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首页> 外文期刊>Journal of applied physiology >Aging and muscle fiber type alter K+ channel contributions to the myogenic response in skeletal muscle arterioles.
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Aging and muscle fiber type alter K+ channel contributions to the myogenic response in skeletal muscle arterioles.

机译:衰老和肌纤维类型会改变K +通道对骨骼肌小动脉肌源性反应的贡献。

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摘要

Aging diminishes myogenic tone in arterioles from skeletal muscle. Recent evidence indicates that both large-conductance Ca2+-activated (BKCa) and voltage-dependent (KV) K+ channels mediate negative feedback control of the myogenic response. Thus we tested the hypothesis that aging increases the contributions of KV and BKCa channels to myogenic regulation of vascular tone. Because myogenic responsiveness differs between oxidative and glycolytic muscles, we predicted that KV and BKCa channel contributions to myogenic responsiveness vary with fiber type. Myogenic responses of first-order arterioles from the gastrocnemius and soleus muscles of 4- and 24-mo-old Fischer 344 rats were evaluated in the presence and absence of 4-aminopyridine (5 mM) or iberiotoxin (30 nM), inhibitors of KV and BKCa, respectively. 4-Aminopyridine enhanced myogenic tone with aging and normalized age-related differences in both muscle types. By contrast, iberiotoxin eliminated age-related differences in soleus arterioles and had no effect in gastrocnemius vessels. KV1.5 is an integral component of KV channels in vascular smooth muscle; therefore, we determined the relative protein expression of KV1.5, as well as BKCa, in soleus and gastrocnemius arterioles. Immunoblot analysis revealed no differences in KV1.5 protein with aging or between variant fiber types, whereas BKCa protein levels declined with age in arterioles from both muscle groups. Collectively, these results suggest that the contribution of BKCa to myogenic regulation of vascular tone changes with age in soleus muscle arterioles, whereas increased KV channel expression and negative feedback regulation of myogenic tone increases with advancing age in arterioles from both oxidative and glycolytic muscles.
机译:衰老减少了骨骼肌小动脉的肌原性。最近的证据表明,大电导的Ca2 +激活(BKCa)和电压依赖性(KV)的K +通道均介导了肌原性反应的负反馈控制。因此,我们检验了以下假设:衰老增加了KV和BKCa通道对血管紧张性肌原性调节的作用。由于氧化和糖酵解肌肉之间的肌反应性不同,因此我们预测KV和BKCa通道对肌反应性的贡献随纤维类型而变化。在存在和不存在KV抑制剂4-氨基吡啶(5 mM)或纤毛毒素(30 nM)的情况下,评估了4和24岁Fischer 344大鼠腓肠肌和比目鱼肌一级小动脉的肌反应。和BKCa。 4-Aminopyridine增强了肌源性肌张力,且两种类型的肌肉均具有衰老和与年龄相关的标准化差异。相比之下,埃博毒素去除比目鱼小动脉的年龄相关差异,并且对腓肠肌血管没有影响。 KV1.5是血管平滑肌中KV通道的组成部分;因此,我们确定了比目鱼肌和腓肠肌小动脉中KV1.5以及BKCa的相对蛋白表达。免疫印迹分析显示,两个肌肉组的小动脉中,KV1.5蛋白随年龄增长或不同纤维类型之间无差异,而BKCa蛋白水平随年龄下降。总体而言,这些结果表明,比目鱼肌小动脉中BKCa对血管紧张度的肌源性调节的作用随年龄的变化而变化,而随着年龄的增加,来自氧化性和糖酵解性肌肉的KV通道表达增加以及对肌源性音调的负反馈调节也随之增加。

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