Sweiry J H, Yudilevich D L
J Physiol. 1985 Sep;366:251-66. doi: 10.1113/jphysiol.1985.sp015795.
Unidirectional influx and efflux of choline into the syncytiotrophoblast were investigated from both maternal and fetal circulations of the perfused guinea-pig placenta by using a single-circulation paired-tracer (extracellular reference and test substrate) dilution technique. Cellular uptake of [3H]choline at 0.05 mM was (mean percentage +/- S.E. of mean, n = 14 placentae) 51 +/- 2 and 49 +/- 2, on maternal and fetal sides, respectively. Kinetics of unidirectional influx (0.05-4.0 mM-choline) indicated the existence of saturable and non-saturable components on both sides: on maternal and fetal interfaces the Km (mM) values were respectively, 0.12 and 0.13, the Vmax (mumol min-1 g-1) values, 0.08 and 0.07 and the apparent linear transfer constants (min-1 g-1) 0.11 and 0.12. Efflux of [3H]choline from the placenta back into the ipsilateral circulation (backflux) was generally fast (20-60% in 5-6 min) and asymmetric with the fetal: maternal ratio usually above unity. Transplacental specific choline transfer in the dually perfused placenta, when observed, was small (less than 10% of the injected dose) following tracer injections in either direction based on the 5-6 min collection of the contralateral circulation (at 0.05 mM-choline). Placental retention of [3H]choline at the end of the 5-6 min period was about 25% of the injected dose when the tracers were injected from either circulation. Analogues of choline such as hemicholinium-3, thiamine, ethanolamine and N,N-dimethylethanolamine inhibited choline unidirectional influx, whereas betaine and acetate had no effect. The absence of the normal sodium gradient (perfusate sodium was replaced by Tris or by lithium) did not inhibit choline transport. The metabolic inhibitors dinitrophenol (1.0 mM) and potassium cyanide (1.0 mM) were essentially ineffective (up to 40 min perfusion). The sulphydryl reagent N-ethylmaleimide did not appear to inhibit the influx, in comparison with its effect on [3H]choline backflux which was greatly accelerated, resulting in a dramatic reduction in placental net uptake of the label. Our findings show that choline transport into the placenta is a rapid carrier-mediated process occurring at both maternal and fetal sides of the trophoblast, at physiological blood concentrations. This cellular uptake is possibly related to the synthesis of acetylcholine, which is known to occur in human placental tissue. Specific transplacental transfer of choline was a very slow process under the conditions of our experiments and this contrasted with the observed fast and high uptake into the trophoblast.
利用单循环配对示踪剂(细胞外参比物和测试底物)稀释技术,从灌注的豚鼠胎盘的母体和胎儿循环两方面研究了胆碱向合体滋养层的单向流入和流出。在0.05 mM时,[3H]胆碱在母体侧和胎儿侧的细胞摄取量(平均百分比±平均值标准误,n = 14个胎盘)分别为51±2和49±2。单向流入(0.05 - 4.0 mM胆碱)的动力学表明两侧均存在可饱和和不可饱和成分:在母体和胎儿界面,Km(mM)值分别为0.12和0.13,Vmax(μmol min-1 g-1)值分别为0.08和0.07,表观线性转运常数(min-1 g-1)分别为0.11和0.12。[3H]胆碱从胎盘回流到同侧循环(反向回流)通常很快(5 - 6分钟内为20 - 60%)且不对称,胎儿与母体的比例通常大于1。在双灌注胎盘中,当从任一方向注射示踪剂后,基于对侧循环5 - 6分钟的收集(在0.05 mM胆碱时),观察到的经胎盘特异性胆碱转运很小(小于注射剂量的10%)。当从任一循环注射示踪剂时,在5 - 6分钟结束时胎盘对[3H]胆碱的保留量约为注射剂量的25%。胆碱类似物如半胱氨酸-3、硫胺素、乙醇胺和N,N-二甲基乙醇胺抑制胆碱单向流入,而甜菜碱和乙酸盐则无作用。正常钠梯度的缺失(灌注液中的钠被Tris或锂替代)并不抑制胆碱转运。代谢抑制剂二硝基苯酚(1.0 mM)和氰化钾(1.0 mM)基本无效(灌注长达40分钟)。与对[3H]胆碱反向回流的影响相比,巯基试剂N-乙基马来酰亚胺似乎不抑制流入,[3H]胆碱反向回流被极大加速,导致胎盘对该标记物的净摄取显著降低。我们的研究结果表明,在生理血液浓度下,胆碱向胎盘的转运是一个快速的载体介导过程,发生在滋养层的母体和胎儿两侧。这种细胞摄取可能与乙酰胆碱的合成有关,已知乙酰胆碱在人胎盘组织中会合成。在我们的实验条件下,胆碱的特异性经胎盘转运是一个非常缓慢的过程,这与观察到的滋养层快速且大量摄取形成对比。