Stable isotopes in biosciences, their measurement and models for amino acid metabolism

被引:24
作者
Bier, DM
机构
[1] Children’s Nutrition Research Center,
[2] Department of Pediatrics,undefined
[3] Baylor College of Medicine,undefined
[4] 1100 Bates Street,undefined
[5] Houston,undefined
[6] TX 77030,undefined
[7] USA,undefined
关键词
leucine; modeling; isotopomer; stable isotopes;
D O I
10.1007/PL00014265
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
In order to follow the movement and quantify the metabolic fates of biologically important molecules in vivo, both tracers and kinetic modeling are required. For the study of intermediary metabolism in children, stable isotopically labeled substrates satisfy both the analytical and ethical requirements for tracer use in children. Stable isotope tracers have been proven safe over more than a half-century of use in humans. In addition, mass spectrometric analysis of stable nuclide molecular position and isotopic enrichment in biological molecules is both highly specific and extraordinarily precise. Using stable isotope data to develop models of biological system dynamics in vivo is an essential element of estimating substrate events that take place in cells or organs otherwise inaccessible for ethical sampling in children. Further, modeling is also a critical component in the development and the testing of hypotheses about the structure of the biological system in question and the mechanisms which control its operational parameters.
引用
收藏
页码:S2 / S8
页数:7
相关论文
共 31 条
  • [1] [Anonymous], 1983, MATH MODELING METABO
  • [2] UNIFORMLY C-13-LABELED ALGAL PROTEIN USED TO DETERMINE AMINO-ACID ESSENTIALITY INVIVO
    BERTHOLD, HK
    HACHEY, DL
    REEDS, PJ
    THOMAS, OP
    HOEKSEMA, S
    KLEIN, PD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (18) : 8091 - 8095
  • [3] INTRINSICALLY DIFFICULT PROBLEMS - THE KINETICS OF BODY PROTEINS AND AMINO-ACIDS IN MAN
    BIER, DM
    [J]. DIABETES-METABOLISM REVIEWS, 1989, 5 (02): : 111 - 132
  • [4] THE USE OF STABLE ISOTOPES IN METABOLIC INVESTIGATION
    BIER, DM
    [J]. BAILLIERES CLINICAL ENDOCRINOLOGY AND METABOLISM, 1987, 1 (04): : 817 - 836
  • [5] VALIDATION OF SIMPLE AND COMPLEX-MODELS IN PHYSIOLOGY AND MEDICINE
    COBELLI, C
    CARSON, ER
    FINKELSTEIN, L
    LEANING, MS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 246 (02): : R259 - R266
  • [6] COMPARTMENTAL MODEL OF LEUCINE KINETICS IN HUMANS
    COBELLI, C
    SACCOMANI, MP
    TESSARI, P
    BIOLO, G
    LUZI, L
    MATTHEWS, DE
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (04): : E539 - E550
  • [7] TRACER-TO-TRACEE RATIO FOR ANALYSIS OF STABLE ISOTOPE TRACER DATA - LINK WITH RADIOACTIVE KINETIC FORMALISM
    COBELLI, C
    TOFFOLO, G
    FOSTER, DM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (06): : E968 - E975
  • [8] Cobelli C, 1990, Horm Metab Res Suppl, V24, P1
  • [9] MODELS TO INTERPRET KINETIC DATA IN STABLE ISOTOPE TRACER STUDIES
    COBELLI, C
    TOFFOLO, G
    BIER, DM
    NOSADINI, R
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (05): : E551 - E564
  • [10] CRAMP DG, 1982, QUANTITATIVE APPROAC