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阻止新生大鼠肝脏中葡萄糖激酶过早出现的因素。

Factors that prevent the premature appearance of glucokinase in neonatal rat liver.

作者信息

Wakelam J O, Allen M B, Walker D G

出版信息

Biochem J. 1980 Mar 15;186(3):817-26. doi: 10.1042/bj1860817.

Abstract
  1. The physiological factors that prevent the precocious appearance of glucokinase activity in the 13-day-old rat that can be induced by oral glucose administration were explored. 2. Evidence is presented that the galactose component of milk sugar is inhibitory. In the absence of this inhibitory galactose, the amount of glucose necessary to effect appreciable induction is greater than that present in milk. 3. The induction is prevented both by administration of mannoheptulose, which inhibits insulin release, and by excess insulin; the amount of insulin available therefore seems to be critical. 4. The inhibition of induction by galactose does not appear to be via competition with glucose but by enhancing insulin release and thereby making this excessive. The relative amounts of glucose and insulin appear to be important in regulating glucokinase induction. 5. The precocious induction of glucokinase by glucose is inhibited by simultaneous treatment with approriate amounts of adrenaline, glucagon, dibutyryl cyclic AMP or isoprenaline but not by vasopressin or angiotensin II. 6. No single cause of glucokinase induction in neonatal rat liver can be recognized. The process is subject to regulation by many factors at a time subsequent to when competence to synthesize the enzyme has been established.
摘要
  1. 对13日龄大鼠中可通过口服葡萄糖诱导的葡萄糖激酶活性过早出现的生理因素进行了探索。2. 有证据表明乳糖中的半乳糖成分具有抑制作用。在没有这种抑制性半乳糖的情况下,实现明显诱导所需的葡萄糖量大于乳汁中所含的葡萄糖量。3. 甘露庚酮糖(抑制胰岛素释放)的给药以及过量胰岛素均会阻止这种诱导;因此,可用的胰岛素量似乎至关重要。4. 半乳糖对诱导的抑制作用似乎不是通过与葡萄糖竞争,而是通过增强胰岛素释放从而使其过量。葡萄糖和胰岛素的相对量在调节葡萄糖激酶诱导方面似乎很重要。5. 用适量的肾上腺素、胰高血糖素、二丁酰环磷腺苷或异丙肾上腺素同时处理可抑制葡萄糖对葡萄糖激酶的过早诱导,但血管加压素或血管紧张素II则无此作用。6. 新生大鼠肝脏中葡萄糖激酶诱导的单一原因无法确定。在建立合成该酶的能力之后的某个时间,该过程受到多种因素的调节。

相似文献

本文引用的文献

1
Artificial Feeding of Neonatal Rats.人工喂养新生大鼠。
Science. 1963 Aug 9;141(3580):517-8. doi: 10.1126/science.141.3580.517.

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