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首页> 外文期刊>Molecular Carcinogenesis >Effects of dietary energy repletion and IGF-1 infusion on the inhibition of mammary carcinogenesis by dietary energy restriction.
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Effects of dietary energy repletion and IGF-1 infusion on the inhibition of mammary carcinogenesis by dietary energy restriction.

机译:饮食能量补充和IGF-1输注对饮食能量限制抑制乳癌发生的影响。

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摘要

Dietary energy restriction (DER) is a potent inhibitor of mammary carcinogenesis, but the responsible mechanisms are not fully understood. In a number of model systems, DER is associated with a decrease in circulating levels of IGF-1. Moreover, we have recently reported that protection against cancer is lost, and plasma IGF-1 levels are restored to control values when animals are re-fed, i.e., energy repleted (DER-REP). Accordingly, an experiment was designed to determine if infusion of IGF-1 could mimic the effect of DER-REP on the carcinogenic response in animals that were DER. Following 1-methyl-1-nitrosourea injection (50 mg/kg), rats were fed either ad libitum (AL) or 40% DER. After 6 wk, the DER group was divided into three groups: (1) continued DER, (2) DER-REP, or (3) continued DER and infused with 120 mug rh-IGF-1/d (INF) for a duration of 8 d. DER reduced mammary cancer incidence and multiplicity (P < 0.01) versus AL rats. In rats that were DER-REP, cancer incidence increased 1.4-fold and multiplicity increased by 3.6-fold versus DER rats. Plasma IGF-1 were reduced by DER (P < 0.01), an effect that was reversed by DER-REP (P < 0.05). INF increased plasma IGF-1 versus DER rats (P < 0.01) but did not reverse the carcinogenic response. Plasma IGFBP-3 levels were reduced by DER (P < 0.01), but elevated by either REP or INF. Thus, an 8-d period of refeeding following chronic DER (DER-REP) reversed the anticancer effects of DER, and 8 d of IGF-1 infusion without refeeding (INF) did not mimic the effects of the DER-REP on the carcinogenic response.
机译:饮食能量限制(DER)是乳癌发生的有效抑制剂,但其作用机理尚未完全明了。在许多模型系统中,DER与IGF-1循环水平的降低有关。此外,我们最近报道,当给动物补饲即补充能量(DER-REP)时,失去了对癌症的保护,血浆IGF-1水平恢复到控制值。因此,设计了一个实验来确定IGF-1的输注是否可以模拟DER-REP对DER动物致癌反应的作用。注射1-甲基-1-亚硝基脲(50 mg / kg)后,随意喂养大鼠(AL)或40%DER。 6周后,DER组分为三组:(1)继续DER,(2)DER-REP或(3)继续DER并持续120杯rh-IGF-1 / d(INF) 8 d。与AL大鼠相比,DER降低了乳腺癌的发病率和多样性(P <0.01)。与DER大鼠相比,在DER-REP大鼠中,癌症发生率增加了1.4倍,多重性增加了3.6倍。血浆IGF-1被DER降低(P <0.01),而DER-REP则被逆转(P <0.05)。与DER大鼠相比,INF增加了血浆IGF-1(P <0.01),但并未逆转致癌反应。血浆IGFBP-3水平被DER降低(P <0.01),但被REP或INF升高。因此,慢性DER(DER-REP)后的8 d补料期逆转了DER的抗癌作用,IGF-1输注8 d不补料(INF)并没有模仿DER-REP的致癌作用响应。

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