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前列腺素通过血脑屏障和血脑脊液屏障的易化转运。

Facilitated transport of prostaglandins across the blood-cerebrospinal fluid and blood-brain barriers.

作者信息

Bito L Z, Davson H, Hollingsworth J R

机构信息

Department of Physiology, University College, London W.C.1.

出版信息

J Physiol. 1976 Apr;256(2):273-85. doi: 10.1113/jphysiol.1976.sp011325.

Abstract
  1. Ventriculo-cisternal perfusions were performed on rabbits with artificial cerebrospinal fluid containing blue dextran and tritium-labelled prostaglandin F(2alpha) ([(3)H]PGF(2alpha)). In order to study the nature of prostaglandin (PG) transfer across the blood-brain barrier, high concentrations of PGF(2alpha) or potential PG transport inhibitors were added to the perfusion fluid after the normal rate of [(3)H]PGF(2alpha) clearance was established.2. The [(3)H]PGF(2alpha) clearance was inhibited by 10(-6) to 10(-3)M PGF(2alpha), PGF(2beta), probenecid, iodipamide or bromcresol green but not by perchlorate.3. The (3)H content of the brain, relative to the (3)H-activity in the ventricular system, was also increased by high concentrations of PGF(2alpha), iodipamide or bromcresol green.4. It is concluded that the removal of PGs from the extracellular fluids of the brain is mediated by saturable, facilitated transport processes across both the choroidal and extrachoroidal regions of the blood-brain barrier system. In the case of the mammalian brain, such facilitated PG transport appears to be the primary mechanism for the termination of the action of these potent, endogenously produced autacoids.
摘要
  1. 用含蓝色葡聚糖和氚标记的前列腺素F(2α)([³H]PGF(2α))的人工脑脊液对家兔进行脑室-脑池灌注。为研究前列腺素(PG)跨越血脑屏障的转运性质,在确定[³H]PGF(2α)的正常清除率后,向灌注液中加入高浓度的PGF(2α)或潜在的PG转运抑制剂。

  2. [³H]PGF(2α)的清除受到10⁻⁶至10⁻³M的PGF(2α)、PGF(2β)、丙磺舒、碘帕醇或溴甲酚绿的抑制,但不受高氯酸盐的抑制。

  3. 相对于脑室系统中的³H活性,高浓度的PGF(2α)、碘帕醇或溴甲酚绿也会使脑中的³H含量增加。

  4. 得出的结论是,PGs从脑的细胞外液中的清除是通过血脑屏障系统脉络丛和脉络丛外区域的可饱和的易化转运过程介导的。就哺乳动物脑而言,这种易化的PG转运似乎是这些内源性产生的强效自分泌物质作用终止的主要机制。

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