Department of Pathophysiology, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang, 050017, Hebei, China.
Department of Neurosurgery, Third Hospital of Shijiazhuang, Beijing, 050011, Hebei, China.
J Mol Med (Berl). 2019 Mar;97(3):281-289. doi: 10.1007/s00109-019-01745-5. Epub 2019 Jan 23.
The accumulation of glutamate (Glu) in the synaptic cleft during cerebral ischemia triggers the death of neurons, causing mental or physical handicap. However, the mechanisms of the alteration in Glu homeostasis and the imbalance between the release and clearance of Glu in ischemia are not yet completely understood. Additionally, the role of Glu transporters in regulating Glu concentration in the synaptic cleft is controversial. This review aims to provide readers with an in-depth understanding of Glu transporters in the early or later stages of ischemic events, or in mild or severe cerebral ischemia via alteration of Glu transporter expression, reversal of Glu transporters function, and trafficking between membrane and cytoplasm, to further clarify whether the Glu transporters are neuroprotective or neurodegenerative during cerebral ischemia. We provide the insights for deeper understanding of the mechanism of Glu transporters regulation after different periods and severities of cerebral ischemia.
谷氨酸(Glu)在脑缺血期间在突触间隙中的积累会触发神经元死亡,导致精神或身体残疾。然而,Glu 动态平衡改变以及缺血时 Glu 释放和清除之间失衡的机制尚不完全清楚。此外,Glu 转运体在调节突触间隙中 Glu 浓度方面的作用存在争议。这篇综述旨在通过改变 Glu 转运体的表达、逆转 Glu 转运体的功能以及在膜和细胞质之间的运输,为读者提供对缺血事件的早期或晚期、轻度或重度脑缺血中 Glu 转运体的深入了解,进一步阐明 Glu 转运体在脑缺血期间是具有神经保护作用还是神经退行性作用。我们为深入了解不同时期和严重程度的脑缺血后 Glu 转运体调节的机制提供了见解。