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谷胱甘肽-SH对代谢后的庆大霉素对离体豚鼠毛细胞毒性作用的特异性抑制

Specific glutathione-SH inhibition of toxic effects of metabolized gentamicin on isolated guinea pig hair cells.

作者信息

Zenner H P, Keiner S, Zimmermann U

机构信息

Department of Otolaryngology, University of Tübingen, Germany.

出版信息

Eur Arch Otorhinolaryngol. 1994;251(2):84-90. doi: 10.1007/BF00179898.

Abstract

The present investigation has shown that only metabolized gentamicin (mG) but not native gentamicin (G) is cytotoxic for isolated guinea pig outer hair cells (OHC). Using FURA-2 fluorescence, both G and mG were found to reduce intracellular free Ca2+ concentrations in unstimulated OHC and inhibit increases in intracellular Ca2+ concentrations during K(+)-induced depolarization. Glutathione-SH (GSH), a detoxificating agent, did not interfere with G and mG effects on intracellular Ca2+ concentration. In non-stimulated OHC, mG but not G induced pathological OHC depolarization, indicating the opening of transduction channels to allow influx of K+ ions. GSH completely inhibited the lytic effect of mG. Electrophysiological investigations also revealed that GSH probably inhibits mG-induced pathological opening of transduction channels. These results suggest that GSH selectively inhibits mG-specific toxic effects on the guinea pig OHC, possibly by enzymatic detoxification.

摘要

目前的研究表明,只有代谢后的庆大霉素(mG)而非天然庆大霉素(G)对分离的豚鼠外毛细胞(OHC)具有细胞毒性。使用FURA-2荧光法,发现G和mG均可降低未受刺激的OHC中的细胞内游离Ca2+浓度,并抑制K(+)诱导的去极化过程中细胞内Ca2+浓度的升高。谷胱甘肽-SH(GSH),一种解毒剂,并不干扰G和mG对细胞内Ca2+浓度的影响。在未受刺激的OHC中,mG而非G诱导了病理性的OHC去极化,表明转导通道开放,允许K+离子内流。GSH完全抑制了mG的裂解作用。电生理研究还表明,GSH可能抑制mG诱导的转导通道病理性开放。这些结果表明,GSH可能通过酶促解毒作用选择性地抑制mG对豚鼠OHC的特异性毒性作用。

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