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Peptides ; 20(7): 829-36, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10477083

RESUMO

Functional angiotensin receptors were characterized in the rat pancreatic acinar cell line AR4-2J. Angiotensin II stimulated a dose-dependent release of amylase and production of inositol phosphates. Results of high-performance liquid chromatography separation of inositol phosphates indicated that angiotensin stimulated the rapid accumulation of inositol 1,3,4-trisphosphate. Angiotensin II and angiotensin III were at least an order of magnitude more potent than angiotensin I in the stimulation of amylase release. The angiotensin II-stimulated amylase release was blocked by losartan, a selective AT1 angiotensin antagonist. The selective AT2 angiotensin receptor ligands CGP42112 did not alter angiotensin II-stimulated amylase released. However, CGP42112 stimulated amylase release at micromolar concentrations with a potency similar to angiotensin I. Analysis of mRNA expression by reverse transcription polymerase chain reaction suggested that AT1A was the predominant type-I angiotensin receptor expressed in the AR4-2J cells.


Assuntos
Pâncreas/metabolismo , Receptores de Angiotensina/metabolismo , Amilases/metabolismo , Angiotensina II/farmacologia , Antagonistas de Receptores de Angiotensina , Animais , Sequência de Bases , Linhagem Celular , Primers do DNA/genética , Fosfatos de Inositol/biossíntese , Cinética , Losartan/farmacologia , Oligopeptídeos/farmacologia , Pâncreas/efeitos dos fármacos , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Ratos , Receptor Tipo 1 de Angiotensina , Receptores de Angiotensina/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa
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