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1.
J Vis Exp ; (180)2022 02 08.
Article in English | MEDLINE | ID: mdl-35225266

ABSTRACT

Liver glycogen is a hyperbranched glucose polymer that is involved in the maintenance of blood sugar levels in animals. The properties of glycogen are influenced by its structure. Hence, a suitable extraction method that isolates representative samples of glycogen is crucial to the study of this macromolecule. Compared to other extraction methods, a method that employs a sucrose density gradient centrifugation step can minimize molecular damage. Based on this method, a recent publication describes how the density of the sucrose solution used during centrifugation was varied (30%, 50%, 72.5%) to find the most suitable concentration to extract glycogen particles of a wide variety of sizes, limiting the loss of smaller particles. A 10 min boiling step was introduced to test its ability to denature glycogen degrading enzymes, thus preserving glycogen. The lowest sucrose concentration (30%) and the addition of the boiling step were shown to extract the most representative samples of glycogen.


Subject(s)
Glycogen , Liver Glycogen , Animals , Liver/chemistry , Liver Glycogen/analysis , Liver Glycogen/chemistry , Sucrose
2.
Carbohydr Polym ; 278: 118991, 2022 Feb 15.
Article in English | MEDLINE | ID: mdl-34973794

ABSTRACT

Liver fibrosis (LF) leads to liver failure and short survival. Liver glycogen is a hyperbranched glucose polymer, comprising individual ß particles, which can bind together to form aggregated α particles. Glycogen functionality depends on its molecular structure. This study compared the molecular structure of liver glycogen from both LF and healthy rats, and explored underlying mechanisms for observed differences. Glycogen from both groups contained α and ß particles; the LF group contained a higher proportion of ß particles, with the glycogen containing fewer long chains than seen in the control group. Both glycogen branching enzyme and glycogen phosphorylase showed a significant decrease of activity in the LF group. Transcriptomics and proteomics revealed a functional deficiency of mitochondria in the LF group, which may lead to changes in glycogen structure. These results provide for the first time an understanding of how liver fibrosis affects liver glycogen metabolism and glycogen structure. HYPOTHESIS: We hypothesized that the molecular structure of liver glycogen from a rat model of liver fibrosis would be altered compared to the control group.


Subject(s)
Liver Cirrhosis/metabolism , Liver Glycogen/metabolism , Animals , Carbohydrate Conformation , Liver Cirrhosis/pathology , Liver Glycogen/chemistry , Male , Rats , Rats, Sprague-Dawley
3.
Carbohydr Polym ; 261: 117887, 2021 Jun 01.
Article in English | MEDLINE | ID: mdl-33766374

ABSTRACT

Liver glycogen is a branched glucose polymer that functions as a blood-sugar buffer in animals. Previous studies have shown that glycogen's molecular structure affects its properties. This makes it important to develop a technique that extracts and purifies a representative sample of glycogen. Here we aim to optimize the sucrose density gradient centrifugation method for preserving glycogen's molecular structure by varying the density of the sucrose solution. The preservation of glycogen's structure involves: 1) minimizing molecular damage and 2) obtaining a structurally representative sample of glycogen. The addition of a 10-minute boiling step was also tested as a means for denaturing any glycogen degrading enzymes. Lower sucrose concentrations and the introduction of the boiling step were shown to be beneficial in obtaining a more structurally representative sample, with the preservation of smaller glycogen particles and decreased glycogen chain degradation.


Subject(s)
Liver Glycogen/chemistry , Liver Glycogen/isolation & purification , Animals , Calibration , Cell Fractionation/methods , Cell Fractionation/standards , Chemical Fractionation/methods , Glycogen/chemistry , Glycogen/isolation & purification , Glycogen/metabolism , Liver/chemistry , Liver/metabolism , Liver Glycogen/metabolism , Male , Mice , Molecular Structure , Tissue and Organ Harvesting/methods , Tissue and Organ Harvesting/standards
4.
Carbohydr Polym ; 243: 116435, 2020 Sep 01.
Article in English | MEDLINE | ID: mdl-32532388

ABSTRACT

Glycogen is a branched glucose polymer involved in sustaining blood glucose homeostasis. Liver glycogen comprises α particles (up to 300 nm in diameter) made of joined ß particles (∼20 nm in diameter). Glycogen α particles in a mouse model for diabetes are molecularly fragile, breaking down into smaller ß particles more readily than in healthy mice. Glycogen phosphorylase (GP), a rate-limiting enzyme in glycogen degradation, is overexpressed in diabetic mice. This study shows that Metformin and Berberine, two common drugs, two common drugs used to treat diabetes, are able to revert the liver glycogen of diabetic mice to the stable structure seen in non-diabetic mice. It is also shown that these drugs reduce the GP level via the cAMP/PKA signaling pathway in diabetic livers and decrease the affinity of GP with the glycogen of db/db mice. These effects of these drugs may slow down the degradation of liver glycogen and improve glucose homeostasis.


Subject(s)
Berberine/therapeutic use , Diabetes Mellitus, Experimental/drug therapy , Glycogenolysis/drug effects , Hypoglycemic Agents/therapeutic use , Liver Glycogen/metabolism , Metformin/therapeutic use , Animals , Drug Therapy, Combination , Liver/drug effects , Liver/metabolism , Liver/pathology , Liver Glycogen/chemistry , Male , Mice , Mice, Inbred C57BL , Molecular Structure
5.
Carbohydr Polym ; 237: 116144, 2020 Jun 01.
Article in English | MEDLINE | ID: mdl-32241436

ABSTRACT

Liver glycogen, a highly branched glucose polymer, is important for blood sugar homeostasis. It comprises α particles which are made of linked ß particles; the molecular structure changes diurnally. In diabetic liver, the α particles are fragile, easily breaking apart into ß particles in chaotropic agents such as dimethyl sulfoxide. We here use size-exclusion chromatography to study how fasting changes liver-glycogen structure in vivo for mice in which type-2 diabetes had previously been induced. Diabetic glycogen degraded enzymatically more quickly in the fasted animals than did glycogen without fasting, with fewer α particles, which however were still fragile. The glycogen had fewer long chains and more shorter chains after fasting. This study gives an overview of the in vivo dynamic changes in α-particles under starvation conditions in both normal and diabetic livers.


Subject(s)
Diabetes Mellitus, Experimental/metabolism , Diabetes Mellitus, Type 2/metabolism , Fasting , Liver Glycogen/chemistry , Animals , Chromatography, Gel , Liver Glycogen/metabolism , Male , Rats, Sprague-Dawley
6.
Carbohydr Polym ; 229: 115526, 2020 Feb 01.
Article in English | MEDLINE | ID: mdl-31826402

ABSTRACT

Glycogen, a highly-branched glucose polymer, functions as a sugar reservoir in many organs and tissues. Liver glycogen comprises small ß particles which can bind to form into large agglomerates (α particles) which readily degrade to ß particles in diabetic livers. Muscle glycogen has only ß particles, optimal for quick energy release. Healthy kidney contains negligible glycogen, but there is an abnormally high accumulation in diabetic kidneys. We here compare the molecular structure of glycogen in diabetic kidneys with that in liver and muscle, using a diabetic rat model. This involved exploring extraction techniques to minimize glycogen degradation. Using size exclusion chromatography and transmission electron microscopy, it was found that there were only ß particles in diabetic kidneys. These are postulated to form during periods of abnormally high blood sugar, the driving force being the need to reduce blood sugar under such circumstances.


Subject(s)
Glycogen/chemistry , Kidney/metabolism , Animals , Blood Glucose/analysis , Chromatography, Gel , Diabetes Mellitus, Experimental/chemically induced , Diabetes Mellitus, Experimental/pathology , Diet, High-Fat , Liver Glycogen/chemistry , Microscopy, Electron, Transmission , Muscle, Skeletal/metabolism , Rats
7.
PLoS One ; 11(3): e0150540, 2016.
Article in English | MEDLINE | ID: mdl-26934359

ABSTRACT

Glycogen is a highly branched glucose polymer which is involved in maintaining blood-sugar homeostasis. Liver glycogen contains large composite α particles made up of linked ß particles. Previous studies have shown that the binding which links ß particles into α particles is impaired in diabetic mice. The present study reports the first molecular structural characterization of human-liver glycogen from non-diabetic patients, using transmission electron microscopy for morphology and size-exclusion chromatography for the molecular size distribution; the latter is also studied as a function of time during acid hydrolysis in vitro, which is sensitive to certain structural features, particularly glycosidic vs. proteinaceous linkages. The results are compared with those seen in mice and pigs. The molecular structural change during acid hydrolysis is similar in each case, and indicates that the linkage of ß into α particles is not glycosidic. This result, and the similar morphology in each case, together imply that human liver glycogen has similar molecular structure to those of mice and pigs. This knowledge will be useful for future diabetes drug targets.


Subject(s)
Liver Glycogen/chemistry , Liver Glycogen/ultrastructure , Aged , Animals , Chromatography, Gel , Female , Humans , Hydrolysis , Male , Mice , Mice, Inbred C57BL , Middle Aged , Molecular Structure , Species Specificity , Swine
8.
Biomed Res Int ; 2015: 535982, 2015.
Article in English | MEDLINE | ID: mdl-26090419

ABSTRACT

This study assessed the effects of individual conjugated linoleic acid isomers, c9t11-CLA and t10c12-CLA, on nonalcoholic fatty liver disease (NAFLD) and systemic endothelial dysfunction in rats fed for four weeks with control or high-fructose diet. The high-fructose diet hampered body weight gain (without influencing food intake), increased liver weight and glycogen storage in hepatocytes, upregulated expression of fatty acid synthase (FAS) and stearoyl-CoA desaturase-1 (SCD-1), and increased saturated fatty acid (SFA) content in the liver. Both CLA isomers prevented excessive accumulation of glycogen in the liver. Specifically, t10c12-CLA decreased concentration of serum triacylglycerols and LDL + VLDL cholesterol, increased HDL cholesterol, and affected liver lipid content and fatty acid composition by downregulation of liver SCD-1 and FAS expression. In turn, the c9t11-CLA decreased LDL+VLDL cholesterol in the control group and downregulated liver expression of FAS without significant effects on liver weight, lipid content, and fatty acid composition. In summary, feeding rats with a high-fructose diet resulted in increased liver glycogen storage, indicating the induction of gluconeogenesis despite simultaneous upregulation of genes involved in de novo lipogenesis. Although both CLA isomers (c9t11 and t10c12) display hepatoprotective activity, the hypolipemic action of the t10c12-CLA isomer proved to be more pronounced than that of c9t11-CLA.


Subject(s)
Linoleic Acids, Conjugated/blood , Liver Glycogen/metabolism , Obesity/blood , Stearoyl-CoA Desaturase/biosynthesis , Animals , Body Weight , Cholesterol/blood , Diet , Fructose , Gene Expression/drug effects , Humans , Isomerism , Lipids/blood , Liver Glycogen/chemistry , Obesity/pathology , Rats , Stearoyl-CoA Desaturase/genetics , Triglycerides/blood
9.
PLoS One ; 10(3): e0121337, 2015.
Article in English | MEDLINE | ID: mdl-25799321

ABSTRACT

Phytoglycogen (from certain mutant plants) and animal glycogen are highly branched glucose polymers with similarities in structural features and molecular size range. Both appear to form composite α particles from smaller ß particles. The molecular size distribution of liver glycogen is bimodal, with distinct α and ß components, while that of phytoglycogen is monomodal. This study aims to enhance our understanding of the nature of the link between liver-glycogen ß particles resulting in the formation of large α particles. It examines the time evolution of the size distribution of these molecules during acid hydrolysis, and the size dependence of the molecular density of both glucans. The monomodal distribution of phytoglycogen decreases uniformly in time with hydrolysis, while with glycogen, the large particles degrade significantly more quickly. The size dependence of the molecular density shows qualitatively different shapes for these two types of molecules. The data, combined with a quantitative model for the evolution of the distribution during degradation, suggest that the bonding between ß into α particles is different between phytoglycogen and liver glycogen, with the formation of a glycosidic linkage for phytoglycogen and a covalent or strong non-covalent linkage, most probably involving a protein, for glycogen as most likely. This finding is of importance for diabetes, where α-particle structure is impaired.


Subject(s)
Glycogen/chemistry , Glycogen/metabolism , Starch/analysis , Zea mays/chemistry , Animals , Diabetes Mellitus/metabolism , Glycogen/analysis , Glycogen/ultrastructure , Humans , Hydrolysis , Liver Glycogen/chemistry , Liver Glycogen/metabolism , Mice , Rats , Starch/chemistry , Starch/metabolism
10.
Am J Physiol Endocrinol Metab ; 304(4): E384-91, 2013 Feb 15.
Article in English | MEDLINE | ID: mdl-23211519

ABSTRACT

Dietary fructose can benefit or hinder glycemic control, depending on the quantity consumed, and these contrasting effects are reflected by alterations in postprandial hepatic glycogen synthesis. Recently, we showed that ²H enrichment of glycogen positions 5 and 2 from deuterated water (²H2O) informs direct and indirect pathway contributions to glycogenesis in naturally feeding rats. Inclusion of position 6(S) ²H enrichment data allows indirect pathway sources to be further resolved into triose phosphate and Krebs cycle precursors. This analysis was applied to six rats that had fed on standard chow (SC) and six rats that had fed on SC plus 35% sucrose in their drinking water (HS). After 2 wk, hepatic glycogenesis sources during overnight feeding were determined by ²H2O administration and postmortem analysis of glycogen ²H enrichment at the conclusion of the dark period. Net overnight hepatic glycogenesis was similar between SC and HS rodents. Whereas direct pathway contributions were similar (403 ± 71 µmol/g dry wt HS vs. 578 ± 76 µmol/g dry wt SC), triose phosphate contributions were significantly higher for HS compared with SC (382 ± 61 vs. 87 ± 24 µmol/g dry wt, P < 0.01) and Krebs cycle inputs lower for HS compared with SC (110 ± 9 vs. 197 ± 32 µmol/g dry wt, P < 0.05). Analysis of plasma glucose ²H enrichments at the end of the feeding period also revealed a significantly higher fractional contribution of triose phosphate to plasma glucose levels in HS vs. SC. Hence, the ²H enrichment distributions of hepatic glycogen and glucose from ²H2O inform the contribution of dietary fructose to hepatic glycogen and glucose synthesis.


Subject(s)
Fructose/metabolism , Liver Glycogen/metabolism , Algorithms , Analytic Sample Preparation Methods , Animals , Blood Glucose/analysis , Body Water/chemistry , Citric Acid Cycle , Deuterium Oxide/metabolism , Dietary Sucrose/administration & dosage , Fructose/blood , Glucose/analogs & derivatives , Glucose/analysis , Glucose/chemistry , Kinetics , Liver/metabolism , Liver Glycogen/chemistry , Male , Nuclear Magnetic Resonance, Biomolecular , Postprandial Period , Random Allocation , Rats , Rats, Wistar , Trioses/chemistry , Trioses/metabolism
11.
Biomacromolecules ; 13(11): 3805-13, 2012 Nov 12.
Article in English | MEDLINE | ID: mdl-23004915

ABSTRACT

Glycogen, a hyperbranched complex glucose polymer, is an intracellular glucose store that provides energy for cellular functions, with liver glycogen involved in blood-glucose regulation. Liver glycogen comprises complex α particles made up of smaller ß particles. The recent discovery that these α particles are smaller and fewer in diabetic, compared with healthy, mice highlights the need to elucidate the nature of α-particle formation; this paper tests various possibilities for binding within α particles. Acid hydrolysis effects, examined using dynamic light scattering and size exclusion chromatography, showed that the binding is not simple α-(1→4) or α-(1→6) glycosidic linkages. There was no significant change in α particle size after the addition of various reagents, which disrupt disulfide, protein, and hydrogen bonds and hydrophobic interactions. The results are consistent with proteinaceous binding between ß particles in α particles, with the inability of protease to break apart particles being attributed to steric hindrance.


Subject(s)
Liver Glycogen/chemistry , Proteins/metabolism , Animals , Diabetes Mellitus , Disulfides/metabolism , Hydrogen Bonding , Hydrophobic and Hydrophilic Interactions , Liver Glycogen/metabolism , Mice , Protein Binding , Swine
12.
Biomacromolecules ; 12(6): 1983-6, 2011 Jun 13.
Article in English | MEDLINE | ID: mdl-21591708

ABSTRACT

Glycogen is a highly branched glucose polymer functioning as a glucose buffer in animals. Multiple-detector size exclusion chromatography and fluorophore-assisted carbohydrate electrophoresis were used to examine the structure of undegraded native liver glycogen (both whole and enzymatically debranched) as a function of molecular size, isolated from the livers of healthy and db/db mice (the latter a type 2 diabetic model). Both the fully branched and debranched levels of glycogen structure showed fundamental differences between glycogen from healthy and db/db mice. Healthy glycogen had a greater population of large particles, with more α particles (tightly linked assemblages of smaller ß particles) than glycogen from db/db mice. These structural differences suggest a new understanding of type 2 diabetes.


Subject(s)
Blood Glucose/metabolism , Diabetes Mellitus, Experimental/metabolism , Liver Glycogen , Animals , Blood Glucose/analysis , Carbohydrate Conformation , Chromatography, Gel , Diabetes Mellitus, Experimental/genetics , Diabetes Mellitus, Experimental/physiopathology , Diabetes Mellitus, Type 2/metabolism , Electrophoresis , Female , Humans , Insulin/metabolism , Liver/chemistry , Liver/metabolism , Liver Glycogen/chemistry , Liver Glycogen/metabolism , Mice , Mice, Inbred C57BL , Mice, Transgenic , Mutation , Receptors, Leptin/genetics , Receptors, Leptin/metabolism
13.
Biomacromolecules ; 11(4): 1094-100, 2010 Apr 12.
Article in English | MEDLINE | ID: mdl-20196533

ABSTRACT

Glycogen is a randomly hyperbranched glucose polymer. Complex branched polymers have two structural levels: individual branches and the way these branches are linked. Liver glycogen has a third level: supramolecular clusters of beta particles which form larger clusters of alpha particles. Size distributions of native glycogen were characterized using size exclusion chromatography (SEC) to find the number and weight distributions and the size dependences of the number- and weight-average masses. These were fitted to two distinct randomly joined reference structures, constructed by random attachment of individual branches and as random aggregates of beta particles. The z-average size of the alpha particles in dimethylsulfoxide does not change significantly with high concentrations of LiBr, a solvent system that would disrupt hydrogen bonding. These data reveal that the beta particles are covalently bonded to form alpha particles through a hitherto unsuspected enzyme process, operative in the liver on particles above a certain size range.


Subject(s)
Chromatography, Gel , Liver Glycogen/chemistry , Liver/metabolism , Particle Size , Animals , Hydrogen Bonding , Liver/ultrastructure , Molecular Weight , Rats , Rats, Sprague-Dawley
14.
J Chromatogr B Analyt Technol Biomed Life Sci ; 877(29): 3638-44, 2009 Nov 01.
Article in English | MEDLINE | ID: mdl-19775945

ABSTRACT

We developed a complete method to measure low [(13)C] enrichments in glycogen. Fourteen rats were fed a control diet. Six of them also ingested either [U-(13)C] glucose (n=2) or a mixture of 20 [U-(13)C] amino acids (n=4). Hepatic glycogen was extracted, digested to glucose and purified on anion-cation exchange resins. After the optimization of methylboronic acid derivatization using GC-MS, [(13)C] enrichment of extracted glucose was measured by GC-C-IRMS. The accuracy was addressed by measuring the enrichment excess of a calibration curve, which observed values were in good agreement with the expected values (R=0.9979). Corrected delta values were -15.6+/-1.6 delta(13)C (per thousand) for control rats (n=8) and increased to -5 to 8 delta(13)C (per thousand) per thousand and 12-14 delta(13)C (per thousand) per thousand after the ingestion of [U-(13)C] amino acids or [U-(13)C] glucose as oral tracers, respectively. The method enabled the determination of dietary substrate transfer into glycogen. The sequestration of dietary glucose in liver glycogen 4 h after the meal was 35% of the ingested dose whereas the transfer of carbon skeletons from amino acids was only 0.25 to 1%.


Subject(s)
Boron Compounds/chemistry , Carbon Isotopes/analysis , Gas Chromatography-Mass Spectrometry/methods , Glucose/chemistry , Liver Glycogen/metabolism , Animals , Liver Glycogen/chemistry , Male , Molecular Structure , Rats , Rats, Wistar
15.
Ukr Biokhim Zh (1999) ; 81(5): 26-32, 2009.
Article in Ukrainian | MEDLINE | ID: mdl-20387644

ABSTRACT

The nature of carbohydrates that accumulate in the cells of photosynthetic green sulphur bacteria of Chlorobium limicola Ya-2002 has been investigated. It is shown by infra-red spectrometry, that carbohydrates accumulated in the cells of bacteria are identical (by 90-95%) to glycogen of the bull liver. Exogenous glucose, saccharose, maltose, did not stimulate formation of glycogen. Growth of glycogen level in the cells of bacteria was observed at addition of acetate or piruvate in the conditions of bacteria cultivation in the light and in the presence CO2 and H2S in the environment. Washed cells of C. limicola Ya-2002 did not use glucose of the environment neither in the conditions of illumination nor in darkness, however acetate and piruvate are actively used in the light. During incubation of the washed cells in darkness the level of glycogen fell down approximately three times. Its amount during cells incubation in the light did not change. The decline of glycogen level in cells during their incubation in darkness was accompanied by piling up of carbonic acids in the environment acetate prevailing among them.


Subject(s)
Carbohydrate Metabolism , Chlorobium/metabolism , Polysaccharides, Bacterial/metabolism , Sulfur/metabolism , Animals , Cattle , Chlorobium/isolation & purification , Glycogen/chemistry , Glycogen/metabolism , Liver Glycogen/chemistry , Liver Glycogen/metabolism , Photosynthesis , Polysaccharides, Bacterial/chemistry , Spectrophotometry, Infrared , Water Microbiology
16.
BMC Physiol ; 8: 19, 2008 Oct 10.
Article in English | MEDLINE | ID: mdl-18847460

ABSTRACT

BACKGROUND: Butyrate naturally produced by intestinal fiber fermentation is the main nutrient for colonocytes, but the metabolic effect of the fraction reaching the liver is not totally known. After glycogen hepatic depletion in the 48-hour fasting rat, we monitored the effect of (butyrate 1.90 mg + glucose 14.0 mg)/g body weight versus isocaloric (glucose 18.2 mg/g) or isoglucidic (glucose 14.0 mg/g) control force-feeding on in vivo changes in hepatic glycogen and ATP contents evaluated ex vivo by NMR in the isolated and perfused liver. RESULTS: The change in glycogen was biphasic with (i) an initial linear period where presence of butyrate in the diet increased (P = 0.05) the net synthesis rate (0.20 +/- 0.01 micromol/min.g(-1) liver wet weight, n = 15) versus glucose 14.0 mg/g only (0.16 +/- 0.01 micromol/min.g(-1) liver ww, n = 14), and (ii) a plateau of glycogen store followed by a depletion. Butyrate delayed the establishment of the equilibrium between glycogenosynthetic and glycogenolytic fluxes from the 6th to 8th hour post-feeding. The maximal glycogen content was then 97.27 +/- 10.59 micromol/g liver ww (n = 7) at the 8th hour, which was significantly higher than with the isocaloric control diet (64.34 +/- 8.49 micromol/g, n = 12, P = 0.03) and the isoglucidic control one (49.11 +/- 6.35 micromol/g liver ww, n = 6, P = 0.003). After butyrate ingestion, ATP content increased from 0.95 +/- 0.29 to a plateau of 2.14 +/- 0.23 micromol/g liver ww at the 8th hour post-feeding (n = 8) [P = 0.04 versus isoglucidic control diet (1.45 +/- 0.19 micromol/g, n = 8) but was not different from the isocaloric control diet (1.70 +/- 0.18 micromol/g, n = 12)]. CONCLUSION: The main hepatic effect of butyrate is a sparing effect on glycogen storage explained (i) by competition between butyrate and glucose oxidation, glucose being preferentially directed to glycogenosynthesis during the post-prandial state; and (ii) by a likely reduced glycogenolysis from the newly synthesized glycogen. This first demonstration of the improvement of liver glycogen storage by acute butyrate supply may be an important contribution to explaining the beneficial effects on glucose homeostasis of nutritional supply increasing butyrate amount such as fiber diets.


Subject(s)
Butyrates/administration & dosage , Eating/drug effects , Eating/physiology , Feeding Behavior/drug effects , Feeding Behavior/physiology , Liver Glycogen/metabolism , Animals , Fasting/metabolism , Liver/chemistry , Liver/metabolism , Liver Glycogen/chemistry , Male , Rats , Rats, Wistar
17.
Biochem J ; 414(1): 1-18, 2008 Aug 15.
Article in English | MEDLINE | ID: mdl-18651836

ABSTRACT

Conversion of glucose into glycogen is a major pathway that contributes to the removal of glucose from the portal vein by the liver in the postprandial state. It is regulated in part by the increase in blood-glucose concentration in the portal vein, which activates glucokinase, the first enzyme in the pathway, causing an increase in the concentration of glucose 6-P (glucose 6-phosphate), which modulates the phosphorylation state of downstream enzymes by acting synergistically with other allosteric effectors. Glucokinase is regulated by a hierarchy of transcriptional and post-transcriptional mechanisms that are only partially understood. In the fasted state, glucokinase is in part sequestered in the nucleus in an inactive state, complexed to a specific regulatory protein, GKRP (glucokinase regulatory protein). This reserve pool is rapidly mobilized to the cytoplasm in the postprandial state in response to an elevated concentration of glucose. The translocation of glucokinase between the nucleus and cytoplasm is modulated by various metabolic and hormonal conditions. The elevated glucose 6-P concentration, consequent to glucokinase activation, has a synergistic effect with glucose in promoting dephosphorylation (inactivation) of glycogen phosphorylase and inducing dephosphorylation (activation) of glycogen synthase. The latter involves both a direct ligand-induced conformational change and depletion of the phosphorylated form of glycogen phosphorylase, which is a potent allosteric inhibitor of glycogen synthase phosphatase activity associated with the glycogen-targeting protein, GL [hepatic glycogen-targeting subunit of PP-1 (protein phosphatase-1) encoded by PPP1R3B]. Defects in both the activation of glucokinase and in the dephosphorylation of glycogen phosphorylase are potential contributing factors to the dysregulation of hepatic glucose metabolism in Type 2 diabetes.


Subject(s)
Glucokinase/metabolism , Liver Glycogen/metabolism , Liver/enzymology , Animals , Glucokinase/chemistry , Glucokinase/physiology , Glucose-6-Phosphate/chemistry , Glucose-6-Phosphate/metabolism , Glucose-6-Phosphate/physiology , Humans , Liver/blood supply , Liver/physiology , Liver Glycogen/chemistry , Liver Glycogen/physiology , Phosphorylation , Signal Transduction/physiology
18.
J Fish Dis ; 26(9): 553-61, 2003 09.
Article in English | MEDLINE | ID: mdl-14575373

ABSTRACT

Withholding feed has been suggested as a strategy to manage infectious disease of channel catfish, Ictalurus punctatus (Rafinesque). In a previous study, we demonstrated that deprivation of feed for as little as 7 days reduced innate resistance of catfish to Flavobacterium columnare. This study was conducted to evaluate the effect of feeding regimens [no feeding (NF), fed once every other day to satiation (FEOD) and fed once daily to satiation (FD)] on organosomatic indices, physiological changes and susceptibility of channel catfish to F. columnare. Fish that were not fed for 2 and 4 weeks had a significant increase (P < 0.05) in gutted weight:-wet weight ratio and decrease in other organosomatic indices [gut index (GI), mesenteric fat index (MFI) and hepatosomatic index (HSI)]. Haematology was not effected by feeding regimen except at week 4, when a significantly higher haemoglobin level was observed in the NF fish. Serum protein did not differ at week 2, but the level at week 4 of the NF fish (35.91 mg mL(-1)) was significantly lower than that of the FD fish (41.77 mg mL(-1)). Significantly lower (P < 0.05) blood glucose (39.5 and 40.3 mg dL(-1)) and liver glycogen (1.7 and 1.8 mg g(-1)) were seen in the NF fish at weeks 2 and 4, respectively, as compared with blood glucose and liver glycogen levels of FD fish (67.5 and 92.8 mg dL(-1) and 46.5 and 52.6 mg g(-1) at weeks 2 and 4, respectively) and FEOD (82.8 and 85.5 mg dL(-1) and 45.1 and 51.4 mg g(-1) at weeks 2 and 4, respectively). Mortality in the NF fish caused by F. columnare (78%) was significantly higher (P < 0.05) than mortality in the FD and FEOD treatments (0.0 and 1.7%, respectively). Blood glucose and liver glycogen showed the same trend of low values for NF fish following challenge (week 6). Blood glucose, liver glycogen, GI and HSI are sensitive indicators for channel catfish deprived of feed (NF) for 4 weeks. Blood glucose and liver glycogen levels around 40 mg dL(-1) and 2 mg g(-1), respectively, are indicative of starvation in juvenile channel catfish. Moreover, NF fish were susceptible to F. columnare infection. Thus, it is suggested that in the absence of natural food, juvenile channel catfish should be fed at least once every other day to apparent satiation to maintain normal physiological function and improve resistance to F. columnare.


Subject(s)
Body Constitution/physiology , Flavobacterium/physiology , Food Deprivation/physiology , Ictaluridae/microbiology , Ictaluridae/physiology , Animals , Aquaculture/methods , Blood Glucose/chemistry , Disease Susceptibility/microbiology , Disease Susceptibility/mortality , Hemoglobins/chemistry , Liver Glycogen/chemistry
19.
NMR Biomed ; 16(1): 36-46, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12577296

ABSTRACT

We studied glycogen synthesis from glucose in perfused livers of fed (n = 4) and 24 h starved (n = 7) rats. Glycogenolysis was inhibited by BAY R3401 (150 microM) and proglycosyn (100 microM). After 60 min, we replaced 99% (13)C-1 glucose by natural abundance glucose. This pulse-chase design allowed us to recognize residual ongoing futile glycogen turnover from the release of initially deposited (13)C-label, into the (13)C-free chase medium. Net residual turnover was less than 2 +/- 0.7% and 0.6 +/- 0.2% of 1-(13)C glycogen deposition rates of 0.31 +/- 0.04 and 0.99 +/- 0.04 micromol glucose g(-1) min(-1), in starved and fed livers, respectively. The 1-(13)C glycogen signal was monitored throughout the experiment with proton-decoupled (13)C NMR spectroscopy and analyzed in the time domain using AMARES. We noticed progressive line-broadening in any single experiment in the chase phase. One or a sum of two to three overlapping Lorentzians, with different exponential damping factors, were fitted to the signal. When the S/N was better than 40, the fit always delivered a small and a broad component. In the chase phase, the fit with a single Lorentzian resulted in a decline of glycogen signal by about 15 +/- 4 and 12 +/- 2% in starved and fed rats, respectively. This apparent decline in 1-(13)C glycogen signal could not be accounted for by the appearance of equivalent amounts of (13)C-labeled metabolites in the perfusate. The fit with a sum of two Lorentzians resulted in a decline of glycogen signal intensity of 7 +/- 5 and 5 +/- 3% in starved and fed rats, respectively, which reduced the apparent turnover to 8 +/- 9% and 6 +/- 4%, respectively. Quantification of the growing (13)C-1 glycogen signal requires a model function that accommodates changes in line shape throughout the period under study.


Subject(s)
Algorithms , Liver Glycogen/analysis , Liver Glycogen/biosynthesis , Liver/metabolism , Magnetic Resonance Spectroscopy/methods , Animals , Carbon Isotopes , Dihydropyridines/pharmacology , Food Deprivation/physiology , Furans/pharmacology , Liver/chemistry , Liver/drug effects , Liver Glycogen/chemistry , Male , Models, Biological , Perfusion , Rats , Rats, Wistar , Signal Processing, Computer-Assisted
20.
Biosci Biotechnol Biochem ; 64(8): 1623-7, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10993148

ABSTRACT

By analyzing the steady state and time-resolved fluorescence anisotropy, the internal motions of chlorophyll a of light-harvesting chlorophyll a/b-protein complex (LHCII) were characterized in a dimyristoylphosphatidylcholine (DMPC) liposome. Corresponding to the thermotropic phase of the membrane, chlorophyll a showed an unique internal motion in LHCII. At the gel phase, two motional components, one fast and the other slow, were observed, which would originate in the heterogeneity of the mutual orientation and the binding site of the chlorophyll a in LHCII. Interestingly, the faster motion was suppressed and only the slower segmental rotation with the larger motional amplitude was allowed on the phase transition to a liquid crystalline phase.


Subject(s)
Chlorophyll/chemistry , Membrane Lipids/chemistry , Photosynthetic Reaction Center Complex Proteins/chemistry , Animals , Chemical Phenomena , Chemistry, Physical , Chlorophyll A , Dimyristoylphosphatidylcholine , Fluorescence Polarization , Light-Harvesting Protein Complexes , Liposomes , Liver Glycogen/chemistry , Rabbits , Temperature
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