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小鼠口腔黏膜对重复剂量博来霉素的反应。

Response of mouse oral mucosa to repeated doses of bleomycin.

作者信息

Dörr W, Hönig M

机构信息

GSF-Institut für Strahlenbiologie, Neuherberg, Germany.

出版信息

Eur J Cancer B Oral Oncol. 1994 Sep;30B(5):312-8. doi: 10.1016/0964-1955(94)90031-0.

Abstract

Bleomycin (BLM) applied at systemically tolerable doses induces denudation of tongue mucosa in the C3H-Neuherberg mouse strain. The dose-incidence curve after single injections has a sigmoid shape with an ED50 of 17.5 mg/kg. In contrast, the dose-response curves to repeated (two, five and 10) drug injections follow triphasic shapes and show dose-effect inversions. The effect initially increases with dose to a maximum of 70-100% at 2 x 7, 5 x 2, and 10 x 0.9 mg/kg. A marked decrease in response is observed at higher doses with a nadir of 10-30% after 2 x 11 mg/kg, 5 x 4 to 5 x 5 mg/kg and 10 x 2 mg/kg, followed by a second rise when dose is further increased. These clinical results were confirmed in a histological study. Variation of the time interval between two drug injections caused marked fluctuations in the treatment efficacy. A clear increase in drug response was induced by splitting total drug doses of 6, 14 or 22 mg/kg, the maximum effect (100%) was seen at intervals of 2 h, 0.5-1 h and 0.25 h between two injections of 3, 7 or 11 mg/kg, respectively. At longer intervals of up to 6 h, a dose-dependent decrease in drug efficacy resulted in an inverse dose-effect. Original tissue tolerance to BLM was restored only in the 2 x 3 mg/kg arm but was still elevated in the other arms after 96 h. The results can be plausibly explained by the dose-dependent induction of detoxifying processes.

摘要

以全身可耐受剂量应用博来霉素(BLM)可导致C3H - Neuherberg小鼠品系的舌黏膜剥脱。单次注射后的剂量 - 发生率曲线呈S形,半数有效剂量(ED50)为17.5毫克/千克。相比之下,重复(两次、五次和十次)药物注射的剂量 - 反应曲线呈三相形状,并显示出剂量 - 效应倒置。效应最初随剂量增加,在2×7、5×2和10×0.9毫克/千克时达到70 - 100%的最大值。在更高剂量下观察到反应明显下降,在2×11毫克/千克、5×4至5×5毫克/千克和10×2毫克/千克后最低点为10 - 30%,随后当剂量进一步增加时出现第二次上升。这些临床结果在组织学研究中得到证实。两次药物注射之间的时间间隔变化导致治疗效果出现明显波动。将6、14或22毫克/千克的总药物剂量分开注射可明显增加药物反应,在两次分别注射3、7或11毫克/千克时,间隔2小时、0.5 - 1小时和0.25小时可观察到最大效应(100%)。在长达6小时的较长间隔下,药物疗效呈剂量依赖性下降,导致剂量 - 效应倒置。仅在2×3毫克/千克组中96小时后原始组织对BLM的耐受性得以恢复,但其他组中仍保持升高。这些结果可以通过解毒过程的剂量依赖性诱导得到合理的解释。

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