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华法林对大鼠诱发结直肠癌的细胞动力学、上皮形态及肿瘤发生率的影响。

Effect of warfarin on cell kinetics, epithelial morphology and tumour incidence in induced colorectal cancer in the rat.

作者信息

Goeting N, Trotter G A, Cooke T, Kirkham N, Taylor I

出版信息

Gut. 1985 Aug;26(8):807-15. doi: 10.1136/gut.26.8.807.

Abstract

The effect of low dose warfarin and high dose warfarin on epithelial cell kinetics (as determined by stathmokinetic techniques), and preneoplastic morphological changes was studied during azoxymethane induced carcinogenesis in the rat. Warfarin, at either low or high dose, had no effect on crypt cell production rate (CCPR) at any time interval whereas tumour incidence in both low dose warfarin and high dose warfarin groups was significantly reduced. Morphological changes were observed using scanning electron microscopy, which by conventional histology were shown to be adenoma precursors. In the control group the number of microadenomas increased with time after starting azoxymethane. In warfarin treated animals, the number of microadenomas also increased with time, but the actual incidence was reduced when compared with controls. These results suggest that the effects of warfarin on tumour development is unrelated to its anticoagulant effect, because increased dose did not result in greater tumour reduction. Furthermore, there was no overall change in CCPR when warfarin was administered. Warfarin may exert a specific effect, by preventing neoplastic change in cells which have undergone morphologically undetectable changes associated with early carcinogenesis.

摘要

在大鼠由氧化偶氮甲烷诱导的致癌过程中,研究了低剂量华法林和高剂量华法林对上皮细胞动力学(通过静止动力学技术测定)以及癌前形态学变化的影响。低剂量或高剂量的华法林在任何时间间隔对隐窝细胞产生率(CCPR)均无影响,而低剂量华法林组和高剂量华法林组的肿瘤发生率均显著降低。使用扫描电子显微镜观察到形态学变化,通过传统组织学显示这些变化为腺瘤前体。在对照组中,开始给予氧化偶氮甲烷后微腺瘤数量随时间增加。在华法林治疗的动物中,微腺瘤数量也随时间增加,但与对照组相比实际发生率降低。这些结果表明,华法林对肿瘤发展的影响与其抗凝作用无关,因为增加剂量并未导致更大程度的肿瘤减少。此外,给予华法林时CCPR没有总体变化。华法林可能通过防止已发生与早期致癌相关的形态学上无法检测到的变化的细胞发生肿瘤性变化而发挥特定作用。

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