Effect of in vivo injection of cholera and pertussis toxin on glucose transport in rat skeletal muscle

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Standard

Effect of in vivo injection of cholera and pertussis toxin on glucose transport in rat skeletal muscle. / Ploug, Thorkil; Han, X; Petersen, L N; Galbo, H.

I: American Journal of Physiology (Consolidated), Bind 272, Nr. 1 Pt 1, 01.1997, s. E7-17.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ploug, T, Han, X, Petersen, LN & Galbo, H 1997, 'Effect of in vivo injection of cholera and pertussis toxin on glucose transport in rat skeletal muscle', American Journal of Physiology (Consolidated), bind 272, nr. 1 Pt 1, s. E7-17.

APA

Ploug, T., Han, X., Petersen, L. N., & Galbo, H. (1997). Effect of in vivo injection of cholera and pertussis toxin on glucose transport in rat skeletal muscle. American Journal of Physiology (Consolidated), 272(1 Pt 1), E7-17.

Vancouver

Ploug T, Han X, Petersen LN, Galbo H. Effect of in vivo injection of cholera and pertussis toxin on glucose transport in rat skeletal muscle. American Journal of Physiology (Consolidated). 1997 jan.;272(1 Pt 1):E7-17.

Author

Ploug, Thorkil ; Han, X ; Petersen, L N ; Galbo, H. / Effect of in vivo injection of cholera and pertussis toxin on glucose transport in rat skeletal muscle. I: American Journal of Physiology (Consolidated). 1997 ; Bind 272, Nr. 1 Pt 1. s. E7-17.

Bibtex

@article{ec448bcff2ed4847ac6216b670c7524c,
title = "Effect of in vivo injection of cholera and pertussis toxin on glucose transport in rat skeletal muscle",
abstract = "Cholera toxin (CTX) and pertussis toxin (PTX) were examined for their ability to inhibit glucose transport in perfused skeletal muscle. Twenty-five hours after an intravenous injection of CTX, basal transport was decreased approximately 30%, and insulin- and contraction-stimulated transport was reduced at least 86 and 49%, respectively, in both the soleus and red and white gastrocnemius muscles. In contrast, PTX treatment was much less efficient. Impairment of glucose transport appeared to develop 10-15 h after CTX administration, which coincided with development of hyperglycemia despite hyperinsulinimia, increased plasma free fatty acid levels, increased adenosine 3',5'-cyclic monophosphate (cAMP) concentrations in muscle, but no difference in plasma catecholamines. Twenty-five hours after CTX treatment, GLUT-4 protein in both soleus and red gastrocnemius muscles was decreased, whereas no change in GLUT-1 protein content was found. In contrast, GLUT-4 mRNA was unchanged, but transcripts for GLUT-1 were increased > or = 150% in all three muscles from CTX-treated rats. The findings suggest that CTX via increased cAMP impairs basal as well as insulin- and contraction-stimulated muscle glucose transport, at least in part from a decrease in intramuscular GLUT-4 protein.",
keywords = "Animals, Biological Transport, Catecholamines, Cholera Toxin, Cyclic AMP, Glucose, Glucose Transporter Type 1, Glucose Transporter Type 4, Injections, Intravenous, Insulin, Male, Monosaccharide Transport Proteins, Muscle Contraction, Muscle Proteins, Muscle, Skeletal, Pertussis Toxin, RNA, Messenger, Rats, Rats, Wistar, Virulence Factors, Bordetella",
author = "Thorkil Ploug and X Han and Petersen, {L N} and H Galbo",
year = "1997",
month = jan,
language = "English",
volume = "272",
pages = "E7--17",
journal = "American Journal of Physiology - Cell Physiology",
issn = "0363-6143",
publisher = "American Physiological Society",
number = "1 Pt 1",

}

RIS

TY - JOUR

T1 - Effect of in vivo injection of cholera and pertussis toxin on glucose transport in rat skeletal muscle

AU - Ploug, Thorkil

AU - Han, X

AU - Petersen, L N

AU - Galbo, H

PY - 1997/1

Y1 - 1997/1

N2 - Cholera toxin (CTX) and pertussis toxin (PTX) were examined for their ability to inhibit glucose transport in perfused skeletal muscle. Twenty-five hours after an intravenous injection of CTX, basal transport was decreased approximately 30%, and insulin- and contraction-stimulated transport was reduced at least 86 and 49%, respectively, in both the soleus and red and white gastrocnemius muscles. In contrast, PTX treatment was much less efficient. Impairment of glucose transport appeared to develop 10-15 h after CTX administration, which coincided with development of hyperglycemia despite hyperinsulinimia, increased plasma free fatty acid levels, increased adenosine 3',5'-cyclic monophosphate (cAMP) concentrations in muscle, but no difference in plasma catecholamines. Twenty-five hours after CTX treatment, GLUT-4 protein in both soleus and red gastrocnemius muscles was decreased, whereas no change in GLUT-1 protein content was found. In contrast, GLUT-4 mRNA was unchanged, but transcripts for GLUT-1 were increased > or = 150% in all three muscles from CTX-treated rats. The findings suggest that CTX via increased cAMP impairs basal as well as insulin- and contraction-stimulated muscle glucose transport, at least in part from a decrease in intramuscular GLUT-4 protein.

AB - Cholera toxin (CTX) and pertussis toxin (PTX) were examined for their ability to inhibit glucose transport in perfused skeletal muscle. Twenty-five hours after an intravenous injection of CTX, basal transport was decreased approximately 30%, and insulin- and contraction-stimulated transport was reduced at least 86 and 49%, respectively, in both the soleus and red and white gastrocnemius muscles. In contrast, PTX treatment was much less efficient. Impairment of glucose transport appeared to develop 10-15 h after CTX administration, which coincided with development of hyperglycemia despite hyperinsulinimia, increased plasma free fatty acid levels, increased adenosine 3',5'-cyclic monophosphate (cAMP) concentrations in muscle, but no difference in plasma catecholamines. Twenty-five hours after CTX treatment, GLUT-4 protein in both soleus and red gastrocnemius muscles was decreased, whereas no change in GLUT-1 protein content was found. In contrast, GLUT-4 mRNA was unchanged, but transcripts for GLUT-1 were increased > or = 150% in all three muscles from CTX-treated rats. The findings suggest that CTX via increased cAMP impairs basal as well as insulin- and contraction-stimulated muscle glucose transport, at least in part from a decrease in intramuscular GLUT-4 protein.

KW - Animals

KW - Biological Transport

KW - Catecholamines

KW - Cholera Toxin

KW - Cyclic AMP

KW - Glucose

KW - Glucose Transporter Type 1

KW - Glucose Transporter Type 4

KW - Injections, Intravenous

KW - Insulin

KW - Male

KW - Monosaccharide Transport Proteins

KW - Muscle Contraction

KW - Muscle Proteins

KW - Muscle, Skeletal

KW - Pertussis Toxin

KW - RNA, Messenger

KW - Rats

KW - Rats, Wistar

KW - Virulence Factors, Bordetella

M3 - Journal article

C2 - 9038845

VL - 272

SP - E7-17

JO - American Journal of Physiology - Cell Physiology

JF - American Journal of Physiology - Cell Physiology

SN - 0363-6143

IS - 1 Pt 1

ER -

ID: 123665900