Bairamian D, Johanson C E, Parmelee J T, Epstein M H
Department of Clinical Neurosciences, Brown University/Rhode Island Hospital, Providence 02902.
J Neurochem. 1991 May;56(5):1623-9. doi: 10.1111/j.1471-4159.1991.tb02060.x.
The effects of loop diuretics and ion substitution on the 2-min uptake of K (86Rb as marker) were analyzed to obtain evidence for K cotransport with Na and Cl in the choroid plexus epithelium. The isolated plexuses, which were excised from lateral ventricles of adult rats, were bathed in artificial cerebrospinal fluid (aCSF). At concentrations of 10(-6) to 10(-4) M, the specific cotransport inhibitors, bumetanide and piretanide, suppressed uptake of K in a dose-dependent manner. Ouabain-insensitive K uptake was stimulated by preincubating the choroid plexus in aCSF very low in [Na] and [K], then incubating it in much higher concentrations of these cations; bumetanide (10(-4)M) blocked this stimulated uptake by 52%. Moreover, tissue preincubation in Na- or Cl-free medium, followed by incubation with normal concentrations of both ions, stimulated the ouabain-insensitive uptake of K from 15 (baseline) to 35 nmol/mg dry weight. This stimulation of K transport depended on the simultaneous presence of both Na and Cl in aCSF, and replacing either ion alone did not stimulate the ouabain-insensitive K uptake. Collectively, these findings, together with those from a previous pharmacological study of 22Na and 36Cl transport, constitute strong evidence for the cotransport of Na, K, and Cl in rat choroid plexus.
分析了袢利尿剂和离子替代对2分钟内K(以86Rb为标记)摄取的影响,以获取脉络丛上皮细胞中K与Na和Cl协同转运的证据。从成年大鼠侧脑室切除的分离脉络丛,置于人工脑脊液(aCSF)中。在10^(-6)至10^(-4)M浓度下,特异性协同转运抑制剂布美他尼和吡咯他尼以剂量依赖性方式抑制K的摄取。哇巴因不敏感的K摄取可通过以下方式刺激:先将脉络丛在[Na]和[K]极低的aCSF中预孵育,然后在这些阳离子浓度高得多的环境中孵育;布美他尼(10^(-4)M)可使这种刺激摄取减少52%。此外,在无Na或无Cl的培养基中对组织进行预孵育,然后用正常浓度的两种离子进行孵育,可使哇巴因不敏感的K摄取从15(基线)增加到35 nmol/mg干重。这种对K转运的刺激取决于aCSF中Na和Cl同时存在,单独替换任何一种离子都不会刺激哇巴因不敏感的K摄取。总的来说,这些发现与先前对22Na和36Cl转运的药理学研究结果一起,构成了大鼠脉络丛中Na、K和Cl协同转运的有力证据。