雌雄肥胖瘦ZSF1大鼠肾损伤与肥胖的关系及高血压的加性效应。

IF 3.7 2区 医学 Q1 PHYSIOLOGY American Journal of Physiology-renal Physiology Pub Date : 2023-07-01 DOI:10.1152/ajprenal.00286.2022
Isabel T N Nguyen, Maarten J Cramer, Jaap A Joles, Marianne C Verhaar
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引用次数: 0

摘要

保留射血分数的心力衰竭(HFpEF)以肥胖、高血压、糖尿病和慢性肾脏疾病为特征。肥胖的ZSF1大鼠,HFpEF的一个模型,表现出多种这样的合并症,可以扰乱心脏功能。很少有人关注这些合并症如何影响ZSF1大鼠的肾脏疾病。HFpEF主要见于肥胖和高血压特别普遍的女性。因此,我们描述了雌性和雄性瘦和肥胖的ZSF1大鼠的肾脏表型,并研究了高血压恶化对疾病严重程度的其他影响。从12周到26周,每两周评估一次收缩压和肾功能。从第19周开始,大鼠被植入醋酸脱氧皮质酮颗粒并喂食高盐饮食(DS),或安慰剂颗粒并喂食正常盐饮食。在26周龄时,通过异氟醚下菊粉清除率评估终末肾小球滤过率。肾切片进行组织学分析。瘦和肥胖的ZSF1大鼠,无论是雌性还是雄性,都有轻度高血压(收缩压:140-150 mmHg)。所有肥胖ZSF1大鼠均出现HFpEF。在正常血糖的雌性ZSF1大鼠中,肥胖与轻度蛋白尿、肾小球滤过率降低和肾小球肥大有关。ds加重的高血压加重蛋白尿并引发肾小球硬化。雄性肥胖ZSF1大鼠出现高血糖、蛋白尿、肾小球肥大、硬化、小管间质损伤。ds加重的高血压加重了雄性ZSF1大鼠的这种表型。综上所述,雌性肥胖ZSF1大鼠出现轻度肾功能障碍,正常血糖的雌性肥胖ZSF1大鼠与高血糖的雄性肥胖ZSF1大鼠一样,ds加重的高血压损害了肾脏功能和结构。慢性肾脏疾病与心力衰竭并发射血分数(HFpEF),与多种合并症和女性相关。我们发现肥胖,轻度高血压的雌性ZSF1大鼠,HFpEF的动物模型,同时发生肾脏疾病和舒张功能障碍。在正常血糖肥胖的雌性ZSF1大鼠和高血糖肥胖的雄性ZSF1大鼠中,高血压的加重(HFpEF中非常普遍的合并症)损害了肾功能和结构。
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Renal injury in relation to obesity and the additive effect of hypertension in female and male obese and lean ZSF1 rats.

Heart failure with preserved ejection fraction (HFpEF) is characterized by obesity, hypertension, diabetes mellitus, and chronic kidney disease. Obese ZSF1 rats, a model of HFpEF, exhibit multiple such comorbidities that can disturb cardiac function. Little attention has been paid to how these comorbidities affect renal disease in ZSF1 rats. HFpEF is found predominantly in women in whom obesity and hypertension are particularly prevalent. Therefore, we characterized the renal phenotype in female and male lean and obese ZSF1 rats and investigated additional effects of worsened hypertension on disease severity. Systolic blood pressure and renal function were assessed biweekly from 12 to 26 wk. From 19 wk, rats were implanted with either a deoxycorticosterone acetate pellet and fed a high-salt diet (DS) or a placebo pellet and fed a normal-salt diet. At 26 wk of age, terminal glomerular filtration rate was assessed via inulin clearance under isoflurane. Renal sections were processed for histological analysis. Lean and obese ZSF1 rats, both female and male, were mildly hypertensive (systolic blood pressure: 140-150 mmHg). All obese ZSF1 rats showed HFpEF. In female normoglycemic ZSF1 rats, obesity associated with mild proteinuria, decreased glomerular filtration rate, and glomerular hypertrophy. DS-worsened hypertension enhanced proteinuria and triggered glomerulosclerosis. Male obese ZSF1 rats were hyperglycemic and showed proteinuria, glomerular hypertrophy and sclerosis, and tubulointerstitial damage. DS-worsened hypertension aggravated this phenotype in male ZSF1 rats. In conclusion, female obese ZSF1 rats develop mild renal dysfunction and DS-worsened hypertension compromises renal function and structure in normoglycemic female obese ZSF1 rats as in hyperglycemic male obese ZSF1 rats.NEW & NOTEWORTHY Chronic kidney disease coexists with heart failure with a preserved ejection fraction (HFpEF), which is associated with multiple comorbidities and the female sex. We showed that obese, mildly hypertensive female ZSF1 rats, an animal model for HFpEF, simultaneously develop renal disease with diastolic dysfunction. Exacerbation of their hypertension, a comorbidity highly prevalent in HFpEF, compromised renal function and structure similarly in normoglycemic obese female ZSF1 rats and hyperglycemic obese male ZSF1 rats.

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来源期刊
CiteScore
8.40
自引率
7.10%
发文量
154
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology - Renal Physiology publishes original manuscripts on timely topics in both basic science and clinical research. Published articles address a broad range of subjects relating to the kidney and urinary tract, and may involve human or animal models, individual cell types, and isolated membrane systems. Also covered are the pathophysiological basis of renal disease processes, regulation of body fluids, and clinical research that provides mechanistic insights. Studies of renal function may be conducted using a wide range of approaches, such as biochemistry, immunology, genetics, mathematical modeling, molecular biology, as well as physiological and clinical methodologies.
期刊最新文献
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