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首页> 外文期刊>Aging cell. >Treatment with the mitochondrial‐targeted antioxidant peptide SS‐31 rescues neurovascular coupling responses and cerebrovascular endothelial function and improves cognition in aged mice
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Treatment with the mitochondrial‐targeted antioxidant peptide SS‐31 rescues neurovascular coupling responses and cerebrovascular endothelial function and improves cognition in aged mice

机译:线粒体靶向抗氧化剂肽SS-31的治疗可挽救神经血管偶联反应和脑血管内皮功能,并改善老年小鼠的认知

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Moment‐to‐moment adjustment of cerebral blood flow (CBF) via neurovascular coupling has an essential role in maintenance of healthy cognitive function. In advanced age, increased oxidative stress and cerebromicrovascular endothelial dysfunction impair neurovascular coupling, likely contributing to age‐related decline of higher cortical functions. There is increasing evidence showing that mitochondrial oxidative stress plays a critical role in a range of age‐related cellular impairments, but its role in neurovascular uncoupling remains unexplored. This study was designed to test the hypothesis that attenuation of mitochondrial oxidative stress may exert beneficial effects on neurovascular coupling responses in aging. To test this hypothesis, 24‐month‐old C57BL/6 mice were treated with a cell‐permeable, mitochondria‐targeted antioxidant peptide (SS‐31; 10?mg?kg?1?day?1, i.p.) or vehicle for 2?weeks. Neurovascular coupling was assessed by measuring CBF responses (laser speckle contrast imaging) evoked by contralateral whisker stimulation. We found that neurovascular coupling responses were significantly impaired in aged mice. Treatment with SS–31 significantly improved neurovascular coupling responses by increasing NO‐mediated cerebromicrovascular dilation, which was associated with significantly improved spatial working memory, motor skill learning, and gait coordination. These findings are paralleled by the protective effects of SS–31 on mitochondrial production of reactive oxygen species and mitochondrial respiration in cultured cerebromicrovascular endothelial cells derived from aged animals. Thus, mitochondrial oxidative stress contributes to age‐related cerebromicrovascular dysfunction, exacerbating cognitive decline. We propose that mitochondria‐targeted antioxidants may be considered for pharmacological microvascular protection for the prevention/treatment of age‐related vascular cognitive impairment (VCI).
机译:通过神经血管偶联的瞬间对脑血流量(CBF)的调节在维持健康的认知功能中起着至关重要的作用。在高龄者中,氧化应激的增加和脑微血管内皮功能障碍会损害神经血管耦合,可能导致与年龄相关的高级皮质功能下降。越来越多的证据表明,线粒体的氧化应激在一系列与年龄有关的细胞损伤中起着关键作用,但其在神经血管解偶联中的作用仍待探索。本研究旨在检验以下假设:线粒体氧化应激的减弱可能会对衰老中的神经血管偶联反应产生有益影响。为了验证这一假设,对24个月大的C57BL / 6小鼠进行了细胞渗透性线粒体靶向抗氧化剂肽(SS-31; 10?mg?kg ?1? day ?1 ,ip)或车辆2周。通过测量对侧晶须刺激引起的CBF反应(激光散斑对比成像)评估神经血管耦合。我们发现老年小鼠的神经血管偶联反应明显受损。 SS–31的治疗通过增加NO介导的脑微血管扩张而显着改善了神经血管偶联反应,这与空间工作记忆,运动技能学习和步态协调性显着改善有关。这些发现与SS–31对源自衰老动物的培养的脑微血管内皮细胞的线粒体活性氧产生和线粒体呼吸的保护作用平行。因此,线粒体的氧化应激会导致与年龄有关的脑微血管功能障碍,加剧认知能力下降。我们建议针对线粒体的抗氧化剂可考虑用于预防/治疗与年龄有关的血管性认知障碍(VCI)的药理微血管。

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