rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1
|
pubmed:dateCreated |
1989-6-16
|
pubmed:abstractText |
The stimulations of ureagenesis and cyclic AMP accumulation induced by glucagon were inhibited by 10 nM vasopressin or 100 nM phorbol 12-myristate 13-acetate (PMA). The maximal accumulation of cyclic AMP induced by glucagon was clearly diminished by these agents without change in the EC50 for the peptide hormone suggesting a non-competitive type of inhibition. H-7 blocked the inhibition of glucagon-stimulated ureagenesis induced by PMA and vasopressin and diminished their effect on the accumulation of cyclic AMP induced by glucagon. It is concluded that activation of protein kinase C inhibits the stimulation of ureagenesis and the accumulation of cyclic AMP induced by glucagon in liver cells from hypothyroid rats; H-7 inhibits the effects of protein kinase C activation.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0158-5231
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
243-9
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:2719714-1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine,
pubmed-meshheading:2719714-Animals,
pubmed-meshheading:2719714-Arginine Vasopressin,
pubmed-meshheading:2719714-Cells, Cultured,
pubmed-meshheading:2719714-Drug Interactions,
pubmed-meshheading:2719714-Female,
pubmed-meshheading:2719714-Glucagon,
pubmed-meshheading:2719714-Hypothyroidism,
pubmed-meshheading:2719714-Isoquinolines,
pubmed-meshheading:2719714-Liver,
pubmed-meshheading:2719714-Piperazines,
pubmed-meshheading:2719714-Protein Kinase C,
pubmed-meshheading:2719714-Rats,
pubmed-meshheading:2719714-Rats, Inbred Strains,
pubmed-meshheading:2719714-Tetradecanoylphorbol Acetate,
pubmed-meshheading:2719714-Urea
|
pubmed:year |
1989
|
pubmed:articleTitle |
Effect of H-7 on the modulation of glucagon actions by activators of protein kinase-C.
|
pubmed:affiliation |
Instituto de Fisiología Celular, UNAM, D.F. Mexico.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|