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        <identifier>oai:www.ideals.illinois.edu:2142/30933</identifier>
        <datestamp>2023-07-10</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_11614</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:subject>Cognition</dc:subject>
          <dc:subject>Medroxyprogesterone Acetate</dc:subject>
          <dc:contributor>Juraska, Janice M.</dc:contributor>
          <dc:contributor>Juraska, Janice M.</dc:contributor>
          <dc:contributor>Schantz, Susan L.</dc:contributor>
          <dc:contributor>Roy, Edward J.</dc:contributor>
          <dc:contributor>Galvez, Roberto</dc:contributor>
          <dc:contributor>Mahoney, Megan M.</dc:contributor>
          <dc:creator>Chisholm, Nioka</dc:creator>
          <dc:date>2012-05-22T00:16:22Z</dc:date>
          <dc:date>2012-05-22T00:16:22Z</dc:date>
          <dc:date>2012-05</dc:date>
          <dc:date>2012-05-22T00:16:22Z</dc:date>
          <dc:date>2012-05</dc:date>
          <dc:description>Although previous research has indicated that hormone replacement therapy benefits memory in
menopausal women, several newer studies have shown no effect or detrimental effects. These
inconsistencies emphasize the need to evaluate the role of hormones in protecting against agerelated
cognitive decline in an animal model. Furthermore, research has found that ovarian
hormones alter brain structure and function. However, many studies evaluating the effects of
estrogen and progesterone on brain structure have used young adult animals and have not
administered medroxyprogesterone acetate (MPA), the most commonly prescribed progestin.
The aging brain may respond differently to the presence of these hormones. Therefore, the
effects of long-term hormone treatment during aging on cognition and neuroanatomy were
investigated. Female Long Evans hooded rats were ovariectomized at middle age (12-14 months)
and placed in one of 5 groups: no replacement, chronic estrogen only, chronic estrogen and
progesterone, chronic estrogen and MPA, and cyclic estrogen. Hormone treatment continued
until sacrifice. Estrogen was administered in the drinking water. Progesterone and MPA were
administered with subcutaneous pellets. Following five months of hormone replacement, animals
were tested on a delayed alternation task in the T-maze. Two weeks after completing the T-maze
animals were tested in the Morris water maze. At approximately 20 months of age, animals were
sacrificed and their brains were sectioned and using immunohistochemistry, stained for tyrosine
hydroxylase and synaptophysin. Adjacent sections were Nissl stained to calculate volume and
quantify neuron number. The medial prefrontal cortex was examined because it is involved in
several cognitive tasks and is known to be sensitive to both aging and ovarian hormones. Using
unbiased stereology and light microscopy, neuron number and synaptophysin labeled boutons
iii
were quantified. Images were acquired of the tyrosine hydroxylase sections using Axiovision
(Zeiss) on a fluorescent microscope and fiber densities were quantified.
Behavioral results found that animals receiving estrogen in combination with MPA acquired the
t-maze faster than no replacement animals, but there were no differences in performance on the
delayed portion of the task. However, on the Morris water maze, animals receiving this hormone
treatment were impaired as compared to other hormone treated groups. Estrogen in combination
with MPA resulted in greater synaptophysin levels in the medial prefrontal cortex. Analysis of
tyrosine hydroxylase fibers found that animals receiving estrogen in combination with MPA
consistently had significantly higher tyrosine hydroxylase pixel densities than no replacement
animals. Hormone treatment did not significantly alter neuron number in the medial prefrontal
cortex.
These results indicate that the effects of long-term hormone treatment are task specific and longterm
hormone treatments alter dopaminergic functioning and synapse number in the medial
prefrontal cortex, providing a possible mechanism by which long-term hormone treatments can
influence cognition. Importantly, these beneficial neural outcomes were observed in groups
receiving estrogen in combination with the controversial progestin, MPA.</dc:description>
          <dc:description>Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2012-04-11T18:49:16Z
Item was in collections:
University of Illinois Theses &amp; Dissertations (ID: 1)
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          <dc:identifier>http://hdl.handle.net/2142/30933</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>Copyright 2012 Nioka Chisholm</dc:rights>
          <dc:subject>Aging</dc:subject>
          <dc:subject>Estrogen</dc:subject>
          <dc:subject>Prefrontal Cortex</dc:subject>
          <dc:subject>hormone Treatment</dc:subject>
          <dc:title>Effects of long-term hormone treatment on cognitive behavior and the structure of the medial prefrontal cortex during aging in female rats</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Psychology</department>
            <departmentCode>1299</departmentCode>
            <discipline>Psychology</discipline>
            <disciplineCode>0338</disciplineCode>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
            <program>PHD:Psychology -UIUC</program>
            <programCode>10KS0338PHD</programCode>
          </degree>
        </thesis>
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