scholarly journals Determination of synthesis, recycling and body mass of glucose in rats and rabbits in vivo with 3H- and 14C-labelled glucose

1974 ◽  
Vol 142 (1) ◽  
pp. 171-183 ◽  
Author(s):  
Joseph Katz ◽  
Arnold Dunn ◽  
Maymie Chenoweth ◽  
Sybil Golden
Keyword(s):  
Body Mass ◽  
Plasma Glucose ◽  
Specific Radioactivity ◽  
Total Body Mass ◽  
Glucose Carbon ◽  
Multicompartmental Model ◽  
Glucose Synthesis ◽  
Total Body

1. Glucose labelled with 3H in position 2 and uniformly with 14C was administered simultaneously to rabbits and rats either as a single injection or by continuous infusion. Plasma glucose specific radioactivity and the yield of 3H in the plasma water were monitored. 2. The rates of synthesis, recycling of carbon and total body mass of glucose were calculated, without assuming a multicompartmental model and without fitting data by exponential expressions. 3. The rate of synthesis of glucose in starved-overnight rabbits was 4mg/min per kg (range 3–4.5mg/min per kg) and 25–35% of the glucose carbon was recycled. The mass of total body glucose in starved rabbits was 290mg/kg (range 220–390mg/kg). About one-third of the total body glucose equilibrates nearly instantaneously with plasma glucose. 4. In rats starved overnight, glucose synthesis was about 10mg/min per kg and recycling of carbon ranged from 30–40%. Total body mass (per kg body weight) is similar to that in rabbits. 5. The activity in plasma water after injection of [2-3H]glucose was determined. The initial rate of 3H2O formation is rapid, indicating that the major site of glucose catabolism is in the rapidly mixing pool. The curve of total body glucose radioactivity was obtained from the 3H2O yield, and total mass of glucose was calculated. This agrees with that obtained from the 3H specific-radioactivity curve.

Determination of gluconeogenesis in vivo with 14C-labeled substrates

1985 ◽  
Vol 248 (4) ◽  
pp. R391-R399 ◽  
Author(s):  
J. Katz
Keyword(s):  
Pyruvate Carboxylase ◽  
Tricarboxylic Acid Cycle ◽  
Specific Radioactivity ◽  
Tricarboxylic Acid ◽  
Pyruvate Metabolism ◽  
Acetyl Coenzyme A ◽  
Glucose Carbon ◽  
Labeling Pattern

A mitochondrial model of gluconeogenesis and the tricarboxylic acid cycle, where pyruvate is metabolized via pyruvate carboxylase and pyruvate dehydrogenase, and pyruvate kinase is examined. The effect of the rate of tricarboxylic acid flux and the rates of the three reactions of pyruvate metabolism on the labeling patterns from [14C]pyruvate and [24C]acetate are analyzed. Expressions describing the specific radioactivities and 14C distribution in glucose as a function of these rates are derived. Specific radioactivities and isotopic patterns depend markedly on the ratio of the rates of pyruvate carboxylation and decarboxylation to the rate of citrate synthesis, but the effect of phosphoenolpyruvate hydrolysis is minor. The effects of these rates on 1) specific radioactivity of phosphoenolpyruvate, 2) labeling pattern in glucose, and 3) contribution of pyruvate, acetyl-coenzyme A, and CO2 to glucose carbon are illustrated. To determine the contribution of lactate or alanine to gluconeogenesis, experiments with two compounds labeled in different carbons are required. Methods in current use to correct for the dilution of 14C in gluconeogenesis from [14C]pyruvate are shown to be erroneous. The experimental design and techniques to determine gluconeogenesis from 14C-labeled precursors are presented and illustrated with numerical examples.

scholarly journals Rates of glucose utilization and glucogenesis in rats in the basal state induced by halothane anaesthesia

1977 ◽  
Vol 162 (3) ◽  
pp. 643-651 ◽  
Author(s):  
D F Heath ◽  
K N Frayn ◽  
J G Rose
Keyword(s):  
Plasma Glucose ◽  
Plasma Insulin ◽  
Glucose Utilization ◽  
Specific Radioactivity ◽  
Specific Effect ◽  
Halothane Anaesthesia ◽  
Rate Coefficients ◽  
Glucose Carbon ◽  
Gluconeogenic Substrates

1. Rates and rate coefficients of glucose utilization and replacement were determined with [5-3H]- and [U-14C]-glucose in rats starved for 24h, either conscious or under halothane anaesthesia, in a thermoneutral environment. Plasma insulin concentrations were also measured. 2. Halothane anaesthesia decreased the turnover rate by 20%, which was similar to previously reported decreases in metabolic rates caused by natural sleep. 3. Fractional recycling of glucose carbon was little affected by halothane. 4. Comparison of values in one rat with those in another, among both conscious rats and those under halothane anaesthesia, showed that rate coefficients were inversely correlated with plasma glucose concentrations. 5. These findings indicated that halothane, in the concentration used (1.25%, v/v), had little specific effect on glucose metabolism. 6. Although equilibrium plasma glucose concentrations in different rats under halothane were widely different (4-8 mmol/l) the rates of utilization were very similar (2.5-3.1 micronmol/min per 100 g), indicating that these rates were determined by the production of glucose from gluconeogenic precursors released by basal metabolism, the rate of which is necessarily similar in different rats. 7. Among rats under halothane anaesthesia plasma insulin concentrations were negatively correlated with rate coefficients, showing that the differences between rate coefficients were mostly accounted for by differences between rats in tissue sensitivities to insulin. Thus in each 24h-starved rat, sleeping or resting, the main regulators of the plasma glucose concentrations were the rate of supply of gluconeogenic substrates from energy metabolism and the intrinsic sensitivity of the tissues to insulin. 8. We found that a commonly used deionization method of purifying glucose for determination of its specific radioactivity was inadequate.

scholarly journals Effects of Somatostatin and Glucagon on the Utilization of [2_14C] Propionate in Glucose Production in Vivo in Sheep

1980 ◽  
Vol 33 (4) ◽  
pp. 457 ◽  
Author(s):  
Ronald P Brockman ◽  
Cindy Greer
Keyword(s):  
Continuous Infusion ◽  
Plasma Glucose ◽  
Control Period ◽  
Specific Radioactivity ◽  
Glucose Production ◽  
Irreversible Loss ◽  
Selective Effect ◽  
Glycogenolytic Effect ◽  
Glucose Synthesis

This study examined the effects of hypoglucagonaemia and hyperglucagonaemia on the incorporation of 14C from [2-14C]propionate into plasma glucose of sheep in vivo. The sheep were adult ewes fed a maintenance diet of lucerne pellets delivered in equal aliquots hourly. The irreversible loss of glucose was determined by the continuous infusion of [6-3H]glucose. During the control period (the hour immediately preceding infusion of hormones) 63 �2 % of the propionate was converted to glucose, accounting for 30�2 % of glucose production. Glucagon deficiency, induced by infusion of somatostatin (100 J1g/h), did not affect gluconeogenesis and the irreversible loss of glucose significantly. However, glucagon infusion at 11 �5 �O� 6 J1g/h significantly increased the irreversible loss of glucose, with the greatest increase occurring in the first 15 min of infusion. The 14C specific radioactivity of glucose and the fraction of glucose derived from propionate decreased significantly during glucagon infusion. The data are consistent with glucagon having a marked glycogenolytic effect initially, but little or no selective effect in promoting the utilization of propionate for glucose synthesis in vivo in sheep.

scholarly journals Evaluation of glucose turnover, body mass and recycling with reversible and irreversible tracers

1974 ◽  
Vol 142 (1) ◽  
pp. 161-170 ◽  
Author(s):  
Joseph Katz ◽  
H. Rostami ◽  
Arnold Dunn
Keyword(s):  
Steady State ◽  
Glucose Metabolism ◽  
Single Injection ◽  
Mean Transit Time ◽  
Specific Radioactivity ◽  
Glucose Turnover ◽  
Glucose Carbon ◽  
Multicompartmental Model ◽  
Labelled Compound ◽  
Total Body

1. Methods are presented for the calculation of rates of synthesis or loss, mean transit time and total body pool of compounds from specific-radioactivity curves, without assuming a multicompartmental model and without fitting the data by exponential expressions. The methods apply to the steady state after either single injection or continuous infusion of a labelled compound. 2. The use of irreversible and reversible tracers and the effects of recycling of carbon on the estimations of the parameters of glucose metabolism are discussed. Methods for quantitatively determining recycling of glucose carbon by the use of glucose doubly labelled with 14C and 3H are presented.

scholarly journals The determination of lactate turnover in vivo with 3H- and 14C-labelled lactate. The significance of sites of tracer administration and sampling

1981 ◽  
Vol 194 (2) ◽  
pp. 513-524 ◽  
Author(s):  
J Katz ◽  
F Okajima ◽  
M Chenoweth ◽  
A Dunn
Keyword(s):  
Specific Radioactivity ◽  
Vena Cava ◽  
Turnover Rates ◽  
High Turnover ◽  
Glucose Carbon ◽  
Lactate Turnover ◽  
Carbon Recycling ◽  
Kinetics Of

L-[3-3H,U-14C]Lactate was administered to starved rats either as a bolus or by continuous infusion. Tracer administration was performed two ways: injection into the vena cava and sampling from the aorta (V-A mode), or injection into the aorta and sampling from the vena cava (A-VC mode). The specific-radioactivity curves after infusion or injection differed markedly with the two procedures. However, the specific radioactivities of 14C-labelled glucose derived from [U-14C]lactate were similar in the two modes. The apparent turnover rates of lactate calculated from the 3H specific-radioactivity curves in the V-A mode were about half those obtained from the 3H specific-radioactivity curves in the A-VC mode. The apparent contribution of lactate carbon to glucose carbon calculated from specific-radioactivity curves of the A-VC mode was greater than that obtained from the V-A mode. The apparent recycling of lactate carbon calculated from the specific radioactivities for [U-14C]- and [3-3H]-lactate was greater in the A-VC mode than the V-A mode. [U-14C] Glucose was administered in the two modes, but in contrast with lactate the specific radioactivities were only slightly different. An analysis to account for these observations is presented. It is shown that the two modes represent sampling from different pools of lactate. The significance of sites of tracer administration and sampling for the interpretation of tracer kinetics of compounds present in intracellular and extracellular spaces, and with a high turnover rate, is discussed. We propose that for such compounds, including lactate, alanine and glycerol, the widely used V-A mode leads to a marked underestimate of replacement, mass and carbon recycling, and that the A-VC mode is the preferred method for the assessment of these parameters.

On the Nature of Hereditary Size Limitation

1929 ◽  
Vol 6 (4) ◽  
pp. 311-324
Author(s):  
R. CUMMING ROBB
Keyword(s):  
Body Weight ◽  
Body Mass ◽  
Physical Significance ◽  
Body Parts ◽  
Total Body Mass ◽  
Organ Growth ◽  
Submaxillary Glands ◽  
Size Limitation ◽  
Similar Association ◽  
Total Body

1. Throughout post-natal life the relative weights of the pituitary body, thyroid, thymus and adrenals in the rabbit may be expressed by the equation y = axk + c. 2. A similar association is indicated in the rat for the weights of eyeballs, liver, pancreas, hypophysis, thyroid, adrenals, submaxillary glands, kidney and fresh skeleton (data from Donaldson, 1924). 3. In giant and pigmy rabbits, the ultimate proportions of body parts are not the same, but (for any given body weight) corresponding tissues in the two groups tend to exhibit an identical relation to total body mass. 4. The adrenals and testes of the Polish rabbits are relatively much larger than those of the Flemish. But in each case the growth of the adrenal approximates to a constant power function of body weight. Moreover, in these two groups and in their hybrids, the growth of the testes adheres to a simple association with adrenal weight identical for each. 5. These data suggest the generalisation that in a growing organism the magnitude of any part tends to be a specific function of the total body mass or of some portion so related to the whole. 6. These associations may be explained by surmising that each tissue is in equilibrium with the internal milieu with regard to the distribution of nutrient growth essentials; that in each case the equilibrium point would be determined by the nature of the cell and after differentiation would tend to remain constant; and that the relative enlargement of each tissue is limited by the excess of the equilibrium value over the katabolic expenditure. 7. According to the above hypothesis of organ growth, the equation y = axk + c may possess a physical significance. Eight types of growth relationships may thus exist, differing because of the apparent inactivity of one or more constants in this equation.

Body size, sexual dimorphism, and seasonal mass fluctuations in a larger sika deer subspecies, the Hokkaido sika deer (Cervus nippon yesoensis Heude, 1884)

2001 ◽  
Vol 79 (1) ◽  
pp. 154-159 ◽  
Author(s):  
Masatsugu Suzuki ◽  
Manabu Onuma ◽  
Mayumi Yokoyama ◽  
Koich Kaji ◽  
Masami Yamanaka ◽  
...  
Keyword(s):  
Sexual Dimorphism ◽  
Body Mass ◽  
Body Length ◽  
Sika Deer ◽  
Cervus Nippon ◽  
Total Body Mass ◽  
Foot Length ◽  
Hind Foot ◽  
Total Body ◽  
Cervus Nippon Yesoensis

Measurements of shoulder height, body length, hind-foot length, and total body mass were collected from 309 Hokkaido sika deer (Cervus nippon yesoensis Heude, 1884) (115 males and 194 females) and analyzed statistically for sexual dimorphism and seasonal body mass fluctuations. The von Bertalanffy equation was fitted to the growth curves that resulted. Asymptotic shoulder height, body length, and hind-foot length were 106.2, 112.6, and 52.9 cm in males and 94.8, 103.9, and 49.4 cm in females, respectively. Total body mass showed distinct seasonal fluctuations, ranging between 102.8 and 151.0 kg in adult males and 68.0 and 99.8 kg in adult females. Male/female ratios in shoulder height, body length, hind-foot length, and total mass were 1.12, 1.08, 1.07, and 1.51, respectively. These results indicate that the Hokkaido sika deer is one of the largest subspecies, at least in skeleton size. A larger body and longer hind foot would seem to be evolutionary adaptations to Hokkaido's cold, snowy environment.

In vivo determination of body fat by measuring total body carbon

1991 ◽  
Vol 53 (6) ◽  
pp. 1339-1344 ◽  
Author(s):  
J J Kehayias ◽  
S B Heymsfield ◽  
A F LoMonte ◽  
J Wang ◽  
R N Pierson
Keyword(s):  
Body Fat ◽  
Body Carbon ◽  
Total Body

scholarly journals Complete and Voluntary Starvation of 50 Days

2016 ◽  
Vol 9 ◽  
pp. CCRep.S39776 ◽  
Author(s):  
Bradley Elliott ◽  
Michelle Mina ◽  
Chrystalla Ferrier
Keyword(s):  
Decision Making ◽  
Body Mass ◽  
Clinical Decision Making ◽  
Clinical Decision ◽  
Activity Levels ◽  
Total Body Mass ◽  
Total Body ◽  
Linear Loss ◽  
Obese Male ◽  
Evidence Based Decision Making

A 34-year-old obese male (96.8 kg; BMI, 30.2 kg m−1) volitionally undertook a 50-day fast with the stated goal of losing body mass. During this time, only tea, coffee, water, and a daily multivitamin were consumed. Severe and linear loss of body mass is recorded during these 50 days (final 75.4 kg; BMI, 23.5 kg mT 1 ). A surprising resilience to effects of fasting on activity levels and physical function is noted. Plasma samples are suggestive of early impairment of liver function, and perturbations to cardiovascular dynamics are also noted. One month following resumption of feeding behavior, body weight was maintained (75.0 kg; BMI, 23.4 kg m−1). Evidence-based decision-making with the fasting or hunger striking patient is limited by a lack of evidence. This case report suggests that total body mass, not mass lost, may be a key observation in clinical decision-making during fasting and starvation.

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