Galicia-Moreno Marina, Monroy-Ramirez Hugo Christian, Caloca-Camarena Fernando, Arceo-Orozco Scarlet, Muriel Pablo, Sandoval-Rodriguez Ana, García-Bañuelos Jesús, García-González Alejandro, Navarro-Partida José, Armendariz-Borunda Juan
Instituto de Biologia Molecular en Medicina y Terapia Génica, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, 44340, Guadalajara, Jalisco, Mexico.
Programa de Doctorado en Farmacología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, 44340, Guadalajara, Jalisco, Mexico.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Mar;398(3):2365-2386. doi: 10.1007/s00210-024-03539-0. Epub 2024 Oct 22.
Liver diseases represent a worldwide health problem accountable for two million deaths per year. Oxidative stress is critical for the development of these diseases. N-acetyl cysteine (NAC) is effective in preventing liver damage, both in experimental and clinical studies, and evidence has shown that the pharmacodynamic mechanisms of NAC are related to its antioxidant nature and ability to modulate key signaling pathways. Here, we provide a comprehensive description of the beneficial effects of NAC in the treatment of liver diseases, addressing the first evidence of its role as a scavenger and precursor of reduced glutathione, along with studies showing its immunomodulatory action, as well as the ability of NAC to modulate epigenetic hallmarks. We searched the PubMed database using the following keywords: oxidative stress, liver disease, epigenetics, antioxidants, NAC, and antioxidant therapies. There was no time limit to gather all available information on the subject. NAC has shown efficacy in treating liver damage, exerting mechanisms of action different from those of free radical scavengers. Like different antioxidant therapies, its effectiveness and safety are related to the administered dose; therefore, designing new pharmacological formulations for this drug is imperative to achieve an adequate response. Finally, there is still much to explore regarding its effect on epigenetic marker characteristics of liver damage, turning it into a drug with broad therapeutic potential. According to the literature reviewed, NAC could be an appropriate option in clinical studies related to hepatic injury and, in the future, a repurposing alternative for treating liver diseases.
肝脏疾病是一个全球性的健康问题,每年导致200万人死亡。氧化应激对这些疾病的发展至关重要。在实验和临床研究中,N-乙酰半胱氨酸(NAC)在预防肝损伤方面均有效,并且有证据表明NAC的药效学机制与其抗氧化性质以及调节关键信号通路的能力有关。在此,我们全面描述了NAC在治疗肝脏疾病中的有益作用,阐述了其作为还原型谷胱甘肽清除剂和前体作用的首个证据,以及显示其免疫调节作用的研究,还有NAC调节表观遗传特征的能力。我们使用以下关键词在PubMed数据库中进行搜索:氧化应激、肝脏疾病、表观遗传学、抗氧化剂、NAC和抗氧化疗法。收集该主题所有可用信息没有时间限制。NAC已显示出治疗肝损伤的疗效,其作用机制不同于自由基清除剂。与不同的抗氧化疗法一样,其有效性和安全性与给药剂量有关;因此,为该药物设计新的药理学制剂对于获得充分的反应至关重要。最后,关于其对肝损伤表观遗传标志物特征的影响仍有许多有待探索之处,这使其成为一种具有广泛治疗潜力的药物。根据所综述的文献,NAC在与肝损伤相关的临床研究中可能是一个合适的选择,并且在未来,是治疗肝脏疾病的一种重新利用的替代药物。