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代谢组学在肾毒性中的应用。

Metabolomics in nephrotoxicity.

出版信息

Adv Clin Chem. 2014;65:69-89.

Abstract

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 environ mental 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.

摘要

肾毒性或肾中毒可能是血流动力学改变、细胞和组织直接损伤、炎症组织损伤和/或肾排泄受阻的结果。肾毒性通常由广泛的治疗药物和环境污染物引起。导致肾毒性的复杂分子和病理生理机制的知识仍然有限,部分原因是历史上的研究集中在单个或相对较少的风险标志物上。因此,目前的肾脏损伤生物标志物在灵敏度和特异性方面都不够充分。相比之下,代谢组学可以使用 NMR 和 MS 同时筛选大量代谢物,以评估它们在肾毒性发展和进展中的作用。对这些生化途径的更全面了解还将为药物开发和治疗至关重要的疾病机制提供有价值的见解。

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