Donta S T
Antimicrob Agents Chemother. 1974 Mar;5(3):240-6. doi: 10.1128/AAC.5.3.240.
Two clonal lines of rat hepatoma cells, in tissue culture, that have steroid-inducible tyrosine aminotransferase (TAT) activities were shown to have different responses to amphotericin B. One of the cell lines (HTC) was relatively resistant to the growth-inhibiting effects of amphotericin B and demonstrated an inhibition of only its steroid-inducible TAT activity when exposed to the antifungal agent. In contrast, not only was the other cell line (MHC) sensitive to amphotericin B during its growth, but uninduced and induced enzyme activities were affected. During the first few hours after the exposure of MHC cells to amphotericin B, both basal and dexamethasone-induced TAT activity were reduced; with continued exposure, enzyme activity increased over that of untreated cells and was superinduced in the presence of maximal, stimulating amounts of steroid. The mechanisms by which enzyme activity is induced by amphotericin B are probably different from those mediated by steroids.
在组织培养中,两种具有类固醇诱导型酪氨酸转氨酶(TAT)活性的大鼠肝癌细胞克隆系对两性霉素B表现出不同的反应。其中一个细胞系(HTC)对两性霉素B的生长抑制作用相对耐药,并且在暴露于抗真菌剂时仅其类固醇诱导型TAT活性受到抑制。相比之下,另一个细胞系(MHC)在生长过程中不仅对两性霉素B敏感,而且未诱导和诱导的酶活性均受到影响。在MHC细胞暴露于两性霉素B后的最初几个小时内,基础和地塞米松诱导的TAT活性均降低;随着持续暴露,酶活性超过未处理细胞并在存在最大刺激量类固醇的情况下被超诱导。两性霉素B诱导酶活性的机制可能与类固醇介导的机制不同。