Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes

Fabregat, I. ; Revilla, E. ; Machado, A.

Amsterdam : Elsevier
ISSN:
0006-291X
Source:
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
Topics:
Biology
Chemistry and Pharmacology
Physics
Type of Medium:
Electronic Resource
URL:
_version_ 1798292248254742529
autor Fabregat, I.
Revilla, E.
Machado, A.
autorsonst Fabregat, I.
Revilla, E.
Machado, A.
book_url http://dx.doi.org/10.1016/0006-291X(87)90618-8
datenlieferant nat_lic_papers
fussnote The short-term activation of the pentose phosphate cycle by insulin in rat adipocytes and hepatocytes has been studied. This NADPH-producing pathway is regulated by the activation or inhibition of different NADPH-consuming pathways. The stimulation of the fatty acid synthesis by insulin produced an increase in the flux through the pentose phosphate cycle. Kynurenate produced a decrease in the fatty acid synthesis and, consequently a diminution in the flux through the pentose phosphate cycle. Incubation of adipocytes and hepatocytes in presence of kynurenate (10 mM and 3 mM respectively) and insulin (5 nM), prevents both insulin activation on fatty acid synthesis and pentose phosphate cycle. These results suggest that insulin actives the pentose phosphate cycle through the activation of fatty acid synthesis.
hauptsatz hsatz_simple
identnr NLZ184184592
issn 0006-291X
journal_name Biochemical and Biophysical Research Communications
materialart 1
package_name Elsevier
publikationsort Amsterdam
publisher Elsevier
reference 146 (1987), S. 920-925
search_space articles
shingle_author_1 Fabregat, I.
Revilla, E.
Machado, A.
shingle_author_2 Fabregat, I.
Revilla, E.
Machado, A.
shingle_author_3 Fabregat, I.
Revilla, E.
Machado, A.
shingle_author_4 Fabregat, I.
Revilla, E.
Machado, A.
shingle_catch_all_1 Fabregat, I.
Revilla, E.
Machado, A.
Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
0006-291X
0006291X
Elsevier
shingle_catch_all_2 Fabregat, I.
Revilla, E.
Machado, A.
Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
0006-291X
0006291X
Elsevier
shingle_catch_all_3 Fabregat, I.
Revilla, E.
Machado, A.
Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
0006-291X
0006291X
Elsevier
shingle_catch_all_4 Fabregat, I.
Revilla, E.
Machado, A.
Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
0006-291X
0006291X
Elsevier
shingle_title_1 Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
shingle_title_2 Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
shingle_title_3 Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
shingle_title_4 Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
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source_archive Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
timestamp 2024-05-06T08:45:30.315Z
titel Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
titel_suche Short-term control of the pentose phosphate cycle by insulin could be modulated by the NADPHNADP ratio in rat adipocytes and hepatocytes
The short-term activation of the pentose phosphate cycle by insulin in rat adipocytes and hepatocytes has been studied. This NADPH-producing pathway is regulated by the activation or inhibition of different NADPH-consuming pathways. The stimulation of the fatty acid synthesis by insulin produced an increase in the flux through the pentose phosphate cycle. Kynurenate produced a decrease in the fatty acid synthesis and, consequently a diminution in the flux through the pentose phosphate cycle. Incubation of adipocytes and hepatocytes in presence of kynurenate (10 mM and 3 mM respectively) and insulin (5 nM), prevents both insulin activation on fatty acid synthesis and pentose phosphate cycle. These results suggest that insulin actives the pentose phosphate cycle through the activation of fatty acid synthesis.
topic W
V
U
uid nat_lic_papers_NLZ184184592