Neurointegrity and europhysiology: astrocyte, glutamate, and carbon monoxide interactions

被引:18
|
作者
Mahan, Vicki L. [1 ]
机构
[1] Drexel Univ, St Christophers Hosp Children, Dept Surg, Div Pediat Cardiothorac Surg,Coll Med, Philadelphia, PA 19104 USA
来源
MEDICAL GAS RESEARCH | 2019年 / 9卷 / 01期
关键词
carbon monoxide; astrocytes; glutamate metabolism in the brain; neuroprotection by carbon monoxide; astrocyte control of glutamate metabolism; gasotransmitters; neurotherapy; neuroprotection; GABA; BRANCHED-CHAIN AMINOTRANSFERASE; KAINATE RECEPTOR SUBUNITS; PERMEABLE AMPA RECEPTORS; NEURONAL-ACTIVITY; APOLIPOPROTEIN-E; HEME OXYGENASE; NMDA RECEPTORS; GLIAL-CELLS; MITOCHONDRIAL DYNAMICS; ENDOPLASMIC-RETICULUM;
D O I
10.4103/2045-9912.254639
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Astrocyte contributions to brain function and prevention of neuropathologies are as extensive as that of neurons. Astroglial regulation of glutamate, a primary neurotransmitter, is through uptake, release through vesicular and non-vesicular pathways, and catabolism to intermediates. Homeostasis by astrocytes is considered to be of primary importance in determining normal central nervous system health and central nervous system physiology - glutamate is central to dynamic physiologic changes and central nervous system stability. Gasotransmitters may affect diverse glutamate interactions positively or negatively. The effect of carbon monoxide, an intrinsic central nervous system gaso-transmitter, in the complex astrocyte homeostasis of glutamate may offer insights to normal brain development, protection, and its use as a neuromodulator and neurotherapeutic. In this article, we will review the effects of carbon monoxide on astrocyte homeostasis of glutamate.
引用
收藏
页码:24 / 45
页数:22
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