The Emerging Role of the DDAH Proteins in Psychiatric Disorders

IF 3.7 Q2 NEUROSCIENCES
Magdalini R. Vareltzoglou , Roman N. Rodionov , Anthony C. Vernon , Nadine Bernhardt
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Abstract

The heterogeneous nature of psychiatric disorders complicates their clinical management and the development of novel treatments, imposing a significant burden on both patients and health care systems. To address these challenges, it is essential to continuously identify new targets involved in their pathogenesis. In this narrative review, we propose the dimethylarginine dimethylaminohydrolase (DDAH) proteins, already known for their significant role in cardiovascular disease, as promising novel treatment targets for psychiatric conditions. The DDAH proteins exist in 2 isoforms, DDAH1 and DDAH2, which both regulate nitric oxide homeostasis. DDAH1 metabolizes the nitric oxide synthase inhibitor asymmetric dimethylarginine (ADMA), while DDAH2 acts through ADMA-independent mechanisms. We synthesize current evidence from systemic studies, genetic analyses, postmortem brain samples, and animal models to evaluate the potential roles of DDAH proteins across psychiatric conditions. Most systemic studies have revealed increased peripheral ADMA levels across several psychiatric disorders, including schizophrenia, depression, bipolar disorder, substance use disorders, and attention-deficit/hyperactivity disorder. Alterations in ADMA levels are also observed in transdiagnostic clinical domains such as cognitive deficits, sleep disturbances, white matter hyperintensities, and oxidative stress. These ADMA changes are evident from early stages of illness and respond to current treatments, suggesting diagnostic potential. Genetic and postmortem brain data further link DDAH1 and DDAH2 to psychiatric symptomatology in patient populations. Finally, fundamental studies in model systems provide insights into their role in neural proliferation, differentiation, cell death, and oxidative stress regulation—key processes in the developing and the adult brain. These data support the view that DDAH proteins may play a role in the molecular mechanisms that underlie psychiatric disorders and merit more investigation as potential therapeutic candidates.
DDAH蛋白在精神疾病中的新作用
精神疾病的异质性使其临床管理和新治疗方法的发展复杂化,给患者和卫生保健系统都带来了沉重的负担。为了应对这些挑战,必须不断确定其发病机制中涉及的新靶点。在这篇叙述性综述中,我们提出了二甲基精氨酸二甲氨基水解酶(DDAH)蛋白,它已经在心血管疾病中发挥了重要作用,作为精神疾病有希望的新治疗靶点。DDAH蛋白存在2种亚型,即DDAH1和DDAH2,它们都能调节一氧化氮的稳态。DDAH1代谢一氧化氮合酶抑制剂不对称二甲基精氨酸(ADMA),而DDAH2通过ADMA独立的机制起作用。我们综合了来自系统研究、遗传分析、死后脑样本和动物模型的现有证据,以评估DDAH蛋白在精神疾病中的潜在作用。大多数系统研究表明,在多种精神疾病中,包括精神分裂症、抑郁症、双相情感障碍、物质使用障碍和注意缺陷/多动障碍,外周ADMA水平升高。ADMA水平的改变也可在认知缺陷、睡眠障碍、白质高信号和氧化应激等跨诊断临床领域观察到。这些ADMA变化从疾病的早期阶段就很明显,并对目前的治疗有反应,表明诊断潜力。遗传和死后脑数据进一步将DDAH1和DDAH2与患者群体的精神症状联系起来。最后,模型系统的基础研究提供了它们在神经增殖、分化、细胞死亡和氧化应激调节中的作用——发育和成人大脑的关键过程。这些数据支持这样一种观点,即DDAH蛋白可能在精神疾病的分子机制中发挥作用,作为潜在的治疗候选物值得更多的研究。
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来源期刊
Biological psychiatry global open science
Biological psychiatry global open science Psychiatry and Mental Health
CiteScore
4.00
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0.00%
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审稿时长
91 days
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