RAPID CHANGES IN CARBOHYDRATE-METABOLISM IN MUSCLE INDUCED BY TRIIODOTHYRONINE - THE ROLE OF GLUCOSE 1,6-BISPHOSPHATE

被引:9
作者
CHENZION, M
BASSUKEVITZ, Y
BEITNER, R
机构
[1] Health Sciences Research Center, Department of Life Sciences, Bar-Ilan University
关键词
D O I
10.1006/bmme.1995.1051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
All of the past research on glucose utilization by muscles focused on the slow action of thyroid hormones. Here we show that experimental hyperthyroidism, which was induced in rats by a single intramuscular injection of 3,3',5-triiodothyronine (T-3) at high concentrations, resulted in rapid changes (within minutes) in carbohydrate metabolism in tibialis anterior muscle, There was an increase in lactate content, in the allosteric activity of soluble phosphofructokinase (the rate-limiting enzyme in glycolysis), and in its product fructose 1,6-bisphosphate, 5 min following the injection of T-3, suggesting stimulation of glycolysis. The allosteric activity of mitochondrial-bound, and, to a lesser extent, of soluble hexokinase, was also enhanced. However, the intracellular distribution of the enzymes was unchanged by the hormone. The allosteric stimulation of hexokinase may be attributed to the decrease in glucose 1,6-bisphosphate, which is a potent inhibitor of hexokinase. The level of glucose 6-phosphate, another known inhibitor of hexokinase, was not changed by the hormone. The activation of phosphofructokinase following T-3 injection may be attributed to the decrease in ATP, an allosteric inhibitor of the enzyme, and the increase in the levels of P-i and fructose 1,6-bisphosphate, allosteric activators of the enzyme. Glycogen content was also significantly decreased in muscle 5 min following the injection of T-3. These results suggest that in hyperthyroidism, muscle reacts rapidly to the excess of thyroid hormones by stimulation of glycogenolysis, glucose phosphorylation, and glycolysis, to provide ATP, which may serve as a compensatory mechanism to ATP depletion. (C) 1995 Academic Press, Inc.
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页码:19 / 25
页数:7
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[31]   UNCOUPLING OF MITOCHONDRIAL OXIDATIVE-PHOSPHORYLATION ABOLISHES THE STIMULATORY ACTION OF INSULIN ON THE BINDING OF GLYCOLYTIC-ENZYMES TO MUSCLE CYTOSKELETON [J].
LIVNAT, T ;
CHENZION, M ;
BEITNER, R .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1993, 25 (07) :993-997
[32]   RAPID STIMULATORY EFFECT OF INSULIN ON BINDING OF GLYCOLYTIC-ENZYMES TO CYTOSKELETON OF C-6 GLIAL-CELLS, AND THE ANTAGONISTIC ACTION OF CALMODULIN INHIBITORS [J].
LIVNAT, T ;
CHENZION, M ;
BRODIE, C ;
BEITNER, R .
ENDOCRINE, 1995, 3 (05) :319-322
[33]   PLATELET-DERIVED GROWTH-FACTOR (PDGF) RAPIDLY STIMULATES BINDING OF GLYCOLYTIC-ENZYMES TO MUSCLE CYTOSKELETON, PREVENTED BY CALMODULIN ANTAGONISTS [J].
LIVNAT, T ;
CHENZION, M ;
BEITNER, R .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1994, 53 (01) :28-33
[34]   STIMULATORY EFFECT OF EPIDERMAL GROWTH-FACTOR ON BINDING OF GLYCOLYTIC-ENZYMES TO MUSCLE CYTOSKELETON AND THE ANTAGONISTIC ACTION OF CALMODULIN INHIBITORS [J].
LIVNAT, T ;
CHENZION, M ;
BEITNER, R .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1993, 50 (01) :24-34
[35]  
LOWRY OH, 1964, J BIOL CHEM, V239, P18
[36]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[37]  
MANSOUR TE, 1972, J BIOL CHEM, V247, P6059
[38]  
MASTERS CJ, 1987, MOL CELL BIOCHEM, V76, P3
[39]  
MOHAN C, 1989, CURR TOP CELL REGUL, V30, P105
[40]  
PASSONNEAU JV, 1969, J BIOL CHEM, V244, P902