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1.
Proc Natl Acad Sci U S A ; 117(39): 24022-24031, 2020 09 29.
Artigo em Inglês | MEDLINE | ID: mdl-32817435

RESUMO

The recently developed new genome-editing technologies, such as the CRISPR/Cas system, have opened the door for generating genetically modified nonhuman primate (NHP) models for basic neuroscience and brain disorders research. The complex circuit formation and experience-dependent refinement of the human brain are very difficult to model in vitro, and thus require use of in vivo whole-animal models. For many neurodevelopmental and psychiatric disorders, abnormal circuit formation and refinement might be at the center of their pathophysiology. Importantly, many of the critical circuits and regional cell populations implicated in higher human cognitive function and in many psychiatric disorders are not present in lower mammalian brains, while these analogous areas are replicated in NHP brains. Indeed, neuropsychiatric disorders represent a tremendous health and economic burden globally. The emerging field of genetically modified NHP models has the potential to transform our study of higher brain function and dramatically facilitate the development of effective treatment for human brain disorders. In this paper, we discuss the importance of developing such models, the infrastructure and training needed to maximize the impact of such models, and ethical standards required for using these models.


Assuntos
Experimentação Animal/ética , Modelos Animais de Doenças , Transtornos Mentais/genética , Doenças do Sistema Nervoso/genética , Primatas/genética , Animais , Transtornos Mentais/fisiopatologia , Doenças do Sistema Nervoso/fisiopatologia , Neurociências/ética , Neurociências/métodos , Primatas/fisiologia
3.
Neuron ; 86(3): 617-31, 2015 May 06.
Artigo em Inglês | MEDLINE | ID: mdl-25950631

RESUMO

One of the great strengths of the mouse model is the wide array of genetic tools that have been developed. Striking examples include methods for directed modification of the genome, and for regulated expression or inactivation of genes. Within neuroscience, it is now routine to express reporter genes, neuronal activity indicators, and opsins in specific neuronal types in the mouse. However, there are considerable anatomical, physiological, cognitive, and behavioral differences between the mouse and the human that, in some areas of inquiry, limit the degree to which insights derived from the mouse can be applied to understanding human neurobiology. Several recent advances have now brought into reach the goal of applying these tools to understanding the primate brain. Here we describe these advances, consider their potential to advance our understanding of the human brain and brain disorders, discuss bioethical considerations, and describe what will be needed to move forward.


Assuntos
Encéfalo/fisiologia , Genes , Primatas/genética , Animais , Evolução Biológica , Humanos , Camundongos , Modelos Biológicos
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