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[抗风湿治疗诱导染色体畸变]

[Induction of chromosome aberrations by antirheumatic therapy].

作者信息

Vormittag W

出版信息

Acta Med Austriaca. 1975;2(4):148-53.

PMID:1224931
Abstract
  1. The comparison between mean structural chromosomal aberration rates after immunosuppressive therapy and the rate of induction of malignant tumours after application of the same cytostatic substances to animals revealed a far-reaching parallelism: Highest mean aberration rates after therapy with procarbazine (Natulan) and cyclophosphamide (Endoxan) - fewer aberrations after mannitol mustard (Degranol) and no definite induction of chromosomal aberrations after azathioprine (Imurel) (8). 2. The possibility of the induction of chromosomal aberrations in lymphocytes of the peripheral blood after injection of gold 198 into the knee-joint, could be confirmed (9). 3. The mean chromosomal aberration rates before and after infusiontherapy with phenylbutazone (Butazolidin; 300 mg + 600 mg/die during 9 days) showed no significant difference (10).
摘要
  1. 免疫抑制治疗后平均结构性染色体畸变率与向动物施用相同细胞毒性物质后恶性肿瘤诱导率之间的比较显示出深远的平行关系:丙卡巴肼(甲基苄肼)和环磷酰胺(癌得星)治疗后的平均畸变率最高——甘露醇氮芥(德格兰诺)治疗后的畸变较少,硫唑嘌呤(依木兰)治疗后未明确诱导染色体畸变(8)。2. 向膝关节注射金198后外周血淋巴细胞中诱导染色体畸变的可能性得到了证实(9)。3. 用保泰松(布他唑立丁;9天内每日300毫克+600毫克)进行输液治疗前后的平均染色体畸变率无显著差异(10)。

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