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Phosphorylation processes mediate rapid changes of brain aromatase activity.
J Balthazart1, M Baillien, G F Ball
1Research Group in Behavioral Neuroendocrinology, Center for Cellular and Molecular Neurobiology, 17 Place Delcour (Bat. L1), University of Liège, B-4020, Liège, Belgium. jbalthazart@ulg.ac.be
The Journal of Steroid Biochemistry and Molecular Biology
|February 19, 2002
Summary
Aromatase enzyme activity in the quail brain is rapidly regulated by calcium and phosphorylation, influencing local estrogen availability for rapid neuronal signaling.
Area of Science:
- Neuroendocrinology
- Molecular Endocrinology
- Reproductive Biology
Background:
- Aromatase (estrogen synthase) is crucial for testosterone's reproductive actions.
- Its regulation in the quail brain, particularly the medial preoptic nucleus (POM), is key to male sexual behavior.
- Understanding estrogen's rapid signaling mechanisms in the brain is important.
Purpose of the Study:
- To investigate the distribution and regulation of aromatase in the quail brain.
- To explore the rapid, calcium-dependent regulation of aromatase activity.
- To understand how local estrogen production impacts neuronal physiology.
Main Methods:
- Radioenzyme assays on microdissected brain areas.
- Immunocytochemistry and in situ hybridization.
- RT-PCR.
- Hypothalamic homogenate and explant studies with calcium and kinase modulators.
Main Results:
- High aromatase activity (AA) is localized in the POM, a steroid-sensitive area critical for male sexual behavior.
- AA is rapidly down-regulated by conditions enhancing protein phosphorylation (Ca2+, Mg2+, ATP).
- AA is rapidly and reversibly regulated by high Ca2+ levels in hypothalamic explants, suggesting neurotransmitter influence.
Conclusions:
- Aromatase synthesis and activity in the quail brain are subject to rapid, calcium-dependent regulation.
- Local estrogen production can be quickly modulated by neuronal activity.
- This rapid regulation allows for non-genomic estrogen signaling, similar to neurotransmitters.