The Neuron in Context

Lux, Vanessa

  • 出版商: Springer
  • 出版日期: 2024-10-01
  • 售價: $2,110
  • 貴賓價: 9.5$2,005
  • 語言: 英文
  • 頁數: 184
  • 裝訂: Quality Paper - also called trade paper
  • ISBN: 3031552318
  • ISBN-13: 9783031552311
  • 海外代購書籍(需單獨結帳)

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商品描述

Neuroscience has largely abandoned its localizationist and mechanistic framework of the 20th century. The plastic, embodied, and network character of our nervous system is widely acknowledged and systems theory approaches to consciousness dominate the field. However, the underlying neuron theory has not changed. The neuron doctrine, conceptualizing the single neuron as atomistic, one-directional source of neural function, still provides the template for our understanding of these basic elements of our nervous system and the material foundation of consciousness. Yet, the single neuron does not exist as an isolated unit. It is embedded within multiple cellular, structural, and functional contexts, and highly depends on them for its development, neural activity, and survival. The book discusses the constraints of the neuron doctrine and its pragmatic reductionism in the light of the growing knowledge about the brain's connectivity, plasticity, and systemic and embodied nature.To overcome these constraints, the author argues for a new neuron theory, depicting the neuron as bidirectional hub which is at the same time source and product of neural function. This bidirectionality is further characterized by spatial and time dimensions, placing the neuron within a multi-level pathway model of psychobiological development from the perspective of Developmental Embodiment Research. Furthermore, the author discusses the potential of neuroepigenetic markers to characterize the neuron and its range of plasticity within this developmental perspective.With its focus on neuroepigenetics, the book addresses a knowledge gap in the current study of the neural foundations of psychological functions. The multi-level and bidirectional perspective is already realized in approaches coming from developmental systems theory, which model neural function at the connectome level, and it also fits with approaches investigating feedback loops underlying neural activity at the single cell level. At both these levels, the spatial and the time dimensions are well characterized, either as changing connectivity patterns across different age groups, or as synaptic feedback loops underlying neural activation patterns. However, for the intermediate level of small neural populations, which is currently the main target for studies investigating the neural basis of specific psychological functions, this characterization turned out to be more challenging. Multi-cell recordings have provided a first glimpse into the complex interaction patterns of these small neural networks, but they are limited to the recording period and do not provide information about the long-term developmental and activation history. Here, neuroepigenetic markers could be of use. Due to their relative stability and, at the same time, environmental sensitivity, neuroepigenetic markers represent an additional layer of information in which, to a certain degree, the cell's metabolic and activation history is aggregated over time. This information is available at the single neuron level but could also be modeled as aggregated information for small neural populations and the supporting cellular context. Looking through this "epigenetic lens" adds to our understanding of the neuron as bidirectional hub by emphasizing the molecular correlates of functional stabilization and their contextual prerequisites. These prerequisites reach from the immediate cellular context to the social-cultural contexts which shape the culturally specific modes of acquisition of psychological functions throughout the lifespan. Accounting for this multilayered contextuality of the neuron and its function affords to repositions the relationship between neuroscience and psychology in their joint effort to unravel the material basis of consciousness. This provides new challenges but also new perspectives for theoretical psychology.

The book presents these current developments and debates to researchers, graduate students, and interested professionals and practitioners working in neuroscience, epigenetics, psychiatry, psychology and psychotherapy. It also provides a basic introduction into neuroepigenetics, its mechanisms, and first findings for graduate students as well as interested professionals and practitioners working in psychiatry, psychology, and psychotherapy.

商品描述(中文翻譯)

神經科學在很大程度上已經放棄了20世紀的區域化和機械化框架。人們普遍承認我們的神經系統具有可塑性、具身性和網絡特徵,而系統理論方法在意識研究中佔據主導地位。然而,基礎的神經元理論並未改變。神經元學說將單一神經元概念化為原子化的、單向的神經功能來源,仍然為我們理解這些神經系統的基本元素及意識的物質基礎提供模板。然而,單一神經元並不存在於孤立的單位中。它嵌入於多重細胞、結構和功能的背景中,並高度依賴這些背景以促進其發展、神經活動和生存。本書討論了神經元學說的限制及其在日益增長的關於大腦連接性、可塑性和系統性及具身性特徵的知識背景下的實用還原主義。為了克服這些限制,作者主張提出一種新的神經元理論,將神經元描繪為雙向的樞紐,同時是神經功能的來源和產物。這種雙向性進一步以空間和時間維度為特徵,將神經元置於發展具身性研究的心理生物發展多層次路徑模型中。此外,作者討論了神經表觀遺傳標記在這一發展視角下表徵神經元及其可塑性範圍的潛力。本書專注於神經表觀遺傳學,填補了當前心理功能神經基礎研究中的知識空白。多層次和雙向的視角已在來自發展系統理論的研究中實現,這些研究在連接組層面上建模神經功能,並且也與調查單細胞層面神經活動背後反饋迴路的研究相符。在這兩個層面上,空間和時間維度都得到了良好的表徵,無論是作為不同年齡組之間變化的連接模式,還是作為神經激活模式背後的突觸反饋迴路。然而,對於小型神經群體的中間層面,這目前是研究特定心理功能神經基礎的主要目標,這種表徵卻顯得更具挑戰性。多細胞記錄提供了對這些小型神經網絡複雜互動模式的初步了解,但它們僅限於記錄期間,並未提供有關長期發展和激活歷史的信息。在這裡,神經表觀遺傳標記可能會有所幫助。由於其相對穩定性和同時對環境的敏感性,神經表觀遺傳標記代表了一層額外的信息,在這一層中,細胞的代謝和激活歷史在一定程度上隨時間聚合。這些信息在單一神經元層面上是可用的,但也可以建模為小型神經群體及其支持的細胞背景的聚合信息。透過這種「表觀遺傳視角」來看,增強了我們對神經元作為雙向樞紐的理解,強調了功能穩定化的分子相關性及其背景前提。這些前提從直接的細胞背景延伸到塑造心理功能文化特定獲得模式的社會文化背景,貫穿整個生命週期。考慮到神經元及其功能的這種多層次背景性,重新定位了神經科學與心理學之間的關係,促進了它們共同努力揭示意識的物質基礎。這為理論心理學提供了新的挑戰,但也帶來了新的視角。

作者簡介

Vanessa Lux PhD is a research fellow at the Department of Genetic Psychology, Faculty of Psychology, Ruhr-Universität Bochum, Germany. Her research interests include the underlying neuroepigenetic mechanisms, but also addresses hormonal regulation and the impact on psychological function.

作者簡介(中文翻譯)

Vanessa Lux 博士是德國魯爾大學波鴻心理學院遺傳心理學系的研究員。她的研究興趣包括潛在的神經表觀遺傳機制,並且也探討荷爾蒙調節及其對心理功能的影響。