Reith M E, Zimanyi I, O'Reilly C A
Center for Neurochemistry, Nathan S. Kline Institute for Psychiatric Research, New York, NY 10035.
Biochem Pharmacol. 1989 Jul 1;38(13):2091-7. doi: 10.1016/0006-2952(89)90062-2.
Plasma membrane vesicle preparations from mouse cerebral cortex actively accumulated [3H]serotonin upon the imposition of a K+ gradient (in greater than out), a Na+ gradient (out greater than in), and the presence of external Cl-. Maximal stimulation of uptake by internal K+ occurred at 15 mM and half-maximal stimulation at 2 mM. Internal K+ did not enhance uptake merely via generation of a membrane potential because simultaneous parallel increases in internal and external K+ concentration also stimulated uptake. External Cl- increased serotonin uptake with a Km of 18 mM and a Hill number of 1.0, suggesting a requirement for one chloride ion for transport. Uptake could not be driven by internal H+ instead of K+. Estimation of the membrane potential by the distribution of triphenylmethylphosphonium ion showed a modest effect of valinomycin (1-20 microM) in increasing the potential from -19 to -31 mV accompanied by an increase in serotonin uptake. Proton ionophores prevented this effect of valinomycin and, by themselves, reduced the potential to -6 mV, but did not affect serotonin transport. A model is proposed for serotonin transport in brain plasma membrane vesicles that is similar to the model for porcine blood platelet vesicles as far as electroneutrality and stimulation by K+, Na+, and Cl- are concerned, but that is different in substitution of internal H+ for K+.
从小鼠大脑皮层制备的质膜囊泡,在施加K⁺梯度(内大于外)、Na⁺梯度(外大于内)以及存在细胞外Cl⁻的情况下,会主动积累[³H]5-羟色胺。内部K⁺对摄取的最大刺激作用出现在15 mM时,半最大刺激作用出现在2 mM时。内部K⁺并非仅仅通过产生膜电位来增强摄取,因为同时平行增加内部和外部K⁺浓度也会刺激摄取。细胞外Cl⁻增加5-羟色胺摄取,其Km为18 mM,希尔系数为1.0,表明转运需要一个氯离子。摄取不能由内部H⁺而非K⁺驱动。通过三苯甲基鏻离子的分布估算膜电位显示,缬氨霉素(1 - 20 μM)对将电位从-19 mV增加到-31 mV有适度影响,同时伴随着5-羟色胺摄取增加。质子离子载体阻止了缬氨霉素的这种作用,并且自身将电位降低到-6 mV,但不影响5-羟色胺转运。提出了一种大脑质膜囊泡中5-羟色胺转运的模型,就电中性以及受K⁺、Na⁺和Cl⁻刺激而言,该模型与猪血小板囊泡的模型相似,但在内部H⁺替代K⁺方面有所不同。