Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Kidney Research Centre, Division of Nephrology, Department of Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
PLoS One. 2023 Feb 2;18(2):e0281123. doi: 10.1371/journal.pone.0281123. eCollection 2023.
Chronic kidney disease (CKD) is a worldwide health burden with increases risk of end-stage renal function if left untreated. CKD induced in the context of metabolic syndrome (MS) increases risks of hypertension, hyperglycemia, excess body fat and dyslipidemia. To test if combining a high-fat diet (HFD) regimen onto the hypertensive/ diabetic phenotype would mimic features of MS induced-CKD in mice, hyperglycemia was induced in genetically hypertensive mice (Lin), followed by HFD regimen. For that, 8-week-old male were subjected to streptozotocin (STZ) intraperitoneal (i.p.) injections (50 mg/kg, 5 days consecutive). LinSTZ were fed a 60% kCal HFD for 8 weeks. Lin mice treated with STZ developed polydipsia, became hypertensive and hyperglycemic. HFD induced weight gain, protected against glomerular hypertrophy, scarring, and albuminuria at endpoint compared to regular diet fed LinSTZ. On the other hand, HFD induced steatosis, liver fibrosis, inflammation, and increase in AST/ALT ratio, characteristics of non-alcoholic liver disease. Taken together, our results show that LinSTZ mice fed a HFD did not lead to a more robust model of MS-induced CKD, protected against kidney injury, but inducing liver damage. More studies are necessary to understand the kidney protective mechanisms of HFD when superimposed with hypertension and type 1 diabetes.
慢性肾脏病(CKD)是一种全球性的健康负担,如果不加以治疗,其终末期肾功能衰竭的风险会增加。代谢综合征(MS)引起的 CKD 会增加高血压、高血糖、体脂过多和血脂异常的风险。为了测试将高脂肪饮食(HFD)方案应用于高血压/糖尿病表型是否会在小鼠中模拟 MS 引起的 CKD 的特征,在遗传高血压小鼠(Lin)中诱导高血糖症,然后进行 HFD 方案。为此,将 8 周龄雄性小鼠进行链脲佐菌素(STZ)腹腔(i.p.)注射(50mg/kg,连续 5 天)。LinSTZ 喂食 60%热量的 HFD 8 周。与接受常规饮食喂养的 LinSTZ 相比,接受 STZ 治疗的 Lin 小鼠出现多饮、高血压和高血糖。HFD 诱导体重增加,在终点时可防止肾小球肥大、瘢痕形成和白蛋白尿。另一方面,HFD 诱导肝脂肪变性、肝纤维化、炎症和 AST/ALT 比值升高,这些都是非酒精性肝病的特征。综上所述,我们的结果表明,LinSTZ 小鼠喂食 HFD 并没有导致更严重的 MS 诱导的 CKD 模型,对肾脏损伤有保护作用,但会导致肝脏损伤。需要进一步研究来了解 HFD 在高血压和 1 型糖尿病的基础上对肾脏的保护机制。