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本文引用的文献

1
Influence of α-adrenergic vasoconstriction on the blunted skeletal muscle contraction-induced rapid vasodilation with aging.α-肾上腺素能血管收缩对衰老时骨骼肌收缩引起的快速血管扩张的迟钝的影响。
J Appl Physiol (1985). 2012 Oct 15;113(8):1201-12. doi: 10.1152/japplphysiol.00734.2012. Epub 2012 Sep 6.
2
Impaired skeletal muscle blood flow control with advancing age in humans: attenuated ATP release and local vasodilation during erythrocyte deoxygenation.随着年龄的增长,人体骨骼肌血流控制受损:在红细胞去氧过程中,ATP 释放和局部血管舒张减弱。
Circ Res. 2012 Jul 6;111(2):220-30. doi: 10.1161/CIRCRESAHA.112.269571. Epub 2012 May 29.
3
Acute reversal of endothelial dysfunction in the elderly after antioxidant consumption.抗氧化剂摄入后老年人内皮功能障碍的急性逆转。
Hypertension. 2012 Apr;59(4):818-24. doi: 10.1161/HYPERTENSIONAHA.111.189456. Epub 2012 Feb 21.
4
Heterogeneous vascular responses to hypoxic forearm exercise in young and older adults.年轻人和老年人在缺氧性前臂运动时血管反应的异质性。
Eur J Appl Physiol. 2012 Aug;112(8):3087-95. doi: 10.1007/s00421-011-2280-x. Epub 2011 Dec 25.
5
Rapid onset vasodilatation is blunted in obese humans.肥胖人群的血管扩张速度会变缓。
Acta Physiol (Oxf). 2012 May;205(1):103-12. doi: 10.1111/j.1748-1716.2011.02370.x. Epub 2011 Nov 5.
6
The function of vascular smooth muscle phosphodiesterase III is preserved in healthy human aging.血管平滑肌磷酸二酯酶 III 的功能在健康的人类衰老中得以保留。
Clin Transl Sci. 2010 Oct;3(5):239-42. doi: 10.1111/j.1752-8062.2010.00232.x.
7
Ageing reduces the compensatory vasodilatation during hypoxic exercise: the role of nitric oxide.衰老降低了低氧运动期间的代偿性血管舒张:一氧化氮的作用。
J Physiol. 2011 Mar 15;589(Pt 6):1477-88. doi: 10.1113/jphysiol.2010.203539. Epub 2011 Jan 31.
8
Nitric oxide, but not vasodilating prostaglandins, contributes to the improvement of exercise hyperemia via ascorbic acid in healthy older adults.一氧化氮,而不是血管扩张性前列腺素,通过抗坏血酸有助于改善健康老年人的运动性充血。
Am J Physiol Heart Circ Physiol. 2010 Nov;299(5):H1633-41. doi: 10.1152/ajpheart.00614.2010. Epub 2010 Sep 3.
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Vasodilatory responsiveness to adenosine triphosphate in ageing humans.在衰老的人类中,对三磷酸腺苷的血管舒张反应性。
J Physiol. 2010 Oct 15;588(Pt 20):4017-27. doi: 10.1113/jphysiol.2010.197814.
10
Blunting of rapid onset vasodilatation and blood flow restriction in arterioles of exercising skeletal muscle with ageing in male mice.雄性小鼠骨骼肌中随增龄导致运动时动脉血管扩张和血流限制的快速反应性减弱。
J Physiol. 2010 Jun 15;588(Pt 12):2269-82. doi: 10.1113/jphysiol.2010.189811. Epub 2010 Apr 7.

一氧化氮在年轻和老年人大鼠收缩诱导的快速血管舒张中的作用。

Contribution of nitric oxide in the contraction-induced rapid vasodilation in young and older adults.

机构信息

Department of Physical Therapy and Rehabilitation Science, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

J Appl Physiol (1985). 2013 Aug 15;115(4):446-55. doi: 10.1152/japplphysiol.00446.2013. Epub 2013 Jun 20.

DOI:10.1152/japplphysiol.00446.2013
PMID:23788575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3742946/
Abstract

We tested the hypothesis that reduced nitric oxide (NO) bioavailability contributes to the attenuated peak and total vasodilation following single-muscle contractions in older adults. Young (n = 10; 24 ± 2 yr) and older (n = 10; 67 ± 2 yr) adults performed single forearm contractions at 10, 20, and 40% of maximum during saline infusion (control) and NO synthase (NOS) inhibition via N(G)-monomethyl-l-arginine. Brachial artery diameters and velocities were measured using Doppler ultrasound and forearm vascular conductance (FVC; in ml·min(-1)·100 mmHg(-1)) was calculated from blood flow (ml/min) and blood pressure (mmHg). Peak and total vasodilator responses [change (Δ) in FVC from baseline] were attenuated in older adults at all intensities (P < 0.05). NOS inhibition reduced the peak ΔFVC at 10% (88 ± 12 vs. 52 ± 9 ml·min(-1)·100 mmHg(-1)), 20% (125 ± 13 vs. 83 ± 13 ml·min(-1)·100 mmHg(-1)), and 40% (207 ± 26 vs. 133 ± 20 ml·min(-1)·100 mmHg(-1)) in young subjects, (P < 0.05 for all) and in older adults at 10% (59 ± 5 vs. 47 ± 7 ml·min(-1)·100 mmHg(-1), P < 0.05) and 20% (88 ± 9 vs. 68 ± 9 ml·min(-1)·100 mmHg(-1), P < 0.05), but not 40% (128 ± 12 vs. 105 ± 11 ml·min(-1)·100 mmHg(-1), P = 0.11). The relative (%) reduction in peak ΔFVC due to NOS inhibition was greater in young vs. older adults at 20% (-36 ± 5 vs. -23 ± 5%, P < 0.05) and 40% (-35 ± 6 vs. -16 ± 7%, P < 0.05). The reduction in the total vasodilator response (area under the curve) with NOS inhibition was also greater in young vs. older adults at all intensities. Our data suggest that contraction-induced rapid vasodilation is mediated in part by NO, and that the contribution of NO is greater in young adults.

摘要

我们检验了这样一个假设,即减少的一氧化氮(NO)生物利用度导致老年人单次肌肉收缩后的峰值和总血管扩张减弱。年轻组(n=10;24±2 岁)和老年组(n=10;67±2 岁)在生理盐水输注期间(对照)和通过 N(G)-单甲基-L-精氨酸抑制一氧化氮合酶(NOS)时,以 10%、20%和 40%的最大程度进行单次前臂收缩。肱动脉直径和速度使用多普勒超声测量,前臂血管传导(FVC;ml·min(-1)·100 mmHg(-1))由血流(ml/min)和血压(mmHg)计算得出。在所有强度下,老年人的峰值和总血管扩张反应[FVC 从基线的变化(Δ)]均减弱(P<0.05)。NOS 抑制降低了年轻人在 10%(88±12 对 52±9 ml·min(-1)·100 mmHg(-1))、20%(125±13 对 83±13 ml·min(-1)·100 mmHg(-1))和 40%(207±26 对 133±20 ml·min(-1)·100 mmHg(-1))时的峰值ΔFVC(所有 P<0.05),以及在老年人的 10%(59±5 对 47±7 ml·min(-1)·100 mmHg(-1),P<0.05)和 20%(88±9 对 68±9 ml·min(-1)·100 mmHg(-1),P<0.05)时的峰值ΔFVC(所有 P<0.05),但在 40%时没有(128±12 对 105±11 ml·min(-1)·100 mmHg(-1),P=0.11)。由于 NOS 抑制,年轻人的峰值ΔFVC 相对(%)减少幅度大于老年人,在 20%(-36±5 对-23±5%,P<0.05)和 40%(-35±6 对-16±7%,P<0.05)时更大。在所有强度下,NOS 抑制引起的总血管扩张反应(曲线下面积)减少幅度也大于年轻人。我们的数据表明,收缩引起的快速血管扩张部分是由 NO 介导的,并且在年轻人中 NO 的贡献更大。