催产素与我们在宇宙中的位置

IF 2.1 Q3 ENDOCRINOLOGY & METABOLISM
Julie R. Korenberg
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引用次数: 0

摘要

催产素-血管加压素(OT-AVP)系统是否是一种看不见的力量的一部分,它巧妙地(以一种巧妙而间接的方式)引导我们人类对自身的迷恋?这种基本驱动力是否可能是个人、家庭和社会为生存和繁衍而进行的基因选择的必然产物?也许是的。但是,同样强烈的体验未知世界的生物动力是相互交织在一起的,它作为 "好奇心 "存在于个体之中。两者对于物种的生存和成功都至关重要。奇怪的是,了解自己的道路、发现的喜悦以及与他人一起踏上通往 OT-AVP 系统的帝国之旅,可能本身就是由同一系统驱动的。出于某种看不见的原因,我被驱使和激励去了解 "我们"。本章讲述了好奇心的驱使和对意义的探寻如何导致了关键的培训和启发式指导,而这些培训和指导对于开发新的基因、细胞和成像技术是必不可少的,这些技术对于加深对 "我们 "的理解是必不可少的。具体而言,本章描述了我对人类 "遗传学 "作为医学枢纽和人类神经生物学语言的认识。然后,我们阐述了四项技术(与重组图谱相结合的高密度全基因组标记阵列;对唐氏综合征和威廉姆斯综合征的大脑和社会行为的不同特征进行基因剖析和定义所需的基因贡献)的原理和顺序发展。这包括生成 1)与重组和基因图谱相结合的高密度基因组标记物全基因组阵列,以确定因一个或多个缺失基因而不同的 WS 罕见病例;2)解析基因对认知和行为数据标准化结果的贡献的分析方法、3) 利用多色和多时间荧光原位杂交技术,确定候选基因在非人灵长类动物(猕猴)大脑中的亚细胞和神经解剖定位;以及 4) 一种将血液神经肽的定时测量和基因组 DNA 序列变异与虔诚的 LDS 教会成员自我报告的宗教经历相结合的方法。通过在细胞、神经系统和生物体水平上进行跨进化和本体的研究,我们怀疑,在过去的 15 亿年中,OT、AVP 及其合作伙伴可能参与了一些宏伟的设计,这些微妙而巧妙的过程将我们物种的生存与我们珍贵的抽象思维能力和灵性联系在了一起。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oxytocin and our place in the universe
Is the oxytocin-vasopressin (OT-AVP) system a part of the unseen force that subtly (in a clever and indirect way) directs our human fascination to ourselves? And is it possible that this fundamental drive is the inevitable handmaiden of the genetic selection for survival and reproduction that is played out at the level of the individual, the family and the society? Perhaps. But an equally intense biological drive to experience the unknown is intertwined and exists in the individual as “curiosity”. Both are essential for survival and success of the species. Curiously, the path to understanding ourselves, the joy of discovery and joining with others on this imperial journey to the OT-AVP system may itself be driven by the same system. I have been driven and inspired to understand “Us” for some unseen reason. This chapter relates how a driving curiosity and search for meaning led to the critical training and inspired mentorship essential for developing novel genetic, cellular and imaging technologies necessary for each advance toward this deeper understanding. Specifically, the chapter describes my recognition of human “Genetics” as the hub of medicine and the language of human neurobiology. We then set out the rationale for and sequential development of four technologies (dense whole genome arrays of genomic markers integrated with the recombination map; needed to genetically dissect and define the genetic contributions to the distinct features of brain and social behavior in Down syndrome and Williams syndrome. These include generation of 1) dense whole genome arrays of genomic markers integrated with the recombination and gene maps for defining rare cases of WS differing by one or more deleted genes, 2) analytic methods for parsing genetic contributions to standardized outcomes of cognitive and behavioral data, 3) technologies using multicolor and multi temporal fluorescence in situ hybridization to define the subcellular and neuroanatomic localization of candidate genes in the non-human primate (macaque) brain, and 4) an approach to integrating timed measures of blood neuropeptides and genomic DNA sequence variants with self-reported religious experience in devout members of the LDS church. Working across evolution and ontogeny at the cellular, neural systems and organismal levels, has led to a suspicion that a bit of the grand design may involve OT, AVP and their partners in the subtle and artful processes of the last one-half billion years that link survival of our species with our prized capacity for abstract thought and spirituality.
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来源期刊
Comprehensive psychoneuroendocrinology
Comprehensive psychoneuroendocrinology Psychiatry and Mental Health
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3.10
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