中度慢性主动脉收缩对大鼠心脏和骨骼肌产生适度的、性别特异性的影响

IF 1.7 Q3 PHYSIOLOGY
William S. Evans , Yuan Liu , Maria Clara Canellas Da Silva , Harry Zichen Li , Steven J. Prior , Sarah Kuzmiak-Glancy
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引用次数: 0

摘要

保留射血分数的心力衰竭(HFpEF)占心力衰竭诊断的约50%,发生在老年人中,女性比男性更普遍,并且高血压是一个因素。我们试图确定雄性和雌性大鼠的长期、中度、横向主动脉收缩是否会诱导心室肥厚和保留射血分数,骨骼肌质量和力量的变化,以及这些结果的性别特异性差异,模拟HFpEF。在4周龄时对雄性和雌性大鼠行主动脉横缩术(TAC),术后40周处死大鼠,并进行超声心动图和握力测量。雄性TAC大鼠的心脏质量比Sham大鼠高12%,心脏与身体质量比高17%;然而,这些参数在雌性TAC大鼠和Sham大鼠之间没有差异。TAC大鼠表现出保留射血分数,TAC对骨骼肌大小和力量没有影响。综上所述,雄性大鼠比雌性大鼠更容易受到tac诱导的压力过载肥大的影响,这种适度的收缩导致射血分数尽管持续时间很长,但仍保持不变。总的来说,这些研究表明,在没有合并症的情况下,压力过载对心肌和骨骼肌产生适度的、性别特异性的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Moderate chronic aortic constriction induces modest, sex-specific effects on rat hearts and skeletal muscle
Heart failure with preserved ejection fraction (HFpEF) accounts for ∼50 % of heart failure diagnoses, occurs in older individuals, is more prevalent in females than males, and includes hypertension as contributing factor. We sought to determine whether a long-term, moderate, transverse aortic constriction in male and female rats induces ventricular hypertrophy and preserved ejection fraction, changes in skeletal muscle mass and strength, and sex-specific differences in these outcomes, mimicking HFpEF. Transverse aortic constriction (TAC) surgery was performed on male and female rats at 4 weeks of age, and rats were sacrificed 40 weeks after surgery, following echocardiography and grip strength measures. Male TAC rats demonstrated a 12 % greater heart mass and 17 % higher heart to body mass ratio than Sham rats; however, these parameters did not differ between female TAC and Sham rats. TAC rats demonstrated a preserved ejection fraction, and TAC had no effect on skeletal muscle size or strength. In summary, male rats were more susceptible to TAC-induced pressure-overload hypertrophy than female rats, and this moderate constriction resulted in preserved ejection fraction despite a long time course. Collectively, these investigations reveal, in the absence of comorbidities, pressure overload produces modest, sex-specific effects in the myocardium and skeletal muscle.
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CiteScore
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