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肌萎缩侧索硬化症的病理发生和病理生理学:星形胶质细胞、肠道微生物组和肌肉通过线粒体褪黑素途径的相互作用的作用,以及草甘膦类除草剂的破坏。

Amyotrophic Lateral Sclerosis Pathoetiology and Pathophysiology: Roles of Astrocytes, Gut Microbiome, and Muscle Interactions via the Mitochondrial Melatonergic Pathway, with Disruption by Glyphosate-Based Herbicides.

机构信息

CRC Scotland & London, Eccleston Square, London SW1V 1PG, UK.

出版信息

Int J Mol Sci. 2022 Dec 29;24(1):587. doi: 10.3390/ijms24010587.

Abstract

The pathoetiology and pathophysiology of motor neuron loss in amyotrophic lateral sclerosis (ALS) are still to be determined, with only a small percentage of ALS patients having a known genetic risk factor. The article looks to integrate wider bodies of data on the biological underpinnings of ALS, highlighting the integrative role of alterations in the mitochondrial melatonergic pathways and systemic factors regulating this pathway across a number of crucial hubs in ALS pathophysiology, namely glia, gut, and the muscle/neuromuscular junction. It is proposed that suppression of the mitochondrial melatonergic pathway underpins changes in muscle brain-derived neurotrophic factor, and its melatonergic pathway mimic, N-acetylserotonin, leading to a lack of metabolic trophic support at the neuromuscular junction. The attenuation of the melatonergic pathway in astrocytes prevents activation of toll-like receptor agonists-induced pro-inflammatory transcription factors, NF-kB, and yin yang 1, from having a built-in limitation on inflammatory induction that arises from their synchronized induction of melatonin release. Such maintained astrocyte activation, coupled with heightened microglia reactivity, is an important driver of motor neuron susceptibility in ALS. Two important systemic factors, gut dysbiosis/permeability and pineal melatonin mediate many of their beneficial effects via their capacity to upregulate the mitochondrial melatonergic pathway in central and systemic cells. The mitochondrial melatonergic pathway may be seen as a core aspect of cellular function, with its suppression increasing reactive oxygen species (ROS), leading to ROS-induced microRNAs, thereby altering the patterning of genes induced. It is proposed that the increased occupational risk of ALS in farmers, gardeners, and sportsmen and women is intimately linked to exposure, whilst being physically active, to the widely used glyphosate-based herbicides. This has numerous research and treatment implications.

摘要

肌萎缩侧索硬化症(ALS)中运动神经元丧失的病理生理学和发病机制仍有待确定,只有一小部分 ALS 患者具有已知的遗传风险因素。本文旨在整合关于 ALS 生物学基础的更广泛的数据,强调线粒体褪黑素途径和调节该途径的系统性因素在 ALS 发病机制中的几个关键枢纽中的整合作用,即神经胶质、肠道和肌肉/运动神经元接头。据推测,线粒体褪黑素途径的抑制是肌肉脑源性神经营养因子及其褪黑素途径模拟物 N-乙酰血清素改变的基础,导致运动神经元接头缺乏代谢营养支持。星形胶质细胞中褪黑素途径的衰减阻止了 Toll 样受体激动剂诱导的促炎转录因子 NF-kB 和阴阳 1 的激活,从而限制了它们同步诱导褪黑素释放所引起的炎症诱导。这种持续的星形胶质细胞激活,加上小胶质细胞反应性增强,是 ALS 中运动神经元易感性的重要驱动因素。两个重要的系统性因素,肠道菌群失调/通透性和松果腺褪黑素,通过上调中枢和全身细胞中的线粒体褪黑素途径,介导许多有益作用。线粒体褪黑素途径可以被视为细胞功能的核心方面,其抑制会增加活性氧物种 (ROS),导致 ROS 诱导的 microRNAs,从而改变诱导基因的模式。据推测,农民、园艺家和运动员在职业中接触并积极活动时,接触广泛使用的草甘膦基除草剂,与 ALS 风险增加密切相关。这有许多研究和治疗意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d8b/9820185/a53cc3e6111b/ijms-24-00587-g001.jpg

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