Department of Health, Exercise and Sport Sciences, Texas Tech University, Lubbock, TX, USA.
J Appl Physiol (1985). 2012 Oct;113(7):1091-100. doi: 10.1152/japplphysiol.00292.2012. Epub 2012 Aug 23.
Skeletal muscle vascular resistance during physical exertion is higher with old age. The purpose of this study was to determine whether 1) aging enhances angiotensin II (ANG II)-induced vasoconstriction; 2) the proinflammatory cytokine tumor necrosis factor (TNF)-α contributes to alterations in ANG II-mediated vasoconstriction with aging; 3) exercise training attenuates putative age-associated increases in ANG II-mediated vasoconstriction; and 4) the mechanism(s) through which aging and exercise training alters ANG II-induced vasoconstriction in skeletal muscle arterioles. Male Fischer 344 rats were assigned to four groups: young sedentary (4 mo), old sedentary (24 mo), young trained, and old trained. In a separate group of young sedentary and old sedentary animals, a TNF type 1 receptor inhibitor was administered subcutaneously for 10 wk. First-order arterioles were isolated from soleus and gastrocnemius muscles for in vitro experimentation. Old age augmented ANG II-induced vasoconstriction in both soleus (young: 27 ± 3%; old: 38 ± 4%) and gastrocnemius (young: 42 ± 6%; old: 64 ± 9%) muscle arterioles; this augmented vasoconstriction was abolished with the removal of the endothelium, N(G)-nitro-l-arginine methyl ester, and chronic inhibition of TNF-α. In addition, exercise training ameliorated the age-induced increase in ANG II vasoconstriction. These findings demonstrate that old age enhances and exercise training diminishes ANG II-induced vasoconstrictor responses in skeletal muscle arterioles through an endothelium-dependent nitric oxide synthase signaling pathway. In addition, the enhancement of ANG II vasoconstriction with old age appears to be related to a proinflammatory state.
在体力活动期间,骨骼肌血管阻力随年龄增长而升高。本研究旨在确定:1)衰老是否增强血管紧张素 II(ANG II)诱导的血管收缩;2)促炎细胞因子肿瘤坏死因子(TNF)-α是否有助于衰老引起的 ANG II 介导的血管收缩改变;3)运动训练是否减弱 ANG II 介导的血管收缩的潜在年龄相关性增加;以及 4)衰老和运动训练改变骨骼肌血管中 ANG II 诱导的血管收缩的机制。雄性 Fischer 344 大鼠分为四组:年轻安静组(4 个月)、年老安静组(24 个月)、年轻训练组和年老训练组。在一组单独的年轻安静和年老安静的动物中,皮下给予 TNF 型 1 受体抑制剂 10 周。第一级小动脉从比目鱼肌和腓肠肌中分离出来进行体外实验。衰老增加了比目鱼肌(年轻:27 ± 3%;年老:38 ± 4%)和腓肠肌(年轻:42 ± 6%;年老:64 ± 9%)肌肉小动脉中 ANG II 诱导的血管收缩;这种增强的血管收缩在去除内皮细胞、N(G)-硝基-L-精氨酸甲酯和慢性抑制 TNF-α后被消除。此外,运动训练改善了衰老引起的 ANG II 血管收缩增加。这些发现表明,衰老通过内皮依赖性一氧化氮合酶信号通路增强,运动训练减弱骨骼肌小动脉中 ANG II 诱导的血管收缩反应。此外,衰老时 ANG II 血管收缩的增强似乎与炎症状态有关。