Villa Emiliano, Albano Claudio, Cappelli Andrea, Favale Emilio, Fugassa Emilia, Gerdoni Ezio, Scarrone Simona, Cupello Aroldo
Molecular Physiology and Bioimaging Institute, CNR, Sezione di Genova, Via De Toni 5, 16132, Genova, Italy.
Neurochem Res. 2005 Nov;30(11):1365-7. doi: 10.1007/s11064-005-8342-x.
The binding of labelled paroxetine to the serotonin transporter (SERT) of platelet membranes has been studied in both venous and mixed venous/arterial blood of the rat. In addition, we studied the inhibition of paroxetine binding to SERT by quipazine and N-methyl-quipazine (NMQ). The results indicate differences in affinity for the two test drugs, quipazine and NMQ, in venous vs. mixed venous/arterial blood. This suggests different post-translational modifications of SERT in platelets of arterial vs. venous blood.
已在大鼠的静脉血以及混合静脉血/动脉血中研究了标记的帕罗西汀与血小板膜5-羟色胺转运体(SERT)的结合。此外,我们还研究了喹哌嗪和N-甲基喹哌嗪(NMQ)对帕罗西汀与SERT结合的抑制作用。结果表明,喹哌嗪和NMQ这两种受试药物在静脉血与混合静脉血/动脉血中的亲和力存在差异。这表明动脉血与静脉血中血小板的SERT存在不同的翻译后修饰。