Differential involvement of signaling pathways in the regulation of growth hormone release by somatostatin and growth hormone-releasing hormone in orange-spotted grouper (Epinephelus coioides) |
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Authors: | Bin Wang Chaobin QinCong Zhang Jirong JiaCaiyun Sun Wensheng Li |
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Affiliation: | State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Province Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, China |
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Abstract: | Somatostatin is the most effective inhibitor of GH release, and GHRH was recently identified as one of the primary GH-releasing factors in teleosts. In this study, we analyzed the possible intracellular transduction pathways that are involved in the mechanisms induced by SRIF and GHRH to regulate GH release. Using a pharmacological approach, the blockade of the PLC/IP/PKC pathway reversed the SRIF-induced inhibition of GH release but did not affect the GHRH-induced stimulation of GH release. Furthermore, SRIF reduced the GH release induced by two PKC activators. Inhibitors of the AC/cAMP/PKA pathway reversed both the SRIF- and GHRH-induced effects on GH release. Moreover, the GH release evoked by forskolin and 8-Br-cAMP were completely abolished by SRIF. The blockade of the NOS/NO pathway attenuated the GHRH-induced GH release but had minimal effects on the inhibitory actions of SRIF. In addition, inhibitors of the sGC/cGMP pathway did not modify the SRIF- or GHRH-induced regulation of GH release. Taken together, these findings indicate that the SRIF-induced inhibition of GH release is mediated by both the PLC/IP/PKC and the AC/cAMP/PKA pathways and not by the NOS/NO/sGC/cGMP pathway. In contrast, the GHRH-induced stimulation of GH secretion is mediated by both the AC/cAMP/PKA and the NOS/NO pathways and is independent of the sGC/cGMP pathway and the PLC/IP/PKC system. |
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Keywords: | GH, growth hormone SRIF, somatotropin release-inhibitory factor GHRH, GH-releasing hormone PACAP, pituitary adenylate cyclase-activating peptide DA, dopamine GnRH, gonadotropin-releasing hormone GPCR, G-protein-coupled receptor SSTR, somatostatin receptor GHRH-R, GHRH receptor PLC, phospholipase C IP, inositol phosphate DAG, diacylglycerol PKC, protein kinase C MAPK, mitogen-activated protein kinase PKA, protein kinase A U73122, 1-[6-((17β-3-Methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl]-1H-pyrrole-2,5-dione GF109203X, 2-[1-(3-Dimethylaminopropyl)-1H-indol-3-yl]-3-(1H-indol-3-yl)-maleimide TPA, phorbol 12-myristate-13-acetate DiC8, 1,2-dioctanoyl-sn-glycerol AC, adenylate cyclase cAMP, adenosine 3&prime ,5&prime -cyclic monophosphate MDL-12,330A, cis-N-(2-Phenylcyclopentyl)azacyclotridec-1-en-2-amine H89, N-[2-((p-bromocinnamyl)amino)ethyl]-5-isoquinolinesulfonamide NO, nitric oxide NOS, nitric oxide synthase SNAP, S-nitroso-N-acetylpenicillamine L-AME, L-arginine methyl ester dihydrochloride L-NAME, Nw-nitro-L-arginine methyl ester hydrochloride sGC, soluble guanylate cyclase cGMP, guanosine 3&prime ,5&prime -cyclic monophosphate LY-83583, 6-fenilanilino-5,8-quinolinedione PBS, phosphate buffered saline FBS, fetal bovine serum BSA, bovine serum albumin |
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