Aickin C C, Brading A F
J Physiol. 1985 Sep;366:267-80. doi: 10.1113/jphysiol.1985.sp015796.
The selectivity of the external site of the Cl transporting mechanism in the guinea-pig vas deferens has been investigated by measurement of 36Cl uptake and efflux and by direct measurement of intracellular pH. Replacing 50% of the Cl in normal Krebs solution inhibited the 15 min uptake of 36Cl in the order NO3 greater than Br greater than SCN greater than F greater than I greater than glucuronate, both in Cl-depleted tissues and tissues pre-incubated in the 50%-Cl solutions (steady-state uptake). After 3 h incubation in these solutions, the total cellular Cl was reduced by the anions in the order Br greater than NO3 greater than I greater than SCN greater than F greater than glucuronate. Br, NO3 and I reduced the cellular Cl to less than 50% of normal, suggesting that they are actively taken up by the cells. The ability of foreign anions to inhibit a 3 min uptake of high specific activity, low concentration Cl (6.5 mM) suggests an apparent affinity series of NO3 greater than Cl = SCN = Br greater than I greater than F at the external site. Addition of NO3, Cl, Br, HCO3, F, SCN or I to a Cl-free, nominally HCO3-free bathing solution accelerated 36Cl efflux. The first four mentioned were powerful stimulants, the other three less potent. However, the exact position of HCO3 in the sequence is uncertain. The rapidity with which CO2 crosses the membrane and forms HCO3 intracellularly may allow competition between HCO3 and Cl at the internal site and so distort the result. The action of F is also questionable since this ion drastically reduces the divalent cation activity and is a metabolic inhibitor. Measurement of intracellular pH provided conclusive evidence that Cl, NO3, Br and I can exchange with HCO3 across the cell membrane. This exchange is as rapid with NO3 as with Cl but slower with Br and considerably slower with I. The results also indicate that SCN ions cross the cell membrane. It is concluded that Cl, HCO3, Br and NO3 are all translocated by the exchange carrier. I and perhaps SCN also interact with the transport mechanism, but the translocation rate is then greatly reduced. The precise order of the affinity of these anions remains uncertain but the following sequence: NO3 greater than Cl = SCN = Br greater than I greater than F is considered to be the most likely.
通过测量³⁶Cl的摄取和流出以及直接测量细胞内pH值,研究了豚鼠输精管中氯离子转运机制外部位点的选择性。在正常的 Krebs 溶液中用50%的其他阴离子取代氯离子,无论是在氯离子缺失的组织还是预先在含50%氯离子溶液中预孵育的组织(稳态摄取)中,³⁶Cl的15分钟摄取受到抑制,抑制顺序为:NO₃>Br>SCN>F>I>葡萄糖醛酸盐。在这些溶液中孵育3小时后,细胞内总氯离子被阴离子按以下顺序减少:Br>NO₃>I>SCN>F>葡萄糖醛酸盐。Br、NO₃和I将细胞内氯离子减少到正常水平的50%以下,表明它们被细胞主动摄取。外来阴离子抑制高比活度、低浓度氯离子(6.5 mM)3分钟摄取的能力表明,在外部位点的表观亲和力顺序为:NO₃>Cl = SCN = Br>I>F。向无氯、名义上无HCO₃的浴液中添加NO₃、Cl、Br、HCO₃、F、SCN或I会加速³⁶Cl的流出。前面提到的前四种是强效刺激剂,后三种效力较小。然而,HCO₃在该序列中的准确位置尚不确定。CO₂穿过膜并在细胞内形成HCO₃的速度很快,这可能导致HCO₃和Cl在内部位点之间发生竞争,从而扭曲结果。F的作用也存在疑问,因为这种离子会大幅降低二价阳离子活性,并且是一种代谢抑制剂。细胞内pH值的测量提供了确凿证据,表明Cl、NO₃、Br和I可以与HCO₃跨细胞膜进行交换。这种交换与NO₃的速度与Cl相同,但与Br较慢,与I则相当慢。结果还表明SCN离子可以穿过细胞膜。结论是Cl、HCO₃、Br和NO₃都是通过交换载体转运的。I以及可能的SCN也与转运机制相互作用,但转运速率会大大降低。这些阴离子亲和力的确切顺序仍不确定,但以下顺序:NO₃>Cl = SCN = Br>I>F被认为是最有可能的。