Oki Chika, Uno Kinuko, Sasase Tomohiko, Tsutsui Takahiro, Sekiguchi Keita, Yamaguchi Ayane, Mandai Kouhei, Shinohara Masami, Sugimoto Miki, Maekawa Tatsuya, Miyajima Katsuhiro, Ohta Takeshi
Biological/Pharmacological Research Laboratories, Takatsuki Research Center, Central Pharmaceutical Research Institute, Japan Tobacco Inc., Osaka, Japan.
Laboratory of Animal Physiology and Functional Anatomy, Graduate School of Agriculture, Kyoto University, Kyoto, Japan.
J Vet Med Sci. 2025 Feb 1;87(2):138-146. doi: 10.1292/jvms.24-0313. Epub 2024 Dec 11.
Many genetic and environmental factors are involved in the development and progression of diabetic kidney disease (DKD), and its pathology shows various characteristics. Animal models of DKD play an important role in elucidating its pathogenesis and developing new therapies. In this study, we investigated the pathophysiological features of two DKD animal models: db/db mice (background of hyperglycemia) and KK-Ay mice (background of hyperinsulinemia). Male and female mice were fed a high-fat/high-sucrose (HFS) diet for eight weeks. Two mouse models fed the HFS diet showed increases in urinary protein, kidney weight, and glomerular size, but these changes were pronounced in KK-Ay mice. Pathological examination revealed tubulointerstitial fibrosis in KK-Ay mice fed the HFS diet, but not in db/db mice. In addition, fat accumulation was observed in the macula densa of db/db mice and in the glomeruli of KK-Ay mice fed with the HFS diet. In conclusion, an HFS diet exacerbates renal lesions with tubulointerstitial fibrosis in KK-Ay mice, and KK-Ay mice fed an HFS diet are expected to be useful as a DKD model.
许多遗传和环境因素参与了糖尿病肾病(DKD)的发生和发展,其病理表现出多种特征。DKD动物模型在阐明其发病机制和开发新疗法方面发挥着重要作用。在本研究中,我们研究了两种DKD动物模型的病理生理特征:db/db小鼠(高血糖背景)和KK-Ay小鼠(高胰岛素血症背景)。雄性和雌性小鼠喂食高脂/高糖(HFS)饮食八周。两种喂食HFS饮食的小鼠模型均出现尿蛋白、肾脏重量和肾小球大小增加,但这些变化在KK-Ay小鼠中更为明显。病理检查显示,喂食HFS饮食的KK-Ay小鼠出现肾小管间质纤维化,而db/db小鼠未出现。此外,在喂食HFS饮食的db/db小鼠的致密斑和KK-Ay小鼠的肾小球中观察到脂肪堆积。总之,HFS饮食会加重KK-Ay小鼠的肾小管间质纤维化肾损伤,喂食HFS饮食的KK-Ay小鼠有望作为DKD模型。