Herrero Pilar, McGill Janet, Lesniak Donna S, Dence Carmen S, Scott Shalonda W, Kisrieva-Ware Zulfia, Gropler Robert J
Division of Radiological Sciences, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St Louis, MO, USA.
J Nucl Cardiol. 2008 Nov-Dec;15(6):791-9. doi: 10.1007/BF03007360.
Our objective was to determine, in the hearts of women with type 1 diabetes mellitus (T1DM), whether the fate of extracted glucose is altered and, if so, what the impact of dobutamine is on myocardial substrate metabolism. In experimental models of T1DM, myocardial glycolysis and glucose oxidation are reduced with the impairment becoming more pronounced with dobutamine. Whether similar changes occur in humans with T1DM is unclear.
Myocardial perfusion, oxygen consumption, and glucose and fatty acid metabolism were measured with positron emission tomography in 19 women, 7 normal volunteers (NVs) and 12 with T1DM. The NVs and 6 T1DM (DM1) patients were studied under baseline metabolic conditions and 6 T1DM patients were studied during hyperinsulinemic-euglycemic clamp (DM1-C), both at rest and during dobutamine. At rest, myocardial glucose uptake, glycolysis, glycogen storage, and oxidation were reduced by similar levels in DM1 patients compared with NVs (P < .05). During dobutamine, although myocardial glucose uptake was not different from DM1 patients at rest, fractional glycolysis was lower compared with NVs or DM1-C patients and reflected a lower glucose oxidation rate (P < .001). Measurements of myocardial glucose metabolism at rest and during dobutamine were comparable between NVs and DM1-C patients. During dobutamine, myocardial fatty acid uptake and oxidation increased in all 3 groups.
In women with T1DM, (1) myocardial glucose metabolism is impaired downstream from initial uptake, (2) these abnormalities become more pronounced with dobutamine and are paralleled by an increase in myocardial fatty acid metabolism, and (3) insulin restores glucose metabolism to levels observed in normal control subjects.
我们的目的是确定1型糖尿病(T1DM)女性患者心脏中摄取的葡萄糖的命运是否改变,以及如果发生改变,多巴酚丁胺对心肌底物代谢有何影响。在T1DM实验模型中,心肌糖酵解和葡萄糖氧化减少,多巴酚丁胺会使这种损害更加明显。T1DM患者中是否发生类似变化尚不清楚。
使用正电子发射断层扫描测量了19名女性的心肌灌注、氧消耗以及葡萄糖和脂肪酸代谢,其中7名是正常志愿者(NVs),12名患有T1DM。NVs和6名T1DM(DM1)患者在基础代谢条件下进行研究,6名T1DM患者在高胰岛素-正常血糖钳夹期间(DM1-C)进行研究,均在静息状态和多巴酚丁胺作用期间进行。静息时,与NVs相比,DM1患者的心肌葡萄糖摄取、糖酵解、糖原储存和氧化减少程度相似(P < 0.05)。在多巴酚丁胺作用期间,尽管心肌葡萄糖摄取与静息时的DM1患者没有差异,但糖酵解分数与NVs或DM1-C患者相比更低,反映出葡萄糖氧化率更低(P < 0.001)。NVs和DM1-C患者在静息时和多巴酚丁胺作用期间的心肌葡萄糖代谢测量结果相当。在多巴酚丁胺作用期间,所有3组的心肌脂肪酸摄取和氧化均增加。
在T1DM女性患者中,(1)心肌葡萄糖代谢在初始摄取后下游受损;(2)这些异常在多巴酚丁胺作用下变得更加明显,同时心肌脂肪酸代谢增加;(3)胰岛素可将葡萄糖代谢恢复到正常对照受试者观察到的水平。