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首页> 外文期刊>Journal of cellular biochemistry. >Cane Toad Skin ExtractInduced Upregulation and Increased Interaction of Serotonin 2A and D-2 Receptors via G(q/11) Signaling Pathway in CLU213 Cells
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Cane Toad Skin ExtractInduced Upregulation and Increased Interaction of Serotonin 2A and D-2 Receptors via G(q/11) Signaling Pathway in CLU213 Cells

机译:Cane蟾蜍皮肤萃取诱导血清素2a和D-2受体通过G(Q / 11)信号通路在CLU213细胞中的相互作用

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Recent evidences show that activation of serotonin 2A receptors (5-HT2AR) by agonists is significant in improving therapeutic activity of disease conditions, such as obsessive-compulsive disorder (OCD). Though the exact molecular mechanism is still not well understood, it is thought to involve agonist-driven, enhanced expression of 5-HT2AR in certain areas of brain, such as the pre-frontal cortex (PFC). Several other reports have also demonstrated association of OCD with lower dopamine receptor (D2R) availability, primarily in the striatum of the brain along with dysfunction of 5-HT2AR-D2R heteromer regulation. We thus hypothesized that compound(s) interacting with this molecular mechanism could be developed as drugs for long-term beneficial effects against OCD. In the present study, we have obtained experimental evidence in cultured neuronal cells (CLU213) that aqueous extract (AE, 50g/mL, P<0.05) of the Australian cane toad skin significantly increased the levels of 5-HT2AR and D2R protein and mRNA expression. AE was also found to enhance the interaction between 5-HT2AR and D2R and formation of expression of 5-HT2AR-D2R heteromer using co-immunoprecipitation and Western blot. Further investigation showed the involvement of classical signaling pathway (G(q/11)-PLC) along with c-FOS transcription factor preferentially in 5-HT2A-mediated agonist activation. These results obtained demonstrated that AE upregulates 5-HT2AR by a mechanism that appears to involve G(q/11)-PLC signaling pathway and c-FOS transcription factor activation. We indicate this enhanced 5-HT2AR and D2R expression and their interaction to induce increased 5-HT2AR-D2R heteromer formation by exposure to AE might provide a molecular mechanism to develop potential novel drug candidates to ameliorate OCD symptoms. J. Cell. Biochem. 118: 979-993, 2017. (c) 2016 Wiley Periodicals, Inc.
机译:最近的证据表明,通过激动剂激活血清素2A受体(5-HT2AR)对于改善疾病病症的治疗活性,例如强迫症(OCD)是显着的。虽然确切的分子机制仍然没有很好地理解,但认为涉及在脑的某些区域中的激动剂驱动,增强的5-HT2AR的表达,例如前额前皮质(PFC)。其他几个报告还表明了OCD与较低的多巴胺受体(D2R)可用性的关联,主要在大脑的纹状体以及5-HT2AR-D2R异构调节的功能障碍。因此,我们假设与这种分子机制相互作用的化合物可以作为针对OCD的长期有益效果的药物开发。在本研究中,我们在培养的神经元细胞(CLU213)中获得了实验证据(CLU213),澳大利亚甘蔗蟾蜍皮肤水性提取物(AE,50g / ml,P <0.05)显着增加了5-HT2AR和D2R蛋白和mRNA的水平表达。还发现AES增强5-HT2AR和D2R之间的相互作用和使用共免疫沉淀和Western印迹的5-HT2AR-D2R异构体的形成。进一步的研究表明,经典信号通路(G(Q / 11)-PLC)的涉及优先于5-HT2A介导的激动剂活化中的C-FOS转录因子。获得的这些结果证明AE通过似乎涉及G(Q / 11)-PLC信号传导途径和C-FOS转录因子激活的机制来推动5-HT2AR。我们指示这种增强的5-HT2AR和D2R表达及其对诱导的5-HT2AR-D2R异构形成通过暴露于AE增加的相互作用可以提供分子机制,以发展潜在的新药候选者以改善OCD症状。 J.Cell。生物学习。 118:979-993,2017。(c)2016年Wiley期刊,Inc。

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