Androgen Modulation of Neurodegeneration in Dopamine Neurons

Project Details

Description

PROBLEM: Parkinson's disease (PD) has a higher prevalence in the human male population. PD is
characterized by motor dysfunction, rigidity, and bradykinesia. Current research suggests that gender plays
a role in this condition, since males have a greater incidence of PD. It is believed that the underlying
mechanism of PD involves oxidative stress leading to cellular apoptosis. In many peripheral cells and some
neuronal cells, androgens have been shown to increase apoptosis. PURPOSE: The goal of these studies is
to determine androgen's effects on dopaminergic cells following oxidative stress by using both in vitro and in
vivo methods. The central hypothesis of this proposal is that androgens increase cellular vulnerability to
oxidative stress-induced neurotoxicity in dopaminergic neurons. RESEARCH QUESTIONS: The first specific
aim of this proposal is to determine the apoptotic signaling pathways activated by androgens in
dopaminergic N27 cells following oxidative stress (hydrogen peroxide). The second specific aim is designed
to evaluate the effects of androgens on estrogen-mediated neuroprotection in dopaminergic N27 neurons
following oxidative stress. These aims will be accomplished through in vitro molecular studies with and
without the presence of astroglia cells and the androgen receptor antagonist, hydroxyflutamide. Lastly, the
third specific aim will characterize the in vivo effects of androgens on tyrosine hydroxylaseexpression,
neuronal death, and motor behavior in aged male rats exposed to 6-OHDA, which induces oxidative stress
and apoptosis in the substantia nigra and striatum. In vivo hormone treatment groups will consist of
gonadectomized aged males, gonadally intact aged males, and gonadectomized aged males plus
replacement androgen (testosterone or dihydrotestosterone) for either a chronic (3 months) or acute (1
week) treatment time length prior to 6-OHDA lesion. Immunocytochemical and behavioral techniques will be
used to accomplish this aim. OUTCOMES: This study will provide basic knowledge on how androgens
modulate dopaminergic cellular vulnerability to oxidative stress. Ultimately, this knowledge can be used to
provide a foundation to understanding the mechanisms underlying sex differences in neurodegenerative
disorders.
PHS 416-1 (Rev. 10/05) Page 2 Number pages consecutively at the bottom throughout Form Page 2
the application. Do not use suffixes such as 2a, 2b
NAME OF APPLICANT (Last, first, middle initial)
Kirschstein-NRSA Individual Fellowship Application
Cunningham, Rebecca, L.
(To be completed by applicant- follow PHS416-1 instructions)
20. GOALS FOR KIRSCHSTEIN-NRSA FELLOWSHIP TRAINING AND CAREER
The training goals of this fellowship include learning scientific approach, troubleshooting, manuscript
preparation, and presentation skills. I believe these goals are critical in maturing as a scientist. As a
researcher it is of utmost importance to have the ability to not only design and perform an experiment, but to
also have the ability to troubleshoot potential problems. The experiments contained within this proposal have
been chosen for their ability to test the hypothesis and extend my knowledge in androgen's mechanisms of
action by utilizing different experimental techniques and model systems. As a researcher it is imperative to
answer "the question." By having a broad knowledge of the tools and techniques available in the scientific
community, the reliability of the data obtained is improved. The skills I wish to acquire while undertaking this
proposal include Western blot analysis, immunocytochemistry, motor behavior analysis, and stereotaxic
surgery. In addition, I wish to expand my knowledge of behavioral studies into the neurodegenerative field of
study and determine what impact androgens have on neurodegeneration.
21. ACTIVITIES PLANNED UNDER THIS AWARD:
instructions.)
Year Research
First 80%
Second 90%
Third 90%
Fourth
Fifth
Approximate percentage of proposed award time in activities identified below. (See
Course Work Teaching Clinical
20% 0% 0%
10% 0% 0%
10% 0% 0%
PREDOCTORAL FELLOWSHIPS ONLY
MD/PhD FELLOWSHIPS ONLY
Sixth
Briefly explain activities other than research and relate them to the proposed research training.
The applicant will participate in several workshops offered by UTHSCSA that include grant and manuscript
writing courses. The applicant has been and plans to continue participating in the weekly department
seminars and journal clubs to expand her knowledge beyond her field of expertise. During the first year of
the fellowship the applicant will take a 1 semester course on Biology of Aging, which is offered by the
Department of Pharmacology.
22. TRAINING SITE(S) (organization, city, state)
University of Texas Health Science Center-San Antonio, Texas
23. HUMAN EMBRYONIC STEM CELLS Kl No Q Yes
If the proposed project involves human embryonic stem cells, list below the registration number of the specific cell line(s) from the following list:
http://stemcells.nih.qov/reqistrv/index.asp. Use continuation pages as needed.
If a specific line cannot be referenced at this time, include a statement that one from the Registry will be used.
Cell Line
PHS 416-1 (Rev. 10/05) Page 3 Form Page 3
Kirschstein-NRSA Individual Fellowship Application NAME OF APPLICANT (Last, first, middle initial)
Table of Contents Cunningham, Rebecca, L.
Page Numbers
(Number pages consecutively at the
_ _ bottom throughout the application.
Section 1 - Applicant Do not use suffixes such as6a, 6b.)
Face Page 1
Sponsor's Contact Information, Description (Form Page 2) 2
Training &Career Goals, Activities Planned Under This Award, Training Site, Human
Embryonic Stem Cells (Form Page 3) 3
Table of Contents (Form Page 4) 4
Biographical Sketch - Applicant/Fellow (Not toexceed four pages) 5-6
Previous Research Experience (Form Page 5) 7-9
Research Training Plan
Introduction to Revised Application (not to exceed 1page)
A. Specific Aims TV. ^ 10
B. Background/Significance !(......(Not to exceed 10pages) J 11
C. Preliminary Studies/Progress Report ../T | 12
D. Research Design andMethods ).. ^ 13
E. Human Subjects (Required if Item 9 on the Face Page is marked "Yes") 20
Protection of Human Subjects (Required if Item 9 on the Face Page is marked "Yes") -
Data and Safety Monitoring Plan (Required if Item 9 on the Face Page is marked "Yes"
and a Phase I, II, or III clinical trial is proposed -
Inclusion of Women and Minorities (Required if Item 9 on the Face Page is marked "Yes"
and is Clinical Research) -
Targeted/Planned Enrollment Table (for new and continuing clinical research studies) -
Inclusion of Children (Required if Item 9 on the Face Page is marked "Yes") -
F. Vertebrate Animals (Required if Item 10on the Face Page is marked "Yes") 20
G. Literature Cited 20
H. Resource Sharing 24
I. Respective Contributions 24
J. Selection of Sponsor and Institution 24
K. Responsible Conduct of Research 24
Section 2 - Sponsor's/Co-Sponsor's Information
Biographical Sketch-Sponsor 25
Research Support Available 29
Previous Trainees 31
Training Plan, Environment, Research Facilities 31
Number of Fellows/Trainees to be Supervised 32
Applicant's Qualifications and Potential 32
Checklist (Completed by Fellow/Applicant &Sponsoring Institution) 33
Section 3 - References (Minimum of 3)
(See instructions for submission of references.)
List full name, institution, and department of individuals submitting reference letters.
1) Marilyn Y. McGinnis, Ph.D., UTHSCSA, Pharmacology 2) William P. Clarke, Ph.D., UTHSCSA,
Pharmacology 3) J. Randy Strong, Ph.D., UTHSCSA, Pharmacology
Other Items (list):
Personal Data Page for Fellowship Applicants
Section 4 - Appendix
(5 collated sets. Nopage numbering necessary. Not to exceed 3 publications;2 for predoctoral candidates.)
E3 Check if Appendix is included
PHS 416-1 (Rev. 10/05) Page 4 Form Page 4
StatusFinished
Effective start/end date1/03/0828/02/11

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