Effects of diabetes and hyperglycemia on the hexosamine synthesis pathway in rat muscle and liver - PubMed (original) (raw)
Effects of diabetes and hyperglycemia on the hexosamine synthesis pathway in rat muscle and liver
K A Robinson et al. Diabetes. 1995 Dec.
Abstract
In vitro studies suggested that increased flux of glucose through the hexosamine biosynthesis pathway (HexNSP) contributes to glucose-induced insulin resistance. Glutamine:fructose-6- phosphate amidotransferase (GFAT) catalyzes glucose flux via HexSNP; its major products are uridine diphosphate (UDP)-N-acetyl hexosamines (UDP-HexNAc). We examined whether streptozotocin (STZ)-induced diabetes (4-10 days) or sustained hyperglycemia (1-2 h) in normal rats alters absolute or relative concentrations of nucleotide-linked sugars in skeletal muscle and liver in vivo. UDP-HexNAc and UDP-hexoses (UDP-Hex) were increased and decreased, respectively, in muscles of diabetic rats, resulting in an approximately 50% increase in the UDP-HexNAc:UDPHex ratio (P < 0.01). No significant changes in nucleotide sugars were observed in livers of diabetic rats. In muscles of normal rats, UDP-HexNAc concentrations increased (P < 0.01) and UDP-Hex decreased (P < 0.01) during hyperglycemia. The UDP-HexNAc:UDP-Hex ratio increased approximately 40% (P < 0.01) and correlated strongly with plasma glucose concentrations. Changes in liver were similar to muscle but were less marked. GFAT activity in muscle and liver was unaffected by 1-2 h of hyperglycemia. GFAT activity decreased 30-50% in muscle, liver, and epididymal fat of diabetic rats, and this was reversible with insulin therapy. No significant change in GFAT mRNA expression was detected, suggesting post-transcriptional regulation. The data suggest that glucose flux via HexNSP increases in muscle during hyperglycemic hyperinsulinemia and that the relative flux of glucose via HexNSP is increased in muscle in STZ-induced diabetes.(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
- Effects of exercise and feeding on the hexosamine biosynthetic pathway in rat skeletal muscle.
Nelson BA, Robinson KA, Koning JS, Buse MG. Nelson BA, et al. Am J Physiol. 1997 May;272(5 Pt 1):E848-55. doi: 10.1152/ajpendo.1997.272.5.E848. Am J Physiol. 1997. PMID: 9176185 - Decreased hexosamine biosynthesis in GH-deficient dwarf rat muscle. reversal with GH, but not IGF-I, therapy.
Robinson KA, Willi SM, Bingel S, Buse MG. Robinson KA, et al. Am J Physiol. 1999 Mar;276(3):E435-42. doi: 10.1152/ajpendo.1999.276.3.E435. Am J Physiol. 1999. PMID: 10070007 - Increased activity of the hexosamine synthesis pathway in muscles of insulin-resistant ob/ob mice.
Buse MG, Robinson KA, Gettys TW, McMahon EG, Gulve EA. Buse MG, et al. Am J Physiol. 1997 Jun;272(6 Pt 1):E1080-8. doi: 10.1152/ajpendo.1997.272.6.E1080. Am J Physiol. 1997. PMID: 9227455 - Hexosamines, insulin resistance, and the complications of diabetes: current status.
Buse MG. Buse MG. Am J Physiol Endocrinol Metab. 2006 Jan;290(1):E1-E8. doi: 10.1152/ajpendo.00329.2005. Am J Physiol Endocrinol Metab. 2006. PMID: 16339923 Free PMC article. Review. - Hexosamines and insulin resistance.
McClain DA, Crook ED. McClain DA, et al. Diabetes. 1996 Aug;45(8):1003-9. doi: 10.2337/diab.45.8.1003. Diabetes. 1996. PMID: 8690144 Review.
Cited by
- Increased O-GlcNAc levels during reperfusion lead to improved functional recovery and reduced calpain proteolysis.
Liu J, Marchase RB, Chatham JC. Liu J, et al. Am J Physiol Heart Circ Physiol. 2007 Sep;293(3):H1391-9. doi: 10.1152/ajpheart.00285.2007. Epub 2007 Jun 15. Am J Physiol Heart Circ Physiol. 2007. PMID: 17573462 Free PMC article. - Decreased UDP-GlcNAc levels abrogate proliferation control in EMeg32-deficient cells.
Boehmelt G, Wakeham A, Elia A, Sasaki T, Plyte S, Potter J, Yang Y, Tsang E, Ruland J, Iscove NN, Dennis JW, Mak TW. Boehmelt G, et al. EMBO J. 2000 Oct 2;19(19):5092-104. doi: 10.1093/emboj/19.19.5092. EMBO J. 2000. PMID: 11013212 Free PMC article. - Nutrient regulation of signaling and transcription.
Hart GW. Hart GW. J Biol Chem. 2019 Feb 15;294(7):2211-2231. doi: 10.1074/jbc.AW119.003226. Epub 2019 Jan 9. J Biol Chem. 2019. PMID: 30626734 Free PMC article. Review. - High-dose thiamine therapy counters dyslipidaemia in streptozotocin-induced diabetic rats.
Babaei-Jadidi R, Karachalias N, Kupich C, Ahmed N, Thornalley PJ. Babaei-Jadidi R, et al. Diabetologia. 2004 Dec;47(12):2235-46. doi: 10.1007/s00125-004-1582-5. Epub 2004 Dec 11. Diabetologia. 2004. PMID: 15662560 - Oligomerization status, with the monomer as active species, defines catalytic efficiency of UDP-glucose pyrophosphorylase.
Martz F, Wilczynska M, Kleczkowski LA. Martz F, et al. Biochem J. 2002 Oct 1;367(Pt 1):295-300. doi: 10.1042/BJ20020772. Biochem J. 2002. PMID: 12088504 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Miscellaneous