Genetic and nongenetic determinants of skeletal muscle glucose transporter 4 messenger ribonucleic acid levels and insulin action in twins
Storgaard, H ; Poulsen, P ; Ling, Charlotte LU
; Groop, Leif
LU
and Vaag, A A
(2006)
In Journal of Clinical Endocrinology and Metabolism
91(2).
p.702-708
- Abstract
- Context: Insulin-stimulated glucose uptake in skeletal muscle is mediated through translocation of the insulin-sensitive glucose transporter 4 ( GLUT4)-containing vesicles to the plasma membrane. Thus, skeletal muscle GLUT4 content plays an important role in whole-body insulin sensitivity. Objectives: The objectives of this study were 1) to examine the relative impact of genetic vs. environmental factors on skeletal muscle GLUT4 mRNA expression using biometric modeling, and 2) to identify factors influencing the expression of GLUT4 and insulin-stimulated whole-body metabolism. Design: We measured GLUT4 mRNA expression in biopsies from young and elderly monozygotic (MZ) and dizygotic (DZ) twins before and during a 2-h hyperinsulinemic... (More)
- Context: Insulin-stimulated glucose uptake in skeletal muscle is mediated through translocation of the insulin-sensitive glucose transporter 4 ( GLUT4)-containing vesicles to the plasma membrane. Thus, skeletal muscle GLUT4 content plays an important role in whole-body insulin sensitivity. Objectives: The objectives of this study were 1) to examine the relative impact of genetic vs. environmental factors on skeletal muscle GLUT4 mRNA expression using biometric modeling, and 2) to identify factors influencing the expression of GLUT4 and insulin-stimulated whole-body metabolism. Design: We measured GLUT4 mRNA expression in biopsies from young and elderly monozygotic (MZ) and dizygotic (DZ) twins before and during a 2-h hyperinsulinemic euglycemic clamp including 3-H-3-tritiated glucose and indirect calorimetry. Participants: A random sample of young (22-31 yr; n = 89) and elderly (57 - 66 yr; n = 69) same sex MZ and DZ twin pairs identified through the Danish Twin Register were studied. Results: We found a major genetic component in the control of basal and insulin-stimulated GLUT4 mRNA expression in young and elderly twins. GLUT4 gene expression increased upon insulin stimulation in both young and elderly twins. Multiple regression analysis revealed that both basal and insulin-stimulated GLUT4 mRNA expressions were positively related to birth weight and total body aerobic capacity and were higher in MZ vs. DZ twins as well as in males vs. females. Both basal and insulin-stimulated expressions of GLUT4 were independently and significantly related to whole-body in vivo insulin action, nonoxidative glucose metabolism, and glucose oxidation. Conclusion: We show that skeletal muscle GLUT4 gene expression in twins is significantly and independently related to glucose metabolism and is determined by both genetic and nongenetic factors, including zygosity and birth weight. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/417792
- author
- Storgaard, H
; Poulsen, P
; Ling, Charlotte
LU
; Groop, Leif
LU
and Vaag, A A
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Clinical Endocrinology and Metabolism
- volume
- 91
- issue
- 2
- pages
- 702 - 708
- publisher
- Oxford University Press
- external identifiers
-
- wos:000235161200054
- pmid:16291707
- scopus:32544445975
- ISSN
- 1945-7197
- DOI
- 10.1210/jc.2005-1172
- language
- English
- LU publication?
- yes
- id
- 753a4ed8-91db-4d07-b6f6-3faca77c3c7f (old id 417792)
- date added to LUP
- 2016-04-01 16:24:09
- date last changed
- 2024-01-11 07:23:00
@article{753a4ed8-91db-4d07-b6f6-3faca77c3c7f,
abstract = {{Context: Insulin-stimulated glucose uptake in skeletal muscle is mediated through translocation of the insulin-sensitive glucose transporter 4 ( GLUT4)-containing vesicles to the plasma membrane. Thus, skeletal muscle GLUT4 content plays an important role in whole-body insulin sensitivity. Objectives: The objectives of this study were 1) to examine the relative impact of genetic vs. environmental factors on skeletal muscle GLUT4 mRNA expression using biometric modeling, and 2) to identify factors influencing the expression of GLUT4 and insulin-stimulated whole-body metabolism. Design: We measured GLUT4 mRNA expression in biopsies from young and elderly monozygotic (MZ) and dizygotic (DZ) twins before and during a 2-h hyperinsulinemic euglycemic clamp including 3-H-3-tritiated glucose and indirect calorimetry. Participants: A random sample of young (22-31 yr; n = 89) and elderly (57 - 66 yr; n = 69) same sex MZ and DZ twin pairs identified through the Danish Twin Register were studied. Results: We found a major genetic component in the control of basal and insulin-stimulated GLUT4 mRNA expression in young and elderly twins. GLUT4 gene expression increased upon insulin stimulation in both young and elderly twins. Multiple regression analysis revealed that both basal and insulin-stimulated GLUT4 mRNA expressions were positively related to birth weight and total body aerobic capacity and were higher in MZ vs. DZ twins as well as in males vs. females. Both basal and insulin-stimulated expressions of GLUT4 were independently and significantly related to whole-body in vivo insulin action, nonoxidative glucose metabolism, and glucose oxidation. Conclusion: We show that skeletal muscle GLUT4 gene expression in twins is significantly and independently related to glucose metabolism and is determined by both genetic and nongenetic factors, including zygosity and birth weight.}},
author = {{Storgaard, H and Poulsen, P and Ling, Charlotte and Groop, Leif and Vaag, A A}},
issn = {{1945-7197}},
language = {{eng}},
number = {{2}},
pages = {{702--708}},
publisher = {{Oxford University Press}},
series = {{Journal of Clinical Endocrinology and Metabolism}},
title = {{Genetic and nongenetic determinants of skeletal muscle glucose transporter 4 messenger ribonucleic acid levels and insulin action in twins}},
url = {{http://dx.doi.org/10.1210/jc.2005-1172}},
doi = {{10.1210/jc.2005-1172}},
volume = {{91}},
year = {{2006}},
}