首页 > 最新文献

Journal of Multiscale Neuroscience最新文献

英文 中文
Journal of Multiscale Neuroscience 多尺度神经科学杂志
Pub Date : 2022-05-28 DOI: 10.56280/1531631243
Ying Zhou, H. Tuckwell, N. Penington
Stress alters neuroendocrine, autonomic, and behavioral processes to cope well with perceived threats that compromise subjective wellbeing. Just as the perception of risk can change the structure and function of brain circuitry, which may result in enduring behavioral changes. There needs to be a greater understanding of how the brain reacts to stress-related disorders and discern how the adaptation mechanisms of the central nervous system under acute stress, as well as how stress-induced adaptation mechanisms are altered under chronic stress conditions that may induce plasticity-related changes in the brain. During this interaction, the brain becomes more capable of resolving stress in a way that is either adaptive or maladaptive, leaving the most critical deficit in the emotion regulation associated with risk for pathological conditions. The essence of this associated risk involves the reciprocal influence between hypothalamic-pituitary-adrenal function, the relay nucleus within the amygdala reactivation, and the hippocampus as essential structures associated with the forebrain pathways mediating stress-induced hormones, and the gamma-aminobutyric acid neurotransmitter system as key mechanisms of regulating stress. Understanding how related emotional experiences occur on the neural level and their impact on cognition and behavior entail tracing the interaction between the hypothalamic-pituitary-adrenal axis, the hormones released by these structures, and the neuroendocrine system's reactivity to stress. The interaction between threat-sensitive brain circuitry and the neuroendocrine stress system is crucial to understanding how related emotions arise on the neural level and their impact on cognition and behavior. The hypothalamic-pituitary-adrenal axis is critical in regulating the synthesis and release of endocrine hormones through its interactions with these structures, collectively referred to as the stress response. The stress system is described in its anatomy and physiology and connections to other brain areas and endocrine systems. We explore the current evidence linking stress with pathophysiologic mechanisms implicated in stressful conditions affecting the neuronal circuitry between endocrine, metabolic, gastrointestinal, and immune systems. Examining the biopsychological contributions provides a conceptual framework for understanding the emergence of emotions and stress-related behaviors.
压力会改变神经内分泌、自主神经和行为过程,从而更好地应对损害主观幸福感的感知威胁。正如对风险的感知可以改变大脑回路的结构和功能,这可能导致持久的行为改变。我们需要更好地了解大脑对压力相关疾病的反应,以及中枢神经系统在急性压力下的适应机制,以及压力诱导的适应机制在慢性压力条件下是如何改变的,这可能会导致大脑中可塑性相关的变化。在这种相互作用中,大脑变得更有能力以一种适应或不适应的方式解决压力,在与病理状况风险相关的情绪调节中留下最关键的缺陷。这种相关风险的本质涉及下丘脑-垂体-肾上腺功能、杏仁核再激活内的中继核和海马之间的相互影响,海马是与前脑通路介导应激诱导激素相关的基本结构,而γ -氨基丁酸神经递质系统是调节应激的关键机制。要了解相关的情绪体验是如何在神经层面上发生的,以及它们对认知和行为的影响,需要追踪下丘脑-垂体-肾上腺轴、这些结构释放的激素和神经内分泌系统对压力的反应之间的相互作用。威胁敏感脑回路和神经内分泌应激系统之间的相互作用对于理解相关情绪如何在神经水平上产生及其对认知和行为的影响至关重要。下丘脑-垂体-肾上腺轴通过与这些结构的相互作用,在调节内分泌激素的合成和释放方面至关重要,这些结构统称为应激反应。应激系统在解剖学和生理学以及与其他脑区和内分泌系统的联系中被描述。我们探索了当前的证据将应激与病理生理机制联系起来,这些机制涉及应激条件影响内分泌、代谢、胃肠道和免疫系统之间的神经回路。检查生物心理学的贡献为理解情绪和压力相关行为的出现提供了一个概念框架。
{"title":"Journal of Multiscale Neuroscience","authors":"Ying Zhou, H. Tuckwell, N. Penington","doi":"10.56280/1531631243","DOIUrl":"https://doi.org/10.56280/1531631243","url":null,"abstract":"Stress alters neuroendocrine, autonomic, and behavioral processes to cope well with perceived threats that compromise subjective wellbeing. Just as the perception of risk can change the structure and function of brain circuitry, which may result in enduring behavioral changes. There needs to be a greater understanding of how the brain reacts to stress-related disorders and discern how the adaptation mechanisms of the central nervous system under acute stress, as well as how stress-induced adaptation mechanisms are altered under chronic stress conditions that may induce plasticity-related changes in the brain. During this interaction, the brain becomes more capable of resolving stress in a way that is either adaptive or maladaptive, leaving the most critical deficit in the emotion regulation associated with risk for pathological conditions. The essence of this associated risk involves the reciprocal influence between hypothalamic-pituitary-adrenal function, the relay nucleus within the amygdala reactivation, and the hippocampus as essential structures associated with the forebrain pathways mediating stress-induced hormones, and the gamma-aminobutyric acid neurotransmitter system as key mechanisms of regulating stress. Understanding how related emotional experiences occur on the neural level and their impact on cognition and behavior entail tracing the interaction between the hypothalamic-pituitary-adrenal axis, the hormones released by these structures, and the neuroendocrine system's reactivity to stress. The interaction between threat-sensitive brain circuitry and the neuroendocrine stress system is crucial to understanding how related emotions arise on the neural level and their impact on cognition and behavior. The hypothalamic-pituitary-adrenal axis is critical in regulating the synthesis and release of endocrine hormones through its interactions with these structures, collectively referred to as the stress response. The stress system is described in its anatomy and physiology and connections to other brain areas and endocrine systems. We explore the current evidence linking stress with pathophysiologic mechanisms implicated in stressful conditions affecting the neuronal circuitry between endocrine, metabolic, gastrointestinal, and immune systems. Examining the biopsychological contributions provides a conceptual framework for understanding the emergence of emotions and stress-related behaviors.","PeriodicalId":230864,"journal":{"name":"Journal of Multiscale Neuroscience","volume":"76 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123222400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Journal of Multiscale Neuroscience 多尺度神经科学杂志
Pub Date : 2022-05-28 DOI: 10.56280/1531676942
R. Poznanski
This paper proposes biophysical principles for why geometric holonomic effects through the geometric vector potential are sentient when harmonized by quantized magnetic vector potential in phase-space. These biophysical principles are based on molecular level electromagnetic resonances in partially holistic molecules where nonintegrated information acts as the consciousness process’s conduit—using the informational structure of physical feelings as a transition into subjectivity. The transformation of internal energies from potential to kinetic as ‘concealed’ motion may measure the causal capacity required to bridge causality for conscious experience. Conformational transitions produce bond-breaking, resulting in boundary conditions and limiting the molecular wavefunction to a partially holistic molecular environment with molecular holonomic effects. The van der Waals energy increases protein conformational activity (re-arrangement of bonds), causing energy transfer and information in protein-protein interactions across the cerebral cortex through the energy transduction process. Energy transitions predetermine molecular level electromagnetic resonances in aromatic residues of amino acids. The energy sharing between various nested molecular level electromagnetic resonances interacting with the intermolecular adhesion of London forces at the nexus between phospholipids and the lipophilic proteins has a key role in constraining the release of energy resulting in a vast array of information-based action through negentropic entanglement. Such information structure, passing from the objectivity of holonomic effects stemming from molecular level electromagnetic resonances, has an inherent ambiguity since meaning cannot be related to context, which constitutes preconscious experienceability. The transition from potentiality to actuality where Coulombic force is expressed as a smear of possible experiences where carriers of evanescent meanings instantly actualize through intermittent dispersion interactions as conscious experiences and return to potentiality in preconscious experienceabilities.
本文提出了通过几何矢量势的几何完整效应在相空间中被量子化磁矢量势协调时是有感知的生物物理原理。这些生物物理原理是基于部分整体分子中的分子水平电磁共振,其中非整合信息充当了意识过程的管道-使用物理感觉的信息结构作为向主体性的过渡。作为“隐藏”运动的内能从势能到动能的转换,可以衡量为意识经验架起因果关系所需的因果能力。构象转变产生键断裂,导致边界条件,并将分子波函数限制在具有分子完整效应的部分整体分子环境中。范德华能增加蛋白质的构象活性(键的重新排列),通过能量转导过程在大脑皮层的蛋白质-蛋白质相互作用中引起能量传递和信息。能量跃迁预先决定了氨基酸芳香残基的分子水平电磁共振。各种嵌套的分子级电磁共振之间的能量共享与磷脂和亲脂蛋白之间的分子间粘附相互作用,在限制能量释放方面起着关键作用,从而通过负熵纠缠产生大量基于信息的作用。这种信息结构源于分子水平电磁共振的完整效应的客观性,具有固有的模糊性,因为意义不能与构成前意识经验的上下文相关。从潜在性到现实性的转变,库仑力被表达为可能经验的涂抹,转瞬即逝的意义的载体通过间歇性的分散相互作用作为意识经验立即实现,并在前意识经验中返回潜在性。
{"title":"Journal of Multiscale Neuroscience","authors":"R. Poznanski","doi":"10.56280/1531676942","DOIUrl":"https://doi.org/10.56280/1531676942","url":null,"abstract":"This paper proposes biophysical principles for why geometric holonomic effects through the geometric vector potential are sentient when harmonized by quantized magnetic vector potential in phase-space. These biophysical principles are based on molecular level electromagnetic resonances in partially holistic molecules where nonintegrated information acts as the consciousness process’s conduit—using the informational structure of physical feelings as a transition into subjectivity. The transformation of internal energies from potential to kinetic as ‘concealed’ motion may measure the causal capacity required to bridge causality for conscious experience. Conformational transitions produce bond-breaking, resulting in boundary conditions and limiting the molecular wavefunction to a partially holistic molecular environment with molecular holonomic effects. The van der Waals energy increases protein conformational activity (re-arrangement of bonds), causing energy transfer and information in protein-protein interactions across the cerebral cortex through the energy transduction process. Energy transitions predetermine molecular level electromagnetic resonances in aromatic residues of amino acids. The energy sharing between various nested molecular level electromagnetic resonances interacting with the intermolecular adhesion of London forces at the nexus between phospholipids and the lipophilic proteins has a key role in constraining the release of energy resulting in a vast array of information-based action through negentropic entanglement. Such information structure, passing from the objectivity of holonomic effects stemming from molecular level electromagnetic resonances, has an inherent ambiguity since meaning cannot be related to context, which constitutes preconscious experienceability. The transition from potentiality to actuality where Coulombic force is expressed as a smear of possible experiences where carriers of evanescent meanings instantly actualize through intermittent dispersion interactions as conscious experiences and return to potentiality in preconscious experienceabilities.","PeriodicalId":230864,"journal":{"name":"Journal of Multiscale Neuroscience","volume":"31 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127494821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Journal of Multiscale Neuroscience 多尺度神经科学杂志
Pub Date : 2022-05-28 DOI: 10.56280/1531632254
A. Pereira Júnior, Vinicius Jonas de Aguiar
Sentience, defined as the capacity of feeling, for example, to experience basic sensations such as hunger, thirst and other types of qualitative mental states, is a psychobiological phenomenon that involves dynamic patterns of electrochemical (below 1Hz) and electromagnetic (above 1Hz) waves in living systems. The science we have called Sentiomics studies unconscious dynamic patterns in the brain that define the capacity for feeling. This paper discusses the explanation of creative processes based on unconscious patterns that combine and constructively interfere, generating a conscious output experienced in the living system's first-person perspective. We claim that the Sentiomics approach to wave interferences helps to explain creative intuition, artistic creativity, the formation of dreams, and related phenomena. We raise a hypothesis – based on available evidence, to be experimentally tested – that the dominance of slower synchronized oscillatory frequencies (such as Delta, Theta and Alpha bands) in scalp electroencephalogram spectra makes more room for constructive electrochemical interferences supporting creativity. This research points to the dynamism of the unconscious mind, since such interferences happen without the need of conscious control but are influenced by the degree of attention focusing. Once those dynamic processes are understood, they can be used to enrich mental life, boost creativity in general, and improve decision-making processes.
感知,被定义为感觉的能力,例如,体验基本的感觉,如饥饿、口渴和其他类型的定性精神状态,是一种心理生物学现象,涉及生命系统中电化学(低于1Hz)和电磁(高于1Hz)波的动态模式。我们称之为感知组学的科学研究大脑中无意识的动态模式,这些模式定义了感觉的能力。本文讨论了基于无意识模式的创造性过程的解释,这些模式结合并建设性地干涉,产生了在生命系统的第一人称视角中体验到的有意识输出。我们声称,波干扰的感知学方法有助于解释创造性直觉、艺术创造力、梦的形成和相关现象。我们提出了一个假设——基于现有的证据,有待实验验证——头皮脑电图频谱中较慢的同步振荡频率(如Delta, Theta和Alpha波段)的主导地位为支持创造力的建设性电化学干扰提供了更多的空间。这项研究指出了无意识思维的活力,因为这种干扰在不需要有意识控制的情况下发生,但受到注意力集中程度的影响。一旦这些动态过程被理解,它们就可以用来丰富精神生活,提高创造力,改善决策过程。
{"title":"Journal of Multiscale Neuroscience","authors":"A. Pereira Júnior, Vinicius Jonas de Aguiar","doi":"10.56280/1531632254","DOIUrl":"https://doi.org/10.56280/1531632254","url":null,"abstract":"Sentience, defined as the capacity of feeling, for example, to experience basic sensations such as hunger, thirst and other types of qualitative mental states, is a psychobiological phenomenon that involves dynamic patterns of electrochemical (below 1Hz) and electromagnetic (above 1Hz) waves in living systems. The science we have called Sentiomics studies unconscious dynamic patterns in the brain that define the capacity for feeling. This paper discusses the explanation of creative processes based on unconscious patterns that combine and constructively interfere, generating a conscious output experienced in the living system's first-person perspective. We claim that the Sentiomics approach to wave interferences helps to explain creative intuition, artistic creativity, the formation of dreams, and related phenomena. We raise a hypothesis – based on available evidence, to be experimentally tested – that the dominance of slower synchronized oscillatory frequencies (such as Delta, Theta and Alpha bands) in scalp electroencephalogram spectra makes more room for constructive electrochemical interferences supporting creativity. This research points to the dynamism of the unconscious mind, since such interferences happen without the need of conscious control but are influenced by the degree of attention focusing. Once those dynamic processes are understood, they can be used to enrich mental life, boost creativity in general, and improve decision-making processes.","PeriodicalId":230864,"journal":{"name":"Journal of Multiscale Neuroscience","volume":"18 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123234403","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Multiscale Neuroscience
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1