Parental obesity predisposes male and female offspring to exacerbated cardiac dysfunction and increased mortality after myocardial infarction.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS American journal of physiology. Heart and circulatory physiology Pub Date : 2025-05-01 Epub Date: 2025-03-20 DOI:10.1152/ajpheart.00827.2024
Jussara M do Carmo, Ana C M Omoto, John E Hall, Xuemei Dai, Emily C Ladnier, Marilia C Mouro, Odecio E S Tosta, Zhen Wang, Xuan Li, Alexandre A da Silva
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Abstract

Acute myocardial infarction (MI) is a leading cause of death worldwide, accounting for >1 million deaths/year in the United States alone. Although parental obesity is a risk factor for offspring cardiovascular diseases, the impact of parental obesity on offspring outcomes after MI is unknown. This study examined if non-obese male and female offspring from obese Sprague-Dawley rat parents fed a high-fat diet (HFD-Offs, n = 11-19/sex) are at greater risk of death and worse cardiac dysfunction after MI, compared with offspring from lean parents fed a normal diet (ND-Offs, n = 12-15/sex). All offspring were fed ND from weaning and subjected to left descending coronary artery ligation at 12 wk of age to induce MI. Survival rate 24 h post-MI was examined, and cardiac function was measured by echocardiography and intraventricular catheterization with a Millar catheter on day 7 post-MI. Compared with ND-Offs, male and female HFD-Offs exhibited increased ventricular fibrillation and reduced survival post-MI (male: 37% vs. 80% and female: 55% vs. 83% for HFD-Offs and ND-Offs, respectively). In surviving rats, systolic dysfunction was more pronounced in male and female HFD-Offs compared with ND-Offs at day 7 post-MI, despite similar infarct size in all groups. We also found reductions in baseline O2 consumption rate and pyruvate-supported mitochondrial respiration, as well as increased mitochondria-derived superoxide production in cardiac fibers from HFD-Offs. Thus, parental obesity is associated with an increased 24-h mortality rate in their offspring after induction of MI and worse systolic function even when the offspring are fed a healthy diet after weaning and remain lean.NEW & NOTEWORTHY A major new finding of this study is that parental obesity markedly reduces survival rate and exacerbates cardiac dysfunction after myocardial infarction in their offspring, and this effect is independent of offspring sex.

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父母肥胖易导致男性和女性后代心肌梗死后心脏功能障碍加重,死亡率增加。
急性心肌梗死(MI)是世界范围内死亡的主要原因,仅在美国每年就有100万人死亡。虽然父母肥胖是后代心血管疾病的危险因素,但父母肥胖对心肌梗死后后代结局的影响尚不清楚。本研究考察了肥胖的spraguedawley大鼠父母喂养高脂肪饮食(hfd - off, n=11-19/性别)的非肥胖雄性和雌性后代是否比喂食正常饮食(nd - off, n=12-15/性别)的瘦父母的后代在心肌梗死后死亡风险更高,心功能障碍更严重。所有子代断奶后饲喂ND, 12周龄时行冠状动脉左降支结扎术诱导心肌梗死。心肌梗死后第7天,通过超声心动图和米勒导管测量心肌梗死后24小时存活率和心功能。与nd - off相比,男性和女性HFD-Off表现出心室颤动增加和心肌梗死后生存率降低(HFD-Off和nd - off患者男性分别为37%和80%,女性分别为55%和83%)。在存活的大鼠中,在心肌梗死后第7天,雄性和雌性hfd - off的收缩功能障碍比nd - off更明显,尽管所有组的梗死面积相似。我们还发现基线氧气消耗率和丙酮酸支持的线粒体呼吸降低,以及hfd - off心脏纤维中线粒体来源的超氧化物产生增加。因此,父母肥胖与诱导心肌梗死后后代24小时死亡率增加和收缩功能恶化有关,即使在断奶后给予健康饮食并保持苗条的情况下也是如此。
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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