Schoeffter P, Ullmer C, Gutierrez M, Weitz-Schmidt G, Lübbert H
Sandoz Pharma Ltd, Basel, Switzerland.
Naunyn Schmiedebergs Arch Pharmacol. 1995 Nov;352(5):580-2. doi: 10.1007/BF00169394.
Pharmacological evidence has suggested the presence of 5-hydroxytryptamine (5-HT, serotonin), 5-HT(1D) receptors on endothelial cells but these receptors have never been identified unambiguously on this type of cells. We now report that human umbilical vein endothelial cells (HUVEC) express 5-HT(1D) receptors coupled to inhibition of cyclic AMP formation. 5-HT and 5-HT(1D) receptor agonists 5-carboxamidotryptamine (5-CT) and sumatriptan were approximately equipotent at inhibiting forskolin-stimulated cyclic AMP accumulation in HUVEC (mean pEC50 7.6-8.2, maximal effect 30% inhibition). The 5-HT(1A) receptor antagonist, 8-OH-DPAT was clearly less potent (pEC50 6.2) and less efficacious. The selective 5-HT(1D) receptor agonist, GR127935 (1 nM) markedly inhibited the effect of 5-HT (apparent pK(B) 10.8). Reverse transcription-polymerase chain reaction analysis showed the mRNA for 5-HT(1D beta) receptors to be expressed in HUVEC. These results demonstrate the presence of functional 5-HT(1D) receptors and the expression of 5-HT(1D beta) receptor mRNA in HUVEC. They support the involvement of 5-HT(1D beta) receptors in endothelial-mediated responses to 5-HT.
药理学证据表明内皮细胞上存在5-羟色胺(5-HT,血清素)、5-HT(1D)受体,但从未在这类细胞上明确鉴定出这些受体。我们现在报告,人脐静脉内皮细胞(HUVEC)表达与抑制环磷酸腺苷形成偶联的5-HT(1D)受体。5-HT和5-HT(1D)受体激动剂5-羧酰胺色胺(5-CT)和舒马曲坦在抑制HUVEC中福斯高林刺激的环磷酸腺苷积累方面效力大致相当(平均pEC50 7.6 - 8.2,最大效应为30%抑制)。5-HT(1A)受体拮抗剂8-OH-DPAT的效力明显较低(pEC50 6.2)且效果较差。选择性5-HT(1D)受体激动剂GR127935(1 nM)显著抑制5-HT的作用(表观pK(B)10.8)。逆转录-聚合酶链反应分析显示HUVEC中表达5-HT(1Dβ)受体的mRNA。这些结果证明HUVEC中存在功能性5-HT(1D)受体以及5-HT(1Dβ)受体mRNA的表达。它们支持5-HT(1Dβ)受体参与内皮介导的对5-HT的反应。