Potential therapeutic uses of L-citrulline beyond genetic urea cycle disorders

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Inherited Metabolic Disease Pub Date : 2024-11-24 DOI:10.1002/jimd.12810
Marshall Summar
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Abstract

L-citrulline (referred to hereafter as citrulline), a non-essential amino acid and an intermediate in the urea cycle, is widely recognized for its role in managing genetic urea cycle disorders (UCDs). Recent studies, however, suggest that citrulline's therapeutic potential extends beyond UCDs, particularly in conditions associated with nitric oxide (NO) deficiency, endothelial dysfunction, and oxidative stress. This review explores citrulline's emerging applications in sickle cell disease (SCD), post-operative pulmonary hypertension (PH), hepatic veno-occlusive disease (HVOD), and bronchopulmonary dysplasia (BPD), as well as its speculative use in asthma and acute respiratory distress syndrome (ARDS). In SCD, citrulline may restore NO bioavailability, potentially reducing the incidence and severity of vaso-occlusive crises and preventing complications like pulmonary hypertension. In the context of post-operative PH, citrulline's capacity to enhance NO production can improve pulmonary vascular resistance, decrease right ventricular strain, and reduce the need for mechanical ventilation. Citrulline's protective effects on endothelial function and its ability to mitigate oxidative stress offer promising adjunctive therapy for HVOD, particularly in patients undergoing bone marrow transplantation. In BPD, citrulline could promote alveolar development, reduce inflammation, and improve long-term respiratory outcomes. Despite these promising findings, further research is necessary to determine optimal dosing strategies and to evaluate long-term efficacy and safety. The potential role of citrulline in modulating NO production in conditions like asthma and ARDS also warrants further investigation. This review underscores the versatile therapeutic potential of citrulline and highlights the need for continued research into its applications across various conditions associated with NO deficiency and endothelial dysfunction.

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除遗传性尿素循环障碍外,L-瓜氨酸的潜在治疗用途
L-瓜氨酸(以下简称瓜氨酸)是一种非必需氨基酸,也是尿素循环的中间体,因其在控制遗传性尿素循环障碍(UCD)方面的作用而得到广泛认可。然而,最近的研究表明,瓜氨酸的治疗潜力并不局限于尿素循环障碍,尤其是与一氧化氮(NO)缺乏、内皮功能障碍和氧化应激相关的疾病。本综述探讨了瓜氨酸在镰状细胞病(SCD)、术后肺动脉高压(PH)、肝静脉闭塞症(HVOD)和支气管肺发育不良(BPD)中的新兴应用,以及其在哮喘和急性呼吸窘迫综合征(ARDS)中的推测用途。在 SCD 中,瓜氨酸可恢复 NO 的生物利用率,从而有可能降低血管闭塞危象的发生率和严重程度,并预防肺动脉高压等并发症。在术后 PH 的情况下,瓜氨酸增强 NO 生成的能力可改善肺血管阻力,降低右心室负荷,减少对机械通气的需求。瓜氨酸对内皮功能的保护作用及其减轻氧化应激的能力为 HVOD 的辅助治疗提供了前景,尤其是对接受骨髓移植的患者。在 BPD 患者中,瓜氨酸可促进肺泡发育、减轻炎症反应并改善长期呼吸预后。尽管这些研究结果令人鼓舞,但仍有必要开展进一步研究,以确定最佳剂量策略并评估长期疗效和安全性。瓜氨酸在哮喘和急性缺氧性呼吸衰竭等疾病中调节 NO 生成的潜在作用也值得进一步研究。本综述强调了瓜氨酸的多功能治疗潜力,并强调了继续研究其在与 NO 缺乏和内皮功能障碍相关的各种疾病中应用的必要性。
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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
期刊最新文献
Reversible white matter changes following a 4-week high phenylalanine exposure in adults with phenylketonuria. Uncommon case of mitochondrial disease: Mild amyotrophy of the legs and symmetrical lipomatosis of the arms. Issue Information Potential therapeutic uses of L-citrulline beyond genetic urea cycle disorders Epidemiology and economic burden of Wilson disease in France: A nationwide population-based study.
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