Department of Endocrinology, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, Shandong, 250014, People's Republic of China.
Department of Endocrinology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012, People's Republic of China.
Mol Med. 2019 Jan 7;25(1):2. doi: 10.1186/s10020-018-0067-9.
Sulfonylurea receptor 1 (SUR1) is primarily responsible for glucose regulation in normal conditions. Here, we sought to investigate the glucose metabolism characteristics of SUR1 rats.
The TALEN technique was used to construct a SUR1 gene deficiency rat model. Rats were grouped by SUR1 gene knockout or not and sex difference. Body weight; glucose metabolism indicators, including IPGTT, IPITT, glycogen contents and so on; and other molecule changes were examined.
Insulin secretion was significantly inhibited by knocking out the SUR1 gene. SUR1 rats showed lower body weights compared to wild-type rats, and even SUR1 males weighed less than wild-type females. Upon SUR1 gene knockout, the rats showed a peculiar plasma glucose profile. During IPGTT, plasma glucose levels were significantly elevated in SUR1 rats at 15 min, which could be explained by SUR1 mainly working in the first phase of insulin secretion. Moreover, SUR1 male rats showed obviously impaired glucose tolerance than before and a better insulin sensitivity in the 12th week compared with females, which might be related with excess androgen secretion in adulthood. Increased glycogen content and GLUT4 expression and the inactivation of GSK3 were also observed in SUR1 rats, which suggested an enhancement of insulin sensitivity.
These results reconfirm the role of SUR1 in systemic glucose metabolism. More importantly, our SUR1 rat model might be applied in other fields, such as for exploring other hypoglycaemic functions of sulfonylureas.
磺酰脲受体 1(SUR1)主要负责正常情况下的葡萄糖调节。在这里,我们试图研究 SUR1 大鼠的葡萄糖代谢特征。
使用 TALEN 技术构建 SUR1 基因缺失大鼠模型。根据 SUR1 基因敲除与否和性别差异对大鼠进行分组。检测体重;葡萄糖代谢指标,包括 IPGTT、IPITT、糖原含量等;以及其他分子变化。
敲除 SUR1 基因可显著抑制胰岛素分泌。与野生型大鼠相比,SUR1 大鼠的体重明显降低,甚至 SUR1 雄性大鼠的体重也低于野生型雌性大鼠。在 SUR1 基因敲除后,大鼠表现出一种特殊的血浆葡萄糖谱。在 IPGTT 中,SUR1 大鼠在 15 分钟时血浆葡萄糖水平显著升高,这可以用 SUR1 主要在胰岛素分泌的第一阶段起作用来解释。此外,与雌性大鼠相比,SUR1 雄性大鼠的葡萄糖耐量明显受损,在第 12 周时胰岛素敏感性更好,这可能与成年后雄激素分泌过多有关。在 SUR1 大鼠中还观察到糖原含量增加、GLUT4 表达增加和 GSK3 失活,提示胰岛素敏感性增强。
这些结果再次证实了 SUR1 在全身葡萄糖代谢中的作用。更重要的是,我们的 SUR1 大鼠模型可能会应用于其他领域,例如探索磺酰脲类药物的其他降血糖功能。