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大鼠肝脏和肾脏中磷酸烯醇丙酮酸羧激酶mRNA浓度的快速变化。胰岛素和环磷酸腺苷的作用。

Rapid changes in the concentration of phosphoenolpyruvate carboxykinase mRNA in rat liver and kidney. Effects of insulin and cyclic AMP.

作者信息

Cimbala M A, Lamers W H, Nelson K, Monahan J E, Yoo-Warren H, Hanson R W

出版信息

J Biol Chem. 1982 Jul 10;257(13):7629-36.

PMID:6282847
Abstract

Starvation and diabetes both caused a marked increase in the concentration of hepatic phosphoenolpyruvate caroboxykinase mRNA while the administration of insulin to diabetic rats or refeeding glucose to starved animals caused a marked reduction in the levels of enzyme mRNA as measured by hybridization using a cDNA probe.l The Administration of dibutyryl cAMP to a starved-refed cat caused an 8-fold induction of phosphoenolpyruvate carboxykinase mRNA in 1 h. Triamcinolone plus acidosis induced the levels of enzyme mRNA in kidney 3-fold within 6 h, however, starvation for 24h had only marginal effects. In all of the above conditions, the levels of phosphoenolpyruvate carboxykinase mRNA measured by hybridization assay agreed well with the relative levels of translatable mRNA for the enzyme. The half-time of phosphoenolpyruvate carboxykinase mRNA, determined after the administration of either alpha-amanitin or cordycepin to starved animals, was approximately 40 min. However, cycloheximide either alone or together with cordycepin, not only prevented the decrease in phosphoenolpyruvate carboxykinase mRNA sequence abundance, but induced it 2-fold. Cycloheximide itself, when injected into 21-day fetal rats in utero caused an induction of enzyme mRNA equal to that noted when dibutyryl cAMP was administered. The mRNA for phosphoenolpyruvate carboxykinase is approximately 2.8 kb in length, but nuclei from the livers of diabetic rats contain a number of putative precursor RNA species for the enzyme, up to 6.5 kb in size, all containing a poly(A) tail. Two hours after refeedng glucose to a starved rat, these nuclear RNA species could no longer be detected by hybridization to our cDNA probe.

摘要

饥饿和糖尿病均导致肝脏磷酸烯醇式丙酮酸羧激酶mRNA浓度显著升高,而给糖尿病大鼠注射胰岛素或给饥饿动物重新喂食葡萄糖后,使用cDNA探针通过杂交检测发现,酶mRNA水平显著降低。给饥饿-再喂食的猫注射二丁酰cAMP,1小时内磷酸烯醇式丙酮酸羧激酶mRNA诱导增加8倍。曲安西龙加酸中毒在6小时内使肾脏中该酶mRNA水平增加3倍,然而,饥饿24小时的影响微乎其微。在上述所有情况下,通过杂交试验测得的磷酸烯醇式丙酮酸羧激酶mRNA水平与该酶可翻译mRNA的相对水平高度一致。给饥饿动物注射α-鹅膏蕈碱或虫草素后测定的磷酸烯醇式丙酮酸羧激酶mRNA半衰期约为40分钟。然而,单独使用放线菌酮或与虫草素一起使用时,不仅可防止磷酸烯醇式丙酮酸羧激酶mRNA序列丰度降低,还可使其增加2倍。将放线菌酮单独注射到21天龄的未出生胎儿大鼠体内时,引起的酶mRNA诱导作用与注射二丁酰cAMP时相当。磷酸烯醇式丙酮酸羧激酶的mRNA长度约为2.8 kb,但糖尿病大鼠肝脏细胞核中含有该酶的一些假定前体RNA种类,大小可达6.5 kb,均含有聚腺苷酸尾。给饥饿大鼠重新喂食葡萄糖2小时后,通过与我们的cDNA探针杂交无法再检测到这些核RNA种类。

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