Differential effects of GH and GH-releasing peptide-6 on astrocytes

被引:22
作者
Baquedano, Eva [1 ,3 ]
Chowen, Julie A. [2 ,3 ]
Argente, Jesus [1 ,2 ,3 ]
Frago, Laura M. [1 ,3 ]
机构
[1] Univ Autonoma Madrid, Dept Pediat, Madrid, Spain
[2] Hosp Infantil Univ Nino Jesus UAM, Dept Endocrinol, Inst Invest La Princesa, Madrid 28009, Spain
[3] Inst Salud Carlos III, Ctr Invest Biomed Red Fisiopatol Obesidad & Nutr, Madrid, Spain
关键词
GH; GHRP-6; hippocampus; hypothalamus; proliferation; differentiation; FIBRILLARY ACIDIC PROTEIN; GROWTH-HORMONE RECEPTOR; HYPOXIC-ISCHEMIC BRAIN; FACTOR-I; THYROID-HORMONE; SECRETAGOGUE RECEPTOR; INHIBITS APOPTOSIS; CELL-PROLIFERATION; SIGNALING PATHWAY; RAT HIPPOCAMPUS;
D O I
10.1530/JOE-13-0053
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
GH and GH secretagogues (GHSs) are involved in many cellular activities such as stimulation of mitosis, proliferation and differentiation. As astrocytes are involved in developmental and protective functions, our aim was to analyse the effects of GH and GH-releasing hexapeptide on astrocyte proliferation and differentiation in the hypothalamus and hippocampus. Treatment of adult male Wistar rats with GH (i.v., 100 mg/day) for 1 week increased the levels of glial fibrillary acidic protein (GFAP) and decreased the levels of vimentin in the hypothalamus and hippocampus. These changes were not accompanied by increased proliferation. By contrast, GH-releasing hexapeptide (i.v., 150 mg/day) did not affect GFAP levels but increased proliferation in the areas studied. To further study the intracellular mechanisms involved in these effects, we treated C6 astrocytoma cells with GH or GH-releasing hexapeptide and the phosphatidylinositol 3'-kinase (PI3K) inhibitor, LY294002, and observed that the presence of this inhibitor reverted the increase in GFAP levels induced by GH and the proliferation induced by GH-releasing hexapeptide. We conclude that although GH-releasing hexapeptide is a GHS, it may exert GH-independent effects centrally on astrocytes when administered i.v., although the effects of both substances appear to be mediated by the PI3K/Akt pathway.
引用
收藏
页码:263 / 274
页数:12
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