with greater reversibility of fibrosis, fetal gene expression, and proteomic alterations. Nevertheless, pressure unloading exposes a more pronounced anti-remodeling effect on the functional level in males, which is attributed to the more progressive functional deterioration in AB animals. The present study is the first to assess the role of sex on pressure unloading-induced reverse and anti-remodeling in a rat model of aortic banding and debanding. Our data indicate that female sex is associated with a greater reversibility of fibrosis, fetal gene expression, and proteomic alterations compared with males. Nevertheless, pressure unloading exposes more anti-remodeling effect on the functional level in males, which is attributed to the more rapid functional deterioration in aortic-banded animals.
在临床情况下,研究性别对减压治疗的影响受到几个非标准化因素的限制。因此,我们试图在实验室条件下研究性别相关的相似性和差异。通过主动脉缩窄(AB)在雄性和雌性大鼠中诱导压力超负荷,持续 6 和 12 周。年龄匹配的假手术动物作为对照。在. 时通过主动脉解缚来实现减压。通过超声心动图、压力-容积分析、组织学、qRT-PCR 和探索性蛋白质组学来描述心肌重构的不同方面。在 AB 组中,在两种性别中,在 时均观察到心肌肥厚、胎儿基因表达增加、间质纤维化和主动松弛延长。然而,只有雄性 AB 大鼠在 时才出现收缩功能失代偿和舒张功能进一步恶化。AB 在两种性别中在 时引起相似的蛋白质组改变,而在 时则发现特征性差异。解缚后,两种性别中肥厚的消退和舒张功能的恢复程度相似。然而,纤维化、β-肌球蛋白到α-肌球蛋白重链比值的转录和心肌蛋白质组改变在雌性中比在雄性中降低得更显著。解缚暴露了两性的抗重构特性,并防止了雄性的功能下降。雌性与纤维化、胎儿基因表达和蛋白质组改变的更大逆转程度相关。然而,在功能水平上,减压暴露了雄性更明显的抗重构作用,这归因于 AB 动物中更渐进的功能恶化。本研究首次评估了性别对主动脉缩窄和解缚大鼠模型中减压诱导的逆转和抗重构的作用。我们的数据表明,与雄性相比,雌性与纤维化、胎儿基因表达和蛋白质组改变的更大逆转程度相关。然而,在功能水平上,减压暴露了雄性更明显的抗重构作用,这归因于 AB 动物中更快速的功能恶化。