THE EFFECTS OF INFUSION OF INSULIN-LIKE GROWTH-FACTOR (IGF)-I, IGF-II, AND INSULIN ON GLUCOSE AND PROTEIN-METABOLISM IN FASTED LAMBS

被引:150
作者
DOUGLAS, RG
GLUCKMAN, PD
BALL, K
BREIER, B
SHAW, JHF
机构
[1] UNIV AUCKLAND, DEPT PAEDIAT, DEV PHYSIOL LAB, PRIVATE BAG, AUCKLAND, NEW ZEALAND
[2] UNIV AUCKLAND, DEPT SURG, AUCKLAND, NEW ZEALAND
关键词
INSULIN; IGF-1; IGF-2; PROTEIN SYNTHESIS; CATABOLISM;
D O I
10.1172/JCI115346
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
In vivo effects of 300-min infusions of recombinant insulinlike growth factor I (IGF-I) and IGF-II on glucose and protein metabolism have been investigated in awake, fasted lambs. Two doses of recombinant human (rh) IGF-I were infused: 6.7 nmol/ kg . h, which induced hypoglycemia, and 2.0 nmol/kg . h, which did not. The effects were compared with an insulin infusion (0.17 nmol/kg . h) that had the same hypoglycemic potential as the high dose rhIGF-I infusion. rhIGF-II was infused at a rate of 6.7 nmol/kg . h. Primed constant infusions of isotopically labeled glucose, urea and leucine tracers were used to determine glucose and protein kinetics. rhIGF-I lowered blood glucose by increasing the rate of glucose clearance (P < 0.01), in contrast to insulin, which both increased clearance and reduced glucose production. Net protein loss was reduced after infusion of low and high dose rhIGF-I and insulin by 11% (P < 0.05), 15% (P < 0.01), and 12% (P < 0.05), respectively. rhIGF-II infusion did not alter the rate of net protein loss. In contrast to insulin, high dose rhIGF-I infusion increased the rate of protein synthesis in skeletal (P < 0.05) and cardiac muscle (P < 0.01) and in hepatic tissue (P < 0.05). We conclude that (a) protein metabolism is more sensitive than glucose metabolism to rhIGF-I infusion, as protein loss was reduced by an rhIGF-I infusion that did not alter glucose kinetics; (b) protein synthesis is increased by rhIGF-I infusion but not by insulin infusion; and (c) rhIGF-II is a less effective anabolic agent than rhIGF-I. We speculate that the effects of rhIGF-I on protein metabolism are not mediated by insulin receptors.
引用
收藏
页码:614 / 622
页数:9
相关论文
共 46 条
[1]   TRANSCAPILLARY PERMEABILITY AND SUBENDOTHELIAL DISTRIBUTION OF ENDOTHELIAL AND AMNIOTIC-FLUID INSULIN-LIKE GROWTH-FACTOR BINDING-PROTEINS IN THE RAT-HEART [J].
BAR, RS ;
CLEMMONS, DR ;
BOES, M ;
BUSBY, WH ;
BOOTH, BA ;
DAKE, BL ;
SANDRA, A .
ENDOCRINOLOGY, 1990, 127 (03) :1078-1086
[2]   SOMATOMEDINS - CHEMICAL AND FUNCTIONAL-CHARACTERISTICS OF THE DIFFERENT MOLECULAR-FORMS [J].
BARRECA, A ;
MINUTO, F .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1989, 12 (04) :279-293
[3]  
BASSETT NS, 1990, J DEV PHYSIOL, V14, P73
[4]   INSULIN-LIKE GROWTH FACTOR-I (IGF-I)-BINDING PROTEIN COMPLEX IS A BETTER MITOGEN THAN FREE IGF-I [J].
BLUM, WF ;
JENNE, EW ;
REPPIN, F ;
KIETZMANN, K ;
RANKE, MB ;
BIERICH, JR .
ENDOCRINOLOGY, 1989, 125 (02) :766-772
[5]   INSULIN-LIKE GROWTH-FACTOR - MODEL FOR TERTIARY STRUCTURE ACCOUNTING FOR IMMUNOREACTIVITY AND RECEPTOR-BINDING [J].
BLUNDELL, TL ;
BEDARKAR, S ;
RINDERKNECHT, E ;
HUMBEL, RE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (01) :180-184
[6]   STUDIES OF ACUTE EFFECTS OF INSULIN-LIKE GROWTH FACTOR-I AND FACTOR-II IN HUMAN FAT-CELLS [J].
BOLINDER, J ;
LINDBLAD, A ;
ENGFELDT, P ;
ARNER, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1987, 65 (04) :732-738
[7]   RADIOIMMUNOASSAY FOR INSULIN-LIKE GROWTH FACTOR-I - SOLUTIONS TO SOME POTENTIAL PROBLEMS AND PITFALLS [J].
BREIER, BH ;
GALLAHER, BW ;
GLUCKMAN, PD .
JOURNAL OF ENDOCRINOLOGY, 1991, 128 (03) :347-357
[8]   CIRCULATING INSULIN-LIKE GROWTH FACTOR-BINDING PROTEINS IN FETAL, NEONATAL AND ADULT SHEEP [J].
BUTLER, JH ;
GLUCKMAN, PD .
JOURNAL OF ENDOCRINOLOGY, 1986, 109 (03) :333-338
[9]   INSULIN-LIKE GROWTH FACTOR-I BINDING IN HEPATOCYTES FROM HUMAN-LIVER, HUMAN HEPATOMA, AND NORMAL, REGENERATING, AND FETAL-RAT LIVER [J].
CARO, JF ;
POULOS, J ;
ITTOOP, O ;
PORIES, WJ ;
FLICKINGER, EG ;
SINHA, MK .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (04) :976-981
[10]  
DAHN MS, 1988, ARCH SURG-CHICAGO, V123, P1409