周细胞介导的毛细血管直径调节:健康和疾病中神经血管耦合的一个组成部分。

Frontiers in neuroenergetics Pub Date : 2010-05-21 eCollection Date: 2010-01-01 DOI:10.3389/fnene.2010.00005
Nicola B Hamilton, David Attwell, Catherine N Hall
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引用次数: 468

摘要

因为局部血流量增加与局部神经活动增加引起的代谢需求增加相关,功能成像研究人员通常假设血流量的变化是潜在神经活动变化的准确读出。了解将神经活动变化与血流变化联系起来的机制,对于评估这一假设的有效性至关重要,对于理解在缺血性中风等疾病状态下可能出错的过程至关重要。许多研究已经调查了小动脉中神经血管调节的机制,但其他证据表明,由于毛细血管壁上存在收缩细胞(周细胞),血流调节也可以发生在毛细血管中。在这里,我们回顾了周细胞可以调节毛细血管直径以响应神经元活动的证据,并评估了在毛细血管水平上神经血管调节对功能成像实验的可能重要性。我们还讨论了表明周细胞在病理性损伤(如缺血、阿尔茨海默病和糖尿病视网膜病变)中对损伤特别敏感的证据,并考虑了周细胞功能障碍可能对治疗干预措施的发展和对这些疾病的功能成像数据的解释的潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pericyte-mediated regulation of capillary diameter: a component of neurovascular coupling in health and disease.

Pericyte-mediated regulation of capillary diameter: a component of neurovascular coupling in health and disease.

Pericyte-mediated regulation of capillary diameter: a component of neurovascular coupling in health and disease.

Pericyte-mediated regulation of capillary diameter: a component of neurovascular coupling in health and disease.

Because regional blood flow increases in association with the increased metabolic demand generated by localized increases in neural activity, functional imaging researchers often assume that changes in blood flow are an accurate read-out of changes in underlying neural activity. An understanding of the mechanisms that link changes in neural activity to changes in blood flow is crucial for assessing the validity of this assumption, and for understanding the processes that can go wrong during disease states such as ischaemic stroke. Many studies have investigated the mechanisms of neurovascular regulation in arterioles but other evidence suggests that blood flow regulation can also occur in capillaries, because of the presence of contractile cells, pericytes, on the capillary wall. Here we review the evidence that pericytes can modulate capillary diameter in response to neuronal activity and assess the likely importance of neurovascular regulation at the capillary level for functional imaging experiments. We also discuss evidence suggesting that pericytes are particularly sensitive to damage during pathological insults such as ischaemia, Alzheimer's disease and diabetic retinopathy, and consider the potential impact that pericyte dysfunction might have on the development of therapeutic interventions and on the interpretation of functional imaging data in these disorders.

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