Literature DB >> 2526729

Decrease in glucose transporter number in skeletal muscle of mildly diabetic (streptozotocin-treated) rats.

T Ramlal1, S Rastogi, M Vranic, A Klip.   

Abstract

Diabetes is associated with a decrease in glucose uptake into muscle, the primary tissue responsible for whole body glucose uptake in the fed state. To study the basis of such a decrease we estimated the number of glucose transporters in skeletal muscle membranes from control and streptozotocin (STZ)-treated rats. Animals were injected with 65 mg STZ/kg and were clearly diabetic (hyperglycemic and glycosuric) at 1 week. After an overnight fast, animals were killed, and skeletal muscle from hind limbs were removed and used to prepare plasma membranes and internal membranes. The number of glucose transporters was determined by D-glucose-protectable equilibrium binding of [3H]cytochalasin-B. STZ-treated rats showed a 37% decrease in the number of glucose transporters per mg protein in crude membranes. The decrease was more pronounced in plasma membranes (average 50% decrease) than in the intracellular membranes (32% decrease). The reduction in the number of glucose transporters was specific, since it was not paralleled by changes in other plasma membrane markers or in total protein, although plasma membrane protein decreased by 15% in STZ-treated rats. When total recoveries of transporters were calculated (i.e. picomoles of transporters recovered per g tissue), the number of transporters in the plasma membrane fraction from STZ-treated rats was decreased by 68% relative to that in control animals. In the intracellular membranes and in total crude membranes from diabetic rats the transporters were decreased by 45%. This suggests that in STZ-treated rats there is an overall decrease in the number of glucose transporters, and that the plasma membrane is further specifically depleted of transporters. The decrease in glucose transporter number in the plasma membrane could at least in part be the cause of the diminished glucose uptake in diabetic muscle and for overall drop in total body glucose utilization of this condition.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2526729     DOI: 10.1210/endo-125-2-890

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  14 in total

1.  Identification and characterization of two distinct intracellular GLUT4 pools in rat skeletal muscle: evidence for an endosomal and an insulin-sensitive GLUT4 compartment.

Authors:  J C Aledo; L Lavoie; A Volchuk; S R Keller; A Klip; H S Hundal
Journal:  Biochem J       Date:  1997-08-01       Impact factor: 3.857

2.  Glycaemia regulates the glucose transporter number in the plasma membrane of rat skeletal muscle.

Authors:  D Dimitrakoudis; T Ramlal; S Rastogi; M Vranic; A Klip
Journal:  Biochem J       Date:  1992-06-01       Impact factor: 3.857

3.  Insulin responsiveness in skeletal muscle is determined by glucose transporter (Glut4) protein level.

Authors:  M Kern; J A Wells; J M Stephens; C W Elton; J E Friedman; E B Tapscott; P H Pekala; G L Dohm
Journal:  Biochem J       Date:  1990-09-01       Impact factor: 3.857

Review 4.  Thirty sweet years of GLUT4.

Authors:  Amira Klip; Timothy E McGraw; David E James
Journal:  J Biol Chem       Date:  2019-06-07       Impact factor: 5.157

5.  Insulin down-regulates expression of the insulin-responsive glucose transporter (GLUT4) gene: effects on transcription and mRNA turnover.

Authors:  J R Flores-Riveros; J C McLenithan; O Ezaki; M D Lane
Journal:  Proc Natl Acad Sci U S A       Date:  1993-01-15       Impact factor: 11.205

6.  Effects of altered glucose homeostasis on glucose transporter expression in skeletal muscle of the rat.

Authors:  R E Bourey; L Koranyi; D E James; M Mueckler; M A Permutt
Journal:  J Clin Invest       Date:  1990-08       Impact factor: 14.808

7.  Glucose rapidly decreases plasma membrane GLUT4 content in rat skeletal muscle.

Authors:  A Marette; D Dimitrakoudis; Q Shi; C D Rodgers; A Klip; M Vranic
Journal:  Endocrine       Date:  1999-02       Impact factor: 3.633

8.  Effects of glycaemia on glucose transport in isolated skeletal muscle from patients with NIDDM: in vitro reversal of muscular insulin resistance.

Authors:  J R Zierath; D Galuska; L A Nolte; A Thörne; J S Kristensen; H Wallberg-Henriksson
Journal:  Diabetologia       Date:  1994-03       Impact factor: 10.122

9.  Insulin resistance in obese Zucker rat (fa/fa) skeletal muscle is associated with a failure of glucose transporter translocation.

Authors:  P A King; E D Horton; M F Hirshman; E S Horton
Journal:  J Clin Invest       Date:  1992-10       Impact factor: 14.808

10.  Mechanisms and time course of impaired skeletal muscle glucose transport activity in streptozocin diabetic rats.

Authors:  R Napoli; M F Hirshman; E S Horton
Journal:  J Clin Invest       Date:  1995-07       Impact factor: 14.808

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.