The Proposed studies are designed to provide information about the mechanisms and physiological significance of interactions among serotonin (5-HT) receptors in the control of female rat lordosis behavior. Emphasis is placed on 5-HT's role in the mediobasal hypothalamus (MBH), especially the ventromedial nucleus of the hypothalamus (VMN).
The specific aims of the present application are to identify mechanisms responsible for this interaction. Studies are also designed to test the hypothesis that 5-HT's dual function within the VMN enables the organism to modulate its behavioral repertoire in a manner conducive to both species and individual survival.
The specific aims of the proposed studies are: To determine the relative distribution of 5-HT1A, 5-HT2A and 5-HT2C receptors within the VMN of proestrous rats and of hormonally-primed, ovariectomized rats. To test intracellular mechanisms responsible for the effects of 5-HT1A and 5-HT2A/2C receptors. Experiments are proposed to test the hypothesis that 5-HT1A receptor-mediated inhibition of cAMP accumulation is involved in the receptor's inhibitory effect on lordosis behavior and that inhibition of cAMP accumulation is involved in the receptor's inibitory effect on lordosis behavior and that 5-HT2 receptors attenuate this inhibition through actions involving protein kinase C. Experiments are proposed to test the hypothesis that 5-HT1A receptors reduce the release of norepinephrine (NE) and that 5-HT2 receptors enhance the release of gamma-aminobutyric acid (GABA); and that these effects of 5-HT on NE and/or GABA contribute to 5-HT's ability to both inhibit and facilitate lordosis behavior. To test a model about the physiological significance of 5-HT's dual role in the control of lordosis behavior. Experiments are designed to evaluate the hypothesis that 5-HT2 receptors reduce inhibition of lordosis behavior (mediated via 5-HT1A receptors) that is initiated by environmental challenge.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
2R01HD028419-08A1
Application #
2903222
Study Section
Special Emphasis Panel (ZRG1-IFCN-1 (01))
Program Officer
De Paolo, Louis V
Project Start
1991-08-01
Project End
2004-06-30
Budget Start
1999-07-12
Budget End
2000-06-30
Support Year
8
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Texas Woman's University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
068979848
City
Denton
State
TX
Country
United States
Zip Code
76201
Uphouse, Lynda; Hiegel, Cindy; Martinez, Giovanny et al. (2015) Repeated estradiol benzoate treatment protects against the lordosis-inhibitory effects of restraint and prevents effects of the antiprogestin, RU486. Pharmacol Biochem Behav 137:1-6
Uphouse, Lynda; Pinkston, Jonathan; Baade, Duane et al. (2015) Use of an operant paradigm for the study of antidepressant-induced sexual dysfunction. Behav Pharmacol 26:697-705
Uphouse, Lynda (2015) Dose-dependent effects of the antiprogestin, RU486, on sexual behavior of naturally cycling Fischer rats. Behav Brain Res 282:95-102
Uphouse, Lynda; Hiegel, Cindy (2014) Allopregnanolone's attenuation of the lordosis-inhibiting effects of restraint is blocked by the antiprogestin, CDB-4124. Pharmacol Biochem Behav 122:16-9
Uphouse, Lynda (2014) Pharmacology of serotonin and female sexual behavior. Pharmacol Biochem Behav 121:31-42
Uphouse, Lynda; Hiegel, Cindy; Adams, Sarah et al. (2014) Prior hormonal treatment, but not sexual experience, reduces the negative effects of restraint on female sexual behavior. Behav Brain Res 259:35-40
Uphouse, Lynda; Hiegel, Cindy (2013) An antiprogestin, CDB4124, blocks progesterone's attenuation of the negative effects of a mild stress on sexual behavior. Behav Brain Res 240:21-5
Miryala, Chandra Suma Johnson; Hiegel, Cindy; Uphouse, Lynda (2013) Comparison of female Fischer and Sprague-Dawley rats in the response to ketanserin. Pharmacol Biochem Behav 114-115:52-7
Uphouse, Lynda; Adams, Sarah; Miryala, Chandra Suma Johnson et al. (2013) RU486 blocks effects of allopregnanolone on the response to restraint stress. Pharmacol Biochem Behav 103:568-72
Miryala, Chandra Suma J; Hiegel, Cindy; Uphouse, Lynda (2013) Sprague-Dawley and Fischer female rats differ in acute effects of fluoxetine on sexual behavior. J Sex Med 10:350-61

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