首页> 外文期刊>Circulation research: a journal of the American Heart Association >Impaired skeletal muscle blood flow control with advancing age in humans: Attenuated ATP release and local vasodilation during erythrocyte deoxygenation
【24h】

Impaired skeletal muscle blood flow control with advancing age in humans: Attenuated ATP release and local vasodilation during erythrocyte deoxygenation

机译:随着年龄的增长,骨骼肌血流控制受损:红细胞脱氧过程中ATP释放减弱和局部血管舒张

获取原文
获取原文并翻译 | 示例
           

摘要

Rationale: Skeletal muscle blood flow is coupled with the oxygenation state of hemoglobin in young adults, whereby the erythrocyte functions as an oxygen sensor and releases ATP during deoxygenation to evoke vasodilation. Whether this function is impaired in humans of advanced age is unknown. Objective: To test the hypothesis that older adults demonstrate impaired muscle blood flow and lower intravascular ATP during conditions of erythrocyte deoxygenation. Methods and Results: We showed impaired forearm blood flow responses during 2 conditions of erythrocyte deoxygenation (systemic hypoxia and graded handgrip exercise) with age, which was caused by reduced local vasodilation. In young adults, both hypoxia and exercise significantly increased venous [ATP] and ATP effluent (forearm blood flow×[ATP]) draining the skeletal muscle. In contrast, hypoxia and exercise did not increase venous [ATP] in older adults, and both venous [ATP] and ATP effluent were substantially reduced compared with young people despite similar levels of deoxygenation. Next, we demonstrated that this could not be explained by augmented extracellular ATP hydrolysis in whole blood with age. Finally, we found that deoxygenation-mediated ATP release from isolated erythrocytes was essentially nonexistent in older adults. Conclusions: Skeletal muscle blood flow during conditions of erythrocyte deoxygenation was markedly reduced in aging humans, and reductions in plasma ATP and erythrocyte-mediated ATP release may be a novel mechanism underlying impaired vasodilation and oxygen delivery during hypoxemia with advancing age. Because aging is associated with elevated risk for ischemic cardiovascular disease and exercise intolerance, interventions that target erythrocyte-mediated ATP release may offer therapeutic potential.
机译:原理:年轻人的骨骼肌血流与血红蛋白的氧合状态有关,因此红细胞起着氧传感器的作用,并在脱氧过程中释放ATP以引起血管舒张。尚不清楚该功能是否在高龄人群中受损。目的:检验以下假设:老年人在红细胞脱氧期间表现出肌肉血流受损和血管内ATP降低。方法和结果:我们发现随着年龄的增长,在两种红细胞脱氧条件下(系统性缺氧和分级握力运动)前臂血流反应受损,这是由于局部血管舒张减少所致。在年轻人中,低氧和运动都显着增加了排出骨骼肌的静脉血[ATP]和ATP流出量(前臂血流量[ATP])。相反,低氧和运动并不会增加老年人的静脉[ATP],尽管年轻人的脱氧水平相近,但与年轻人相比,静脉[ATP]和ATP流出量均大大减少。接下来,我们证明了这不能通过随着年龄的增长而增加全血中的细胞外ATP水解来解释。最后,我们发现在老年人中从分离的红细胞中脱氧介导的ATP释放基本上不存在。结论:衰老的人在红细胞脱氧条件下的骨骼肌血流量明显减少,血浆ATP和红细胞介导的ATP释放的减少可能是低氧血症随着年龄的增长而损害血管舒张和氧气输送的新机制。由于衰老与缺血性心血管疾病和运动不耐症的风险升高相关,因此针对红细胞介导的ATP释放的干预措施可能具有治疗潜力。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号