Diabetes Obes Metab. 2012 Oct;14(10):960-2. doi: 10.1111/j.1463-1326.2012.01616.x. Epub 2012 May 28.
The Goto-Kakizaki (GK) rat, a type 2 diabetes model, has increased pancreatic islet and white adipose tissue (WAT) blood flow, and this can be normalized by acute administration of SR59230A, a β₃ -adrenoceptor antagonist. We now implanted osmotic pumps which allowed a constant release of saline or SR59230A (0.6 mg/kg × day) for 2 weeks. A decrease in islet blood flow was seen also after 2 weeks of continuous SR59230A treatment in the GK rat. However, no improvement in glucose tolerance was seen in the GK rats. Neither did SR59230A affect insulin secretion from isolated islets in vitro. WAT blood flow was not affected by the 2-week SR59230A treatment. Thus, the increased islet blood flow seen in the GK rat can be normalized for up to 2 weeks, which opens the possibilities for further studies on the long-term functional role on the islet blood flow increase in this type 2 diabetes model.
Goto-Kakizaki (GK) 大鼠是一种 2 型糖尿病模型,其胰岛和白色脂肪组织(WAT)的血流量增加,而这种增加可以通过急性给予β₃-肾上腺素受体拮抗剂 SR59230A 来正常化。我们现在植入了渗透型泵,使生理盐水或 SR59230A(0.6mg/kg×天)持续释放 2 周。在 GK 大鼠连续接受 SR59230A 治疗 2 周后,也观察到胰岛血流减少。然而,在 GK 大鼠中,葡萄糖耐量没有得到改善。SR59230A 也没有影响离体胰岛的胰岛素分泌。WAT 血流不受 2 周 SR59230A 治疗的影响。因此,在 GK 大鼠中观察到的增加的胰岛血流可以在 2 周内正常化,这为进一步研究这种 2 型糖尿病模型中胰岛血流增加的长期功能作用提供了可能性。