Korean J Physiol Pharmacol.  2008 Apr;12(2):37-41. 10.4196/kjpp.2008.12.2.37.

Melatonin Induces Akt Phosphorylation through Melatonin Receptor- and PI3K-Dependent Pathways in Primary Astrocytes

• Kong PJ
• Byun JS
• Lim SY
• Lee JJ
• Hong SJ
• Kwon KJ
• Kim SS

• KMID: 1486141
• DOI: http://doi.org/10.4196/kjpp.2008.12.2.37

Abstract

Melatonin has been reported to protect neurons from a variety of neurotoxicity. However, the underlying mechanism by which melatonin exerts its neuroprotective property has not yet been clearly understood. We previously demonstrated that melatonin protected kainic acid-induced neuronal cell death in mouse hippocampus, accompanied by sustained activation of Akt, a critical mediator of neuronal survival. To further elucidate the neuroprotective action of melatonin, we examined in the present study the causal mechanism how Akt signaling pathway is regulated by melatonin in a rat primary astrocyte culture model. Melatonin resulted in increased astrocytic Akt phosphorylation, which was significantly decreased with wortmannin, a specific inhibitor of PI3K, suggesting that activation of Akt by melatonin is mediated through the PI3K-Akt signaling pathway. Furthermore, increased Akt activation was also significantly decreased with luzindole, a non-selective melatonin receptor antagonist. As downstream signaling pathway of Akt activation, increased levels of CREB phoshorylation and GDNF expression were observed, which were also attenuated with wortmannin and luzindole. These results strongly suggest that melatonin exerts its neuroprotective property in astrocytes through the activation of plasma membrane receptors and then PI3K-Akt signaling pathway.

Keyword

Melatonin; Akt phosphorylation; Melatonin receptor; luzindole; PI3K; Primary astrotyctes

MeSH Terms

Androstadienes
Animals
Astrocytes
Cell Death
Cell Membrane
Glial Cell Line-Derived Neurotrophic Factor
Hippocampus
Melatonin
Mice
Neurons
Phosphorylation
Rats
Receptors, Melatonin
Tryptamines
Androstadienes
Glial Cell Line-Derived Neurotrophic Factor
Melatonin
Receptors, Melatonin
Tryptamines

Figure

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  Fig. 1. Time-course of melatonin-stimulated Akt phosphorylation at Ser473 in primary cultures of rat cortical astrocytes. Quiescent astrocytes were treated with melatonin (10μM) for indicated time periods. Data are representative of four independent experiments. The phospho-Akt and total Akt bands of the samples were densitometrically evaluated and phospho-Akt/total Akt ratio was expressed as mean±SEM. ∗p<0.05 and ∗∗p<0.01 indicate statistically significant difference from the control group.

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  Fig. 2. Effects of PI3K inhibition and melatonin receptor blockade on melatonin-induced Akt phosphorylation. Melatonin (10μM) was applied to primary cultures for 12 hr in the absence or presence of wortmannin or luzindole. Concentrations and preincubation times of these compounds were as follows: wortmannin (W), 10μM, 1 hr; luzindole (L), 100μM, 1 hr. Right panel represents quantitative analysis. The phospho-Akt/Akt ratio was determined and expressed as mean±SEM. Akt phosphorylation by melatonin was inhibited by pretreatment of the cells with wortmannin or luzindole. ∗p<0.05 and ∗∗p<0.01 indicate statistically significant difference from the melatonin treated group.

• 

  Fig. 3. Time-course of melatonin-stimulated CREB phosphorylation in primary cultures of rat cortical astrocytes. Quiescent cultured astrocytes were treated with melatonin (10μM) for indicated time periods. CREB phosphorylation in mouse hippocampus was increased by melatonin treatment. Left panel is the representative blot, and right panel shows quantitative verification. The phospho-CREB/CREB ratio was expressed as mean±SEM. ∗p<0.05 indicates statistically significant difference from the control group.

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  Fig. 4. Effects of PI3K inhibition and melatonin receptor blockade on melatonin-induced CREB phosphorylation. Melatonin (10μM) was applied to primary cultures for 12 hr in the absence or presence of the inhibitor indicated. Left panel is the representative blot, and right panel shows quantitative verification. The phospho-CREB/CREB ratio was expressed as mean±SEM. CREB phosphorylation by melatonin was partially inhibited by pretreatment of the cells with wortmannin or luzindole. ∗p<0.05 indicates statistically significant difference from the melatonin treated group.

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  Fig. 5. Effects of PI3K inhibition or melatonin receptor blockade on melatonin-induced neurotrophic factors expression. Melatonin (10 μM) was applied to primary cultures for 24 hr in the absence or presence of the agents indicated. Left panel is a representative blot, and right panel shows quantitative verification. The GDNF/β-actin ratio was expressed as mean±SEM. GDNF expression by melatonin was inhibited by pretreatment of the cells with wortmannin and luzindole. ∗∗p < 0.01 indicates statistically significant difference from the melatonin treated group.

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