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首页> 外文期刊>Physiological Research >Acute Glycemic Changes in Brain and Subcutaneous Tissue Measured by Continuous Glucose Monitoring System in Hereditary Hypertriglyceridemic Rat
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Acute Glycemic Changes in Brain and Subcutaneous Tissue Measured by Continuous Glucose Monitoring System in Hereditary Hypertriglyceridemic Rat

机译:胎儿高温甘油泛患者连续葡萄糖监测系统测量脑和皮下组织急性血糖变化

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Parallel glucose measurements in blood and other different tissues give us knowledge about dynamics of glycemia changes, which depend on vascularization, distribution space and local utilization by tissues. Such information is important for the understanding of glucose homeostasis and regulation. The aim of our study was to determine the time-lag between blood, brain, and adipose tissue during rapid glucose changes in a male hHTG rat (n=15). The CGMS sensor Guardian RT (Minimed/Medtronic, USA) was inserted into the brain and into the abdominal subcutaneous tissue. Fixed insulin and variable rate of glucose infusion was used to maintain euglycemia during sensor calibration period. At 0 min, 0.5 g/kg of bolus of glucose was administered, and at 50 min, 5 IU/kg of bolus of insulin was administered. Further glucose and insulin infusion was stopped at this time. The experiment was finished at 130 min and animals were euthanized. The time-shift between glycemia changes in blood, brain, and subcutaneous tissue was calculated by identification of the ideal correlation function. Moreover, the time to achieve 90 % of the maximum glucose excursion after intervention (T90) was measured to compare our data with the literature. The time-lag blood vs. brain and blood vs. subcutaneous tissue was 10 (10; 15) min and 15 (15; 25) min, respectively. The difference was statistically significant (P=0.01). T90 after glucose bolus in brain and subcutaneous tissue was 10 min (8.75; 15) and 15 min (13.75; 21.25), respectively. T90 after insulin bolus in brain and subcutaneous tissue was 10 min (10; 15) and 20 min (20; 27.5), respectively. To the contrary, with literature, our results showed earlier glucose level changes in brain in comparison with subcutaneous tissue after glucose and insulin boluses. Our results suggest that glucose dynamics is different within monitored tissues under rapid changing glucose level and we can expect similar behavior in humans. Improved knowledge about glucose
机译:血液和其他不同组织中的平行葡萄糖测量使我们了解糖血症变化的动态,这取决于血管化,分布空间和组织的局部利用。这些信息对于了解葡萄糖稳态和监管很重要。我们的研究目的是在雄性HHTG大鼠的快速葡萄糖变化期间确定血液,脑和脂肪组织之间的时间延迟(n = 15)。将CGMS传感器Guardian RT(最小/ Medtronic,USA)插入脑中并进入腹部皮下组织。固定胰岛素和可变血液输注术期间的葡萄糖输注在传感器校准期间维持晚期性。在0分钟时,施用0.5g / kg葡萄糖推注,施用50分钟,施用5例Iu / kg胰岛素。此时停止了进一步的葡萄糖和胰岛素输注。实验在130分钟后完成,并使动物安乐死。通过识别理想的相关函数计算血液,脑和皮下组织之间的血糖变化的时移。此外,测量了在干预后(T90)之后的最大葡萄糖偏移的90%的时间,以将数据与文献进行比较。时间滞后血液与脑和血液与皮下组织分别为10(10; 15)分钟,分别为15(15; 25)分钟。差异有统计学意义(p = 0.01)。 T90分别在脑和皮下组织中葡萄糖推注后10分钟(8.75; 15)和15分钟(13.75; 21.25)。 T90脑内胰岛素胰腺炎术后,皮下组织为10分钟(10; 15)和20分钟(20; 27.5)。相反,随着文献,我们的结果表明,与葡萄糖和胰岛素推注后,与皮下组织相比,脑内的早期血糖水平变化。我们的研究结果表明,在快速变化的葡萄糖水平下监测组织内葡萄糖动力学不同,我们可以期待人类的类似行为。改进了关于葡萄糖的知识

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