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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Glial cells dilate and constrict blood vessels: a mechanism of neurovascular coupling.
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Glial cells dilate and constrict blood vessels: a mechanism of neurovascular coupling.

机译:胶质细胞扩张和收缩血管:神经血管偶联机制。

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摘要

Neuronal activity evokes localized changes in blood flow. Although this response, termed neurovascular coupling, is widely used to monitor human brain function and diagnose pathology, the cellular mechanisms that mediate the response remain unclear. We investigated the contribution of glial cells to neurovascular coupling in the acutely isolated mammalian retina. We found that light stimulation and glial cell stimulation can both evoke dilation or constriction of arterioles. Light-evoked and glial-evoked vasodilations were blocked by inhibitors of cytochrome P450 epoxygenase, the synthetic enzyme for epoxyeicosatrienoic acids. Vasoconstrictions, in contrast, were blocked by an inhibitor of omega-hydroxylase, which synthesizes 20-hydroxyeicosatetraenoic acid. Nitric oxide influenced whether vasodilations or vasoconstrictions were produced in response to light and glial stimulation. Light-evoked vasoactivity was blocked when neuron-to-glia signaling was interrupted by a purinergic antagonist. These results indicate that glial cells contribute to neurovascular coupling and suggest that regulation of blood flow may involve both vasodilating and vasoconstricting components.
机译:神经元活动唤起血流的局部变化。虽然这种反应称为神经血管偶联,广泛用于监测人脑功能和诊断病理学,但介导响应的细胞机制仍然不清楚。我们调查了胶质细胞在急性分离的哺乳动物视网膜中对神经血管偶联的贡献。我们发现光刺激和胶质细胞刺激可以引起大菌的扩张或收缩。通过细胞色素P450环氧树脂的抑制剂,环氧基硅酸的合成酶被抑制剂阻断了光诱发和胶质血管舒张。相比之下,血管收缩以ω-羟化酶的抑制剂封闭,其合成20-羟基辛酸四烯酸。一氧化氮影响是否响应于光和胶质刺激而产生血管沉积或血管科。当神经元拮抗剂中断神经元到胶质增长信号时,曝光的血管活性被阻断。这些结果表明,胶质细胞有助于神经血管偶联,并表明血流调节可能涉及血管舒张和血管电脑的组分。

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