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褪黑素对环磷酸腺苷及囊性纤维化跨膜传导调节因子离子通道的受体增强作用。

Melatonin receptor potentiation of cyclic AMP and the cystic fibrosis transmembrane conductance regulator ion channel.

作者信息

Nelson C S, Marino J L, Allen C N

机构信息

Center for Research on Occupational and Environmental Toxicology, Department of Psychiatry, Oregon Health Sciences University, Portland 97201, USA.

出版信息

J Pineal Res. 1999 Mar;26(2):113-21. doi: 10.1111/j.1600-079x.1999.tb00571.x.

Abstract

We have used the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel as a model system to study the cAMP signal transduction pathways coupled to the Xenopus melatonin receptor. During forskolin (Fsk) stimulation, melatonin reduced the amplitude of the CFTR currents in oocytes injected with in vitro transcribed cRNAs for the Xenopus melatonin receptor and CFTR. Pertussis toxin (Ptx) treatment eliminated melatonin inhibition of Fsk stimulated CFTR currents. In oocytes injected with cRNA for melatonin receptors, serotonin receptors (5-HT7), and CFTR Cl- channels, application of melatonin together with serotonin (5-HT) activated an additional inward current showing potentiation of adenylyl cyclases by melatonin receptors. Subthreshold activation of 5-HT7 receptors was sufficient and necessary to permit activation of CFTR channels by melatonin. Preexposure to melatonin desensitized the melatonin receptor mediated response. Therefore, based on this model system, the effects of melatonin in vivo could be either positive or negative modulation of other neuronal inputs, depending on the mode of adenylyl cyclase stimulation.

摘要

我们已使用囊性纤维化跨膜传导调节因子(CFTR)氯离子通道作为模型系统,来研究与非洲爪蟾褪黑素受体偶联的环磷酸腺苷(cAMP)信号转导途径。在福斯高林(Fsk)刺激过程中,褪黑素降低了注射了非洲爪蟾褪黑素受体和CFTR体外转录cRNA的卵母细胞中CFTR电流的幅度。百日咳毒素(Ptx)处理消除了褪黑素对Fsk刺激的CFTR电流的抑制作用。在注射了褪黑素受体、5-羟色胺受体(5-HT7)和CFTR氯离子通道cRNA的卵母细胞中,褪黑素与5-羟色胺(5-HT)共同作用激活了另一种内向电流,表明褪黑素受体增强了腺苷酸环化酶的活性。5-HT7受体的阈下激活对于褪黑素激活CFTR通道而言是充分且必要的。预先暴露于褪黑素会使褪黑素受体介导的反应脱敏。因此,基于该模型系统,褪黑素在体内的作用可能是对其他神经元输入的正向或负向调节,这取决于腺苷酸环化酶的刺激模式。

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