Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Islets. 2012 Sep-Oct;4(5):343-8. doi: 10.4161/isl.22283. Epub 2012 Sep 1.
Adenylyl cyclase 3 (AC3) is expressed in pancreatic islets of the Goto-Kakizaki (GK) rat, a spontaneous animal model of type 2 diabetes (T2D), and also exerts genetic effects on the regulation of body weight in man. In addition to pancreatic islets, the central nervous system (CNS) plays an important role in the pathogenesis of T2D and obesity by regulating feeding behavior, body weight and glucose metabolism. In the present study, we have investigated AC3 expression in pancreatic islets, striatum and hypothalamus of GK rats to evaluate its role in the regulation of glucose homeostasis. GK and Wistar rats at the age of 2.5 mo were used. A group of GK rats were implanted with sustained insulin release chips for 15 d. Plasma glucose and serum insulin levels were measured. AC3 gene expression levels in pancreatic islets, striatum and hypothalamus were determined by using real-time RT-PCR. Results indicated that plasma glucose levels in Wistar rats were found to be similar to insulin-treated GK rats, and significantly lower compared with non-treated GK rats. AC3 expression levels in pancreatic islets, striatum and hypothalamus of GK rats were higher compared with Wistar rats, while the levels were intermediate in insulin-treated GK rats. The AC3 expression display patterns between pancreatic islets and striatum-hypothalamus were similar. The present study thus provides the first evidence that AC3 is overexpressed in the regions of striatum and hypothalamus of brain, and similarly in pancreatic islets of GK rats suggesting that AC3 plays a role in regulation of glucose homeostasis via CNS and insulin secretion.
腺苷酸环化酶 3(AC3)在 Goto-Kakizaki(GK)大鼠的胰岛中表达,GK 大鼠是 2 型糖尿病(T2D)的自发性动物模型,并且对人体体重调节也具有遗传影响。除了胰岛外,中枢神经系统(CNS)通过调节摄食行为、体重和葡萄糖代谢在 T2D 和肥胖的发病机制中发挥重要作用。在本研究中,我们研究了 GK 大鼠胰岛、纹状体和下丘脑的 AC3 表达,以评估其在葡萄糖稳态调节中的作用。使用 2.5 月龄的 GK 和 Wistar 大鼠。一组 GK 大鼠被植入持续释放胰岛素的芯片 15 天。测量血浆葡萄糖和血清胰岛素水平。通过实时 RT-PCR 测定胰岛、纹状体和下丘脑的 AC3 基因表达水平。结果表明,Wistar 大鼠的血浆葡萄糖水平与胰岛素处理的 GK 大鼠相似,明显低于未处理的 GK 大鼠。与 Wistar 大鼠相比,GK 大鼠的胰岛、纹状体和下丘脑的 AC3 表达水平较高,而胰岛素处理的 GK 大鼠的表达水平居中。胰岛和纹状体-下丘脑之间的 AC3 表达模式相似。本研究首次提供了证据表明,AC3 在 GK 大鼠的纹状体和下丘脑区域以及胰岛中过度表达,这表明 AC3 通过中枢神经系统和胰岛素分泌在葡萄糖稳态调节中发挥作用。