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Transgenic nonhuman primates for neurodegenerative diseases

机译:转基因非人类灵长类动物神经退行性疾病

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Animal models that represent human diseases constitute an important tool in understanding the pathogenesis of the diseases, and in developing effective therapies. Neurodegenerative diseases are complex disorders involving neuropathologic and psychiatric alterations. Although transgenic and knock-in mouse models of Alzheimer's disease, (AD), Parkinson's disease (PD) and Huntington's disease (HD) have been created, limited representation in clinical aspects has been recognized and the rodent models lack true neurodegeneration. Chemical induction of HD and PD in nonhuman primates (NHP) has been reported, however, the role of intrinsic genetic factors in the development of the diseases is indeterminable. Nonhuman primates closely parallel humans with regard to genetic, neuroanatomic, and cognitive/behavioral characteristics. Accordingly, the development of NHP models for neurodegenerative diseases holds greater promise for success in the discovery of diagnoses, treatments, and cures than approaches using other animal species. Therefore, a transgenic NHP carrying a mutant gene similar to that of patients will help to clarify our understanding of disease onset and progression. Additionally, monitoring disease onset and development in the transgenic NHP by high resolution brain imaging technology such as MRI, and behavioral and cognitive testing can all be carried out simultaneously in the NHP but not in other animal models. Moreover, because of the similarity in motor repertoire between NHPs and humans, it will also be possible to compare the neurologic syndrome observed in the NHP model to that in patients. Understanding the correlation between genetic defects and physiologic changes (e.g. oxidative damage) will lead to a better understanding of disease progression and the development of patient treatments, medications and preventive approaches for high risk individuals. The impact of the transgenic NHP model in understanding the role which genetic disorders play in the development of efficacious interventions and medications is foreseeable.
机译:代表人类疾病的动物模型是理解疾病发病机理和开发有效疗法的重要工具。神经退行性疾病是涉及神经病理学和精神病学改变的复杂疾病。尽管已经创建了阿尔茨海默氏病(AD),帕金森氏病(PD)和亨廷顿氏病(HD)的转基因和敲入小鼠模型,但在临床方面的代表性有限,啮齿动物模型缺乏真正的神经变性。已经报道了在非人类灵长类动物(NHP)中对HD和PD的化学诱导作用,但是,内在遗传因素在疾病发展中的作用尚不确定。在遗传,神经解剖学和认知/行为特征方面,非人类灵长类动物与人类极为相似。因此,与使用其他动物物种的方法相比,用于神经退行性疾病的NHP模型的开发对成功发现诊断,治疗和治愈方法具有更大的希望。因此,携带与患者相似的突变基因的转基因NHP将有助于阐明我们对疾病发作和进展的了解。此外,通过高分辨率脑成像技术(例如MRI)监测转基因NHP中疾病的发作和发展以及行为和认知测试,都可以在NHP中同时进行,而不能在其他动物模型中进行。此外,由于NHP和人类之间的运动库相似,因此也有可能将NHP模型中观察到的神经系统综合症与患者进行比较。理解遗传缺陷和生理变化(例如氧化损伤)之间的相关性将使人们更好地了解疾病的进展以及对高风险个体的患者治疗,药物和预防方法的发展。可以预见,转基因NHP模型在了解遗传性疾病在有效干预措施和药物开发中的作用方面会产生影响。

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