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Relation of potassium transport to oxidative metabolism in isolated brain capillaries

机译:钾转运与孤立脑毛细血管氧化代谢的关系

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摘要

1. The uptake of K by a capillary suspension isolated from rat brain was studied with the radioactive analogue 86Rb.2. Rb uptake was dependent upon the presence of oxygen and could be markedly inhibited with ouabain.3. The ouabain sensitive Rb uptake was measured at varying external concentrations of K. Uptake of K (as 86Rb) was half-maximal when the K concentration was 3·0 mM. This in vitro affinity of the transport carrier for K is similar to that found in previous in vivo studies of K efflux from brain to blood.4. I propose that the ouabain sensitive K pump is located on the antiluminal plasma membrane of brain capillary endothelial cells and that this pump contributes to the maintenance of a constant concentration (i.e. 3 mM) of K in brain interstitial fluid.5. Glucose and palmitate were tested as possible energy substrates for the support of active Rb uptake by isolated brain capillaries. The rate of Rb uptake increased 40% when 0·25 mM-palmitate was added to a capillary suspension containing 5 mM-glucose. This stimulation of Rb uptake could be blocked by 1 mM-4-pentenoic acid, an inhibitor of fatty acid oxidation. In contrast, the fraction of Rb uptake supported by glucose was not altered by 4-pentenoic acid.6. The rates of [U-14C]glucose and [U-14C]palmitate oxidation to CO2 were measured in isolated brain capillaries and compared to their oxidation by brain slices and synaptosomes. Palmitate was the source of 28% of the 14CO2 produced by the capillaries but only 0·5% of the 14CO2 produced by the brain slices and synaptosomes.7. It is concluded that brain capillaries are similar to renal tubules in their polar distribution of ouabain sensitive K transport carriers, dependence on oxidative metabolism for active ion transport, and use of fatty acids as energy substrates. These features may underlie the vulnerability of brain capillaries in several metabolic diseases that cause brain oedema.
机译:1.用放射性类似物 86 Rb研究了从大鼠脑中分离的毛细血管悬浮液对钾的吸收。 Rb的吸收取决于氧气的存在,并且可能被哇巴因抑制。3。在不同的外部K浓度下测量了哇巴因对Rb的吸收。当K浓度为3·0 mM时,K的吸收( 86 Rb)最大。转运载体对钾的这种体外亲和力类似于先前体内从脑到血液的钾外排研究中发现的亲和力4。我建议对哇巴因敏感的K泵位于脑毛细血管内皮细胞的管腔质膜上,并且该泵有助于维持脑组织液中K的恒定浓度(即3 mM).5。测试葡萄糖和棕榈酸酯作为可能的能量底物,以支持离体的脑毛细血管吸收活性Rb。当将0·25 mM棕榈酸酯添加到含有5 mM葡萄糖的毛细管悬浮液中时,Rb吸收率增加40%。 Rb摄取的这种刺激可被1 mM-4-戊烯酸(一种脂肪酸氧化抑制剂)阻断。相反,葡萄糖支持的Rb吸收比例并未被4-戊烯酸改变。6。在分离的脑毛细血管中测量[U- 14 C]葡萄糖和[U- 14 C]棕榈酸氧化成CO2的速率,并与脑切片和脑片进行比较突触小体。棕榈酸酯是毛细血管产生的 14 CO2的28%,而脑切片和突触小体产生的 14 CO2的只有0·5%。7。结论是,脑毛细血管在哇巴因敏感的K转运载体的极性分布,依赖于氧化代谢进行活性离子转运以及使用脂肪酸作为能量底物方面与肾小管相似。这些特征可能是脑毛细血管在几种引起脑水肿的代谢疾病中的脆弱性的基础。

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