Artículos de revistas
In vivo activation of insulin receptor tyrosine kinase by melatonin in the rat hypothalamus
Registro en:
Journal Of Neurochemistry. Blackwell Publishing Ltd, v. 90, n. 3, n. 559, n. 566, 2004.
0022-3042
WOS:000222720500005
10.1111/j.1471-4159.2004.02514.x
Autor
Anhe, GF
Caperuto, LC
Pereira-Da-Silva, M
Souza, LC
Hirata, AE
Velloso, LA
Cipolla-Neto, J
Carvalho, CRO
Institución
Resumen
Melatonin is the pineal hormone that acts via a pertussis toxin-sensitive G-protein to inhibit adenylate cyclase. However, the intracellular signalling effects of melatonin are not completely understood. Melatonin receptors are mainly present in the suprachiasmatic nucleus (SCN) and pars tuberalis of both humans and rats. The SCN directly controls, amongst other mechanisms, the circadian rhythm of plasma glucose concentration. In this study, using immunoprecipitation and immunoblotting, we show that melatonin induces rapid tyrosine phosphorylation and activation of the insulin receptor beta-subunit tyrosine kinase (IR) in the rat hypothalamic suprachiasmatic region. Upon IR activation, tyrosine phosphorylation of IRS-1 was detected. In addition, melatonin induced IRS-1/PI(3)-kinase and IRS-1/SHP-2 associations and downstream AKT serine phosphorylation and MAPK (mitogen-activated protein kinase) phosphorylation, respectively. These results not only indicate a new signal transduction pathway for melatonin, but also a potential cross-talk between melatonin and insulin. 90 3 559 566