Department of Pharmacology, Physiology and Toxicology, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25755, USA.
Endocrine. 2011 Dec;40(3):379-85. doi: 10.1007/s12020-011-9528-4. Epub 2011 Aug 31.
The TALLYHO/JngJ (TH) mouse is a novel polygenic model of type 2 diabetes and exhibits obesity, hyperglycemia (males), hyperinsulinemia, hyperlipidemia, and enlarged pancreatic islets. Since the kidney is damaged by hyperglycemia in other animal models, the present study aimed to determine the kidney phenotype of TH mice using immunoblot and histological analyses of the kidneys of 6-week-old (prediabetic) and 16-week-old TH mice. Interestingly, even 6-week-old male TH mice showed significant increases in kidney weight, compared to C57BL/B6 (B6) mice. Cuboidal parietal epithelium was observed in the Bowman's capsule in male TH mice at the prediabetic age. Water accumulated inside the kidneys of male TH mice in an age-dependent manner, but not in B6 mice. Since Swr/J mice are reported to develop diabetes insipidus and share 86.8% genotype homology with TH mice, the expression level of arginine vasopressin receptor 2 (AVPR2), a candidate protein for diabetes insipidus, was examined and determined to be significantly reduced in the kidneys of prediabetic male TH mice, compared to B6 mice. Aldehyde dehydrogenase (ALDH) activity in the kidneys of prediabetic male TH mice was significantly lower than that in age-matched male B6 mice, while there were no differences between female TH and B6 mice. These results suggest that the kidney phenotype of prediabetic TH mice occurs only in males, accompanied by a reduction in ALDH activity and AVPR2 expression. The kidney phenotype of male TH mice at a prediabetic age becomes evident before the onset of diabetes.
TALLYHO/JngJ (TH) 小鼠是一种新型的 2 型糖尿病多基因模型,表现出肥胖、高血糖(雄性)、高胰岛素血症、高血脂和胰岛增大。由于其他动物模型中的肾脏因高血糖而受损,本研究旨在使用免疫印迹和肾脏组织学分析来确定 6 周龄(糖尿病前期)和 16 周龄 TH 小鼠的肾脏表型。有趣的是,即使是 6 周龄的雄性 TH 小鼠的肾脏重量也明显高于 C57BL/B6 (B6) 小鼠。在糖尿病前期,雄性 TH 小鼠的鲍曼氏囊中观察到立方状壁层上皮。雄性 TH 小鼠的肾脏随年龄增长而出现水分积聚,但 B6 小鼠则没有。由于 Swr/J 小鼠被报道会发生尿崩症,并且与 TH 小鼠共享 86.8%的基因型同源性,因此检查了血管加压素受体 2 (AVPR2) 的表达水平,AVPR2 是尿崩症的候选蛋白,并确定与 B6 小鼠相比,糖尿病前期雄性 TH 小鼠的肾脏中 AVPR2 的表达水平显著降低。糖尿病前期雄性 TH 小鼠肾脏中的醛脱氢酶 (ALDH) 活性明显低于同龄雄性 B6 小鼠,而雌性 TH 小鼠和 B6 小鼠之间没有差异。这些结果表明,糖尿病前期 TH 小鼠的肾脏表型仅在雄性中发生,伴随着 ALDH 活性和 AVPR2 表达的降低。糖尿病前期雄性 TH 小鼠的肾脏表型在糖尿病发作前就已经明显。