Todd J H, Hottendorf G H
Pathology Department, West Virginia University, Robert C. Byrd Health Sciences Center, Morgantown 26506, USA.
Toxicol Lett. 1997 Feb 7;90(2-3):217-21. doi: 10.1016/s0378-4274(96)03858-1.
Cultured human proximal tubule cell monolayers maintained on permeable supports were treated simultaneously with the aminoglycoside antibiotic, gentamicin, and poly-L-aspartic acid (PAA), an inhibitor of aminoglycoside nephrotoxicity. Following 4 days of exposure, cell monolayers were placed into Ussing chambers to allow monitoring of transepithelial electrical properties. For each of the three cell isolates examined, aminoglycoside-induced alterations in electrogenic transport, reflected by changes in short-circuit current (Isc), as well as alterations in paracellular properties, indicated by changes in transepithelial electrical resistance (RT), were diminished in the presence of PAA. Alterations resulting from selective basolateral exposure to gentamicin were unchanged in the case of apically applied PAA and attenuated only when PAA acid was added basolaterally. This is the first demonstration of PAA inhibition of aminoglycoside-induced cellular alterations involving human cells.
在可渗透支持物上维持培养的人近端肾小管细胞单层,同时用氨基糖苷类抗生素庆大霉素和氨基糖苷类肾毒性抑制剂聚-L-天冬氨酸(PAA)进行处理。暴露4天后,将细胞单层放入尤斯灌流小室中,以监测跨上皮电特性。对于所检测的三种细胞分离株中的每一种,在存在PAA的情况下,氨基糖苷类诱导的电生成转运改变(通过短路电流(Isc)变化反映)以及细胞旁特性改变(通过跨上皮电阻(RT)变化指示)均减少。在顶端应用PAA的情况下,由选择性基底外侧暴露于庆大霉素引起的改变没有变化,仅当基底外侧添加PAA酸时才减弱。这是PAA抑制涉及人类细胞的氨基糖苷类诱导的细胞改变的首次证明。