Malmgren R
Acta Pharmacol Toxicol (Copenh). 1981 Oct;49(4):277-84. doi: 10.1111/j.1600-0773.1981.tb00906.x.
The 5-HT uptake mechanism in human platelets was studied in undiluted platelet-rich plasma (PRP). The kinetic data obtained, which were based on 5-HT concentrations ranging from 0.17 to 1.7 mumol/l, were analyzed according to Lineweaver-Burk, Eadie-Hofstee, Scatchard and Sips. In undiluted PRP all the analyses revealed a strict linearity between 5-HT concentrations and initial uptake velocities. Only one site for active transport seemed to be involved and no passive diffusion was present. The apparent Km and Vmax in a 95 per cent confidence interval (n = 25) were 1.20 +/- 0.14 mumol/l and 1.40 +/- 0.15 pmol/10(6) platelets and minutes, respectively. Dilution of PRP with autologous platelet-poor plasma or Ringer's solution markedly influenced the active 5-HT transport mechanism. The addition of minute amounts of supernatant from lysed autologous platelets to PRP totally impaired the active 5-HT uptake. It is concluded that relevant studies on the active 5-HT transport can be performed only in fresh undiluted PRP. The commonly used Lineweaver-Burk analysis does not discriminate sufficiently between fully saturable and non-saturable transport mechanism and therefore cannot be used for the detection of irregularities in the 5-HT transport.
在未稀释的富血小板血浆(PRP)中研究了人血小板中的5-羟色胺(5-HT)摄取机制。根据Lineweaver-Burk、Eadie-Hofstee、Scatchard和Sips方法分析了基于0.17至1.7μmol/L的5-HT浓度获得的动力学数据。在未稀释的PRP中,所有分析均显示5-HT浓度与初始摄取速度之间存在严格的线性关系。似乎仅涉及一个主动转运位点,不存在被动扩散。在95%置信区间(n = 25)中的表观Km和Vmax分别为1.20±0.14μmol/L和1.40±0.15 pmol/10⁶个血小板/分钟。用自体贫血小板血浆或林格氏溶液稀释PRP会显著影响5-HT的主动转运机制。向PRP中添加微量来自裂解的自体血小板的上清液会完全损害5-HT的主动摄取。结论是,关于5-HT主动转运的相关研究只能在新鲜未稀释的PRP中进行。常用的Lineweaver-Burk分析不能充分区分完全可饱和和不可饱和的转运机制,因此不能用于检测5-HT转运中的异常情况。