Increased insulin sensitivity and maintenance of glucose utilization rates in fetal sheep with placental insufficiency and intrauterine growth restriction

被引:149
作者
Limesand, Sean W.
Rozance, Paul J.
Smith, Danielle
Hay, William W., Jr.
机构
[1] Univ Arizona, Dept Anim Sci, Agr Res Complex, Tucson, AZ 85719 USA
[2] Univ Colorado, Hlth Sci Ctr, Perinatal Res Ctr, Dept Pediat, Aurora, CO USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2007年 / 293卷 / 06期
关键词
pregnancy; fetus; glucose oxidation;
D O I
10.1152/ajpendo.00459.2007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this study we determined body weight-specific fetal (umbilical) glucose uptake (UGU), utilization (GUR), and production rates (GPR) and insulin action in intrauterine growth-restricted (IUGR) fetal sheep. During basal conditions, UGU from the placenta was 33% lower in IUGR fetuses, but GUR was not different between IUGR and control fetuses. The difference between glucose utilization and UGU rates in the IUGR fetuses demonstrated the presence and rate of fetal GPR (41% of GUR). The mRNA concentrations of the gluconeogenic enzymes glucose-6-phophatase and PEPCK were higher in the livers of IUGR fetuses, perhaps in response to CREB activation, as phosphorylated CREB/total CREB was increased 4.2-fold. A hyperglycemic clamp resulted in similar rates of glucose uptake and utilization in IUGR and control fetuses. The nearly identical GURs in IUGR and control fetuses at both basal and high glucose concentrations occurred at mean plasma insulin concentrations in the IUGR fetuses that were similar to 70% lower than controls, indicating increased insulin sensitivity. Furthermore, under basal conditions, hepatic glycogen content was similar, skeletal muscle glycogen was increased 2.2-fold, the fraction of fetal GUR that was oxidized was 32% lower, and GLUT1 and GLUT4 concentrations in liver and skeletal muscle were the same in IUGR fetuses compared with controls. These results indicate that insulin-responsive fetal tissues (liver and skeletal muscle) adapt to the hypoglycemic-hypoinsulinemic IUGR environment with mechanisms that promote glucose utilization, particularly for glucose storage, including increased insulin action, glucose production, shunting of glucose utilization to glycogen production, and maintenance of glucose transporter concentrations.
引用
收藏
页码:E1716 / E1725
页数:10
相关论文
共 92 条
[1]  
ALEXANDER G, 1964, J REPROD FERTIL, V7, P307, DOI 10.1530/jrf.0.0070307
[2]   Placental transport of threonine and its utilization in the normal and growth-restricted fetus [J].
Anderson, AH ;
Fennessey, PV ;
Meschia, G ;
Wilkening, RB ;
Battaglia, FC .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 272 (05) :E892-E900
[3]   Effects of acute hyperinsulinemia on insulin signal transduction and glucose transporters in ovine fetal skeletal muscle [J].
Anderson, MS ;
Thamotharan, M ;
Kao, D ;
Devaskar, SU ;
Qiao, LP ;
Friedman, JE ;
Hay, WW .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2005, 288 (02) :R473-R481
[4]   Effects of selective hyperglycemia and hyperinsulinemia on glucose transporters in fetal ovine skeletal muscle [J].
Anderson, MS ;
He, J ;
Flowers-Ziegler, J ;
Devaskar, SU ;
Hay, WW .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2001, 281 (04) :R1256-R1263
[5]  
[Anonymous], 1998, Mother, Babies and Health in Later Life
[6]   RELEASE OF GLUCOSE FROM THE LIVER OF FETAL AND POSTNATAL SHEEP BY PORTAL-VEIN INFUSION OF CATECHOLAMINES OR GLUCAGON [J].
APATU, RSK ;
BARNES, RJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1991, 436 :449-468
[7]  
Ausubel FM, 1995, CURRENT PROTOCOLS MO
[8]   Activation of liver G-6-Pase in response to insulin-induced hypoglycemia or epinephrine infusion in the rat [J].
Bady, I ;
Zitoun, C ;
Guignot, L ;
Mithieux, G .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 282 (04) :E905-E910
[9]  
Barry JS, 2006, EXP BIOL MED, V231, P566
[10]   Prevention of hypoinsulinemia modifies catecholamine effects in fetal sheep [J].
Bassett, JM ;
Hanson, C .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2000, 278 (05) :R1171-R1181