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Galanin and galanin receptors.

机译:甘丙肽和甘丙肽受体。

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摘要

The development of a strain of galanin knockout mice has provided confirmation of a neuroendocrine role for galanin, as well as supporting results of previous physiological investigations indicating a role for galanin in analgesia and neuropathic pain, and potentially in neuronal growth and regeneration processes. Whether elevation of galanin expression in neurodegenerative disorders such as Alzheimer's disease represents a survival response or exacerbates functional deficit in afflicted individuals remains to be determined. More detailed analysis of the phenotype of the galanin knockout mouse should provide insights into the physiological role of galanin in memory and learning processes, as well as in hypothalamic function and other aspects of neuroendocrine regulation. Biochemical and molecular cloning efforts have demonstrated that the multiplicity of actions of galanin is matched by complexity in the distribution and regulation of galanin and its receptors. A focus on characterisation of galanin receptors has resulted in the molecular cloning of three receptor subtypes to date. The distribution and functional properties of these receptors have not yet been fully elucidated, currently precluding assignment of discrete functions of galanin to any one receptor subtype. It is not currently possible to reconcile available pharmacological data using analogs of galanin and chimeric peptides in functional assay systems with the pharmacological properties of cloned receptor subtypes. This highlights the value of further knockout approaches targeting galanin receptor subtypes, but also raises the possibility of the existence of additional receptor subtypes that have yet to be cloned, or that receptor activity may be modulated by regulatory molecules that remain to be identified. The development of receptor subtype-specific compounds remains a high priority to advance work in this area. The ability to selectively modulate the many different actions of galanin, through a clearer understanding of receptor structure-function relationships and neuronal distribution, promises to provide important insights into the molecular and cellular basis of galanin action in normal physiology, and may provide lead compounds with therapeutic application in the prevention and treatment of a range of disorders.
机译:甘丙肽敲除小鼠品系的发展已证实了甘丙肽的神经内分泌作用,并支持先前的生理学研究结果,表明甘丙肽在镇痛和神经性疼痛以及潜在的神经元生长和再生过程中起作用。神经退行性疾病例如阿尔茨海默氏病中甘丙肽表达的升高是否代表存活反应或加重患病个体的功能障碍尚待确定。甘丙肽敲除小鼠的表型的更详细的分析应提供深入了解甘丙肽在记忆和学习过程,以及下丘脑功能和神经内分泌调节的其他方面的生理作用。生化和分子克隆研究表明,甘丙肽的多种作用与甘丙肽及其受体的分布和调节的复杂性相匹配。聚焦于甘丙肽受体的表征已经导致了迄今为止三种受体亚型的分子克隆。这些受体的分布和功能特性尚未完全阐明,目前排除了甘丙肽的离散功能分配给任何一种受体亚型。目前尚不可能在功能测定系统中使用甘丙肽和嵌合肽的类似物与克隆的受体亚型的药理特性来调节可用的药理数据。这突出了针对甘丙肽受体亚型的进一步敲除方法的价值,但也增加了可能存在尚未克隆的其他受体亚型存在的可能性,或者受体活性可能由尚待鉴定的调节分子调节。受体亚型特异性化合物的开发仍然是推进该领域工作的高度优先事项。通过更清楚地了解受体结构-功能关系和神经元分布来选择性调节甘丙肽许多不同作用的能力有望为正常生理中甘丙肽作用的分子和细胞基础提供重要见解,并可能为先导化合物提供在预防和治疗一系列疾病中的治疗应用。

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