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Dexamethasone impairs growth hormone (GH)-stimulated growth by suppression of local insulin-like growth factor (IGF)-I production and expression of GH- and IGF-I-receptor in cultured rat chondrocytes.

Jux, C (författare)
Leiber, K (författare)
H?gel, U (författare)
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Blum, W. F. (författare)
Ohlsson, Claes, 1965 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för internmedicin,Institute of Internal Medicine, Dept of Medicine
Klaus, G (författare)
Mehls, O (författare)
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 (creator_code:org_t)
1998
1998
Engelska.
Ingår i: Endocrinology. - 0013-7227. ; 139:7, s. 3296-305
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Growth depression as a side effect of glucocorticoid therapy in childhood is partially mediated by alterations of the somatotropic hormone axis. The mechanisms of interaction between glucocorticoids and somatotropic hormones on the cellular and molecular level are poorly understood. In an experimental model of primary cultured rat growth plate chondrocytes, basal as well as GH (40 ng/ml) or insulin-like growth factor (IGF)-I (60 ng/ml)-stimulated growth was suppressed dose dependently (10(-l2)-10(-7)M) by dexamethasone (Dexa). An IGF-I antibody specifically and dose dependently inhibited the GH- but not the basic fibroblast growth factor (bFGF)-stimulated cell proliferation. GH increased the IGF-I concentration in conditioned serum-free culture medium; this was reversed by concomitant Dexa. Dexa time dependently suppressed the transcription of GH receptor (GHR) messenger RNA (mRNA) and down-regulated the basal and GH-stimulated expression of GHR. Whereas no suppressive effect on basal type I IGF-receptor (IGFR) was observed, Dexa blocked the IGF-I induced increase of IGF binding. These results were confirmed by GHR and IGFR immunostaining. We conclude that Dexa impairs the GH-induced stimulation of local secretion and paracrine action of IGF-I and reduces the homologous increase of IGFR and GHR expression. The above experiments give further insight on the interaction between GH and glucocorticoids on the cellular and molecular level of growth plate chondrocytes.

Nyckelord

Animals
Cartilage
cytology
metabolism
Cell Division
drug effects
Cells
Cultured
DNA
biosynthesis
Dexamethasone
pharmacology
Epiphyses
cytology
metabolism
Glucocorticoids
pharmacology
Human Growth Hormone
pharmacology
Humans
Insulin-Like Growth Factor I
antagonists & inhibitors
metabolism
Rats
Rats
Sprague-Dawley
Receptors
Somatomedin
antagonists & inhibitors
metabolism
Receptors
Somatotropin
antagonists & inhibitors
genetics
metabolism
Transcription
Genetic
physiology

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