In vivo glucose uptake and glucose transporter proteins GLUT1 and GLUT4 in heart and various types of skeletal muscle from streptozotocin-diabetic rats - PubMed (original) (raw)
In vivo glucose uptake and glucose transporter proteins GLUT1 and GLUT4 in heart and various types of skeletal muscle from streptozotocin-diabetic rats
H Kainulainen et al. Biochim Biophys Acta. 1994.
Abstract
The in vivo glucose uptake and the levels of two glucose transporter proteins (GLUT1 and GLUT4) were measured in heart and in various types of skeletal muscle from streptozotocin-diabetic rats. Diabetes (12-16 weeks) reduced the in vivo glucose uptake (glucose metabolic index, GMI), and the levels of GLUT1 and GLUT4 in heart by 75%, 60% and 70%, respectively. In diaphragm consisting of approximately equal amounts of type I (slow-contracting oxidative), IIa (fast-contracting oxidative) and IIb (fast-contracting glycolytic) fibers, GMI and GLUT4 levels were reduced by 60% and 40%, respectively, with no change in GLUT1 levels. In muscle consisting mainly of type I fibers (e.g., m. soleus), GMI and GLUT4 levels were reduced by 60% and 30%, respectively, whereas GLUT1 levels were unaltered. In mixed-type muscle consisting of type IIa and IIb fibers (e.g., m. plantaris and red part of m. gastrocnemius), GMI and GLUT1 levels were unchanged, whereas GLUT4 levels were decreased by 45%. In contrast, GMI was increased by 100% in type IIb fibers (e.g., the white part of m. gastrocnemius), probably reflecting the 4-fold increase in blood glucose levels, whereas GLUT4 levels were lowered by 55% with no change in GLUT1 levels. These data demonstrate a marked difference in the response of in vivo glucose uptake to long-term hypoinsulinemia between oxidative (type I) and glycolytic (type IIb) fibers. Furthermore, in contrast to the GLUT4, GLUT1 levels are regulated differentially in heart and skeletal muscle in response to streptozotocin-induced diabetes.
Similar articles
- Dissociation of the effects of training on oxidative metabolism, glucose utilisation and GLUT4 levels in skeletal muscle of streptozotocin-diabetic rats.
Kainulainen H, Komulainen J, Joost HG, Vihko V. Kainulainen H, et al. Pflugers Arch. 1994 Jul;427(5-6):444-9. doi: 10.1007/BF00374259. Pflugers Arch. 1994. PMID: 7971142 - In-vivo glucose uptake and glucose transporter proteins GLUT1 and GLUT3 in brain tissue from streptozotocin-diabetic rats.
Kainulainen H, Schürmann A, Vilja P, Joost HG. Kainulainen H, et al. Acta Physiol Scand. 1993 Oct;149(2):221-5. doi: 10.1111/j.1748-1716.1993.tb09615.x. Acta Physiol Scand. 1993. PMID: 8266811 - Decreased in vivo glucose uptake but normal expression of GLUT1 and GLUT4 in skeletal muscle of diabetic rats.
Kahn BB, Rossetti L, Lodish HF, Charron MJ. Kahn BB, et al. J Clin Invest. 1991 Jun;87(6):2197-206. doi: 10.1172/JCI115254. J Clin Invest. 1991. PMID: 2040701 Free PMC article. - Effects of hyperglycemia on glucose transporters of the muscle: use of the renal glucose reabsorption inhibitor phlorizin to control glycemia.
Dimitrakoudis D, Vranic M, Klip A. Dimitrakoudis D, et al. J Am Soc Nephrol. 1992 Nov;3(5):1078-91. doi: 10.1681/ASN.V351078. J Am Soc Nephrol. 1992. PMID: 1482748 Review. - Effect of diabetes on glucoregulation. From glucose transporters to glucose metabolism in vivo.
Klip A, Marette A, Dimitrakoudis D, Ramlal T, Giacca A, Shi ZQ, Vranic M. Klip A, et al. Diabetes Care. 1992 Nov;15(11):1747-66. doi: 10.2337/diacare.15.11.1747. Diabetes Care. 1992. PMID: 1468312 Review.
Cited by
- In vivo effects of vanadium on GLUT4 translocation in cardiac tissue of STZ-diabetic rats.
Li SH, McNeill JH. Li SH, et al. Mol Cell Biochem. 2001 Jan;217(1-2):121-9. doi: 10.1023/a:1007224828753. Mol Cell Biochem. 2001. PMID: 11269655 - Influence of GLP-1 on myocardial glucose metabolism in healthy men during normo- or hypoglycemia.
Gejl M, Lerche S, Mengel A, Møller N, Bibby BM, Smidt K, Brock B, Søndergaard H, Bøtker HE, Gjedde A, Holst JJ, Hansen SB, Rungby J. Gejl M, et al. PLoS One. 2014 Jan 6;9(1):e83758. doi: 10.1371/journal.pone.0083758. eCollection 2014. PLoS One. 2014. PMID: 24400077 Free PMC article. Clinical Trial. - P-glycoprotein is strongly expressed in the luminal membranes of the endothelium of blood vessels in the brain.
Beaulieu E, Demeule M, Ghitescu L, Béliveau R. Beaulieu E, et al. Biochem J. 1997 Sep 1;326 ( Pt 2)(Pt 2):539-44. doi: 10.1042/bj3260539. Biochem J. 1997. PMID: 9291129 Free PMC article. - Long-term and rapid regulation of ob mRNA levels in adipose tissue from normal (Sprague Dawley rats) and obese (db/db mice, fa/fa rats) rodents.
Igel M, Kainulainen H, Brauers A, Becker W, Herberg L, Joost HG. Igel M, et al. Diabetologia. 1996 Jul;39(7):758-65. doi: 10.1007/s001250050508. Diabetologia. 1996. PMID: 8817099 - Cellular and molecular regulation of cardiac glucose transport.
Young LH, Coven DL, Russell RR 3rd. Young LH, et al. J Nucl Cardiol. 2000 May-Jun;7(3):267-76. doi: 10.1016/s1071-3581(00)70016-x. J Nucl Cardiol. 2000. PMID: 10888399 Review. No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous