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环境诱发神经疾病的太平洋范式:临床、流行病学及分子视角

Pacific paradigms of environmentally-induced neurological disorders: clinical, epidemiological and molecular perspectives.

作者信息

Garruto R M

机构信息

Laboratory of Central Nervous System Studies, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Neurotoxicology. 1991 Fall;12(3):347-77.

PMID:1745428
Abstract

During the past quarter century biomedical scientists have begun to recognize the unique opportunities for studying disease etiology and mechanisms of pathogenesis in non-Western anthropological populations with focal, endemic diseases. Such natural experiments as they are called, are important paradigms for solving etiological and epidemiological problems of widespread medical significance, with an ultimate goal towards treatment and prevention. The systematic search for etiological factors and mechanisms of pathogenesis of neurodegenerative disorders is perhaps nowhere better exemplified than in the western Pacific. During the past three decades, the opportunistic and multidisciplinary study of hyperendemic foci of amyotrophic lateral sclerosis and parkinsonism-dementia which occur in different cultures, in different ecological zones and among genetically divergent populations have served as natural models that have had a major impact on our thinking and enhanced our understanding of these and other neurodegenerative disorders such as Alzheimer disease and the process of early neuronal aging. Our cross-disciplinary approach to these intriguing neurobiological problems and the accumulated epidemiological, genetic, cellular and molecular evidence strongly implicates environmental factors in their causation, specifically the role of aluminum and its interaction with calcium in neuronal degeneration. As a direct consequence of our studies in these Pacific populations, we have undertaken the long-term development of experimental models of neuronal degeneration, in an attempt to understand the cellular and molecular mechanisms by which these toxicants affect the central nervous system. Our experimental studies have resulted in the establishment of an aluminum-induced chronic myelopathy in rabbits and the development of neurofilamentous lesions after low-dose aluminum administration in cell culture. These studies clearly demonstrate the philosophy that chronic rather than acute experimental models of toxicity are necessary in order to enhance our understanding of human neurodegenerative disorders with long-latency and slow progression. Finally, the ultimate significance of these Pacific paradigms may well depend on our ability to comprehensively evaluate and synthesize the growing body of relevant scientific data from other human disorders and from widely divergent academic fields, as well as our ability to recognize emerging new models in nature.

摘要

在过去的四分之一个世纪里,生物医学科学家们开始认识到,在患有局部性、地方性疾病的非西方人类学群体中,研究疾病病因和发病机制存在独特的机会。这些被称为自然实验的研究,是解决具有广泛医学意义的病因和流行病学问题的重要范例,其最终目标是治疗和预防疾病。对神经退行性疾病病因和发病机制的系统性探索,或许没有比西太平洋地区体现得更好的了。在过去三十年里,对肌萎缩侧索硬化症和帕金森病 - 痴呆症的高度地方性病灶进行的机会性多学科研究,这些病灶出现在不同文化、不同生态区域以及基因不同的人群中,已成为自然模型,对我们的思维产生了重大影响,并加深了我们对这些以及其他神经退行性疾病(如阿尔茨海默病)和早期神经元衰老过程的理解。我们对这些引人入胜的神经生物学问题采用的跨学科方法,以及积累的流行病学、遗传学、细胞和分子证据,强烈表明环境因素在其病因中起作用,特别是铝及其与钙在神经元变性中的相互作用。作为我们在这些太平洋人群中研究的直接结果,我们着手长期开发神经元变性的实验模型,试图了解这些毒物影响中枢神经系统的细胞和分子机制。我们的实验研究导致在兔子身上建立了铝诱导的慢性脊髓病,并在细胞培养中低剂量给予铝后出现了神经丝病变。这些研究清楚地表明,为了加深我们对具有长潜伏期和缓慢进展的人类神经退行性疾病的理解,慢性而非急性毒性实验模型是必要的。最后,这些太平洋范例的最终意义很可能取决于我们全面评估和综合来自其他人类疾病以及广泛不同学术领域的越来越多相关科学数据的能力,以及我们识别自然界中新兴新模型的能力。

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