Modulation of growth hormone signal transduction in kidneys of streptozotocin-induced diabetic animals: effect of a growth hormone receptor antagonist
Autor: | Ana C P, Thirone, John A, Scarlett, Alessandra L, Gasparetti, Eliana P, Araujo, Maria H L, Lima, Carla R O, Carvalho, Lício A, Velloso, Mario J A, Saad |
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Rok vydání: | 2002 |
Předmět: |
Blood Glucose
Male Src Homology 2 Domain-Containing Transforming Protein 1 Kidney Diabetes Mellitus Experimental src Homology Domains Reference Values Proto-Oncogene Proteins Animals Rats Wistar Adaptor Proteins Signal Transducing GRB2 Adaptor Protein Body Weight Proteins Organ Size Receptors Somatotropin Janus Kinase 2 Protein-Tyrosine Kinases Phosphoproteins Immunohistochemistry Rats Adaptor Proteins Vesicular Transport Amino Acid Substitution Shc Signaling Adaptor Proteins Growth Hormone Insulin Receptor Substrate Proteins Signal Transduction |
Zdroj: | Diabetes. 51(7) |
ISSN: | 0012-1797 |
Popis: | Growth hormone (GH) and IGFs have a long distinguished history in diabetes, with possible participation in the development of renal complications. The implicated effect of GH in diabetic end-stage organ damage may be mediated by growth hormone receptor (GHR) or postreceptor events in GH signal transduction. The present study investigates the effects of diabetes induced by streptozotocin (STZ) on renal GH signaling. Our results demonstrate that JAK2, insulin receptor substrate (IRS)-1, Shc, ERKs, and Akt are widely distributed in the kidney, and after GH treatment, there is a significant increase in phosphorylation of these proteins in STZ-induced diabetic rats compared with controls. Moreover, the GH-induced association of IRS-1/phosphatidylinositol 3-kinase, IRS-1/growth factor receptor bound 2 (Grb2), and Shc/Grb2 are increased in diabetic rats as well. Immunohistochemical studies show that GH-induced p-Akt and p-ERK activation is apparently more pronounced in the kidneys of diabetic rats. Administration of G120K-PEG, a GH antagonist, in diabetic mice shows inhibitory effects on diabetic renal enlargement and reverses the alterations in GH signal transduction observed in diabetic animals. The present study demonstrates a role for GH signaling in the pathogenesis of early diabetic renal changes and suggests that specific GHR blockade may present a new concept in the treatment of diabetic kidney disease. |
Databáze: | OpenAIRE |
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