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大鼠中他莫昔芬及其代谢物的测定以及与二甲基苯并蒽诱导的乳腺肿瘤反应的关系。

The measurement of tamoxifen and metabolites in the rat and relationship to the response of DMBA-induced mammary tumours.

作者信息

Daniel C P, Gaskell S J, Nicholson R I

出版信息

Eur J Cancer Clin Oncol. 1984 Jan;20(1):137-43. doi: 10.1016/0277-5379(84)90045-2.

Abstract

The concentrations of tamoxifen and two of its metabolites, N-desmethyltamoxifen and 4'-hydroxytamoxifen (metabolite B), have been measured in rat plasma and DMBA-induced tumours using gas chromatography-mass spectrometry. At a dose of 100 micrograms/day all three compounds produced tumour regression and, in the case of tamoxifen, the number and extent of regressions and the inhibition of new tumours were dependent upon dosage. No correlation was observed, however, between tumour regression and the concentrations of tamoxifen or N-desmethyltamoxifen in the plasma of individual animals. When tamoxifen, N-desmethyltamoxifen and metabolite B were measured in oestrogen-receptor-positive tumours a correlation was found between reduction in tumour and the tamoxifen concentration in cytosol fractions. The concentrations of all three compounds in both nuclear and cytosol fractions were higher than could be accounted for by binding to the oestrogen receptor. The mechanistic significance of these high values is, at present, unclear.

摘要

已使用气相色谱 - 质谱法测定了大鼠血浆和二甲基苯并蒽(DMBA)诱导的肿瘤中他莫昔芬及其两种代谢物N - 去甲基他莫昔芬和4'-羟基他莫昔芬(代谢物B)的浓度。在每日剂量为100微克时,所有三种化合物均使肿瘤消退,就他莫昔芬而言,消退的数量和程度以及对新肿瘤的抑制作用取决于剂量。然而,在个体动物的血浆中,未观察到肿瘤消退与他莫昔芬或N - 去甲基他莫昔芬浓度之间的相关性。当在雌激素受体阳性肿瘤中测定他莫昔芬、N - 去甲基他莫昔芬和代谢物B时,发现肿瘤缩小与胞浆部分中他莫昔芬浓度之间存在相关性。核部分和胞浆部分中所有三种化合物的浓度均高于与雌激素受体结合所能解释的浓度。目前,这些高值的机制意义尚不清楚。

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