Mariana Charleaux de Ponte, Vanessa Gerolde Cardoso, Juliana Martins da Costa-Pessoa, Guilherme Lopes-Gonçalves, Beatriz Maria Veloso Pereira, Karina Thieme, Maria Oliveira-Souza
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引用次数: 0
Abstract
Acute kidney injury (AKI) is a public health concern associated with high rates of mortality, even in milder cases. One of the reasons for the difficulty in managing AKI in patients is due to its association with pre-existing comorbidities, such as diabetes. In fact, diabetes increases the susceptibility to develop more severe AKI after renal ischemia. However, the long-term effects of this association are not known. Thus, an experimental model was designed to evaluate the chronic effects of renal ischemia/reperfusion (IR) in streptozotocin (STZ)-treated mice. We focused on the glomerular and tubulointerstitial damage, as well as kidney function and metabolic profile. It was found that pre-existing diabetes may potentiate progressive kidney disease after AKI, mainly by exacerbating proinflammatory and sustaining fibrotic responses and altering renal glucose metabolism. To our knowledge, this is the first report that highlights the long-term effects of renal IR on diabetes. The findings of this study can support the management of AKI in clinical practice.NEW & NOTEWORTHY This study demonstrated that early diabetes potentiates progressive kidney disease after ischemia/reperfusion (IR)-induced acute kidney injury, mainly by exacerbating pro-inflammatory and sustaining fibrotic responses and altering renal glucose metabolism. Thus, these findings will contribute to the therapeutic support of patients with type 1 diabetes with eventual renal IR intervention in clinical practice.
急性肾损伤(AKI)是一个与高死亡率相关的公共卫生问题,即使是较轻的病例也是如此。患者急性肾损伤难以控制的原因之一是它与糖尿病等原有合并症有关。事实上,糖尿病会增加肾缺血后发生更严重 AKI 的可能性。然而,这种关联的长期影响尚不清楚。因此,我们分析了一个实验模型,以评估 STZ 处理的小鼠肾缺血/再灌注(IR)的慢性影响。我们重点研究了肾小球和肾小管间质损伤,以及肾功能和代谢状况。研究发现,原有的糖尿病可能会加剧 AKI 后肾脏疾病的进展,主要是通过加剧促炎症反应和维持纤维化反应以及改变肾脏葡萄糖代谢。据我们所知,这是第一份强调肾脏红外对糖尿病长期影响的报告。这项研究的结果可为临床实践中的 AKI 管理提供支持。
期刊介绍:
The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.