Glucose kinetics

De Gaetano A, Mingrone G, Castagneto M. NONMEM improves group parameter estimation for the minimal model of glucose kinetics. Am J Physiol 1996 271 E932-7. 

G. Velho, P. Froguel, D. R. Thevenot, and G. Reach, In vivo calibration of a subcutaneous glucose sensor for determination of subcutaneous glucose kinetics, Diabetes Nutr. Metab Clin, Exp. 1, 227-233 (1988). 

Figure 1.4 Glucose kinetics three-compartment model. Gex, exogenous glucose Gend, glucose produced by gluconeogenesis Gk, glucose eliminated via the kidney BG, blood glucose IG, subcutaneous interstitial glucose. (See the color version of this figure in Color Plates section.)...

Two methods of ozonolysis of glucose, kinetic-static and ozone-bubbling, have been compared for kinetic measurements and the former... 

Immobilized enzyme microreactor for the continuously-referenced monitoring of isoenz3mie activities of creatine kin after liquid-chromatographic separation Evaluation of the analytical performance of the enzyme-containing coils, adapted for use with the Technicon SMAC analyser in the determination of D-glucose Kinetic studies of active immobilized enzyme... 

FIGURE9.3 The linear compartmental model of glucose kinetics by Cobelli et al. [1984b]. 

Cobelli, C., Toffolo, G., and Ferrannini, E. 1984b. A model of glucose kinetics and their control by insulin. 

Cobelli, C. and Thomaseth, K. 1988b. Optimal equidose inputs and role of measurement error for estimating the parameters of a compartmental model of glucose kinetics from continuous-and discrete-time optimal samples. Math. Biosci. 89 135-147. 

Cobelli, C. and Ruggeri, A. 1989. Optimal design of sampling schedules for studying glucose kinetics with tracers. Am. J. Physiol. 257 E444-E450. 

Topp, B., Promislow, K., de Vries, G., Miura, R.M. and Finegood, D.T. (2000) A model of P-cell mass, insluin and glucose kinetics pathways to diabetes. Journal of Theoretical Biology 206,605-19. 

Berneis, K., Ninnis, R., Haussinger, D., and Keller, U., Effects of hyper- and hypoos-molality on whole body protein and glucose kinetics in humans. Am J Physiol, 276, E188, 1999. 

Schiavon M, Dalla Man C, Dube S, Slama M, Kudva YC, Peyser T, Basu A, Basu R, Cobelli C (2015) Modeling plasma-to-interstitium glucose kinetics from multitracer plasma and microdialysis data. Diabetes Technol TTict 17(11) 825—831... 

The linear model. Equation 9.6, has become very useful in applications due to an important result the kinetics of a tracer in a constant steady-state system, linear or nonlinear, are linear with constant coefficients. An example is shown in Figure 9.3 where the three-compartment model by Cobelli et al. [1984b] for studying tracer glucose kinetics in steady state at the whole-body level is depicted. Linear compartmental models in conjunction with tracer experiments have been extensively used in studying distribution of materials in living systems both at whole-body, organ and cellular level. Examples and references can be found in Carson et al. [1983], Jacquez [1996], and Cobelli et al. [2000], Carson and Cobelli [2001]. 

Protein supply, glucose kinetics and mUk yield in dairy cows... 

Where can amino acids alter glucose kinetics ... 

Konig, B.A., J.D. Oldham and D.S. Parker, 1984. The effect of abomasal infusion of casein on acetate, pahnitate and glucose kinetics in cows during early lactation. Br. J. Nutr. 52, 319-328. 

Though in this system also the products of inactivation of cozymase have not been determined chemically, the ability of components of the cozymase molecule to serve as precursors of the substance has been demonstrated. Cozymase production by yeast in aqueous suspension at 25°C. for some 22 hours was markedly increased by added adenine, adenosine, or nicotinic acid, and still further by mixtures of these or by glucose. Kinetic experiments comparing the production of cozymase from such substances with production from the unknown products of inactivation were not reported, results quoted (58) referring to cozymase extracted from the cells at one time only but the rates of production are unlikely to differ greatly. The spontaneous reactivation at 25° was at a rate of about 2.5 m/xM per... 

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