Homeostasis to Allostasis: Prefrontal Astrocyte Roles in Cognitive Flexibility and Stress Biology.

Q3 Neuroscience Advances in neurobiology Pub Date : 2024-01-01 DOI:10.1007/978-3-031-64839-7_6
Bolati Wulaer, Mika A Holtz, Jun Nagai
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Abstract

In the intricate landscape of neurophysiology, astrocytes have been traditionally cast as homeostatic cells; however, their mechanistic involvement in allostasis-particularly how they modulate the adaptive response to stress and its accumulative impact that disrupts cognitive functions and precipitates psychiatric disorders-is now starting to be unraveled. Here, we address the gap by positing astrocytes as crucial allostatic players whose molecular adaptations underlie cognitive flexibility in stress-related neuropsychiatric conditions. We review how astrocytes, responding to stress mediators such as glucocorticoid and epinephrine/norepinephrine, undergo morphological and functional transformations that parallel the maladaptive changes. Our synthesis of recent findings reveals that these glial changes, especially in the metabolically demanding prefrontal cortex, may underlie some of the neuropsychiatric mechanisms characterized by the disruption of energy metabolism and astrocytic networks, compromised glutamate clearance, and diminished synaptic support. We argue that astrocytes extend beyond their homeostatic role, actively participating in the brain's allostatic response, especially by modulating energy substrates critical for cognitive functions.

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从平衡到失衡:前额叶星形胶质细胞在认知灵活性和应激生物学中的作用
在错综复杂的神经生理学领域,星形胶质细胞历来被认为是平衡细胞;然而,它们参与异稳态的机理--尤其是它们如何调节对压力的适应性反应以及压力的累积影响,从而破坏认知功能并诱发精神疾病--现在已开始被揭开谜底。在这里,我们将星形胶质细胞假设为关键的异稳态参与者,其分子适应性是压力相关神经精神疾病中认知灵活性的基础,从而填补了这一空白。我们回顾了星形胶质细胞如何对糖皮质激素和肾上腺素/去甲肾上腺素等应激介质做出反应,并发生与适应不良变化平行的形态和功能转变。我们对最新研究结果的综合分析表明,这些神经胶质的变化,尤其是在需要大量新陈代谢的前额叶皮质中,可能是一些神经精神机制的基础,这些机制的特点是能量代谢和星形胶质细胞网络被破坏、谷氨酸清除能力受损以及突触支持减弱。我们认为,星形胶质细胞的作用超出了其平衡作用的范围,它们积极参与大脑的异质反应,尤其是通过调节对认知功能至关重要的能量基质。
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来源期刊
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
CiteScore
2.80
自引率
0.00%
发文量
0
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