Literature DB >> 3510923

Glucose utilization rates and insulin sensitivity in vivo in tissues of virgin and pregnant rats.

A Leturque, P Ferre, A F Burnol, J Kande, P Maulard, J Girard.   

Abstract

In vivo studies have shown that insulin resistance in late pregnancy results from a decreased sensitivity of liver and peripheral tissues. In the present study, measurements of the rates of glucose utilization by skeletal muscles (soleus, extensor digitorum longus, epitrochlearis, and diaphragm), white adipose tissue, and brain of virgin and 19-day pregnant rats were performed in the basal condition and during a euglycemic, hyperinsulinemic (400 microU/ml) clamp to quantify the partition of glucose utilization and to identify the tissues other than liver responsible for insulin resistance. Fetal and placental glucose utilization rates were also measured in pregnant rats. The fetal glucose utilization rate (22 mg/min/kg) was very high and was not stimulated by physiologic maternal hyperinsulinemia. By contrast, the placental glucose utilization rate (29 mg/min/kg) was increased by 30% during hyperinsulinemia. The glucose utilization rate of the conceptus represented 23% of the maternal glucose utilization rate in the basal state. Glucose utilization rates in the basal condition were not statistically altered by pregnancy in brain, skeletal muscles, and white adipose tissue. During hyperinsulinemia (400 microU/ml), glucose utilization rates in extensor digitorum longus, epitrochlearis, and white adipose tissue were 30-70% lower in pregnant than in virgin rats. Insulin sensitivity of glucose metabolism in all the tissues tested other than brain was 50% lower in pregnant than in virgin rats. We conclude that skeletal muscles and, to a smaller extent, adipose tissue are involved in the insulin resistance of late pregnancy.

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Year:  1986        PMID: 3510923     DOI: 10.2337/diab.35.2.172

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  17 in total

1.  Evidence for the lack of spare high-affinity insulin receptors in skeletal muscle.

Authors:  M Camps; A Gumà; F Viñals; X Testar; M Palacín; A Zorzano
Journal:  Biochem J       Date:  1992-08-01       Impact factor: 3.857

2.  Changes in activity and intra-acinar distribution of glucose-6-phosphate dehydrogenase and malic enzyme during pregnancy in rat liver.

Authors:  A P Newham; K Krieger; I P Maly; D Sasse
Journal:  Histochemistry       Date:  1991

3.  Hyperthyroidism impairs pancreatic beta cell adaptations to late pregnancy and maternal liporegulation in the rat.

Authors:  M J Holness; G K Greenwood; N D Smith; M C Sugden
Journal:  Diabetologia       Date:  2005-10-05       Impact factor: 10.122

4.  Implication of low level inflammation in the insulin resistance of adipose tissue at late pregnancy.

Authors:  J de Castro; J Sevillano; J Marciniak; R Rodriguez; C González-Martín; M Viana; O H Eun-suk; S Hauguel de Mouzon; E Herrera; M P Ramos
Journal:  Endocrinology       Date:  2011-09-13       Impact factor: 4.736

5.  Suboptimal protein nutrition in early life later influences insulin action in pregnant rats.

Authors:  M J Holness; M C Sugden
Journal:  Diabetologia       Date:  1996-01       Impact factor: 10.122

6.  Tyrosine kinase activity of liver insulin receptor is inhibited in rats at term gestation.

Authors:  C Martínez; P Ruiz; A Andrés; J Satrústegui; J M Carrascosa
Journal:  Biochem J       Date:  1989-10-01       Impact factor: 3.857

Review 7.  Maternal cardiac metabolism in pregnancy.

Authors:  Laura X Liu; Zolt Arany
Journal:  Cardiovasc Res       Date:  2014-01-20       Impact factor: 10.787

8.  The set point for maternal glucose homeostasis is lowered during late pregnancy in the rat: the role of the islet beta-cell and liver.

Authors:  C J Nolan; J Proietto
Journal:  Diabetologia       Date:  1996-07       Impact factor: 10.122

9.  Pregnancy impairs baroreflex control of heart rate in rats: role of insulin sensitivity.

Authors:  Virginia L Brooks; Julia M Mulvaney; Afaf S Azar; Ding Zhao; Robert K Goldman
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-11-25       Impact factor: 3.619

10.  Physiological modulation of the uptake and fate of glucose in brown adipose tissue.

Authors:  M C Sugden; M J Holness
Journal:  Biochem J       Date:  1993-10-01       Impact factor: 3.857

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