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肿瘤启动剂12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯和苯巴比妥在体内诱导大鼠肝脏鸟氨酸脱羧酶活性与多胺腐胺、亚精胺和精胺水平之间的关系;乙酸视黄酯的不同作用。

Relation between induction of rat hepatic ornithine decarboxylase activity by tumor promoters 12-O-tetradecanoylphorbol-13-acetate and phenobarbital and levels of the polyamines putrescine, spermidine and spermine, in vivo; differential effects of retinyl-acetate.

作者信息

Van Rooijen L A, Derks H J, Van Wijk R, Bisschop A

出版信息

Carcinogenesis. 1984 Feb;5(2):225-9. doi: 10.1093/carcin/5.2.225.

Abstract

A single i.p. injection of 12-O-tetradecanoylphorbol-13-acetate (TPA) induced a transient increase in the levels of rat liver putrescine, spermidine and spermine. These polyamine concentrations continuously increased until 6 h, immediately following administration of the tumor promoter. Phenobarbital (PB) induced an increase of the putrescine and spermidine concentrations during the 8 h post administration studied, while spermine reached a plateau after 4 h. When retinyl-acetate (RA) was injected one hour prior to TPA, the increases of the polyamines were considerably inhibited. This treatment with RA partially inhibited further increase of putrescine and spermine by PB. These findings are discussed in respect to the concomitant ornithine decarboxylase (ODC) activities, we have previously reported. I.p. injection of RA alone caused an elevation of ODC activity as well as putrescine and spermidine concentration within 2 h of exposure.

摘要

腹腔注射一次12 - O - 十四酰佛波醇 - 13 - 乙酸酯(TPA)可使大鼠肝脏腐胺、亚精胺和精胺水平短暂升高。在给予肿瘤启动子后,这些多胺浓度持续升高直至6小时。在研究的给药后8小时内,苯巴比妥(PB)可使腐胺和亚精胺浓度升高,而精胺在4小时后达到平台期。当在TPA注射前1小时注射视黄醇乙酸酯(RA)时,多胺的升高受到显著抑制。RA的这种处理部分抑制了PB引起的腐胺和精胺的进一步升高。结合我们之前报道的鸟氨酸脱羧酶(ODC)活性,对这些发现进行了讨论。单独腹腔注射RA会在暴露后2小时内导致ODC活性以及腐胺和亚精胺浓度升高。

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