Zedde Marialuisa, Pascarella Rosario
Neurology Unit, Stroke Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123 Reggio Emilia, Italy.
Neuroradiology Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123 Reggio Emilia, Italy.
Brain Sci. 2024 Sep 28;14(10):983. doi: 10.3390/brainsci14100983.
The delivery of nutrients to the brain is provided by a 600 km network of capillaries and microvessels. Indeed, the brain is highly energy demanding and, among a total amount of 100 billion neurons, each neuron is located just 10-20 μm from a capillary. This vascular network also forms part of the blood-brain barrier (BBB), which maintains the brain's stable environment by regulating chemical balance, immune cell transport, and blocking toxins. Typically, brain microvascular endothelial cells (BMECs) have low turnover, indicating a stable cerebrovascular structure. However, this structure can adapt significantly due to development, aging, injury, or disease. Temporary neural activity changes are managed by the expansion or contraction of arterioles and capillaries. Hypoxia leads to significant remodeling of the cerebrovascular architecture and pathological changes have been documented in aging and in vascular and neurodegenerative conditions. These changes often involve BMEC proliferation and the remodeling of capillary segments, often linked with local neuronal changes and cognitive function. Cerebrovascular plasticity, especially in arterioles, capillaries, and venules, varies over different time scales in development, health, aging, and diseases. Rapid changes in cerebral blood flow (CBF) occur within seconds due to increased neural activity. Prolonged changes in vascular structure, influenced by consistent environmental factors, take weeks. Development and aging bring changes over months to years, with aging-associated plasticity often improved by exercise. Injuries cause rapid damage but can be repaired over weeks to months, while neurodegenerative diseases cause slow, varied changes over months to years. In addition, if animal models may provide useful and dynamic in vivo information about vascular plasticity, humans are more complex to investigate and the hypothesis of glymphatic system together with Magnetic Resonance Imaging (MRI) techniques could provide useful clues in the future.
由600公里长的毛细血管和微血管网络为大脑输送营养物质。事实上,大脑对能量的需求极高,在总共1000亿个神经元中,每个神经元距离毛细血管仅10 - 20微米。这个血管网络也是血脑屏障(BBB)的一部分,它通过调节化学平衡、免疫细胞运输和阻挡毒素来维持大脑的稳定环境。通常,脑微血管内皮细胞(BMECs)的更新率较低,这表明脑血管结构稳定。然而,由于发育、衰老、损伤或疾病,这种结构会发生显著变化。短暂的神经活动变化通过小动脉和毛细血管的扩张或收缩来调节。缺氧会导致脑血管结构的显著重塑,并且在衰老以及血管和神经退行性疾病中已记录到病理变化。这些变化通常涉及BMEC增殖和毛细血管段的重塑,这往往与局部神经元变化和认知功能相关。脑血管可塑性,尤其是在小动脉、毛细血管和小静脉中,在发育、健康、衰老和疾病的不同时间尺度上有所不同。由于神经活动增加,脑血流量(CBF)会在数秒内迅速变化。受持续环境因素影响,血管结构的长期变化需要数周时间。发育和衰老会在数月至数年的时间里带来变化,与衰老相关的可塑性通常通过运动得到改善。损伤会导致快速损伤,但可在数周至数月内修复,而神经退行性疾病则会在数月至数年的时间里导致缓慢且多样的变化。此外,如果动物模型可以提供有关血管可塑性的有用且动态的体内信息,那么对人类进行研究则更为复杂,未来淋巴系统假说与磁共振成像(MRI)技术可能会提供有用的线索。