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5-羟色胺1D受体亚型参与血清素对人小细胞肺癌细胞增殖的刺激作用。

5-HT1D receptor type is involved in stimulation of cell proliferation by serotonin in human small cell lung carcinoma.

作者信息

Cattaneo M G, Palazzi E, Bondiolotti G, Vicentini L M

机构信息

Department of Pharmacology, School of Medicine, University of Milan, Italy.

出版信息

Eur J Pharmacol. 1994 Aug 16;268(3):425-30. doi: 10.1016/0922-4106(94)90068-x.

Abstract

Serotonin (5-hydroxytryptamine, 5-HT), a neurotransmitter and vasoactive agent, is contained in two small cell lung carcinoma cell lines GLC8 and NCI-N-592 and is released in the culture medium. It also stimulates DNA synthesis in the same cell lines. In GLC8 cells this mitogenic effect is not counteracted by ketanserin, ICS 205-930 and GR 113-808 which are antagonists of the 5-HT2, 5-HT3 and 5-HT4 receptors, respectively. On the contrary, the antagonists metergoline, methysergide, SDZ 21-009 and methiothepin inhibit the 5-HT-stimulated incorporation of [3H]thymidine in GLC8 cells. The 5-HT1D agonist sumatriptan is capable of mimicking 5-HT action on cell proliferation. Both sumatriptan and 5-HT inhibit adenylate cyclase activity at doses which correlate with the mitogenic effect. We conclude that a 5-HT1D receptor type contributes to the mitogenic effect of 5-HT in GLC8 cells. This is the first demonstration of an involvement of the 5-HT1D receptor type in human cell proliferation. The design of specific antagonists for this type of receptor might be useful for the growth control of this very aggressive tumor.

摘要

血清素(5-羟色胺,5-HT)是一种神经递质和血管活性物质,存在于两种小细胞肺癌细胞系GLC8和NCI-N-592中,并释放到培养基中。它还能刺激相同细胞系中的DNA合成。在GLC8细胞中,这种促有丝分裂作用不会被酮色林、ICS 205-930和GR 113-808所抵消,它们分别是5-HT2、5-HT3和5-HT4受体的拮抗剂。相反,拮抗剂麦角林、甲基麦角新碱、SDZ 21-009和甲硫噻平抑制5-HT刺激的GLC8细胞中[3H]胸腺嘧啶核苷的掺入。5-HT1D激动剂舒马曲坦能够模拟5-HT对细胞增殖的作用。舒马曲坦和5-HT在与促有丝分裂作用相关的剂量下均抑制腺苷酸环化酶活性。我们得出结论,5-HT1D受体类型促成了5-HT在GLC8细胞中的促有丝分裂作用。这是首次证明5-HT1D受体类型参与人类细胞增殖。针对这种受体类型设计特异性拮抗剂可能对控制这种极具侵袭性的肿瘤的生长有用。

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