Acylated and unacylated ghrelin attenuate isoproterenol-induced lipolysis in isolated rat visceral adipocytes through activation of phosphoinositide 3-kinase γ and phosphodiesterase 3B

被引:33
作者
Baragli, Alessandra [1 ,2 ]
Ghe, Corrado [1 ]
Arnoletti, Elisa [1 ]
Granata, Riccarda [2 ]
Ghigo, Ezio [2 ]
Muccioli, Giampiero [1 ]
机构
[1] Univ Torino, Div Med Pharmacol, Dept Anat Pharmacol & Forens Med, I-10125 Turin, Italy
[2] Univ Torino, Dept Internal Med, Div Endocrinol Diabetol & Metab, I-10126 Turin, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2011年 / 1811卷 / 06期
关键词
Ghrelin; Isoproterenol; Insulin; Lipolysis; Phosphodiesterase; 3B; Phosphoinositide 3-kinase gamma; HORMONE SECRETAGOGUE RECEPTOR; PROTEIN-KINASE-A; IN-VITRO; CELLS; GROWTH; INHIBITION; MECHANISMS; PI3K-GAMMA; INSULIN; PDE3B;
D O I
10.1016/j.bbalip.2011.03.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The acylated peptide ghrelin (AG) and its endogenous non-acylated isoform (UAG) protect cardiomyocytes, pancreatic beta-cells, and preadipocytes from apoptosis, and induce preadipocytes differentiation into adipocytes. These events are mediated by AG and UAG binding to a still unidentified receptor, which determines the activation of phosphoinositide 3-kinase (PI3K), protein kinase B (AKT), and mitogen-activated protein kinase (MAPK) ERK1/2. AG and UAG also possess antilipolytic activity in vitro, but the underlying mechanism remains unknown. Thus, the objective of the current study was to characterize the molecular events involved in AG/UAG receptor signaling cascade. We treated rat primary visceral adipocytes with isoproterenol (ISO) and forskolin (FSK) to stimulate lipolysis, simultaneously incubating them with or without AG or UAG. Both peptides blocked ISO- and FSK-induced lipolysis. By direct measurement of cAMP intracellular content, we demonstrated that AG/UAG effect was associated to a reduction of ISO-induced cAMP accumulation. Moreover, the cAMP analog 8Br-cAMP abolished AG/UAG effect. As AG and UAG were ineffective against lipolysis induced by db-cAMP, another poorly hydrolyzable cAMP analog, phosphodiesterase (PDE) involvement was hypothesized. Indeed, cilostamide, a specific PDE3B inhibitor, blocked AG/UAG effect on ISO-induced lipolysis. Furthermore, the P13K inhibitor wortmannin and AKT inhibitor 1,3-dihydro-1-(1-((4-(6-phenyl-1H-imidazo(4,5-g)quinoxalin-7-yl)phenyl) methyl)-4piperidiny1)-2H-benzimidazol-2-one trifluoroacetate also blocked AG/UAG action, suggesting a role in PDE3B activation. In particular, PI3K isoenzyme gamma (PI3K gamma) selective inhibition through the compound A5605240 prevented AG/UAG effect on ISO-stimulated lipolysis, hampering AKT phosphorylation on Ser(473). Taken together, these data demonstrate for the first time that AG/UAG attenuation of ISO-induced lipolysis involves PI3K gamma/AKT and PDE3B. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:386 / 396
页数:11
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