Murphy V A, Johanson C E
Laboratory of Neurosciences, National Institute on Aging, Bethesda, MD.
Biochim Biophys Acta. 1989 Feb 27;979(2):187-92. doi: 10.1016/0005-2736(89)90434-3.
Cerebrospinal fluid (CSF) production results from active transport of Na+ from blood to CSF, which is followed by H2O and anions. Amiloride reduces Na+ movement in epithelial tissues. To ascertain if amiloride alters transport of Na+ in the choroid plexus, the drug was administered either i.p. to male Sprague-Dawley rats that were bilaterally nephrectomized to determine in vivo effects, or added to artificial CSF to incubate the choroid plexus in vitro. Choroid cell [Na+] was reduced after amiloride treatment both in vivo and in vitro. In addition, the rate of 22Na uptake into the CSF and choroid plexus (CP) was decreased after amiloride. Alterations in choroid cell [Na+] and 22Na penetration into CSF and CP occurred at relatively high doses of drug (1 mumol/ml, in vitro and 100 micrograms/g in vivo), but lower doses were less effective (0.1 mumol/ml in vitro and 10 micrograms/g in vivo). It is concluded that the effects of amiloride on Na+ distribution and transport in the CP are due to inhibition of basolateral Na+-H+ exchange.
脑脊液(CSF)的产生源于Na⁺从血液到脑脊液的主动转运,随后是水和阴离子。氨氯地平可减少上皮组织中Na⁺的移动。为确定氨氯地平是否会改变脉络丛中Na⁺的转运,将该药物经腹腔注射给予双侧肾切除的雄性Sprague-Dawley大鼠以确定其体内效应,或将其添加到人工脑脊液中以体外孵育脉络丛。氨氯地平处理后,体内和体外脉络丛细胞中的[Na⁺]均降低。此外,氨氯地平处理后,CSF和脉络丛(CP)对²²Na的摄取速率降低。脉络丛细胞[Na⁺]的改变以及²²Na进入CSF和CP的情况发生在相对高剂量的药物作用下(体外为1 μmol/ml,体内为100 μg/g),但较低剂量的效果较差(体外为0.1 μmol/ml,体内为10 μg/g)。得出的结论是,氨氯地平对CP中Na⁺分布和转运的影响是由于抑制了基底外侧Na⁺-H⁺交换。