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从LLC-PK1分离的克隆细胞系中,新霉素的细胞毒性降低。

Decreased cellular toxicity of neomycin in a clonal cell line isolated from LLC-PK1.

作者信息

Hori R, Okuda M, Ohishi Y, Yasuhara M, Inui K, Takano M

机构信息

Department of Pharmacy, Kyoto University Hospital, Faculty of Medicine, Japan.

出版信息

Pharm Res. 1993 Apr;10(4):573-6. doi: 10.1023/a:1018954204094.

Abstract

We have previously shown in LLC-PK1 cells, that apical membrane enzyme activity was inhibited by aminoglycoside antibiotics (Am. J. Physiol. 254, C251-C257, 1988). In the present study, the relationship between the lethal cytotoxic effect of aminoglycoside and its effect on apical membrane enzyme was examined by establishing aminoglycoside resistant cells. A clonal cell line, LLC-PK1/NRa3, was isolated from parent LLC-PK1 cells in the presence of neomycin. Neomycin inhibited colony formation and increased the number of floating dead cells in parent LLC-PK1 cultures. In contrast, these cytotoxic effects of neomycin were negligible or less pronounced in NRa3 cells, indicating that NRa3 cells were more resistant to neomycin compared with the parent cells. The inhibitory effect of neomycin on apical enzyme activity was significantly weaker in NRa3 cells than in the parent cells. These results suggest that a common mechanism is involved in the aminoglycoside-induced reductions in the apical enzyme activity and in cell viability of LLC-PK1 cells.

摘要

我们之前在LLC-PK1细胞中发现,氨基糖苷类抗生素可抑制顶膜酶活性(《美国生理学杂志》254卷,C251 - C257页,1988年)。在本研究中,通过建立氨基糖苷类耐药细胞,研究了氨基糖苷类的致死细胞毒性作用与其对顶膜酶作用之间的关系。在新霉素存在的情况下,从亲代LLC-PK1细胞中分离出一个克隆细胞系LLC-PK1/NRa3。新霉素抑制亲代LLC-PK1培养物中的集落形成并增加漂浮死细胞的数量。相比之下,新霉素的这些细胞毒性作用在NRa3细胞中可忽略不计或不太明显,这表明与亲代细胞相比,NRa3细胞对新霉素更具抗性。新霉素对顶膜酶活性的抑制作用在NRa3细胞中明显弱于亲代细胞。这些结果表明,氨基糖苷类诱导的LLC-PK1细胞顶膜酶活性降低和细胞活力降低涉及共同机制。

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