Kastin A J, Akerstrom V, Hackler L
VA Medical Center and Tulane University School of Medicine, New Orleans, LA 70112-1262, USA.
Neuroendocrinology. 2001 Dec;74(6):423-32. doi: 10.1159/000054708.
Galanin-like peptide (GALP) was recently isolated from the hypothalamus, where its expression is influenced by leptin and food deprivation. Since leptin crosses the blood-brain barrier (BBB) by a saturable transport system that is downregulated by fasting, we examined the effect of leptin and fasting on the entry of GALP into mouse brain. Multiple-time regression analysis showed that the basal influx of 125I-GALP from blood was rapid (K(i) = 9.49 +/- 0.72 x 10(-4) ml/g x min). This influx was not affected by leptin but was significantly decreased by food deprivation for 24 or 48 h, accompanied by decreased immunoreactive plasma GALP at 48 h, but not at 24 h. By contrast, pretreatment of mice fasted for 24 h with glucose resulted in a significant increase in the blood-to-brain influx of GALP that was not accompanied by increased immunoreactive plasma GALP. HPLC showed that most of the GALP crossed the BBB in an intact form, and capillary depletion studies showed that more than 93% of the GALP crossing entered the parenchyma of the brain rather than being bound to the endothelial cells of the capillaries composing the BBB or being reversibly associated with the vasculature. Efflux of 125I-GALP occurred at the rate of the normal reabsorption of CSF, and the octanol-buffer partition coefficient showed insufficient lipophilicity to explain the fast rate of influx. When 125I-GALP was perfused in blood-free buffer, the self-inhibition characteristic of a saturable transport system was evident even though capillary gel electrophoresis showed GALP aggregating as a trimer. Capillary zone electrophoresis showed protein binding of GALP in serum, perhaps facilitating its interactions at the BBB. In particular, these studies show for the first time (1) that immunoreactive GALP is present in blood where (2) its concentrations are reduced by food deprivation, and (3) that there is a rapid blood-to-brain influx of intact GALP (4) which is decreased by fasting and (5) increased by pretreatment with glucose.
甘丙肽样肽(GALP)最近是从下丘脑分离出来的,其在下丘脑的表达受瘦素和食物剥夺的影响。由于瘦素通过一种可饱和转运系统穿过血脑屏障(BBB),而这种转运系统在禁食时会下调,我们研究了瘦素和禁食对GALP进入小鼠脑内的影响。多元回归分析表明,125I - GALP从血液中的基础流入速度很快(K(i) = 9.49 +/- 0.72 x 10(-4) ml/g x min)。这种流入不受瘦素影响,但在禁食24或48小时后显著降低,48小时时伴有免疫反应性血浆GALP降低,但24小时时没有。相比之下,用葡萄糖对禁食24小时的小鼠进行预处理,导致GALP从血液到脑内的流入显著增加,且免疫反应性血浆GALP没有增加。高效液相色谱法显示,大多数GALP以完整形式穿过血脑屏障,毛细血管耗竭研究表明,超过93%穿过血脑屏障的GALP进入脑实质,而不是与构成血脑屏障的毛细血管内皮细胞结合或与脉管系统可逆性结合。125I - GALP的流出速率与脑脊液的正常重吸收速率相同,辛醇 - 缓冲液分配系数显示其亲脂性不足以解释快速的流入速率。当在无血缓冲液中灌注125I - GALP时,即使毛细管凝胶电泳显示GALP以三聚体形式聚集,可饱和转运系统的自我抑制特性也很明显。毛细管区带电泳显示GALP在血清中有蛋白质结合,这可能促进了它在血脑屏障处的相互作用。特别是,这些研究首次表明:(1)血液中存在免疫反应性GALP;(2)食物剥夺会降低其浓度;(3)完整的GALP存在从血液到脑内的快速流入;(4)禁食会使其减少;(5)葡萄糖预处理会使其增加。