NOX-NOS crosstalk in the liver-brain axis: Novel insights for redox regulation and neurodegenerative diseases.

IF 11.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sang-Seop Lee,Yung-Choon Yoo
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引用次数: 0

Abstract

The liver-brain axis is an emerging concept linking liver dysfunction and brain disease. Hepatic metabolic abnormalities induce systemic oxidative stress and endothelial dysfunction, which contribute to central nervous system (CNS) inflammation and neurodegeneration. Redox regulation plays a key role in the liver-brain axis, with NADPH oxidase (NOX) and nitric oxide synthase (NOS) being involved in the generation of various reactive oxygen species (ROS) and reactive nitrogen species (RNS), respectively, thereby inducing oxidative stress and disrupting the NADPH/NADP balance. Dysregulation of NOX-NOS cross-signaling not only amplifies oxidative stress, but also disrupts endothelial homeostasis and exacerbates neuroinflammation, leading to progressive neurodegeneration. For instance, reactive carbonyl species such as methylglyoxal (MGO) and acrolein can upregulate NOX isoforms and stimulate NLRP (NOD like receptor protein) inflammasomes activation, illustrating disease-relevant links between hepatic redox imbalance and CNS pathology. Mechanistically, superoxide (O2•-) generated by NOX readily reacts with nitric oxide (•NO) derived from NOS to form peroxynitrite (ONOO-), a highly reactive oxidant that exacerbates vascular and neuronal injury. Despite extensive research on NOX and NOS, their interactive contributions to redox imbalance and the progression of neurodegenerative diseases remain poorly understood. In this review, we introduce the NOX-NOS axis as a key regulator of the liver-brain axis, and highlight the roles of NOX and NOS in linking hepatic metabolic dysfunction to central nervous system pathology through intermediary metabolites in the exacerbation of neuroinflammation and oxidative stress. We also explore therapeutic strategies targeting NOX-NOS interactions, including selective NOX inhibitors, NOS modulators, and redox homeostasis regulators, providing new insights into redox regulation and the management of metabolic neurodegenerative diseases.
肝脑轴一氧化氮-一氧化氮串扰:氧化还原调节和神经退行性疾病的新见解
肝脑轴是一个将肝功能障碍和脑部疾病联系起来的新兴概念。肝脏代谢异常会引起全身氧化应激和内皮功能障碍,从而导致中枢神经系统(CNS)炎症和神经变性。氧化还原调控在肝-脑轴中起关键作用,NADPH氧化酶(NOX)和一氧化氮合酶(NOS)分别参与各种活性氧(ROS)和活性氮(RNS)的生成,从而诱导氧化应激,破坏NADPH/NADP平衡。一氧化氮-一氧化氮交叉信号的失调不仅会放大氧化应激,还会破坏内皮稳态,加剧神经炎症,导致进行性神经退行性变。例如,活性羰基物质如甲基乙二醛(MGO)和丙烯醛可以上调NOX亚型并刺激NLRP (NOD样受体蛋白)炎症小体的激活,说明肝脏氧化还原失衡与中枢神经系统病理之间存在疾病相关联系。从机制上讲,NOX产生的超氧化物(O2•-)很容易与NOX衍生的一氧化氮(•NO)反应形成过氧亚硝酸盐(ONOO-),这是一种高活性氧化剂,会加剧血管和神经元损伤。尽管对NOX和NOS进行了广泛的研究,但它们在氧化还原失衡和神经退行性疾病进展中的相互作用仍知之甚少。在这篇综述中,我们介绍了NOX-NOS轴作为肝-脑轴的关键调节因子,并强调了NOX和NOS通过中间代谢物在神经炎症和氧化应激加剧中将肝脏代谢功能障碍与中枢神经系统病理联系起来的作用。我们还探索了针对NOX-NOS相互作用的治疗策略,包括选择性NOX抑制剂,NOS调节剂和氧化还原稳态调节剂,为氧化还原调节和代谢性神经退行性疾病的管理提供了新的见解。
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来源期刊
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
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