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FASEB J ; 26(3): 1251-60, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22075645

RESUMO

The plant hormone abscisic acid (ABA) is released from glucose-challenged human pancreatic ß cells and stimulates insulin secretion. We investigated whether plasma ABA increased during oral and intravenous glucose tolerance tests (OGTTs and IVGTTs) in healthy human subjects. In all subjects undergoing OGTTs (n=8), plasma ABA increased over basal values (in a range from 2- to 9-fold). A positive correlation was found between the ABA area under the curve (AUC) and the glucose AUC. In 4 out of 6 IVGTTs, little or no increase of ABA levels was observed. In the remaining subjects, the ABA increase was similar to that recorded during OGTTs. GLP-1 stimulated ABA release from an insulinoma cell line and from human islets, by ∼10- and 2-fold in low and high glucose, respectively. Human adipose tissue also released ABA in response to high glucose. Nanomolar ABA stimulated glucose uptake, similarly to insulin, in rat L6 myoblasts and in murine 3T3-L1 cells differentiated to adipocytes, by increasing GLUT-4 translocation to the plasma membrane. Demonstration that a glucose load in humans is followed by a physiological rise of plasma ABA, which can enhance glucose uptake by adipose tissues and muscle cells, identifies ABA as a new mammalian hormone involved in glucose metabolism.


Assuntos
Ácido Abscísico/sangue , Adipócitos/efeitos dos fármacos , Glucose/farmacologia , Hiperglicemia/sangue , Mioblastos/efeitos dos fármacos , Células 3T3-L1 , Ácido Abscísico/metabolismo , Adipócitos/citologia , Adipócitos/metabolismo , Tecido Adiposo/citologia , Tecido Adiposo/metabolismo , Adolescente , Adulto , Animais , Glicemia/metabolismo , Western Blotting , Linhagem Celular Tumoral , Diabetes Mellitus Tipo 1/sangue , Feminino , Citometria de Fluxo , Receptor do Peptídeo Semelhante ao Glucagon 1 , Glucose/farmacocinética , Teste de Tolerância a Glucose , Transportador de Glucose Tipo 4/metabolismo , Humanos , Camundongos , Pessoa de Meia-Idade , Mioblastos/citologia , Mioblastos/metabolismo , Interferência de RNA , Receptores de Glucagon/genética , Receptores de Glucagon/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Adulto Jovem
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