Suppr超能文献

阿片受体激动剂对T47D人乳腺癌细胞系的抗增殖作用部分是通过阿片受体介导的。

The antiproliferative effect of opioid receptor agonists on the T47D human breast cancer cell line, is partially mediated through opioid receptors.

作者信息

Hatzoglou A, Bakogeorgou E, Castanas E

机构信息

Laboratory of Experimental Endocrinology, University of Crete, Greece.

出版信息

Eur J Pharmacol. 1996 Jan 25;296(2):199-207. doi: 10.1016/0014-2999(95)00703-2.

Abstract

In the present study, we investigated the action of opioid receptor agonists on the proliferation of cells of the T47D human breast cancer cell line, grown in the absence of exogenously added steroids and growth factors. We found that the opioid receptor agonists ethylketocyclazocine, morphine, [D-Ala2,D-Leu5]enkephalin (DADLE), [D-Ser2,Leu5]enkephalin-Thr6 (DSLET) and etorphine inhibit dose dependently cell proliferation. The opioid receptor antagonist diprenorphine had no significant effect per se, but it was able to reverse the action of all opioid receptor agonists except morphine. In order to investigate the mechanism of action of opioids on T47D cells, we characterised the opioid receptors present on this cell line, by saturation binding, using radiolabelled [D-Ala2,N-Me-Phe4-Gly5-ol]enkephalin (DAGO, mu-opioid receptor agonist), ethylketocyclazocine (kappa 1-, kappa 2-, mu- and delta-opioid receptor agonist), diprenorphine (kappa 2-, kappa 3-, delta- and mu-opioid receptor antagonist), DADLE (delta- and mu-opioid receptor agonist), and effectors. We identified opioid binding sites belonging mainly to the kappa-type (kappa 1, kappa 2 and kappa 3), a few delta-opioid receptor sites, but no mu-opioid receptors. Our results indicate that the inhibitory effect of opioids on T47D cell growth is mediated through kappa- and delta-opioid receptors. The effect of mu-acting morphine might not be mediated through opioid receptors.

摘要

在本研究中,我们调查了阿片受体激动剂对T47D人乳腺癌细胞系细胞增殖的作用,这些细胞在无外源性添加类固醇和生长因子的情况下培养。我们发现阿片受体激动剂乙基酮环唑新、吗啡、[D-丙氨酸2,D-亮氨酸5]脑啡肽(DADLE)、[D-丝氨酸2,亮氨酸5]脑啡肽-苏氨酸6(DSLET)和埃托啡剂量依赖性地抑制细胞增殖。阿片受体拮抗剂二丙诺啡本身无显著作用,但它能够逆转除吗啡外所有阿片受体激动剂的作用。为了研究阿片类药物对T47D细胞的作用机制,我们通过饱和结合,使用放射性标记的[D-丙氨酸2,N-甲基苯丙氨酸4-甘氨酸5-醇]脑啡肽(DAGO,μ阿片受体激动剂)、乙基酮环唑新(κ1、κ2、μ和δ阿片受体激动剂)、二丙诺啡(κ2、κ3、δ和μ阿片受体拮抗剂)、DADLE(δ和μ阿片受体激动剂)以及效应器,对该细胞系上存在的阿片受体进行了表征。我们鉴定出主要属于κ型(κ1、κ2和κ3)的阿片结合位点、少数δ阿片受体位点,但没有μ阿片受体。我们的结果表明,阿片类药物对T47D细胞生长的抑制作用是通过κ和δ阿片受体介导的。μ作用的吗啡的作用可能不是通过阿片受体介导的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验