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Utility of genetically modified mice for understanding the neurobiology of substance use disorders

机译:转基因小鼠用于了解物质使用障碍的神经生物学的用途

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Advances in our ability to modify the mouse genome have enhanced our understanding of the genetic and neurobiological mechanisms contributing to addiction-related behaviors underlying substance use and abuse. These experimentally induced manipulations permit greater spatial and temporal specificity for modification of gene expression within specific cellular populations and during select developmental time periods. In this review, we consider the current mouse genetic model systems that have been employed to understand aspects of addiction and highlight significant conceptual advances achieved related to substance use and abuse. The mouse models reviewed herein include conventional knockout and knockin, conditional knockout, transgenic, inducible transgenic, mice suitable for optogenetic control of discrete neuronal populations, and phenotype-selected mice. By establishing a reciprocal investigatory relationship between genetic findings in humans and genomic manipulations in mice, a far better understanding of the discrete neuromechanisms underlying addiction can be achieved, which is likely to provide a strong foundation for developing and validating novel therapeutics for the treatment of substance abuse disorders.
机译:我们修饰小鼠基因组能力的进步增强了我们对遗传和神经生物学机制的理解,这些机制促成了物质使用和滥用的成瘾相关行为。这些实验诱导的操纵允许更大的空间和时间特异性,以修饰特定细胞群体内和选定的发育时期内的基因表达。在这篇综述中,我们考虑了目前用于理解成瘾方面的小鼠遗传模型系统,并重点介绍了与药物使用和滥用相关的重要概念进展。本文综述的小鼠模型包括常规敲除和敲除,条件敲除,转基因,诱导型转基因,适合于离散神经元群体的光遗传学控制的小鼠和表型选择的小鼠。通过在人类的遗传发现和小鼠的基因组操作之间建立相互的调查关系,可以更好地理解成瘾的离散神经机制,这很可能为开发和验证用于治疗物质的新疗法提供坚实的基础。虐待障碍。

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