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Tonic Local Brain Blood Flow Control by Astrocytes Independent of Phasic Neurovascular Coupling

机译:星形胶质细胞与阶段性神经血管耦合无关的补品局部脑血流量控制。

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摘要

According to the current model of neurovascular coupling, blood flow is controlled regionally through phasic changes in the activity of neurons and astrocytes that signal to alter arteriole diameter. Absent in this model, however, is how brain blood flow is tonically regulated independent of regional changes in activity. This is important because a large fraction of brain blood flow is required to maintain basal metabolic needs. Using two-photon fluorescence imaging combined with patch-clamp in acute rat brain slices of sensory-motor cortex, we demonstrate that reducing resting Ca2+ in astrocytes with intracellular BAPTA causes vasoconstriction in adjacent arterioles. BAPTA-induced vasoconstriction was eliminated by a general COX blocker and the effect is mimicked by a COX-1, but not COX-2, antagonist, suggesting that astrocytes provide tonic, steady-state vasodilation by releasing prostaglandin messengers. Tonic vasodilation was insensitive to TTX, as well as a variety of synaptic and extrasynaptic receptor antagonists, indicating that the phenomenon operates largely independent of neural activity. Using in vivo two-photon fluorescence imaging of the barrel cortex in fully awake mice, we reveal that acute COX-1 inhibition reduces resting arteriole diameter but fails to affect vasodilation in response to vibrissae stimulation. Our findings demonstrate that astrocytes provide tonic regulation of arterioles using resting intracellular Ca2+ in a manner that is independent of phasic, neuronal-evoked vasodilation.>SIGNIFICANCE STATEMENT The brain requires both phasic and tonic regulation of its blood supply to service energy needs over various temporal windows. While many mechanisms have been described for phasic blood flow regulation, how the brain accomplishes tonic control is largely unknown. Here we describe a way in which astrocytes contribute to the management of basal brain blood flow by providing steady-state vasodilation to arterioles via resting astrocyte Ca2+ and the continuous release of prostaglandin messengers. This phenomenon may be important for understanding the declines in basal brain blood flow that occur in aging and dementia, as well as for the interpretation of fMRI data.
机译:根据当前的神经血管偶联模型,通过信号改变小动脉直径的神经元和星形胶质细胞活动的阶段性变化来局部控制血流。然而,在该模型中缺少的是如何独立于活动区域变化来调节脑血流量。这很重要,因为需要大量的脑血流来维持基础代谢需求。使用双光子荧光成像结合膜片钳在大鼠感觉运动皮层的急性脑切片中,我们证明减少具有细胞内BAPTA的星形胶质细胞中的静息Ca 2 + 会导致邻近小动脉的血管收缩。 BAPTA诱导的血管收缩可通过一般的COX阻滞剂消除,其作用可通过COX-1拮抗剂(而非COX-2拮抗剂)模仿,这表明星形胶质细胞通过释放前列腺素使者提供强直的稳态血管舒张作用。补药性血管舒张作用对TTX以及各种突触和突触外受体拮抗剂均不敏感,这表明该现象在很大程度上与神经活动无关。使用完全清醒的小鼠的桶状皮质的体内双光子荧光成像,我们揭示了急性COX-1抑制可减少静息小动脉直径,但不能影响对触须刺激的血管舒张作用。我们的发现表明,星形胶质细胞利用静息的细胞内Ca 2 + 来调节小动脉的强直性,其方式与阶段性,神经元诱发的血管舒张无关。>重要意义声明调节其血液供应的相位和张力,以在各种时间范围内满足能量需求。尽管已经描述了用于调节阶段性血流的许多机制,但是大脑如何完成补品控制仍然是未知的。在这里,我们描述了一种星形胶质细胞通过静息星形胶质细胞Ca 2 + 并持续释放前列腺素使者,为小动脉提供稳态血管舒张,从而有助于基础脑血流的管理。该现象对于理解衰老和痴呆中发生的基础脑血流量下降以及对fMRI数据的解释可能很重要。

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