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下丘脑甘丙肽:受脂肪代谢信号调控

Hypothalamic galanin: control by signals of fat metabolism.

作者信息

Wang J, Akabayashi A, Yu H J, Dourmashkin J, Alexander J T, Silva I, Lighter J, Leibowitz S F

机构信息

The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.

出版信息

Brain Res. 1998 Aug 31;804(1):7-20. doi: 10.1016/s0006-8993(98)00632-5.

Abstract

The peptide, galanin (GAL), is known to stimulate eating behavior, reduce energy expenditure and affect the release of metabolic hormones. Further, the activity of this peptide in the hypothalamus is modulated, in turn, by these hormones as well as by the ingestion of nutrients. The focus of this investigation is on signals related to nutrient metabolism that may also affect GAL production and, through these neurochemical events, control the ingestion of specific nutrients. Three experiments were performed in normal-weight male, Sprague-Dawley rats. In Experiment 1, the impact of food deprivation (24 and 48 h) was examined. Experiment 2 tested the effects of the compound, 2-deoxy-D-glucose (2-DG, 200 and 400 mg/kg), which blocks glucose utilization, whereas Experiment 3 studied mercaptoacetate (MA, 200 and 600 micromol/kg), which blocks fatty acid oxidation. Eating behavior was examined in some rats, whereas hypothalamic GAL activity was measured in others using radioimmunoassay, immunohistochemistry and in situ hybridization. Both food deprivation and MA (600 micromol/kg), but not 2-DG, affected GAL in the hypothalamus, in one specific area. This is the anterior parvocellular region of the paraventricular nucleus (aPVN), which has a dense concentration of GAL-containing neurons and terminals. GAL gene expression and peptide immunoreactivity in this area is enhanced by food deprivation; in contrast, it is reduced by injection of MA. Other hypothalamic sites with dense concentrations of GAL-containing neurons or fibers are unaffected by food deprivation or MA, and the antimetabolite 2-DG has no impact on GAL in any area. Behavioral measurements indicate that these shifts in GAL activity are accompanied by specific changes in eating behavior. Food deprivation which enhances aPVN GAL produces a marked increase in fat ingestion, whereas MA which reduces aPVN GAL causes a specific reduction in fat ingestion along with a stimulation of protein intake. In contrast, 2-DG preferentially enhances ingestion of carbohydrate. These findings suggest a possible relationship between GAL activity in the aPVN and the metabolic and behavioral processes of fat metabolism and ingestion.

摘要

肽类物质甘丙肽(GAL)已知可刺激进食行为、降低能量消耗并影响代谢激素的释放。此外,该肽在下丘脑中的活性又会反过来受到这些激素以及营养物质摄入的调节。本研究的重点是与营养物质代谢相关的信号,这些信号可能也会影响甘丙肽的产生,并通过这些神经化学事件控制特定营养物质的摄入。在正常体重的雄性斯普拉格-道利大鼠身上进行了三项实验。实验1研究了禁食(24小时和48小时)的影响。实验2测试了化合物2-脱氧-D-葡萄糖(2-DG,200和400毫克/千克)的作用,该化合物会阻断葡萄糖的利用,而实验3研究了巯基乙酸盐(MA,200和600微摩尔/千克)的作用,其会阻断脂肪酸氧化。在一些大鼠中检测进食行为,而在另一些大鼠中使用放射免疫分析、免疫组织化学和原位杂交技术测量下丘脑甘丙肽的活性。禁食和MA(600微摩尔/千克),而非2-DG,会影响下丘脑一个特定区域的甘丙肽。这个区域是室旁核的前小细胞区(aPVN),这里含有密集的含甘丙肽神经元和终末。禁食会增强该区域的甘丙肽基因表达和肽免疫反应性;相反,注射MA会使其降低。其他含有密集的含甘丙肽神经元或纤维的下丘脑部位不受禁食或MA的影响,抗代谢物2-DG对任何区域的甘丙肽都没有影响。行为测量表明,甘丙肽活性的这些变化伴随着进食行为的特定改变。增强aPVN甘丙肽的禁食会使脂肪摄入量显著增加,而降低aPVN甘丙肽的MA会导致脂肪摄入量特定减少,同时刺激蛋白质摄入。相比之下,2-DG优先增强碳水化合物的摄入。这些发现表明aPVN中甘丙肽的活性与脂肪代谢和摄入的代谢及行为过程之间可能存在关联。

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