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多烯大环内酯类抗生素对中国仓鼠细胞体外协同作用的差异控制

Differential control of synergistic effect with polyene macrolide antibiotics upon Chinese hamster cells in vitro.

作者信息

Hidaka K, Matsui K, Endo H, Akiyama S I, Kuwano M

出版信息

Cancer Res. 1978 Dec;38(12):4650-3.

PMID:82481
Abstract

An amphotericin B-resistant cell (AMBR-1), which was isolated from aneuploid Chinese hamster cells (V79), was found to show much higher resistance than the parent V79 cells to other polyene antibiotics, such as pentamycin and filipin. To obtain the 50 to 60% inhibition of the control protein synthesis activity by a synergistic combination of fusidic acid and amphotericin B, 50 microgram fusidic acid per ml were combined with 10 microgram amphotericin B in V79 cells, whereas in AMBR cells 50 microgram fusidic acid per ml were combined with 100 microgram polyene antibiotic per ml. Bleomycin (10 microgram/ml), which alone did not affect cellular DNA synthesis, inhibited DNA synthesis of V79 cells by more than 90% of the control activity when combined with only 1 microgram pentamycin per ml, whereas a similar extent of inhibition in AMBR cells was observed by combination with more than 5 microgram pentamycin per ml.

摘要

从非整倍体中国仓鼠细胞(V79)中分离出的一株对两性霉素B耐药的细胞(AMBR-1),被发现对其他多烯类抗生素(如戊霉素和菲律宾菌素)的耐药性比亲本V79细胞高得多。为了通过夫西地酸和两性霉素B的协同组合使对照蛋白合成活性受到50%至60%的抑制,在V79细胞中,每毫升50微克夫西地酸与10微克两性霉素B组合,而在AMBR细胞中,每毫升50微克夫西地酸与每毫升100微克多烯类抗生素组合。博来霉素(10微克/毫升)单独使用时不影响细胞DNA合成,但与每毫升仅1微克戊霉素组合时,可使V79细胞的DNA合成抑制超过对照活性的90%,而在AMBR细胞中,与每毫升超过5微克戊霉素组合时,观察到类似程度的抑制。

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