Synaptic sensitization in the anterior cingulate cortex sustains the consciousness of pain via synchronized oscillating electromagnetic waves

IF 2.4 3区 医学 Q3 NEUROSCIENCES Frontiers in Human Neuroscience Pub Date : 2024-09-11 DOI:10.3389/fnhum.2024.1462211
Richard Ambron
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Abstract

A recent report showed that experiencing pain requires not only activities in the brain, but also the generation of electric fields in a defined area of the anterior cingulate cortex (ACC). The present manuscript presents evidence that electromagnetic (EM) waves are also necessary. Action potentials (APs) encoding information about an injury stimulate thousands synapses on pyramidal neurons within the ACC resulting in the generation of synchronized oscillating (EM) waves and the activation of NMDA receptors. The latter induces a long-term potentiation (LTP) in the pyramidal dendrites that is necessary to experience both neuropathic and visceral pain. The LTP sensitizes transmission across the synapses that sustains the duration of the waves and the pain, EM waves containing information about the injury travel throughout the brain and studies using transcranial stimulation indicate that they can induce NMDA-mediated LTP in distant neuronal circuits. What is ultimately experienced as pain depends on the almost instantaneous integration of information from numerous neuronal centers, such as the amygdala, that are widely separated in the brain. These centers also generate EM waves and I propose that the EM waves from these centers interact to rapidly adjust the intensity of the pain to accommodate past and present circumstances. Where the waves are transformed into a consciousness of pain is unknown. One possibility is the mind which, according to contemporary theories, is where conscious experiences arise. The hypothesis can be tested directly by blocking the waves from the ACC. If correct, the waves would open new avenues of research into the relationship between the brain, consciousness, and the mind.
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前扣带回皮层的突触敏化通过同步振荡电磁波维持疼痛意识
最近的一份报告显示,体验疼痛不仅需要大脑的活动,还需要在前扣带回皮层(ACC)的特定区域产生电场。本手稿提供的证据表明,电磁波(EM)也是必要的。编码损伤信息的动作电位(AP)刺激 ACC 中锥体神经元上的数千个突触,从而产生同步振荡(EM)波并激活 NMDA 受体。后者在锥体树突中诱导长期电位(LTP),这是体验神经痛和内脏痛所必需的。LTP 使突触间的传导变得敏感,从而维持了电波和疼痛的持续时间。含有损伤信息的电磁波会传遍整个大脑,经颅刺激研究表明,它们可以在远处的神经元回路中诱导 NMDA 介导的 LTP。最终体验到的疼痛取决于来自大脑中相距甚远的众多神经元中枢(如杏仁核)的信息的几乎瞬时整合。这些中枢也会产生电磁波,我认为来自这些中枢的电磁波相互作用,迅速调整疼痛的强度,以适应过去和现在的环境。至于这些电磁波在哪里转化为疼痛意识,目前还不得而知。一种可能是心灵,根据当代理论,心灵是产生意识体验的地方。可以通过阻断来自 ACC 的电波来直接验证这一假设。如果假说正确,那么这些电波将为研究大脑、意识和心灵之间的关系开辟新的途径。
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来源期刊
Frontiers in Human Neuroscience
Frontiers in Human Neuroscience 医学-神经科学
CiteScore
4.70
自引率
6.90%
发文量
830
审稿时长
2-4 weeks
期刊介绍: Frontiers in Human Neuroscience is a first-tier electronic journal devoted to understanding the brain mechanisms supporting cognitive and social behavior in humans, and how these mechanisms might be altered in disease states. The last 25 years have seen an explosive growth in both the methods and the theoretical constructs available to study the human brain. Advances in electrophysiological, neuroimaging, neuropsychological, psychophysical, neuropharmacological and computational approaches have provided key insights into the mechanisms of a broad range of human behaviors in both health and disease. Work in human neuroscience ranges from the cognitive domain, including areas such as memory, attention, language and perception to the social domain, with this last subject addressing topics, such as interpersonal interactions, social discourse and emotional regulation. How these processes unfold during development, mature in adulthood and often decline in aging, and how they are altered in a host of developmental, neurological and psychiatric disorders, has become increasingly amenable to human neuroscience research approaches. Work in human neuroscience has influenced many areas of inquiry ranging from social and cognitive psychology to economics, law and public policy. Accordingly, our journal will provide a forum for human research spanning all areas of human cognitive, social, developmental and translational neuroscience using any research approach.
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