Estimation of glucose turnover and recycling in rabbits using various [3H, 14C]glucose labels

1976 ◽  
Vol 230 (4) ◽  
pp. 1159-1162 ◽  
Author(s):  
A Dunn ◽  
J Katz ◽  
S Golden ◽  
M Chenoweth
Keyword(s):  
Glucose Metabolism ◽  
Transit Time ◽  
Phosphate Level ◽  
Glucose Turnover ◽  
Replacement Rate ◽  
Carbon Recycling ◽  
Futile Cycling ◽  
Mean Glucose

The glucose replacement rate, percent carbon recycling, mean glucose transit time, and the glucose mass were determined in fasted unanesthetized rabbits after administration of [2-3H,U-14C]-, [3-3H,U-14C]-, [5-3H,U-14C]- or [6-3H,U-14C]glucose using the procedures of Katz et al. (10). The glucose replacement rates and carbon recycling determined with [2-3H,U-14C] and [5-3H,U-14C]glucose are equivalent and greater than those obtained with [3-3H,U-14C]- and [6-3H,U-14C]glucose. Although the means of the glucose replacement rates and percent carbon recycling obtained using [3-3H,U-14C]- and [6-3H,U-14C]glucose are similar, greater variation resulted using the former tracer. Comparisons of detritiation rates and percent carbon recycling using [2-3H,U-14C]- and [6-3H,U-14C]glucose suggest that about 10% of tritium is lost from carbon 2 via futile cycling at the glucose 6-phosphate level. Similarly, comparisons of [5-3H,U-14C]- and [6-3H,U-14C]glucose metabolism suggest that about 10% of tritium lost from carbon 5 occurs via futile cycling at the fructose diphosphate level and/or via the transaldolase reaction. Our results indicate that [6-3H,U-14C]glucose is the more suitable tracer for determining the glucose replacement rate and carbon recycling in vivo.

GLUT2 and hexokinase control proximodistal gradient of intestinal glucose metabolism in the newborn pig

1997 ◽  
Vol 272 (6) ◽  
pp. G1530-G1539 ◽  
Author(s):  
C. Cherbuy ◽  
B. Darcy-Vrillon ◽  
L. Posho ◽  
P. Vaugelade ◽  
M. T. Morel ◽  
...  
Keyword(s):  
Glucose Metabolism ◽  
Glucose Transporter ◽  
Glucose Utilization ◽  
Specific Effect ◽  
Glucose Consumption ◽  
Utilization Rate ◽  
Glucose Turnover ◽  
Proximal Jejunum ◽  
A Site

We have reported previously that a high glycolytic capacity develops soon after birth in enterocytes isolated from suckling newborn pigs. In the present work, we investigated whether such metabolic changes could affect intestinal glucose utilization in vivo and examined possible variations in glucose metabolism along the small intestine. Glucose utilization by individual tissues was assessed using the 2-deoxyglucose technique. The overall glucose utilization rate was doubled in suckling vs. fasting 2-day-old pigs because of significantly higher rates in all tissues studied, except for the brain. In parallel, enterocytes were isolated from the proximal, medium, or distal jejunoileum of newborn vs. 2-day-old pigs and assessed for their capacity to utilize, transport, and phosphorylate glucose. Intestinal glucose consumption accounted for approximately 15% of glucose turnover rate in suckling vs. 8% in fasting pigs. Moreover, there was a proximal-to-distal gradient of glucose utilization in the intestinal mucosa of suckling pigs. Such a gradient was also evidenced on isolated enterocytes. The stimulation of both hexokinase activity (HK2 isoform) and basolateral glucose transporter (GLUT2), as observed in the proximal jejunum, could account for such a site-specific effect of suckling.

Impact of in vivo fatty acid oxidation blockade on glucose turnover and muscle glucose metabolism during low-dose AICAR infusion

2006 ◽  
Vol 291 (5) ◽  
pp. E1131-E1140 ◽  
Author(s):  
Michael Christopher ◽  
Christian Rantzau ◽  
Zhi-Ping Chen ◽  
Rodney Snow ◽  
Bruce Kemp ◽  
...  
Keyword(s):  
Fatty Acid ◽  
Glucose Metabolism ◽  
Fatty Acid Oxidation ◽  
Low Dose ◽  
Whole Body ◽  
Glucose Turnover ◽  
Acid Oxidation ◽  
Metabolic Clearance ◽  
The Impact

AMPK plays a central role in influencing fuel usage and selection. The aim of this study was to analyze the impact of low-dose AMP analog 5-aminoimidazole-4-carboxamide-1-β-d-ribosyl monophosphate (ZMP) on whole body glucose turnover and skeletal muscle (SkM) glucose metabolism. Dogs were restudied after prior 48-h fatty acid oxidation (FAOX) blockade by methylpalmoxirate (MP; 5 × 12 hourly 10 mg/kg doses). During the basal equilibrium period (0–150 min), fasting dogs ( n = 8) were infused with [3-3H]glucose followed by either 2-h saline or AICAR (1.5–2.0 mg·kg−1·min−1) infusions. SkM was biopsied at completion of each study. On a separate day, the same protocol was undertaken after 48-h in vivo FAOX blockade. The AICAR and AICAR + MP studies were repeated in three chronic alloxan-diabetic dogs. AICAR produced a transient fall in plasma glucose and increase in insulin and a small decline in free fatty acid (FFA). Parallel increases in hepatic glucose production (HGP), glucose disappearance (Rd tissue), and glycolytic flux (GF) occurred, whereas metabolic clearance rate of glucose (MCRg) did not change significantly. Intracellular SkM glucose, glucose 6-phosphate, and glycogen were unchanged. Acetyl-CoA carboxylase (ACC∼pSer221) increased by 50%. In the AICAR + MP studies, the metabolic responses were modified: the glucose was lower over 120 min, only minor changes occurred with insulin and FFA, and HGP and Rd tissue responses were markedly attenuated, but MCRg and GF increased significantly. SkM substrates were unchanged, but ACC∼pSer221 rose by 80%. Thus low-dose AICAR leads to increases in HGP and SkM glucose uptake, which are modified by prior FAox blockade.

Amino acid gluconeogenesis and glucose turnover in kelp bass (Paralabrax sp.)

1981 ◽  
Vol 240 (3) ◽  
pp. R246-R252 ◽  
Author(s):  
K. Bever ◽  
M. Chenoweth ◽  
A. Dunn
Keyword(s):  
Amino Acid ◽  
Body Mass ◽  
The Body ◽  
High Rate ◽  
Glucose Turnover ◽  
Replacement Rate ◽  
Kelp Bass ◽  
Gluconeogenesis From Alanine ◽  
Relationship Of

The glucose replacement rate, plasma glucose concentration, glucose body mass, and amino acid gluconeogenesis were determined in vivo in fed and fasted kelp bass (Paralabrax clathratus) using [6-3H]glucose administered with [U-14C]glutamate, [U-14C]aspartate, or [U-14C]alanine. Fasting (14 days) and prolonged starvation (72 days) do not produce changes in the replacement rate, body mass, or plasma concentration of glucose. The removal of amino acids from the circulation is rapid in both fed and fasting states with nearly 50% of the administered 14Ctracer disappearing by 5 min. The incorporation of [14C]amino acid carbon into the body glucose mass is also rapid with significant amounts of tracer appearing within 15 min after administration. Gluconeogenesis from alanine and glutamate is increased by fasting whereas that from aspartate is diminished. The gluconeogenic rate is comparable to that previously observed in rats (Dunn, A., M. Chenoweth, and J. G. Hemington. The relationship of adrenal glucocorticoids to transaminase activity and gluconeogenesis in the intact rat. Biochim. Biophys. Acta 237: 192-202, 1971), although the glucose replacement rate is significantly lower. We propose that the paradoxically high rate of gluconeogenesis in fish may serve to provide carbohydrate precursors for mucus synthesis in these carnivorous animals with limited carbohydrate intake.

scholarly journals Glucose metabolism in vivo in fed and 48 h starved goats during pregnacy and lactation

1982 ◽  
Vol 47 (1) ◽  
pp. 87-94 ◽  
Author(s):  
N. Chaiyabutr ◽  
Anne Faulkner ◽  
M. Peaker
Keyword(s):  
Plasma Concentration ◽  
Glucose Metabolism ◽  
Continuous Infusion ◽  
Plasma Glucose ◽  
Glucose Turnover ◽  
Pregnancy And Lactation ◽  
Glucose Synthesis

1. Glucose turnover (i.e. glucose entry and utilization rates) in fed and 48 h starved goats during pregnancy and lactation was determined using a continuous infusion of [U-14C]- and [3-3H]glucose.2. Glucose synthesis and utilization increased during pregnancy and lactation in fed but not in starved goats.3. Recycling of giucosc-C was approximately 10% in fed animals and 15–20% in starved animals and was unaffected by the stage of pregnancy or lactation.4. Plasma glucose concentrations were maintained during pregnancy and lactation in fed goats but decreased during 48 h starvation in pregnant goats. Little change was seen in the plasma concentration of lipids and their metabolites during pregnancy and lactation in fed goats, but increases were observed after 48 h starvation.5. The control of glucose metabolism in ruminants during pregnancy and lactation is discussed.

scholarly journals Glucose metabolism in the developing rat. Studies in vivo

1972 ◽  
Vol 127 (3) ◽  
pp. 521-529 ◽  
Author(s):  
Richard G. Vernon ◽  
Deryck G. Walker
Keyword(s):  
Glucose Metabolism ◽  
Turnover Rate ◽  
Relative Size ◽  
Specific Radioactivity ◽  
Liver Glycogen ◽  
Glucose Turnover ◽  
Newborn Rat ◽  
Old Rats ◽  
Developing Rat

1. The specific radioactivity of plasma d-glucose and the incorporation of 14C into plasma l-lactate, liver glycogen and skeletal-muscle glycogen was measured as a function of time after the intraperitoneal injection of d-[6-14C]glucose and d-[6-3H]glucose into newborn, 2-, 10- and 30-day-old rats. 2. The log of the specific radioactivity of both plasma d-[6-14C]- and d-[6-3H]-glucose of the 2-, 10- and 30-day-old rats decreased linearly with time for at least 60min after injection of labelled glucose. The specific radioactivity of both plasma d-[6-14C]- and d-[6-3H]-glucose of the newborn rat remained constant for at least 75min after injection. 3. The glucose turnover rate of the 30-day-old rat was significantly greater than (approximately twice) that of the 2- and 10-day-old rats. The relative size of both the glucose pool and the glucose space decreased with age. Less than 10% of the glucose utilized in the 2-, 10- and 30-day-old rats was recycled via the Cori cycle. 4. The results are discussed in relationship to the availability of dietary glucose and other factors that may influence glucose metabolism in the developing rat.

scholarly journals Effects of exogenous glucose on glucose metabolism in the lactating goat in vivo

1983 ◽  
Vol 49 (1) ◽  
pp. 159-165 ◽  
Author(s):  
N. Chaiyabutr ◽  
Anne Faulkner ◽  
M. Peaker
Keyword(s):  
Glucose Metabolism ◽  
Plasma Insulin ◽  
Pentose Phosphate ◽  
Glucose Turnover ◽  
Glucose Load ◽  
Glucose Loading ◽  
Exogenous Glucose ◽  
Lactating Goats ◽  
Glucose Supply

1. Glucose turnover in fed and 48 h-starved lactating goats was determined during a glucose load of 500 μmol/min using a continuous infusion of [U-14C]- and [3-3H]glucose.2. Endogenous rates of irreversible glucose turnover (i.e. total rates of irreversible glucose turnover minus the rate of exogenous glucose supply) were depressed during glucose loading by 14 and 62% in the fed and starved animals respectively.3. Plasma glucose concentrations increased significantly by 57 and 88% in the fed and starved goats respectively. Plasma insulin concentrations increased by 108 and 128% in the fed and starved animals respectively.4. Milk yields increased significantly (41%) in the starved animals during glucose loading, but were unaffected in fed animals.5. In both the fed and 48 h-starved goats, mammary glucose metabolism via glycolysis and the pentose phosphate pathway appeared to be stimulated by glucose loading.

scholarly journals Peroxisome proliferator-activated receptor α deficiency modifies glucose handling by isolated mouse adipocytes

2007 ◽  
Vol 193 (1) ◽  
pp. 39-43 ◽  
Author(s):  
C G Walker ◽  
M C Sugden ◽  
G F Gibbons ◽  
M J Holness
Keyword(s):  
Glucose Metabolism ◽  
High Glucose ◽  
Ex Vivo ◽  
Whole Body ◽  
Glucose Turnover ◽  
Peroxisome Proliferator ◽  
Peroxisome Proliferator Activated Receptor ◽  
Total Glucose ◽  
The Impact

Peroxisome proliferator-activated receptor α (PPARα) is a transcription factor that regulates enzymes involved in fatty acid (FA) utilisation. PPARα null mice have recently been demonstrated to have increased whole-body glucose turnover in vivo. This has been attributed to increased glucose uptake by adipose tissue, but the impact of PPARα deficiency on the characteristics of glucose handling by isolated adipocytes ex vivo is unknown. To determine directly the impact of PPARα deficiency on adipocyte glucose handling, thereby excluding any influence of humoral/neuronal factors, we examined total glucose metabolism as well as glucose disposition towards alternative fates in epididymal adipocytes isolated from wild-type and PPARαnull mice. Total glucose metabolism (oxidation, incorporation into FA and glycerol moieties of triglyceride (TAG) and conversion to lactate) was measured under basal conditions (low glucose) and ‘stimulated lipogenic’ conditions (high glucose + insulin). Adipocytes from PPARα null mice had higher rates of glucose metabolism under both basal and stimulated lipogenic conditions, with increased glucose utilisation both for oxidation and entry into the synthesis of the FA and glycerol components of lipid. In particular, the capacity of adipocytes from PPARα-deficient mice to utilise glucose for synthesis of the glycerol backbone of TAG was greatly enhanced under stimulated (high glucose + insulin) conditions. The increased use of glucose for the glycerol moiety of adipocyte TAG may therefore contribute to, and provide explanation for, enhanced glucose turnover in PPARα null mice.

Effects of amylin on glucose metabolism and glycogenolysis in vivo and in vitro.

1990 ◽  
Vol 259 (3) ◽  
pp. E457 ◽  
Author(s):  
D A Young ◽  
R O Deems ◽  
R W Deacon ◽  
R H McIntosh ◽  
J E Foley
Keyword(s):  
Glucose Metabolism ◽  
Glucose Uptake ◽  
Glucose Turnover ◽  
Metabolic Clearance ◽  
Tissue Samples ◽  
Glucose Levels ◽  
Blood Glucose Levels ◽  
Glucose Phosphorylation

The effects of amylin on glucose metabolism and glycogenolysis were examined in vivo and in vitro. Eighteen-hour-fasted rats were infused with 5 nmol.kg-1.min-1 amylin and [3-3H]glucose for 120 min. Blood glucose levels increased an average of 45% during the infusion. Glucose turnover measurements indicated that the overall rate of glucose appearance (Ra) did not change, but the metabolic clearance rate of glucose was decreased by 42%. Samples of liver, gastrocnemius, and soleus muscles were freeze-clamped at the end of the infusion period and analyzed for glycogen and glucose 6-phosphate levels. Glycogen levels were decreased in all tissue samples, whereas glucose 6-phosphate was elevated in gastrocnemius and soleus muscles. Isolated soleus muscles were incubated in vitro with 200 microU/ml of insulin and 1, 10, or 100 nM amylin. Amylin treatment had no effect on 3-O-methyl-D-glucose transport; however, 2-deoxy-D-glucose uptake was inhibited by 33 or 48% at 10 or 100 nM amylin, respectively. Glycogen levels were also decreased after treatment with 10 and 100 nM amylin. Glucose 6-phosphate levels were not affected by amylin treatment in the presence of insulin but were increased nearly twofold in its absence. The data suggest that amylin stimulates glycogenolysis and inhibits glucose uptake both in vivo and in vitro and that the inhibition of glucose uptake is due to inhibition of glucose phosphorylation (i.e., hexokinase).

Glucose and lactate kinetics and interrelations in an antarctic bird (emperor penguin)

1982 ◽  
Vol 242 (5) ◽  
pp. R458-R464 ◽  
Author(s):  
R. Groscolas ◽  
A. Rodriguez
Keyword(s):  
Body Mass ◽  
Transit Time ◽  
Plasma Glucose ◽  
Glucose Concentration ◽  
Lactate Concentration ◽  
Plasma Glucose Concentration ◽  
Emperor Penguin ◽  
Replacement Rate ◽  
Lactate Kinetics ◽  
Mean Glucose

The isotope single-injection method was used to investigate the glucose and lactate kinetics and the interrelationships between the glucose and lactate pools in fasting emperor penguins. In these remarkably fast-resistant birds, mean lactate concentration, replacement rate, pool, space, and transit time were 1.5 mmol.1-1,53 mumol.min-1.kg-1, 900 mumol.kg-1, 60% of body mass, and 17 min, respectively. Mean glucose concentration, replacement rate, pool, space, and transit time were 20 mmol.1-1, 23 mumol.min-1.kg-1, 4,300 mumol.kg-1, 24% of body mass, and 196 min, respectively. Maximum conversions of lactate into glucose and of glucose into lactate were 29 +/- 2.9% and 75.5 +/- 4.2%, respectively, which indicates that lactate is an effective gluconeogenic precursor and a major fate of glucose metabolism in fasting penguins. The lactate replacement rate and incorporation into glucose were related to the plasma lactate concentration, which suggests that the rate of formation of glucose from lactate is dependent on the availability of lactate. The glucose replacement rate and reduction into lactate were related with the plasma glucose concentration, suggesting that the rate of lactate formation from glucose is dependent on the plasma glucose concentration. These data suggest that in the fasting emperor penguin glucose and lactate availability is capable of regulating the rate at which these substrates are utilized and interconverted. To our knowledge, this is the first evidence for such regulatory capacities in birds.

Melatonin modifies tumor hypoxia and metabolism by inhibiting HIF-1α and energy metabolic pathway in the in vitro and in vivo models of breast cancer

2019 ◽  
Vol 2 (4) ◽  
pp. 83-98 ◽  
Author(s):  
André De Lima Mota ◽  
Bruna Vitorasso Jardim-Perassi ◽  
Tialfi Bergamin De Castro ◽  
Jucimara Colombo ◽  
Nathália Martins Sonehara ◽  
...  
Keyword(s):  
Breast Cancer ◽  
Glucose Metabolism ◽  
Tumor Growth ◽  
Tumor Cells ◽  
Carbonic Anhydrases ◽  
In Vivo Models ◽  
Ca Ix ◽  
Gene And Protein Expression

Breast cancer is the most common cancer among women and has a high mortality rate. Adverse conditions in the tumor microenvironment, such as hypoxia and acidosis, may exert selective pressure on the tumor, selecting subpopulations of tumor cells with advantages for survival in this environment. In this context, therapeutic agents that can modify these conditions, and consequently the intratumoral heterogeneity need to be explored. Melatonin, in addition to its physiological effects, exhibits important anti-tumor actions which may associate with modification of hypoxia and Warburg effect. In this study, we have evaluated the action of melatonin on tumor growth and tumor metabolism by different markers of hypoxia and glucose metabolism (HIF-1α, glucose transporters GLUT1 and GLUT3 and carbonic anhydrases CA-IX and CA-XII) in triple negative breast cancer model. In an in vitro study, gene and protein expressions of these markers were evaluated by quantitative real-time PCR and immunocytochemistry, respectively. The effects of melatonin were also tested in a MDA-MB-231 xenograft animal model. Results showed that melatonin treatment reduced the viability of MDA-MB-231 cells and tumor growth in Balb/c nude mice (p <0.05). The treatment significantly decreased HIF-1α gene and protein expression concomitantly with the expression of GLUT1, GLUT3, CA-IX and CA-XII (p <0.05). These results strongly suggest that melatonin down-regulates HIF-1α expression and regulates glucose metabolism in breast tumor cells, therefore, controlling hypoxia and tumor progression. 

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