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Insulin resistance and vasodilation in essential hypertension. Studies with adenosine.

机译:原发性高血压患者的胰岛素抵抗和血管舒张作用。用腺苷研究。

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摘要

Insulin-mediated vasodilation has been proposed as a determinant of in vivo insulin sensitivity. We tested whether sustained vasodilation with adenosine could overcome the muscle insulin resistance present in mildly overweight patients with essential hypertension. Using the forearm technique, we measured the response to a 40-min local intraarterial infusion of adenosine given under fasting conditions (n = 6) or superimposed on a euglycemic insulin clamp (n = 8). In the fasting state, adenosine-induced vasodilation (forearm blood flow from 2.6 +/- 0.6 to 6.0 +/- 1.2 ml min-1dl-1, P < 0.001) was associated with a 45% rise in muscle oxygen consumption (5.9 +/- 1.0 vs 8.6 +/- 1.7 mumol min-1dl-1, P < 0.05), and a doubling of forearm glucose uptake (0.47 +/- 0.15 to 1.01 +/- 0.28 mumol min-1dl-1, P < 0.05). The latter effect remained significant also when expressed as a ratio to concomitant oxygen balance (0.08 +/- 0.03 vs 0.13 +/- 0.04 mumol mumol-1, P < 0.05), whereas for all other metabolites (lactate, pyruvate, FFA, glycerol, citrate, and beta-hydroxybutyrate) this ratio remained unchanged. During euglycemic hyperinsulinemia, whole-body glucose disposal was stimulated (to 19 +/- 3 mumol min-1kg-1), but forearm blood flow did not increase significantly above baseline (2.9 +/- 0.2 vs 3.1 +/- 0.2 ml min-1dl-1, P = NS). Forearm oxygen balance increased (by 30%, P < 0.05) and forearm glucose uptake rose fourfold (from 0.5 to 2.3 mumol min-1dl-1, P < 0.05). Superimposing an adenosine infusion into one forearm resulted in a 100% increase in blood flow (from 2.9 +/- 0.2 to 6.1 +/- 0.9 ml min-1dl-1, P < 0.001); there was, however, no further stimulation of oxygen or glucose uptake compared with the control forearm. During the clamp, the ratio of glucose to oxygen uptake was similar in the control and in the infused forearms (0.27 +/- 0.11 and 0.23 +/- 0.09, respectively), and was not altered by adenosine (0.31 +/- 0.9 and 0.29 +/- 0.10). We conclude that in insulin-re15-76sistant patients with hypertension, adenosine-induced vasodilation recruits oxidative muscle tissues and exerts a modest, direct metabolic effect to promote muscle glucose uptake in the fasting state. Despite these effects, however, adenosine does not overcome muscle insulin resistance.
机译:已经提出胰岛素介导的血管舒张作为体内胰岛素敏感性的决定因素。我们测试了用腺苷持续进行血管舒张是否可以克服轻度超重原发性高血压患者的肌肉胰岛素抵抗。使用前臂技术,我们测量了在禁食条件下(n = 6)或叠加在血糖正常的胰岛素钳夹(n = 8)上对腺苷40分钟局部动脉内输注的反应。在空腹状态下,腺苷诱导的血管舒张(前臂血流从2.6 +/- 0.6到6.0 +/- 1.2 ml min-1dl-1,P <0.001)与肌肉耗氧量增加45%(5.9 + /-1.0与8.6 +/- 1.7摩尔-1 min-1dl-1,P <0.05),前臂葡萄糖摄入量翻倍(0.47 +/- 0.15至1.01 +/- 0.28 mol-1 min-1dl-1,P <0.05 )。当以相对氧平衡的比率(0.08 +/- 0.03 vs 0.13 +/- 0.04 mumol mumol-1,P <0.05)表示时,后一种效果仍然很明显,而对于所有其他代谢物(乳酸,丙酮酸,FFA,甘油) ,柠檬酸盐和β-羟基丁酸酯)的比例保持不变。在正常血糖高胰岛素血症期间,全身葡萄糖处置受到刺激(至19 +/- 3μmol·min-1kg-1),但前臂血流量并未明显高于基线(2.9 +/- 0.2 vs. 3.1 +/- 0.2 ml / min) -1dl-1,P = NS)。前臂氧平衡增加(增加30%,P <0.05),前臂葡萄糖摄取增加四倍(从0.5到2.3 mumol min-1dl-1,P <0.05)。将腺苷输注叠加到一个前臂中会导致血流量增加100%(从2.9 +/- 0.2毫升增加到6.1 +/- 0.9毫升min-1dl-1,P <0.001);然而,与对照前臂相比,没有进一步刺激氧或葡萄糖的摄取。在钳夹过程中,对照组和输注的前臂中葡萄糖与氧气吸收的比率相似(分别为0.27 +/- 0.11和0.23 +/- 0.09),并且腺苷不会改变(0.31 +/- 0.9和0.29 +/- 0.10)。我们得出的结论是,在胰岛素抵抗15-76的高血压患者中,腺苷诱导的血管舒张募集氧化性肌肉组织,并发挥适度的直接代谢作用,以促进空腹状态下肌肉葡萄糖的摄取。尽管有这些作用,腺苷仍不能克服肌肉胰岛素抵抗。

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