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首页> 外文期刊>Expert opinion on therapeutic targets >6th International Symposium on Aldosterone and ENaC: from gene to disease. 3-7 October 2007, Zermatt, Switzerland.
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6th International Symposium on Aldosterone and ENaC: from gene to disease. 3-7 October 2007, Zermatt, Switzerland.

机译:第六届醛固酮和ENaC国际研讨会:从基因到疾病。 2007年10月3日至7日,瑞士采尔马特。

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BACKGROUND: Failure of sodium homeostasis contributes to a range of pathologies, particularly hypertension and cardiovascular disease but also respiratory diseases such as cystic fibrosis. As such the pathways involved in sodium homeostasis are now well recognised as important therapeutic targets. OBJECTIVE: The 6th International Symposium on Aldosterone and ENaC explored recent developments in aldosterone synthesis and action, particularly with regard to its influence on the regulation of the epithelial sodium channel (ENaC). METHODS: Although aldosterone biosynthesis, and indeed the mineralocorticoid receptor (MR), can be explored in isolation as can many aspects of the structure and function of the ENaC, the strength of the meeting was bringing these two topics together to explore the mechanisms of regulation of ENaC, including those mediated by activation of the MR. RESULTS/CONCLUSION: Given the number of individual presentations, any synthesis of the meeting will not do justice to all of the exciting work that was presented, however several themes emerged. The availability of crystal structures for the MR ligand-binding domain and a member of the ENaC family of channels have facilitated a number of structure function studies. The regulation of the activity of ENaC by the MR involves an interplay of factors which include transcriptional regulation, posttranslational modification and channel turnover. Several of these represent potential novel targets for the modulation of sodium homeostasis.
机译:背景:钠稳态失灵导致多种病理,尤其是高血压和心血管疾病,还包括呼吸系统疾病,如囊性纤维化。因此,现在已经充分认识到钠稳态所涉及的途径是重要的治疗靶标。目的:第六届国际醛固酮和ENaC研讨会探讨了醛固酮合成和作用的最新进展,特别是对醛固酮对上皮钠通道(ENaC)调节的影响。方法:尽管醛固酮的生物合成以及盐皮质激素受体(MR)以及ENaC的结构和功能的许多方面都可以单独进行探索,但这次会议的强度是将这两个主题结合在一起以探讨调节机制的ENaC,包括那些由MR激活介导的。结果/结论:鉴于个人演讲的数量众多,会议的任何综述都将无法与所有令人兴奋的工作相提并论,但是出现了几个主题。 MR配体结合域和ENaC通道家族成员的晶体结构的可用性促进了许多结构功能的研究。 MR对ENaC活性的调节涉及多种因素的相互作用,包括转录调节,翻译后修饰和通道更新。这些中的几个代表了调节钠稳态的潜在新靶标。

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