Gene interactions and pathways from curated databases and text-mining
Endocrinology 2004, PMID: 14630710

Glucocorticoids differentially modulate insulin-mediated protein and glycogen synthetic signaling downstream of protein kinase B in rat myocardium.

Wu, Yangsong; Barrett, Eugene J; Long, Wen; Liu, Zhenqi

Insulin and protein kinase B (or Akt) play critical roles in cardiomyocytic growth and survival. High concentrations of glucocorticoids antagonize insulin's action. To examine whether endogenous glucocorticoids modulate insulin's effect on Akt signaling in the protein and glycogen synthetic pathways in myocardium, we studied three groups of rats (n = 12 each) 4 d after either a bilateral adrenalectomy (ADX), ADX with physiological stress dose dexamethasone treatment (ADX + DEX), or a sham operation. Rats received either a saline infusion or a 3 mU/kg.min euglycemic insulin clamp for 3 h. ADX had no effect on myocardial Akt or GSK-3 [glycogen synthase (GS) kinase 3] phosphorylation, but it decreased the phosphorylation of eukaryotic initiation factor 4E binding protein 1 (4E-BP1) and ribosomal protein S6 kinase (p70(S6K)) (P < 0.003 for both). Insulin enhanced the phosphorylation of Akt (P < 0.04), 4E-BP1 (P < 0.002), and p70(S6K) (P < 0.0001) in ADX, but not in sham rats. Dexamethasone restored the levels of 4E-BP1 and p70(S6K) phosphorylation and abrogated the insulin-stimulated Akt, 4E-BP1, and p70(S6K) phosphorylation. ADX rats had higher GS activity (P = 0.058) and lower glycogen content (P < 0.0001) than sham rats. GSK-3 phosphorylation after insulin infusion was greater in ADX rats. Insulin did not alter GS activity. Although insulin did not change the glycogen content in sham or ADX rats, it increased glycogen content by approximately 50% in ADX + DEX rats (P < 0.02). We conclude that endogenous glucocorticoids differentially modulate the regulation of Akt-4E-BP1/p70(S6K) and Akt-GSK-3-GS signaling pathways in heart by physiologic hyperinsulinemia over a range from deficiency to physiological stress concentrations.

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Text Mining Data

Akt — insulin: " To examine whether endogenous glucocorticoids modulate insulin 's effect on Akt signaling in the protein and glycogen synthetic pathways in myocardium, we studied three groups of rats ( n = 12 each ) 4 d after either a bilateral adrenalectomy ( ADX ), ADX with physiological stress dose dexamethasone treatment ( ADX + DEX ), or a sham operation "

4E-BP1 → Insulin: " Insulin enhanced the phosphorylation of Akt ( P < 0.04 ), 4E-BP1 ( P < 0.002 ), and p70 ( S6K ) ( P < 0.0001 ) in ADX, but not in sham rats "

Akt → Insulin: " Insulin enhanced the phosphorylation of Akt ( P < 0.04 ), 4E-BP1 ( P < 0.002 ), and p70 ( S6K ) ( P < 0.0001 ) in ADX, but not in sham rats "

p70 → Insulin: " Insulin enhanced the phosphorylation of Akt ( P < 0.04 ), 4E-BP1 ( P < 0.002 ), and p70 ( S6K ) ( P < 0.0001 ) in ADX, but not in sham rats "

4E-BP1 → insulin: " Dexamethasone restored the levels of 4E-BP1 and p70 ( S6K ) phosphorylation and abrogated the insulin stimulated Akt, 4E-BP1 , and p70 ( S6K ) phosphorylation "

Akt → insulin: " Dexamethasone restored the levels of 4E-BP1 and p70 ( S6K ) phosphorylation and abrogated the insulin stimulated Akt , 4E-BP1, and p70 ( S6K ) phosphorylation "

p70 → insulin: " Dexamethasone restored the levels of 4E-BP1 and p70 ( S6K ) phosphorylation and abrogated the insulin stimulated Akt, 4E-BP1, and p70 ( S6K ) phosphorylation "

Manually curated Databases

No curated data.