Abstract
It has been over 60years since the first studies have been published describing the effects of steroid hormones on brain function. For over 30years, estrogen has been presumed to directly affect gene expression and protein synthesis through a specific receptor. More than 20years ago, the first estrogen receptor was cloned and identified as a transcription factor. Yet, throughout their course of study, estrogens have also been observed to affect nervous system function via mechanisms independent of intracellular receptor regulation of gene expression. Up until recently, the membrane estrogen receptors responsible for these rapid actions have remained elusive. Recent studies have demonstrated that a large number of these rapid, membrane-initiated actions of estradiol are due to surface expression of classical estrogen receptors. This review focuses on the importance of membrane estrogen receptor interactions with metabotropic glutamate receptors for understanding rapid estradiol signaling mechanisms and downstream effectors, as well as their significance in a variety of physiological processes.
Original language | English (US) |
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Pages (from-to) | 66-77 |
Number of pages | 12 |
Journal | Molecular neurobiology |
Volume | 38 |
Issue number | 1 |
DOIs | |
State | Published - Aug 2008 |
Bibliographical note
Funding Information:Acknowledgment This work was supported by NIH grants DA013185 and HD042635 (PEM) and NS41302 (PGM). The authors would like to thank Dr. Marissa Boulware for providing the experimental data found within this review and Jessie Luoma for her technical assistance regarding the preparation of this manuscript.
Keywords
- Estradiol
- Estrous cycle
- Lordosis
- MGluR
- Membrane
- Nociception
- Pain
- Rapid actions