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Keywords: glucose
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Biochem J (2015) 466 (2): 203–218.
Published: 20 February 2015
...Guy A. Rutter; Timothy J. Pullen; David J. Hodson; Aida Martinez-Sanchez Insulin release from pancreatic β-cells is required to maintain normal glucose homoeostasis in man and many other animals. Defective insulin secretion underlies all forms of diabetes mellitus, a disease currently reaching...
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Biochem J (2014) 460 (3): 353–361.
Published: 29 May 2014
... advantage of the high temporal resolution of recently available FRET nanosensors for glucose, lactate and ATP. The activity of the Na + pump was assessed in parallel with the Na + -sensitive dye SBFI AM (Na + -binding benzofuran isophthalate acetoxymethyl ester). OXPHOS (oxidative phosphorylation...
Includes: Supplementary data
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Biochem J (2013) 452 (3): 489–497.
Published: 31 May 2013
... to glucose by activating the Hxt5p (hexose transporter 5) glucose transporter, which provides an advantage during early phases after glucose resupply. cAMP and glucose FRET (fluorescence resonance energy transfer) sensors were used to identify three signalling pathways that co-operate in the anticipatory...
Includes: Supplementary data
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Biochem J (2013) 449 (2): 497–506.
Published: 14 December 2012
... or organelles. In response to nutrient deprivation, e.g. depletion of amino acids or serum, autophagy is induced and most of these signals converge on the kinase mTOR (mammalian target of rapamycin). It is commonly accepted that glucose inhibits autophagy, since its deprivation from cells cultured in full...
Includes: Supplementary data
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Biochem J (2012) 443 (3): 829–839.
Published: 16 April 2012
... activity and lower blood glucose levels in the fed, but not the fasted, state. PDHK4 deficiency caused similar effects, but only after fasting. Double deficiency intensified these effects in both the fed and fasted states. PDHK2 deficiency had no effect on glucose tolerance, PDHK4 deficiency produced only...
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Biochem J (2011) 440 (2): 203–215.
Published: 14 November 2011
...Bogumil Zelent; Stella Odili; Carol Buettger; Dorothy K. Zelent; Pan Chen; Deborah Fenner; Joseph Bass; Charles Stanley; Monique Laberge; Jane M. Vanderkooi; Ramakanth Sarabu; Joseph Grimsby; Franz M. Matschinsky GK (glucokinase) is activated by glucose binding to its substrate site, is inhibited...
Includes: Supplementary data
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Biochem J (2011) 435 (1): 285–296.
Published: 15 March 2011
...-resolved metabolomics) to determine the metabolic effects of tunicamycin. Glucose was found to be the major carbon source for energy production and anabolic metabolism. Following tunicamycin exposure, glucose uptake and lactate production are greatly reduced. Decreased 13 C labelling in several cellular...
Includes: Supplementary data
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Biochem J (2010) 431 (3): 381–390.
Published: 11 October 2010
... semialdehyde is increased by 2-oxoglutarate, generated in α-keto acid transamination to its corresponding α-amino acid. The present work was aimed at investigating whether glucose also promotes islet GABA metabolism and whether the latter contributes to the stimulation of insulin secretion. Glucose (20 mM...
Includes: Supplementary data
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Biochem J (2009) 424 (3): 459–466.
Published: 10 December 2009
... for the control of glucose-stimulated insulin secretion. AGC1 or Aralar1 (aspartate–glutamate carrier 1) is a key component of the malate–aspartate shuttle. Overexpression of AGC1 increases the capacity of the malate–aspartate shuttle, resulting in enhanced metabolism–secretion coupling, both in INS-1E cells...
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Biochem J (2009) 421 (3): 371–376.
Published: 15 July 2009
... glucose levels were unchanged in 16-week-old, 6 h fasted animals of either gender; however, plasma insulin concentrations were reduced in both female (∼31%) and male (∼47%) ZnT-8 −/− mice. Intraperitoneal glucose tolerance tests demonstrated no impairment in glucose clearance in male ZnT-8 −/− mice...
Includes: Supplementary data
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Biochem J (2008) 415 (1): 1–10.
Published: 12 September 2008
... to changes in blood glucose levels. The synthesis of insulin is regulated by blood glucose levels at the transcriptional and post-transcriptional levels. Although many transcription factors have been implicated in the regulation of insulin gene transcription, three β-cell-specific transcriptional regulators...
Includes: Multimedia, Supplementary data
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Biochem J (2008) 414 (2): 177–187.
Published: 12 August 2008
... © The Authors Journal compilation © 2008 Biochemical Society 2008 galactose glucose haem meiosis oxygen The Zn(II) 2 Cys 6 family of proteins are defined by a conserved motif. This motif is composed of six cysteine residues in the form of: -Cys-X 2 -Cys-X 6 -Cys-X 5-12 -Cys-X 2...
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Biochem J (2008) 411 (2): 261–270.
Published: 27 March 2008
...Nikolas G. Tsatsos; Michael N. Davies; Brennon L. O'callaghan; Howard C. Towle In the liver, induction of genes encoding enzymes involved in de novo lipogenesis occurs in response to increased glucose metabolism. ChREBP (carbohydrate-response-element-binding protein) is a basic helix–loop–helix...
Includes: Supplementary data
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Biochem J (2007) 408 (2): 251–258.
Published: 14 November 2007
... glycation end-products) in various tissues, including the lens. Nevertheless, glycation of α-crystallin with various sugars has resulted in divergent results. In the present in vitro study, we have investigated the effect of glucose, fructose, G6P (glucose 6-phosphate) and MGO (methylglyoxal), which...
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Biochem J (2006) 400 (1): 81–89.
Published: 27 October 2006
.... The L -[U- 14 C]-Glutamine (at 0.5 and 10.0 mM) conversion to 14 CO 2 was enhanced by 10 mM OMP within 30% and 70% respectively. Gabaculine (250 μM), a GABA transaminase inhibitor, suppressed OMP-induced oxygen consumption but not L -leucine- or glucose-stimulated respiration. It also suppressed the OMP...
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Biochem J (2006) 399 (2): e11.
Published: 27 September 2006
... phosphorylation of glucose-derived Amadori products suggests that intracellular glycation could be deleterious under certain circumstances. In order to approach the question of the biological relevance of intracellular glycation, in this issue of the Biochemical Journal , Veiga-da-Cunha and colleagues generated...
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Biochem J (2005) 392 (3): 633–639.
Published: 06 December 2005
... of blood glucose levels, while high GSK3 activity has been reported in Type II diabetes. Insulin inhibits GSK3 by promoting phosphorylation of a serine residue (Ser-21 in GSK3α, Ser-9 in GSK3β), thereby relieving GSK3 inhibition of glycogen synthesis in muscle. GSK3 inhibition in liver reduces expression...
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Biochem J (2004) 381 (3): 905–909.
Published: 27 July 2004
... resistance to current treatments. To study new potential targets, we have functionally characterized two natural variants of the hexose transporter of P. vivax (PvHT) after heterologous expression in Xenopus oocytes. We show that PvHT transports both glucose and fructose. Differences in the affinity...
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Biochem J (2003) 375 (2): 385–393.
Published: 15 October 2003
... TGF-β receptor (TβRII) induced by high glucose might contribute to distal tubular hypertrophy [Yang, Guh, Yang, Lai, Tsai, Hung, Chang and Chuang (1998) J. Am. Soc. Nephrol. 9 , 182–193]. We have elucidated the mechanism by using cultured Madin–Darby canine kidney cells. Enhancer assay...
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Biochem J (2003) 374 (3): 677–685.
Published: 15 September 2003
...Hong YAN; Antony C. WILLIS; John J. HARDING Several mechanisms have been proposed for the way in which glucose and its metabolites cause cataract, retinopathy and other complications of diabetes, the most convincing being glycation. Glycation, the reaction of sugars with free amino groups...
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Biochem J (2002) 364 (1): 309–315.
Published: 08 May 2002
...Michael GUPPY; Peter LEEDMAN; XinLin ZU; Victoria RUSSELL For the past 70 years the dominant perception of cancer metabolism has been that it is fuelled mainly by glucose (via aerobic glycolysis) and glutamine. Consequently, investigations into the diagnosis, treatment and the basic metabolism...
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Biochem J (2001) 360 (2): 265–276.
Published: 26 November 2001
...Ronaldo P. FERRARIS The Na + -dependent glucose transporter SGLT1 and the facilitated fructose transporter GLUT5 absorb sugars from the intestinal lumen across the brush-border membrane into the cells. The activity of these transport systems is known to be regulated primarily by diet...
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Biochem J (2000) 351 (3): 811–816.
Published: 24 October 2000
...Roger R. GOMIS; Juan C. FERRER; Joan J. GUINOVART We have used recombinant adenoviruses (AdCMV-RLGS and AdCMV-GK) to overexpress the liver isoforms of glycogen synthase (GS) and glucokinase (GK) in primary cultured rat hepatocytes. Glucose activated overexpressed GS in a dose-dependent manner...
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Biochem J (2000) 349 (3): 667–688.
Published: 25 July 2000
...Antonio ZORZANO; César FANDOS; Manuel PALACÍN Muscle plays a major role in metabolism. Thus it is a major glucose-utilizing tissue in the absorptive state, and changes in muscle insulin-stimulated glucose uptake alter whole-body glucose disposal. In some conditions, muscle preferentially uses lipid...
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Biochem J (2000) 347 (1): 23–27.
Published: 27 March 2000
...-assisted laster-desorption ionization-MS and NMR. CMA gradually increased in collagen during incubation with glucose and the yield reached about 8 mol/mol of collagen, which is 100 times higher than that of pentosidine. This result suggests that CMA is a major AGE in collagen. Biochem. J. (2000) 347, 23 27...
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Biochem J (1999) 344 (2): 433–441.
Published: 24 November 1999
... that their activation by insulin requires the presence, in the medium in which the cells are maintained, of both amino acids and glucose: insulin only induced activation of eIF2B and the dephosphorylation of eEF2 when cells were exposed to both types of nutrient. Other translational regulators, e.g. the 70 kDa...
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