Metabolomics in Nephrotoxicity

被引:77
作者
Zhao, Ying-Yong [1 ]
Lin, Rui-Chao [2 ]
机构
[1] NW Univ Xian, Coll Life Sci, Minist Educ, Key Lab Resource Biol & Biotechnol Western China, Xian 710069, Shaanxi, Peoples R China
[2] Beijing Univ Chinese Med, Sch Chinese Materia Med, Beijing, Peoples R China
来源
ADVANCES IN CLINICAL CHEMISTRY, VOL 65 | 2014年 / 65卷
关键词
ACUTE KIDNEY INJURY; LIQUID CHROMATOGRAPHY/MASS SPECTROMETRY; CISPLATIN-INDUCED NEPHROTOXICITY; MORNING GLORY SEED; GENTAMICIN-INDUCED NEPHROTOXICITY; MAGNETIC-RESONANCE-SPECTROSCOPY; ACID-INDUCED NEPHROTOXICITY; DRUG-INDUCED NEPHROTOXICITY; ARISTOLOCHIC ACID; RENAL TOXICITY;
D O I
10.1016/B978-0-12-800141-7.00003-6
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Nephrotoxicity or renal toxicity can be a result of hemodynamic changes, direct injury to cells and tissue, inflammatory tissue injury, and/or obstruction of renal excretion. Nephrotoxicity is frequently induced by a wide spectrum of therapeutic drugs and environmental pollutants. Knowledge of the complex molecular and pathophysiologic mechanisms leading to nephrotoxicity remains limited, in part, by research that historically focused on single or relatively few risk markers. As such, current kidney injury biomarkers are inadequate in terms of sensitivity and specificity. In contrast, metabolomics enables screening of a vast array of metabolites simultaneously using NMR and MS to assess their role in nephrotoxicity development and progression. A more comprehensive understanding of these biochemical pathways would also provide valuable insight to disease mechanisms critical for drug development and treatment.
引用
收藏
页码:69 / 89
页数:21
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