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首页> 外文期刊>The Journal of Physiology >Vasodilatory responsiveness to adenosine triphosphate in ageing humans.
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Vasodilatory responsiveness to adenosine triphosphate in ageing humans.

机译:老年人对三磷酸腺苷的血管舒张反应性。

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Endothelium-dependent vasodilatation is reduced with advancing age in humans, as evidenced by blunted vasodilator responsiveness to acetylcholine (ACh). Circulating adenosine triphosphate (ATP) has been implicated in the control of skeletal muscle vascular tone during mismatches in oxygen delivery and demand (e.g. exercise) via binding to purinergic receptors (P2Y) on the endothelium evoking subsequent vasodilatation, and ageing is typically associated with reductions in muscle blood flow under such conditions. Therefore, we tested the hypothesis that ATP-mediated vasodilatation is impaired with age in healthy humans. We measured forearm blood flow (venous occlusion plethysmography) and calculated vascular conductance (FVC) responses to local intra-arterial infusions of ACh, ATP, and sodium nitroprusside (SNP) before and during ascorbic acid (AA) infusion in 13 young and 13 older adults. The peak increase in FVC to ACh was significantly impaired in older compared with young adults (262 +/- 71% vs. 618 +/- 97%; P < 0.05), and this difference was abolished during AA infusion (510 +/- 82% vs. 556 +/- 71%; not significant, NS). In contrast, peak FVC responses were not different between older and young adults to either ATP (675 +/- 105% vs. 734 +/- 126%) or SNP (1116 +/- 111% vs. 1138 +/- 148%) and AA infusion did not alter these responses in either age group (both NS). In another group of six young and six older adults, we determined whether vasodilator responses to adenosine and ATP were influenced by P1-receptor blockade via aminophylline. The peak FVC responses to adenosine were not different in young (350 +/- 65%) versus older adults (360 +/- 80%), and aminophylline blunted these responses by approximately 50% in both groups. The peak FVC responses to ATP were again not different in young and older adults, and aminophylline did not impact the vasodilatation in either group. Thus, in contrast to the observed impairments in ACh responses, the vasodilatory response to exogenous ATP is not reduced with age in healthy humans. Further, our data also indicate that adenosine mediated vasodilatation is not reduced with age, and that ATP-mediated vasodilatation is independent of P1-receptor stimulation in both young and older adults.
机译:随着年龄的增长,内皮依赖性血管舒张作用降低,这可由对乙酰胆碱(ACh)的血管舒张反应迟钝来证明。循环中的三磷酸腺苷(ATP)通过与内皮上的嘌呤能受体(P2Y)结合,引起随后的血管舒张,从而在氧气输送和需求(例如运动)不匹配的过程中参与骨骼肌血管紧张度的控制,而衰老通常与减少有关在这种情况下肌肉的血液流动。因此,我们测试了健康人中ATP介导的血管舒张随着年龄而受损的假设。我们测量了13位年轻和13岁以上的抗坏血酸(AA)输注之前和期间对前肢动脉内ACh,ATP和硝普钠(SNP)的局部动脉内输注的前臂血流量(静脉阻塞体积描记法),并计算了血管电导(FVC)反应大人。与年轻人相比,老年人中FVC向ACh的峰值增加明显受损(262 +/- 71%对618 +/- 97%; P <0.05),并且在AA输注期间消除了这种差异(510 +/- 82%对556 +/- 71%;不显着,NS)。相比之下,老年人和年轻人对ATP(675 +/- 105%vs. 734 +/- 126%)或SNP的峰值FVC反应没有差异(1116 +/- 111%vs. 1138 +/- 148%) )和AA输注在两个年龄段(均为NS)中均未改变这些反应。在另一组由六名年轻成年人和六名成年人组成的小组中,我们确定了对腺苷和ATP的血管舒张反应是否受到氨茶碱对P1受体阻滞的影响。年轻人(350 +/- 65%)与老年人(360 +/- 80%)对腺苷的峰值FVC反应无差异,两组中氨茶碱使这些反应减弱约50%。 FATP对ATP的峰值反应在年轻人和老年人中也没有差异,氨茶碱对两组的血管舒张均无影响。因此,与观察到的ACh反应障碍相反,在健康人中,对外源性ATP的血管舒张反应并未随年龄而降低。此外,我们的数据还表明,腺苷介导的血管舒张并不会随着年龄的增长而减少,并且ATP介导的血管舒张在年轻人和老年人中均独立于P1受体刺激。

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