磁共振成像和光谱学方法揭示食欲调节过程中的下丘脑代谢区隔。

Frontiers in neuroenergetics Pub Date : 2013-06-13 eCollection Date: 2013-01-01 DOI:10.3389/fnene.2013.00006
Blanca Lizarbe, Ania Benitez, Gerardo A Peláez Brioso, Manuel Sánchez-Montañés, Pilar López-Larrubia, Paloma Ballesteros, Sebastián Cerdán
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引用次数: 31

摘要

我们回顾了通过磁共振成像(MRI)和光谱学(MRS)方法检测的神经胶质区隔和跨细胞神经递质循环在下丘脑食欲调节中的作用。我们首先讨论下丘脑神经内分泌调节的神经化学基础,以及控制食欲的厌氧和厌氧反馈回路。然后,我们检查了主要的MRI和MRS策略,已用于研究食欲调节。锰增强磁共振成像(MEMRI)、血氧水平依赖对比(BOLD)和弥散加权磁共振成像(DWI)分别显示禁食条件下下丘脑的Mn(2+)积累、氧消耗增加和星形细胞肿胀。体内高场(1)H磁共振显示,与其他大脑结构相比,下丘脑肌醇浓度升高。(1)H和(13)C高分辨率魔角旋转(HRMAS)显示,在缺氧刺激下,神经胶质氧化代谢和糖酵解代谢增加,下丘脑谷氨酸能和gaba能神经递质增加。我们在此提出了对所有这些发现的综合解释,表明食欲的神经内分泌调节是由重要的离子和代谢跨细胞通量支持的,这些跨细胞通量始于三方食氧间隙,并通过星形细胞网络在下丘脑中扩展,最终通过MRI和MRS检测到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Hypothalamic metabolic compartmentation during appetite regulation as revealed by magnetic resonance imaging and spectroscopy methods.

We review the role of neuroglial compartmentation and transcellular neurotransmitter cycling during hypothalamic appetite regulation as detected by Magnetic Resonance Imaging (MRI) and Spectroscopy (MRS) methods. We address first the neurochemical basis of neuroendocrine regulation in the hypothalamus and the orexigenic and anorexigenic feed-back loops that control appetite. Then we examine the main MRI and MRS strategies that have been used to investigate appetite regulation. Manganese-enhanced magnetic resonance imaging (MEMRI), Blood oxygenation level-dependent contrast (BOLD), and Diffusion-weighted magnetic resonance imaging (DWI) have revealed Mn(2+) accumulations, augmented oxygen consumptions, and astrocytic swelling in the hypothalamus under fasting conditions, respectively. High field (1)H magnetic resonance in vivo, showed increased hypothalamic myo-inositol concentrations as compared to other cerebral structures. (1)H and (13)C high resolution magic angle spinning (HRMAS) revealed increased neuroglial oxidative and glycolytic metabolism, as well as increased hypothalamic glutamatergic and GABAergic neurotransmissions under orexigenic stimulation. We propose here an integrative interpretation of all these findings suggesting that the neuroendocrine regulation of appetite is supported by important ionic and metabolic transcellular fluxes which begin at the tripartite orexigenic clefts and become extended spatially in the hypothalamus through astrocytic networks becoming eventually MRI and MRS detectable.

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