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Arteriolar network architecture and vasomotor function with ageing in mouse gluteus maximus muscle

机译:小鼠臀大肌衰老的小动脉网络结构和血管舒缩功能

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摘要

Physical diminishes with ageing, but little is known of how the microvascular supply to skeletal muscle fibres is affected. To test the hypothesis that ageing alters blood flow control, we investigated network architecture and vasomotor responses of arterioles in the gluteus maximus muscle of young (2–3 months), adult (12–14 months) and old (18–20 months) C57BL6 male mice (n = 83) (Young, Adult and Old, respectively). Microvascular casts revealed that the total number, length and surface area of arteriolar segments (diameter, 10–50 μm) were not significantly different across age-groups. However, for arterioles with diameter of 30 μm, tortuosity and branch angles increased with age (P < 0.05). In anaesthetized mice, second-order (2A) distributing arterioles had similar resting (17 ± 1 μm) and maximal (37 ± 1 μm) diameters and similar responsiveness to cumulative (10−10–10−4m) superfusion of acetylcholine or phenylephrine. With superfusate oxygen level raised from 0 to 21%, 2A arteriolar constriction in Young (11 ± 1 μm) was greater (P < 0.05) than Adult and Old (5 ± 1 μm). Observed 1 mm upstream from microiontophoresis of ACh (1 μA, 1 s), conducted vasodilatation was 10 ± 1 μm in Young, 17 ± 1 μm in Adult and 6 ± 1 μm in Old (P < 0.05). With muscle contractions (2, 4 and 8 Hz; 30 s) arteriolar diameter increased similarly across age-groups (6 ± 1, 11 ± 1 and 18 ± 1 μm, respectively). Muscle mass and active tension were similar across age-groups yet postcontraction vasodilatation recovered more rapidly in Old versus Adult and Young (P < 0.05). With arteriolar network architecture maintained during ageing, the impairment in conducted vasodilatation and attenuation of postcontraction vasodilatation may compromise exercise tolerance.
机译:身体会随着年龄的增长而减少,但是人们对骨骼肌纤维的微血管供应受到怎样的影响知之甚少。为了检验衰老会改变血流控制的假设,我们研究了C57BL6的年轻人(2-3个月),成年人(12-14个月)和老年人(18-20个月)的臀大肌的网络结构和小动脉的血管舒缩反应。雄性小鼠(n = 83)(分别为年轻,成年和老年)。微血管模型显示,不同年龄段的小动脉节段的总数,长度和表面积(直径10–50μm)没有显着差异。然而,对于直径为30μm的小动脉,曲折度和分支角随年龄增长而增加(P <0.05)。在麻醉的小鼠中,二阶(2A)分布的小动脉具有相似的静息(17±1μm)和最大(37±1μm)直径,并对累积(10 −10 –10 −4 m)乙酰胆碱或去氧肾上腺素的融合。随着超融合液含氧量从0%升高到21%,年轻人(11±1μm)的2A小动脉收缩比成人和老人(5±1μm)大(P <0.05)。在ACh的微离子电泳上游1毫米处观察到(1μA,1 s),年轻时进行的血管扩张为10±1μm,成人时为17±1μm,老年人为6±1μm(P <0.05)。随着肌肉的收缩(2、4和8 Hz; 30 s),小动脉直径在各个年龄段(分别为6±1、11±1和18±1μm)相似地增加。各个年龄段的肌肉质量和活动紧张程度相似,但老年人比成年人和年轻人的收缩后血管舒张恢复更快(P <0.05)。在衰老过程中保持小动脉网络结构的情况下,传导性血管舒张功能的损害和收缩后血管舒张功能的减弱可能会损害运动耐力。

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