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雄性和雌性肥胖 ZSF1 大鼠在肥胖诱导的射血分数保留性心力衰竭中都会出现心功能障碍。

Both male and female obese ZSF1 rats develop cardiac dysfunction in obesity-induced heart failure with preserved ejection fraction.

机构信息

Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht, The Netherlands.

Division of Experimental Cardiology, Department of Cardiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

出版信息

PLoS One. 2020 May 6;15(5):e0232399. doi: 10.1371/journal.pone.0232399. eCollection 2020.

Abstract

Heart failure with a preserved ejection fraction (HFpEF) is associated with multiple comorbidities, such as old age, hypertension, type 2 diabetes and obesity and is more prevalent in females. Although the male obese ZSF1 rat has been proposed as a suitable model to study the development of diastolic dysfunction and early HFpEF, studies in female animals have not been performed yet. Therefore, we aimed to characterize the cardiac phenotype in female obese ZSF1 rats and their lean counterparts. Additionally, we aimed to investigate whether differences exist in disease progression in obese male and female ZSF1 rats. Therefore, male and female ZSF1 rats, lean as well as obese (N = 6-9/subgroup), were used. Every two weeks, from 12 to 26 weeks of age, systolic blood pressure and echocardiographic measurements were performed, and venous blood was sampled. Female obese ZSF1 rats, as compared to female lean ZSF1 rats, developed diastolic dysfunction with cardiac hypertrophy and fibrosis in the presence of severe dyslipidemia, increased plasma growth differentiation factor 15 and mild hypertension, and preservation of systolic function. Although obese female ZSF1 rats did not develop hyperglycemia, their diastolic dysfunction was as severe as in the obese males. Taken together, the results from the present study suggest that the female obese ZSF1 rat is a relevant animal model for HFpEF with multiple comorbidities, suitable for investigating novel therapeutic interventions.

摘要

射血分数保留的心力衰竭(HFpEF)与多种合并症相关,如老年、高血压、2 型糖尿病和肥胖症,并且在女性中更为常见。尽管雄性肥胖 ZSF1 大鼠已被提议作为研究舒张功能障碍和早期 HFpEF 发展的合适模型,但尚未在雌性动物中进行研究。因此,我们旨在描述雌性肥胖 ZSF1 大鼠及其瘦型对照的心脏表型,并探讨肥胖雄性和雌性 ZSF1 大鼠的疾病进展是否存在差异。因此,使用了雄性和雌性 ZSF1 大鼠,包括瘦型和肥胖型(每组 6-9 只)。从 12 到 26 周龄,每两周进行一次收缩压和超声心动图测量,并采集静脉血样。与雌性瘦型 ZSF1 大鼠相比,雌性肥胖型 ZSF1 大鼠在严重血脂异常、血浆生长分化因子 15 增加和轻度高血压的情况下出现舒张功能障碍、心脏肥大和纤维化,并且保留了收缩功能。尽管肥胖雌性 ZSF1 大鼠没有发生高血糖,但它们的舒张功能障碍与肥胖雄性大鼠一样严重。综上所述,本研究结果表明,雌性肥胖 ZSF1 大鼠是一种具有多种合并症的 HFpEF 的相关动物模型,适合研究新的治疗干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df6d/7202634/9e2922b6cd6f/pone.0232399.g001.jpg

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