Anatomy and Embryology Department, College of Medicine, Tanta University, Tanta 31511, Egypt.
Medical Biochemistry and Molecular Biology Department, College of Medicine, Kafrelsheikh University, Kafrelsheikh 33516, Egypt.
Biomed Pharmacother. 2021 Jul;139:111624. doi: 10.1016/j.biopha.2021.111624. Epub 2021 Apr 26.
Acute kidney injury (AKI) is a sudden insult of the kidney that happens within a short period of time, which is associated with poor prognosis in diabetic patients with myocardial infarction (MI). Subclinical AKI is a condition in which tubular damage biomarkers [Neutrophil gelatinase-associated lipocalin (NGAL) and kidney injury molecule-1(KIM-1)] are positive even in the absence of elevated serum creatinine. Recent studies reported that SGLT-2 inhibitors could protect against subclinical AKI in diabetic patients by elevating the level of β-Hydroxybutyric acid (βOHB). This study aims to examine the reno-protective potential of empagliflozin (EMPA) against MI associated AKI in diabetic rats. Eighty Albino Wistar rats were divided into: (1) nondiabetic sham group (CS), (2) nondiabetic + myocardial infarction group (CM), (3) diabetic + myocardial infarction group (DM) and (4) diabetic + myocardial infarction + empagliflozin group (DME). At the end of the experiment, blood samples and kidneys were collected for biochemical analysis, histopathological, and immunohistochemical studies. After induction of myocardial infarction, there was a significant decrease in serum creatinine and NGAL levels in DME. After EMPA administration, mesangial matrix index and glomerular area were lowered in DME if compared to DM group. As a marker for tubular injury, we used anti-NGAL and anti-KIM-1 immunohistochemistry. Strong positive reaction was noticed in DM group if compared to DME group which showed weak positive reaction. Levels of renal mRNAs [NGAL; KIM-1; Nox-2,4; TLR-2,4; MyD88; TNF- α and IL-1 β, 18] in DME group were reduced significantly compared to DM group. In conclusion, empagliflozin can protect against subclinical acute kidney injury in diabetic albino Wistar rats after myocardial infarction induction, which could improve the clinical outcome of SGLT-2 inhibitors in diabetic patients.
急性肾损伤(AKI)是肾脏在短时间内受到的急性损伤,与伴有心肌梗死(MI)的糖尿病患者的预后不良有关。亚临床 AKI 是一种管状损伤生物标志物[中性粒细胞明胶酶相关脂质运载蛋白(NGAL)和肾损伤分子 1(KIM-1)]呈阳性的情况,即使在血清肌酐没有升高的情况下也是如此。最近的研究表明,SGLT-2 抑制剂通过提高β-羟基丁酸(βOHB)的水平,可以预防糖尿病患者的亚临床 AKI。本研究旨在探讨恩格列净(EMPA)对糖尿病大鼠 MI 相关 AKI 的肾脏保护作用。80 只白化 Wistar 大鼠分为:(1)非糖尿病假手术组(CS)、(2)非糖尿病+心肌梗死组(CM)、(3)糖尿病+心肌梗死组(DM)和(4)糖尿病+心肌梗死+恩格列净组(DME)。实验结束时,采集血样和肾脏进行生化分析、组织病理学和免疫组织化学研究。在诱导心肌梗死后,DME 组血清肌酐和 NGAL 水平显著下降。与 DM 组相比,DME 组经 EMPA 治疗后系膜基质指数和肾小球面积降低。作为管状损伤的标志物,我们使用抗-NGAL 和抗-KIM-1 免疫组织化学。与 DME 组相比,DM 组的反应明显为强阳性,而 DME 组的反应为弱阳性。与 DM 组相比,DME 组肾组织的 mRNAs[NGAL;KIM-1;Nox-2、4;TLR-2、4;MyD88;TNF-α和 IL-1β、18]水平显著降低。结论:恩格列净可预防糖尿病白化 Wistar 大鼠心肌梗死后的亚临床急性肾损伤,这可能改善 SGLT-2 抑制剂在糖尿病患者中的临床疗效。