Stimulation of serotonin transport by the cyclic GMP phosphodiesterase-5 inhibitor sildenafil

被引:38
|
作者
Zhu, CB
Hewlett, WA
Francis, SH
Corbin, JD
Blakely, RD [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Psychiat, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Mol Physiol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Dept Biophys, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Sch Med, Dept Pharmacol, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Sch Med, Ctr Mol Neurosci, Nashville, TN 37232 USA
关键词
serotonin; transporter; cGMP; PKG; sildenafil; PDE5;
D O I
10.1016/j.ejphar.2004.09.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The serotonin (5-hydroxtryptamine, 5-HT) transporter (SERT) plays a critical role in the inactivation of synaptic 5-HT and has been implicated in multiple psychiatric and peripheral disorders. SERT regulation studies demonstrate that activation of cyclic guanosine monophosphate (cGMP)/protein kinase G (PKG)-linked pathways can increase SERT activity. As cGMP actions are limited by cGMP-specific phosphodiesterase (PDEs), we investigated whether the cGMP-specific PDE5 inhibitor sildenafil (Viagra(R)) can stimulate 5-HT uptake and potentiate cGMP-mediated regulation. In RBL-2H3 cells, SERT activity was stimulated by sildenafil in a concentration- and time-dependent manner. Sildenafil also enhanced the stimulation of SERT triggered by the adenosine receptor agonist 5'-N-ethylcarboxamidoadenosine (NECA), effects blocked by the PKG inhibitor N-[2-(methylamino)ethy]-5-isoquinoline-sulfonamide (H8). Sildenafil stimulation of 5-HT uptake arises from an increase in 5-HT transport Vmax and is paralleled by elevated SERT surface antagonist binding, also H8-sensitive. These findings implicate cGMP-targeted PDEs in limiting the regulation of antidepressant-sensitive 5-HT transport. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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