首页> 美国卫生研究院文献>American Journal of Physiology - Heart and Circulatory Physiology >Small Vessels-Big Problems: Novel Insights into Microvascular Mechanisms of Diseases: Pathways for insulin access to the brain: the role of the microvascular endothelial cell
【2h】

Small Vessels-Big Problems: Novel Insights into Microvascular Mechanisms of Diseases: Pathways for insulin access to the brain: the role of the microvascular endothelial cell

机译:小血管-大问题:微血管疾病机制的新见解:胰岛素进入大脑的途径:微血管内皮细胞的作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Insulin affects multiple important central nervous system (CNS) functions including memory and appetite, yet the pathway(s) by which insulin reaches brain interstitial fluid (bISF) has not been clarified. Recent studies demonstrate that to reach bISF, subarachnoid cerebrospinal fluid (CSF) courses through the Virchow-Robin space (VRS) which sheaths penetrating pial vessels down to the capillary level. Whether insulin predominantly enters the VRS and bISF by local transport through the blood-brain barrier, or by being secreted into the CSF by the choroid plexus, is unknown. We injected 125I-TyrA14-insulin or regular insulin intravenously and compared the rates of insulin reaching subarachnoid CSF with its plasma clearance by brain tissue samples (an index of microvascular endothelial cell binding/uptake/transport). The latter process was more than 40-fold more rapid. We then showed that selective insulin receptor blockade or 4 wk of high-fat feeding each inhibited microvascular brain 125I-TyrA14-insulin clearance. We further confirmed that 125I-TyrA14-insulin was internalized by brain microvascular endothelial cells, indicating that the in vivo tissue association reflected cellular transport, not simply microvascular tracer binding.
机译:胰岛素影响多种重要的中枢神经系统(CNS)功能,包括记忆和食欲,但胰岛素到达脑组织间质液(bISF)的途径尚不清楚。最近的研究表明,要达到bISF,蛛网膜下腔脑脊液(CSF)会通过Virchow-Robin空间(VRS)穿行,该鞘将穿透脉管的鞘层向下渗透到毛细血管水平。胰岛素是通过血脑屏障的局部转运还是通过脉络丛分泌到CSF中而主要进入VRS和bISF是未知的。我们静脉注射 125 I-TyrA14-胰岛素或常规胰岛素,并通过脑组织样本比较了到达蛛网膜下腔CSF的胰岛素的比率及其血浆清除率(微血管内皮细胞结合/摄取/转运的指数)。后者的处理速度提高了40倍以上。然后我们表明选择性胰岛素受体阻滞或高脂喂养4周分别抑制了微血管脑 125 I-TyrA14-胰岛素清除。我们进一步证实, 125 I-TyrA14-胰岛素被脑微血管内皮细胞内化,表明体内组织的结合反映了细胞运输,而不仅仅是微血管示踪剂的结合。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号