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The separate roles of glucose and insulin in the induction of glucokinase in hepatocytes isolated from neonatal rats.葡萄糖和胰岛素在新生大鼠分离肝细胞中诱导葡萄糖激酶的各自作用。
Biochem J. 1981 May 15;196(2):383-90. doi: 10.1042/bj1960383.
2
Factors that prevent the premature appearance of glucokinase in neonatal rat liver.阻止新生大鼠肝脏中葡萄糖激酶过早出现的因素。
Biochem J. 1980 Mar 15;186(3):817-26. doi: 10.1042/bj1860817.
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Regulation of the gene expression of glucokinase and L-type pyruvate kinase in primary cultures of rat hepatocytes by hormones and carbohydrates.
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4
Insulin and tri-iodothyronine induce glucokinase mRNA in primary cultures of neonatal rat hepatocytes.胰岛素和三碘甲状腺原氨酸可诱导新生大鼠肝细胞原代培养物中的葡萄糖激酶信使核糖核酸。
Biochem J. 1990 Nov 1;271(3):585-9. doi: 10.1042/bj2710585.
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Initial expression of glucokinase gene in cultured hepatocytes from suckling rats is linked to the synthesis of an insulin-dependent protein.
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De novo synthesis of glucokinase in hepatocytes isolated from neonatal rats.新生大鼠分离肝细胞中葡萄糖激酶的从头合成
FEBS Lett. 1980 Feb 25;111(1):115-9. doi: 10.1016/0014-5793(80)80774-5.
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Insulin signalling and regulation of glucokinase gene expression in cultured hepatocytes.
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Role of insulin, glucose, and cyclic GMP in the regulation of glucokinase in cultured hepatocytes.胰岛素、葡萄糖和环磷酸鸟苷在培养肝细胞中对葡萄糖激酶调节的作用。
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Induction of glucokinase by insulin under the permissive action of dexamethasone in primary rat hepatocyte cultures.在原代大鼠肝细胞培养物中,地塞米松的允许作用下胰岛素对葡萄糖激酶的诱导作用。
Biochem Biophys Res Commun. 1979 May 14;88(1):23-9. doi: 10.1016/0006-291x(79)91691-7.
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Transcriptional induction of glucokinase gene by insulin in cultured liver cells and its repression by the glucagon-cAMP system.
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引用本文的文献

1
Mike Wakelam: an appreciation.迈克·韦克拉姆:赞颂
Essays Biochem. 2020 Sep 23;64(3):397-399. doi: 10.1042/EBC20200042.
2
Hepatic glucokinase activity and circulating insulin concentrations in two inbred mouse strains.两种近交系小鼠品系的肝脏葡萄糖激酶活性和循环胰岛素浓度。
Diabetologia. 1983 Aug;25(2):114-9. doi: 10.1007/BF00250898.
3
Biochemistry of liver development in the perinatal period.围生期肝脏发育的生物化学
Experientia. 1983 May 15;39(5):473-83. doi: 10.1007/BF01965164.
4
Insulin and tri-iodothyronine induce glucokinase mRNA in primary cultures of neonatal rat hepatocytes.胰岛素和三碘甲状腺原氨酸可诱导新生大鼠肝细胞原代培养物中的葡萄糖激酶信使核糖核酸。
Biochem J. 1990 Nov 1;271(3):585-9. doi: 10.1042/bj2710585.

本文引用的文献

1
Nutrition of animal cells in tissue culture; initial studies on a synthetic medium.组织培养中动物细胞的营养;对合成培养基的初步研究。
Proc Soc Exp Biol Med. 1950 Jan;73(1):1-8. doi: 10.3181/00379727-73-17557.
2
Induction of glucokinase in vitro in hepatocytes from neonatal rats [proceedings].新生大鼠肝细胞中葡萄糖激酶的体外诱导[会议论文集]
Biochem Soc Trans. 1980 Jun;8(3):384-5. doi: 10.1042/bst0080384.
3
Factors that prevent the premature appearance of glucokinase in neonatal rat liver.阻止新生大鼠肝脏中葡萄糖激酶过早出现的因素。
Biochem J. 1980 Mar 15;186(3):817-26. doi: 10.1042/bj1860817.
4
De novo synthesis of glucokinase in hepatocytes isolated from neonatal rats.新生大鼠分离肝细胞中葡萄糖激酶的从头合成
FEBS Lett. 1980 Feb 25;111(1):115-9. doi: 10.1016/0014-5793(80)80774-5.
5
Glucoreceptor mechanisms and the control of insulin release and biosynthesis.葡萄糖受体机制与胰岛素释放及生物合成的调控
Diabetologia. 1980 Jan;18(1):5-15. doi: 10.1007/BF01228295.
6
Purification and properties of adenosine 5'-triphospae-D-glucose 6-phosphotransferase from rat liver.大鼠肝脏腺苷5'-三磷酸-D-葡萄糖6-磷酸转移酶的纯化及性质
Biochem J. 1966 May;99(2):266-74. doi: 10.1042/bj0990266.
7
The development of hepatic glucokinase in the neonatal rat.新生大鼠肝脏葡萄糖激酶的发育
Biochem J. 1965 Dec;97(3):845-54. doi: 10.1042/bj0970845.
8
The secretion of serum protein and the synthesis of albumin and total protein in regenerating rat liver.再生大鼠肝脏中血清蛋白的分泌以及白蛋白和总蛋白的合成。
J Biol Chem. 1971 Jul 25;246(14):4531-8.
9
Paper disc estimation of radioactive RNA: studies on the presence and elimination of metabolically generated artifacts from labeled purine and pyrimidine precursors.
Anal Biochem. 1971 Feb;39(2):319-21. doi: 10.1016/0003-2697(71)90420-9.
10
Hormonal control of hexokinase activity in animal tissues.动物组织中己糖激酶活性的激素调控。
Biochim Biophys Acta. 1970 Sep 22;215(3):461-76. doi: 10.1016/0304-4165(70)90097-8.

葡萄糖和胰岛素在新生大鼠分离肝细胞中诱导葡萄糖激酶的各自作用。

The separate roles of glucose and insulin in the induction of glucokinase in hepatocytes isolated from neonatal rats.

作者信息

Wakelam M J, Walker D G

出版信息

Biochem J. 1981 May 15;196(2):383-90. doi: 10.1042/bj1960383.

DOI:10.1042/bj1960383
PMID:6274313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1163009/
Abstract
  1. The specificity of the effect of glucose on the induction of glucokinase activity that occurs when hepatocytes freshly isolated from 13-day-old rats are incubated in Medium 199 together with insulin [Wakelam & Walker (1980) FEBS Lett. 111, 115-119] was examined. A pattern that is different from other known effects of glucose is found, and metabolism of this compound is not necessarily to account for this particular effect. 2. The effects of a raised glucose concentration and of insulin on the induction can be separated. The hexose initiates the process in the absence of insulin in a manner that is sensitive to actinomycin D but not to cycloheximide. The subsequent effect of insulin is dependent on the prior effect of glucose or other positive analogue, does not require the presence of glucose and is inhibited by cycloheximide but not by actinomycin D. 3. Induction of glucokinase in vitro in hepatocytes from neonatal animals is inhibited by adrenaline, glucagon and dibutyryl cyclic AMP, but not by vasopressin or angiotensin II. The inhibition by cyclic AMP is on the stage requiring insulin and is comparatively specific, because total protein synthesis is not apparently diminished. 4. The implications of these results are discussed with reference to possible mechanisms of induction and to the situation in vivo.
摘要
  1. 研究了葡萄糖对从13日龄大鼠新鲜分离的肝细胞与胰岛素一起在199培养基中孵育时发生的葡萄糖激酶活性诱导作用的特异性[Wakelam和Walker(1980年),《欧洲生物化学学会联合会快报》111,115 - 119]。发现了一种与葡萄糖的其他已知作用不同的模式,并且该化合物的代谢不一定能解释这种特定作用。2. 升高的葡萄糖浓度和胰岛素对诱导作用的影响可以分开。在没有胰岛素的情况下,己糖以对放线菌素D敏感但对环己酰亚胺不敏感的方式启动该过程。胰岛素的后续作用取决于葡萄糖或其他正性类似物的先前作用,不需要葡萄糖的存在,并且被环己酰亚胺抑制但不被放线菌素D抑制。3. 新生动物肝细胞中葡萄糖激酶的体外诱导受到肾上腺素、胰高血糖素和二丁酰环磷腺苷的抑制,但不受血管加压素或血管紧张素II的抑制。环磷腺苷的抑制作用发生在需要胰岛素的阶段,并且具有相对特异性,因为总蛋白质合成显然没有减少。4. 参照可能的诱导机制和体内情况讨论了这些结果的意义。