Great progress has been made in the analysis of hormonal, neural and genetic mechanisms underlying a simple sex behavior, lordosis. Now, it would be exciting to understand the flow of behaviors leading up to mating. Also, to explore the behavioral dispositions underlying these proceptive behaviors by the female. We have discovered active approach and pacing behaviors, previously thought to be absent, in female mice. New experiments with mice will allow for 'state of the art' genetic elucidation.
(Aim I.) : To finish carefully characterizing these locomotor, approach, proceptive and pacing behaviors. Included are quantitative analyses in seminatural environments which encourage a full range of social behaviors by the female, in their natural form. We have already discovered Direct Approaches, Head Turns, Hop-and-Stops, and Dart/Return Pacing responses. This is almost finished and will not take long.
(Aim II.) : We will determine their hormonal facilitation. For the first time in mice, the relative importance of estrogens (E), progestins (P) and their combination will be explored. New data comparing the roles of P and the gene for PRs in small shoebox cages compared to a semi-natural environment already show us the importance of context in discerning hormone/gene/behavior causal relations.
(Aim III) : We will discover the CNS sites of hormone action and genetic influences. For the genetics, primarily, a novel antisense technology will be used. Both hormonal experiments and antisense DNA experiments will include the use of a new 'microsphere' delivery system for hormones and for antisense DNA reagents. The antisense and microsphere techniques, well documented elsewhere, can be applied for the first time to the mouse CNS. Using female mice allows us to apply novel genetic tools. Analyzing the entire sequence of behaviors preceding lordosis, we can address scientifically exciting questions about reproductive behaviors which are not simple and which are biologically important. These behaviors bring together, at the right time, conspecifics who are competent to reproduce. Further, increasing attention to broader, hormone-dependent behavioral dispositions brings us one step closer to issues important for women's health.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37HD005751-34
Application #
7218577
Study Section
Special Emphasis Panel (ZRG1-IFCN-2 (01))
Program Officer
Lamar, Charisee A
Project Start
1978-05-01
Project End
2008-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
34
Fiscal Year
2007
Total Cost
$356,279
Indirect Cost
Name
Rockefeller University
Department
Biology
Type
Other Domestic Higher Education
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Kow, Lee-Ming; Pataky, Stefan; Dupré, Christophe et al. (2016) Analyses of rapid estrogen actions on rat ventromedial hypothalamic neurons. Steroids 111:100-112
Kow, Lee-Ming; Pfaff, Donald W (2016) Rapid estrogen actions on ion channels: A survey in search for mechanisms. Steroids 111:46-53
Ribeiro, Ana C; Ågmo, Anders; Musatov, Sergei et al. (2016) Silencing Estrogen Receptor-? with siRNA in the Intact Rodent Brain. Methods Mol Biol 1366:343-352
Faustino, Larissa C; Gagnidze, Khatuna; Ortiga-Carvalho, Tania M et al. (2015) Impact of Thyroid Hormones on Estrogen Receptor ?-Dependent Transcriptional Mechanisms in Ventromedial Hypothalamus and Preoptic Area. Neuroendocrinology 101:331-46
Keenan, Daniel M; Quinkert, Amy W; Pfaff, Donald W (2015) Stochastic modeling of mouse motor activity under deep brain stimulation: the extraction of arousal information. PLoS Comput Biol 11:e1003883
Gore, Andrea C; Martien, Katherine M; Gagnidze, Khatuna et al. (2014) Implications of prenatal steroid perturbations for neurodevelopment, behavior, and autism. Endocr Rev 35:961-91
Gagnidze, K; Weil, Z M; Faustino, L C et al. (2013) Early histone modifications in the ventromedial hypothalamus and preoptic area following oestradiol administration. J Neuroendocrinol 25:939-55
Vasudevan, Nandini; Morgan, Maria; Pfaff, Donald et al. (2013) Distinct behavioral phenotypes in male mice lacking the thyroid hormone receptor ?1 or ? isoforms. Horm Behav 63:742-51
Hunter, Richard G; Murakami, Gen; Dewell, Scott et al. (2012) Acute stress and hippocampal histone H3 lysine 9 trimethylation, a retrotransposon silencing response. Proc Natl Acad Sci U S A 109:17657-62
Ribeiro, Ana C; Musatov, Sergei; Shteyler, Anna et al. (2012) siRNA silencing of estrogen receptor-ýý expression specifically in medial preoptic area neurons abolishes maternal care in female mice. Proc Natl Acad Sci U S A 109:16324-9

Showing the most recent 10 out of 29 publications