Ryoko HIroi, PhD - US grants

[unreadable] DESCRIPTION (provided by applicant): Ovarian hormones, such as estrogen (E), are thought to play a significant role in regulation of anxiety, perhaps via modulating the serotonin (5-HT) system emanating from the dorsal raphe nucleus (DRN). In support of this hypothesis, we have recently found that chronic E treatment in ovariectomized (OVX) rats increases the mRNA level of tryptophan hydroxylase-2 (TPH2; the rate-limiting enzyme for 5-HT synthesis and one of the key control points in regulation of the serotonergic system) selectively in the mid-ventromedial and caudal DRN and also decreases anxiety-like behavior in the open field. In particular, increased TPH2 mRNA in the caudal DRN was correlated with decreased anxiety-like behavior in the open field, whereas in the rostral DRN was correlated with increased anxiety behavior. These results suggest that E may decrease anxiety by increasing the synthetic capacity of 5-HT in the caudal DRN. The proposed study will examine the overarching hypothesis that E increases TpH2 mRNA in caudal DRN, and this in turn reduces anxiety. I will test this hypothesis by investigating the whether TPH2 mRNA knockdown or overexpression in the caudal DRN will block or mimic, respectively, the effects of E on anxiety-like behavior in the open field and the elevated plus maze. This study seeks to elucidate the role of the DRN 5-HT system in hormone regulation of anxiety behaviors. Most importantly, findings from this study have significant clinical implications for treatment of mood disorders in women. [unreadable] [unreadable] [unreadable]

DESCRIPTION (provided by applicant): Ovarian Hormones, such as estrogen, are thought to play a significant role in regulation of affective disorders. This may occur through modulation of serotonin (5-HT) system emanating from the midbrain dorsal raphe nucleus (DRN). In support of this hypothesis, we have found that chronic estradiol (E2) treatment in ovariectomized rats increases the expression of tryptophan hydroxylase-2 (TpH2), the rate-limiting enzyme for 5-HT biosynthesis, selectively in the caudal DRN and this increase is critical for the anxiolytic effects of E2. E2- induced increases of TpH2 mRNA are mediated via estrogen receptor beta (ER2), and activation of local ER2 in the DRN is sufficient for this increase in TpH2 mRNA and for antidepressant effects of E2. As ER2 is found on serotonergic neurons in the caudal DRN, these studies lend credence to the hypothesis that E2 acts directly on the 5-HT neurons to increase TpH2 mRNA via ER2. However, exact mechanisms underlying this E2 effect on TpH2 are yet to be elucidated. Therefore, the proposed study will investigate the overarching hypothesis that that estrogen increases TpH2 mRNA directly via ER2, and address the possibility that estrogen activates the transcriptional region of the TpH2 promoter via interaction with ER2 and its co-regulator proteins. We will test this idea by first examining the functional effects of estrogen interaction with ER2 on the TpH promoter-luciferase construct using reporter gene assay in vitro. Second, we will identify the regulatory regions of the estrogen and ER2 induced activation of the TpH2 promoter by using progressive 5'deletions of the TpH2 promoter, followed by site directed mutagenesis of potential regulatory elements. Finally, we will explore the array of possible co- regulatory factors and mechanisms involved in ER2 mediated activation of TpH2 by using chromatin immunoprecipitation assay, triple labeled immunohistochemistry and antisense oligonucleotide knockdown. PUBLIC HEALTH RELEVANCE: The proposed study will elucidate the genetic and molecular mechanisms underlying the interaction between estrogen receptor beta and the tryptophan hydroxylase 2 (TpH2) gene promoter. This interaction activates gene expression of the rate-limiting enzyme for serotonin biosynthesis, TpH2, which has been implicated in the etiology of affective disorders. This study will address the possibility that estrogen regulates TpH2 expression through direct interactions of estrogen receptor with distinct regulatory regions of the TpH2 promoter. Understanding the exact mechanisms of the estrogen regulation of this gene may lead to novel targets for treatment of affective disorders in women.