患有线粒体疾病的儿童和青少年的内皮功能障碍以及补充精氨酸和瓜氨酸的效果。

IF 2.6 Q2 CLINICAL NEUROLOGY Journal of Central Nervous System Disease Pub Date : 2020-02-29 eCollection Date: 2020-01-01 DOI:10.1177/1179573520909377
Fatma Al Jasmi, Nuha Al Zaabi, Khalid Al-Thihli, Amal M Al Teneiji, Jozef Hertecant, Ayman W El-Hattab
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引用次数: 0

摘要

背景:除了线粒体疾病特有的能量生成减少外,还可能出现一氧化氮(NO)缺乏症。血管内皮细胞产生的一氧化氮能使血管平滑肌松弛,导致血管扩张,从而保持小血管的通畅,促进微血管中的血流。由于血管内皮细胞无法产生足够的 NO 以维持充分的血管舒张,导致内皮功能障碍,从而导致各种组织的微血管灌注减少,引发线粒体疾病患者的多种并发症。氨基酸精氨酸和瓜氨酸是 NO 的前体:增加它们的浓度有可能恢复 NO 的生成:在这项研究中,我们评估了患有线粒体疾病的儿童和青少年的内皮功能障碍。我们还研究了补充精氨酸和瓜氨酸对这些人内皮功能障碍的影响。我们使用外周动脉测压法测量反应性充血指数(RHI),当内皮功能障碍时RHI较低:结果:研究结果表明,线粒体疾病患者的反应性高血容量指数较低,表明其存在内皮功能障碍。补充精氨酸或瓜氨酸可提高 RHI,这表明补充 NO 前体可通过提高 NO 的产生来改善内皮功能障碍:本研究首次在线粒体疾病中使用外周动脉测压法。本研究结果为线粒体疾病的内皮功能障碍提供了证据,并证明补充精氨酸或瓜氨酸可缓解内皮功能障碍,为这些氨基酸在线粒体疾病中的潜在治疗作用提供了更多证据。
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Endothelial Dysfunction and the Effect of Arginine and Citrulline Supplementation in Children and Adolescents With Mitochondrial Diseases.

Background: In addition to the reduced energy production, characteristic of mitochondrial disorders, nitric oxide (NO) deficiency can occur as well. The NO produced by vascular endothelial cells relaxes vascular smooth muscles, resulting in vasodilation that maintains the patency of small blood vessels and promotes blood flow through microvasculature. Endothelial dysfunction due to inability of vascular endothelium to generate enough NO to maintain adequate vasodilation can result in decreased perfusion in the microvasculature of various tissues, contributing to many complications seen in individuals with mitochondrial diseases. The amino acids arginine and citrulline are NO precursors: increasing their concentrations could potentially restore NO production.

Methods: In this study, we assessed endothelial dysfunction in children and adolescents with mitochondrial diseases. We also investigated the effect of arginine and citrulline supplementation on endothelial dysfunction in these individuals. We used peripheral arterial tonometry to measure the reactive hyperemic index (RHI), which is low when there is endothelial dysfunction.

Results: The results demonstrated low RHI in individuals with mitochondrial diseases, indicating endothelial dysfunction. RHI increased with arginine or citrulline supplementation suggesting that supplementation with NO precursors can improve endothelial dysfunction by enhancing NO production.

Conclusions: This study is the first one to use peripheral arterial tonometry methodology in mitochondrial diseases. The results of this study provide evidence for endothelial dysfunction in mitochondrial diseases and demonstrate that arginine or citrulline supplementation can alleviate the endothelial dysfunction, providing more evidence for the potential therapeutic utility of these amino acids in mitochondrial diseases.

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CiteScore
6.90
自引率
0.00%
发文量
39
审稿时长
8 weeks
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