| Autor: |
Tesfai J; Department of Biochemistry, Loma Linda University School of Medicine, Loma Linda, CA 92350, USA., Crane L, Baziard-Mouysset G, Kennedy W, Edwards LP |
| Jazyk: |
angličtina |
| Zdroj: |
Pharmacological reports : PR [Pharmacol Rep] 2011; Vol. 63 (6), pp. 1442-9. |
| DOI: |
10.1016/s1734-1140(11)70708-3 |
| Abstrakt: |
The I(1)-imidazoline receptor is a novel target for drug development for hypertension and insulin resistance, major disorders associated with type 2 diabetes. In the present study, we examined the effects of a novel imidazoline agonist S43126, on phosphorylation of protein kinase B (PKB/Akt) and extracellular signal-regulated kinase (ERK1/2) in PC12 cells. We further examined the effects of S43126 on insulin stimulated PKB and ERK phosphorylation. PC12 cells were treated with varying doses of S43126 (10(-10) to 10(-6) M) or insulin (10(-10) to 10(-6) M) or combination treatment with insulin (10(-6) M) and varying doses of S43126 (10(-6) - 10(-11) M) for 10 min. Western blot analysis of treated samples showed that S43126 increased both ERK1/2 and PKB phosphorylation by 5 fold. Combination treatment with insulin (10(-6) M) and varying doses of S43126 (10(-6) - 10(-11) M) enhanced phosphorylation of PKB and ERK1/2 above the level of insulin alone, in a dose and time dependent manner. Treatment with siRNA against Nischarin (mouse homologue of I(1)-imidazoline receptor) reduced the phosphorylation of both ERK and PKB following combination treatments. These results indicate that S43126 has the potential to augment insulin action and should be further studied as a possible candidate drug for the treatment of insulin resistance states. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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