Laustsen Christoffer, Lipsø Kasper, Ostergaard Jakob Appel, Nørregaard Rikke, Flyvbjerg Allan, Pedersen Michael, Palm Fredrik, Ardenkjær-Larsen Jan Henrik
Department of Clinical Medicine, MR Research Centre, Aarhus University, Aarhus, Denmark.
Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark Department of Electrical Engineering, Technical University of Denmark, Kgs. Lyngby, Denmark.
Physiol Rep. 2014 Dec 11;2(12). doi: 10.14814/phy2.12233. Print 2014 Dec 1.
Good glycemic control is crucial to prevent the onset and progression of late diabetic complications, but insulin treatment often fails to achieve normalization of glycemic control to the level seen in healthy controls. In fact, recent experimental studies indicate that insufficient treatment with insulin, resulting in poor glycemic control, has an additional effect on progression of late diabetic complications, than poor glycemic control on its own. We therefore compared renal metabolic alterations during conditions of poor glycemic control with and without suboptimal insulin administration, which did not restore glycemic control, to streptozotocin (STZ)-diabetic rats using noninvasive hyperpolarized (13)C-pyruvate magnetic resonance imaging (MRI) and blood oxygenation level-dependent (BOLD) (1)H-MRI to determine renal metabolic flux and oxygen availability, respectively. Suboptimal insulin administration increased pyruvate utilization and metabolic flux via both anaerobic and aerobic pathways in diabetic rats even though insulin did not affect kidney oxygen availability, HbA1c, or oxidative stress. These results imply direct effects of insulin in the regulation of cellular substrate utilization and metabolic fluxes during conditions of poor glycemic control. The study demonstrates that poor glycemic control in combination with suboptimal insulin administration accelerates metabolic alterations by increasing both anaerobic and aerobic metabolism resulting in increased utilization of energy substrates. The results demonstrate the importance of tight glycemic control in insulinopenic diabetes, and that insulin, when administered insufficiently, adds an additional burden on top of poor glycemic control.
良好的血糖控制对于预防晚期糖尿病并发症的发生和发展至关重要,但胰岛素治疗往往无法使血糖控制恢复到健康对照者的正常水平。事实上,最近的实验研究表明,胰岛素治疗不足导致血糖控制不佳,相比于单纯血糖控制不佳,对晚期糖尿病并发症的进展有额外影响。因此,我们使用无创超极化(13)C-丙酮酸磁共振成像(MRI)和血氧水平依赖(BOLD)(1)H-MRI分别测定肾脏代谢通量和氧可用性,比较了血糖控制不佳且胰岛素给药未恢复血糖控制的情况下与未给药时,链脲佐菌素(STZ)诱导的糖尿病大鼠的肾脏代谢改变。尽管胰岛素不影响肾脏氧可用性、糖化血红蛋白(HbA1c)或氧化应激,但次优胰岛素给药增加了糖尿病大鼠通过无氧和有氧途径的丙酮酸利用和代谢通量。这些结果表明,在血糖控制不佳的情况下,胰岛素对细胞底物利用和代谢通量的调节有直接作用。该研究表明,血糖控制不佳与次优胰岛素给药相结合,通过增加无氧和有氧代谢加速代谢改变,导致能量底物利用增加。结果证明了在胰岛素缺乏型糖尿病中严格控制血糖的重要性,以及胰岛素给药不足时,会在血糖控制不佳的基础上增加额外负担。