Aging and restriction of dietary calories increases insulin receptor mRNA, and aging increases glucocorticoid receptor mRNA in the liver of female C3B10RF1 mice.
Aging and restriction of dietary calories increases insulin receptor mRNA, and aging increases glucocorticoid receptor mRNA in the liver of female C3B10RF1 mice.
复制标题
衰老和饮食热量限制会增加雌性 C3B10RF1 小鼠肝脏中胰岛素受体 mRNA 的含量,而衰老会增加肝脏中糖皮质激素受体 mRNA 的含量。
DOI:
10.1093/geronj/46.6.b233
复制
发表时间:
1991
期刊:
影响因子:
--
通讯作者:
Mote,PL
中科院分区:
文献类型:
--
作者:
Spindler,SR;Grizzle,JM;Walford,RL;Mote,PL
We investigated the influence of age and a 20% or 52% reduction in dietary calories (caloric restriction) on expression of mRNA for a number of transcription factors and signal-transducing proteins using4,16, and 30-monthold female mice of the long-lived c3B10RF, strain. In all age groups, 52% caloric restriction, which extends maximum life span by approximately 33%, increased insulin receptor mRNA by 15% to 25% over the levels in animals fed ad libitum. Aging increased insulin receptor mRNA and glucocorticoid receptor mRNA in all dietary groups. A similar increase in glucocorticoid receptor mRNA was not observed for male mice of three other strains, suggesting the change is sex-or strain-specific and not a general feature of aging. These changes appear to be specific. Neither caloric restriction nor age had an effect on the level of mRNA for insulin-like growth factor-I, RNA polymerase II elongation-factor S-II, or transcription factors SPL, CCAAT and enhancer binding protein, or proto-oncogene c-jun.