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在腐胺存在的情况下预防3,4-苯并芘致癌作用。

Prevention of 3,4-benzopyrene carcinogenesis in presence of putrescine.

作者信息

Kallistratos G, Fasske E

出版信息

Z Krebsforsch Klin Onkol Cancer Res Clin Oncol. 1976 Sep 24;87(1):81-92. doi: 10.1007/BF00285076.

Abstract

The 3,4-Benzopyrene (3,4-BP) carcinogenesis can be postponed or even completely inhibited in the presence of Putrescine (P). A single s.c. injection of 2.52 mg 3,4-BP in 0.5 ml tricaprylin on female mice (NMRI-strains, 4--5 weeks old, 20--25 g of body weight) induced locally malignant tumors (sarcomas and carcinomas) up to 97% of the animals treated. (132 mice with tumors from 136 animals treated). Animals injected with 3,4-BP plus 10 mg putrescine showed a considerable reduction of tumor incidence. Only three from 38 mice treated developed tumors (8%). The prevention of tumor could not be further improved with higher putrescine amounts, for example 15 mg and 20 mg P. These concentrations were moreover toxic to the animals. Histologically, the tumors developed in the presence of putrescine were rather poor in malignant cells and mitoses were also rare, in contrast to the usual 3,4-BP tumors which were rich in polymorph cells and mitoses.

摘要

在腐胺(P)存在的情况下,3,4-苯并芘(3,4-BP)致癌作用可被延缓甚至完全抑制。对雌性小鼠(NMRI品系,4 - 5周龄,体重20 - 25克)皮下注射0.5毫升三辛酸甘油酯中含2.52毫克3,4-BP,高达97%接受治疗的动物诱发了局部恶性肿瘤(肉瘤和癌)。(136只接受治疗的动物中有132只出现肿瘤)。注射3,4-BP加10毫克腐胺的动物肿瘤发生率显著降低。38只接受治疗的小鼠中只有3只出现肿瘤(8%)。使用更高剂量的腐胺(例如15毫克和20毫克P)并不能进一步提高肿瘤预防效果。此外,这些浓度对动物有毒。组织学上,与通常富含多形细胞和有丝分裂的3,4-BP肿瘤相比,在腐胺存在下形成的肿瘤恶性细胞较少,有丝分裂也很少见。

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