Combined sedentarism and high-fat diet induce early signs of kidney injury in C57BL/6J mice.

Precious C Opurum, Stephen T Decker, Deborah Stuart, Alek D Peterlin, Venisia L Paula, Piyarat Siripoksup, Micah J Drummond, Alejandro Sanchez, Nirupama Ramkumar, Katsuhiko Funai
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Abstract

Chronic kidney disease (CKD) is a progressive disorder marked by a decline in kidney function. Obesity and sedentary behavior contribute to the development of CKD, though mechanisms by which this occurs are poorly understood. This knowledge gap is worsened by the lack of a reliable murine CKD model that does not rely on injury, toxin, or gene deletion to induce a reduction in kidney function. High-fat diet (HFD) feeding alone is insufficient to cause reduced kidney function until later in life. Here, we used a small mouse cage (SMC), a recently developed mouse model of sedentariness, to study its effect on kidney function. Wild-type C57BL/6J male mice were housed in sham or SMC housing for 6 mo with HFD in room (22°C) or thermoneutral (30°C) conditions. Despite hyperinsulinemia induced by the SMC + HFD intervention, kidneys from these mice displayed normal glomerular filtration rate. However, the kidneys showed early signs of kidney injury, including increases in collagen I and neutrophil gelatinase-associated lipocalin transcripts, as well as fibrosis by histology, primarily in the inner medullary/papilla region. High-resolution respirometry and fluorometry experiments showed no statistically significant changes in the capacities for respiration, ATP synthesis, or electron leak. These data confirm the technical challenge in modeling human CKD. They further support the notion that obesity and a sedentary lifestyle make the kidneys more vulnerable, but additional insults are likely required for the pathogenesis of CKD.NEW & NOTEWORTHY Physical inactivity is a risk factor for chronic kidney disease. Our laboratory recently developed a new mouse model of physical inactivity (small mouse cage housing) that more closely recapitulates the metabolic disturbances that occur with sedentary behavior. In this paper, we performed an in-depth phenotyping of kidney function and metabolic parameters in response to small mouse cage housing.

久坐与高脂饮食联合可诱导C57BL/6J小鼠肾损伤的早期症状。
慢性肾脏疾病(CKD)是一种以肾功能下降为特征的进行性疾病。肥胖和久坐行为有助于CKD的发展,尽管其发生的机制尚不清楚。由于缺乏一种不依赖于损伤、毒素或基因缺失来诱导肾功能下降的可靠的小鼠CKD模型,这一知识差距进一步加剧。高脂肪饮食(HFD)单独喂养不足以导致肾功能下降,直到晚年。在这里,我们采用了一个小老鼠笼(SMC),一种最近开发的久坐小鼠模型,来研究它对肾功能的影响。野生型C57BL/6J雄性小鼠分别在假或SMC房中饲养6个月,室温(22°C)或热中性(30°C)条件下进行HFD。尽管SMC+HFD干预导致高胰岛素血症,这些小鼠的肾脏显示正常的肾小球滤过率(GFR)。然而,肾脏表现出肾损伤的早期迹象,包括Col1a1和NGAL转录物的增加,以及组织学上的纤维化,主要发生在髓内/乳头区域。高分辨率呼吸测定和荧光测定实验显示,呼吸能力、ATP合成或电子泄漏没有统计学上显著的变化。这些数据证实了人类CKD建模的技术挑战。他们进一步支持肥胖和久坐不动的生活方式使肾脏更脆弱的观点,但CKD的发病机制可能需要额外的损害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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