Alterations in hepatic amino acid metabolism related to MASLD in individuals with obesity.

IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Armando J Pérez-Díaz, Inmaculada Ros-Madrid, María A Martínez-Sánchez, Sara Rico-Chazarra, Alba Oliva-Bolarín, Andrés Balaguer-Román, Virginia E Fernández-Ruiz, Carlos M Martínez, José E Yuste, Mercedes Ferrer-Gómez, Camilo J Llamoza-Torres, María D Frutos, María Á Núñez-Sánchez, Bruno Ramos-Molina
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引用次数: 0

Abstract

Deregulation of amino acid (AA) metabolism has been reported in several pathological conditions, including metabolic diseases (e.g., obesity and diabetes), cardiovascular diseases, and cancer. However, the role of alterations in AA levels in chronic liver disorders such as metabolic dysfunction-associated steatotic liver disease (MASLD) remains largely unexplored. In this study we aimed to evaluate the hepatic AA composition in patients with different stages of MASLD, and their relationship with MASLD-related risk factors. A case-control study was conducted in 40 patients with obesity undergoing bariatric surgery at Virgen de la Arrixaca University Hospital (Murcia, Spain), where MASLD diagnosis was confirmed by histological analysis of liver biopsies, and hepatic AA levels were measured using ultra-performance liquid chromatography high-resolution time-of-flight mass spectrometry. Our results revealed that the hepatic AA profile was significantly altered in patients with MASLD. More specifically, comparison between MASLD patients revealed a significant increase in hepatic levels of arginine, glycine and cystine in MASH samples compared to steatotic livers. In addition, hepatic concentrations of arginine, lysine and cystine positively correlated with histopathological diagnosis and other MASLD-related parameters, including transaminases and CK-18 levels. These findings suggest that alterations in certain hepatic AA levels such as arginine, lysine, glycine and cystine in MASLD patients could have translational relevance in understanding the onset of this disease.

肥胖患者与MASLD相关的肝脏氨基酸代谢改变
氨基酸(AA)代谢的失调已经在几种病理条件下被报道,包括代谢性疾病(如肥胖和糖尿病)、心血管疾病和癌症。然而,AA水平的改变在慢性肝脏疾病(如代谢功能障碍相关的脂肪变性肝病(MASLD))中的作用在很大程度上仍未被探索。在本研究中,我们旨在评估不同阶段MASLD患者的肝脏AA组成及其与MASLD相关危险因素的关系。在Virgen de la Arrixaca大学医院(西班牙穆尔西亚)对40例接受减肥手术的肥胖患者进行了病例对照研究,通过肝脏活检的组织学分析证实了MASLD的诊断,并使用超高效液相色谱高分辨率飞行时间质谱法测量了肝脏AA水平。我们的研究结果显示,MASLD患者的肝脏AA谱明显改变。更具体地说,MASLD患者之间的比较显示,与脂肪变性肝相比,MASH样本中肝脏精氨酸、甘氨酸和胱氨酸水平显著升高。此外,肝脏精氨酸、赖氨酸和胱氨酸浓度与组织病理学诊断和其他masld相关参数(包括转氨酶和CK-18水平)呈正相关。这些发现表明,MASLD患者中某些肝脏AA水平(如精氨酸、赖氨酸、甘氨酸和胱氨酸)的改变可能与理解该疾病的发病具有翻译相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of physiology and biochemistry
Journal of physiology and biochemistry 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
86
审稿时长
6-12 weeks
期刊介绍: The Journal of Physiology and Biochemistry publishes original research articles and reviews describing relevant new observations on molecular, biochemical and cellular mechanisms involved in human physiology. All areas of the physiology are covered. Special emphasis is placed on the integration of those levels in the whole-organism. The Journal of Physiology and Biochemistry also welcomes articles on molecular nutrition and metabolism studies, and works related to the genomic or proteomic bases of the physiological functions. Descriptive manuscripts about physiological/biochemical processes or clinical manuscripts will not be considered. The journal will not accept manuscripts testing effects of animal or plant extracts.
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