Physiological processes underpinning the ubiquitous benefits and interactions of melatonin, butyrate and green tea in neurodegenerative conditions

George Anderson
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Abstract

There is a growing dissatisfaction at the lack of progress in treating neurodegenerative conditions, such as Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. No current pharmaceuticals have any significant impact on the pathophysiological changes occurring in such neurodegenerative conditions. More promising has been the utilization of nutraceuticals, a number of which show preventative and treatment benefits. This article reviews the beneficial effects of melatonin, sodium butyrate and epigallocatechin gallate (EGCG) in the management of the pathophysiological changes underpinning neurodegenerative conditions. It is proposed that all three nutraceuticals upregulate the tryptophan-melatonin pathway, which may be particularly important in astrocytes given astrocyte regulation of neuronal energy supply and antioxidants, including released melatonin. Alterations in the tryptophan-melatonin pathway are intimately intertwined with changes in the kynurenine pathway and its neuroregulatory products, including kynurenic acid and quinolinic acid. This article places these changes in the tryptophan-melatonin pathways within a novel circadian-systemic interaction, involving the regulation of the night-time rise in cortisol culminating in the morning cortisol awakening response that mediates effects via glucocorticoid receptor (GR) activation. The night-time and morning GR activation is suppressed by melatonin, gut microbiome derived butyrate and bcl2-associated athanogene (BAG)-1. As melatonin, butyrate and BAG-1 decrease over age, there is a heightened level of GR nuclear translocation with age at night and early morning. This is exemplified by the 10-fold decrease in pineal melatonin in people in their 9th, versus 2nd, decade of life. The ‘battle’ of melatonin/butyrate/EGCG versus cortisol/GR for influence on cellular function, microenvironment homeostasis and systemic system (immune) regulation at night and early morning shapes how the body and brain are prepared for the coming day and drives the emergence of aging associated neurodegenerative conditions. It is upon such processes that melatonin, butyrate and EGCG have their impacts.    
褪黑素、丁酸盐和绿茶对神经退行性疾病的普遍益处和相互作用的生理过程
人们对阿尔茨海默病、帕金森病和肌萎缩侧索硬化症等神经退行性疾病的治疗缺乏进展日益感到不满。目前没有任何药物能对这类神经退行性疾病的病理生理变化产生明显影响。更有前景的是对营养保健品的利用,其中一些保健品显示出预防和治疗功效。本文回顾了褪黑素、丁酸钠和表没食子儿茶素没食子酸酯(EGCG)在治疗神经退行性疾病的病理生理变化方面的有益作用。鉴于星形胶质细胞对神经元能量供应和抗氧化剂(包括释放的褪黑激素)的调节作用,这三种营养保健品可能对星形胶质细胞尤为重要。色氨酸-褪黑激素途径的变化与犬尿氨酸途径及其神经调节产物(包括犬尿酸和喹啉酸)的变化密切相关。这篇文章将色氨酸-褪黑激素通路的这些变化置于一种新的昼夜节律-系统相互作用中,其中涉及到对夜间皮质醇上升的调节,最终导致早晨皮质醇唤醒反应,这种反应通过糖皮质激素受体(GR)的激活产生作用。褪黑激素、肠道微生物组产生的丁酸盐和 bcl2 相关基因(BAG)-1 会抑制夜间和早晨的 GR 激活。随着年龄的增长,褪黑激素、丁酸盐和 BAG-1 会减少,夜间和清晨的 GR 核转位水平也会随着年龄的增长而提高。例如,松果体褪黑激素在人的第 9 个 10 年比第 2 个 10 年减少了 10 倍。在夜间和清晨,褪黑激素/丁酸/EGCG 与皮质醇/GR 的 "斗争 "对细胞功能、微环境稳态和全身系统(免疫)调节的影响,决定了身体和大脑如何为即将到来的一天做好准备,并推动了与衰老相关的神经退行性疾病的出现。褪黑激素、丁酸盐和 EGCG 正是对这些过程产生影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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