Department of Pharmacy, 71213The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Hum Exp Toxicol. 2022 Jan-Dec;41:9603271221119178. doi: 10.1177/09603271221119178.
Drug-induced nephrotoxicity is widespread and seriously affects human health. Vancomycin is a classical glycopeptide antibiotic. Vancomycin is widely used for severe infections caused by Gram-positive bacteria, especially methicillin-resistant but its obvious nephrotoxicity affects the safety of its clinical application. However, the etiology of vancomycin induced kidney injury is not well understood. This study aimed to explore the potential mechanism of vancomycin-induced nephrotoxicity in rats. Vancomycin (400 mgkg) was used to establish kidney injury models in rats. A metabonomic approach was employed using ultra-performance liquid chromatography coupled with quadrupole-time-of-flight mass spectrometry (UHPLC-Q-TOF/MS) to delineate metabolic alterations. As a result, 15, 22, and 37 biomarkers were identified in urine samples from the treatment group compared to the control model on D2, D4, and D7, respectively. Changes in the levels of these metabolites indicated that amino acid metabolism and energy metabolism were disturbed in rats with vancomycin-associated nephrotoxicity. This study revealed the kidney effect of vancomycin, which may provide novel and promising research approaches to vancomycin-induced renal toxicity.
药物诱导的肾毒性很普遍,严重影响人类健康。万古霉素是一种经典的糖肽类抗生素。万古霉素被广泛用于治疗由革兰氏阳性菌引起的严重感染,特别是耐甲氧西林的细菌感染,但它明显的肾毒性影响了其临床应用的安全性。然而,万古霉素诱导肾损伤的病因尚不清楚。本研究旨在探讨万古霉素诱导大鼠肾毒性的潜在机制。使用万古霉素(400mg/kg)建立大鼠肾损伤模型。采用超高效液相色谱-四极杆飞行时间质谱联用(UHPLC-Q-TOF/MS)技术进行代谢组学研究,以描绘代谢变化。结果表明,与对照组相比,在第 2、4 和 7 天,治疗组的尿液样本中分别有 15、22 和 37 种生物标志物。这些代谢物水平的变化表明,在万古霉素相关肾毒性大鼠中,氨基酸代谢和能量代谢受到干扰。本研究揭示了万古霉素的肾脏作用,为研究万古霉素诱导的肾毒性提供了新的有前途的研究方法。