In multiple neuronal populations, growth factors attenuate cell death induced by a variety of insults. Because of the wide range of protective effects of growth factors they are currently being considered as potential therapeutic agents for stroke, amyotrophic lateral sclerosis, Parkinson's disease, and other neurodegenerative conditions. However, to date, and for a variety of reasons, the results of clinical trials using neurotrophic factors have been disappointing. Furthermore, while most in vitro and animal studies have shown protective effects of growth factors against neuronal cell death, there have also been a number of studies showing injury enhancing effects of growth factors. The hypothesis to be tested in this proposal is that, under specific definable conditions, many growth factors will have injury potentiating effects. Preliminary data indicates that while growth factors are consistently protective against insults, which induce apoptotic cell death, they potentiate some forms of necrotic cell death. It follows that to maximize the therapeutic usefulness of growth factors it is necessary to determine the mechanism(s) by which the injury enhancing effects occur. Study of the mechanism(s) of growth factor potentiation of cell death will focus on expanding preliminary results which suggest a role for increased mitochondrial free radical formation, increased calcium influx, and altered neurotransmitter release. Preliminary studies have focused on the effects of brain derived neurotrophic factor on oxygen-glucose deprivation in cortical cultures. Proposed experiments will use neuronal cultures prepared from selected brain regions, and with specific growth factors, each chosen because of known mechanisms of cell death and relevance to disease conditions. It is believed that these studies will aid in determining under what conditions growth factor induced potentiation of cell death may be of concern regarding their therapeutic use, and how those concerns may be addressed.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
1R01AG016708-01A2
Application #
6196788
Study Section
Special Emphasis Panel (ZRG1-BDCN-3 (01))
Program Officer
Wise, Bradley C
Project Start
2000-08-01
Project End
2005-06-30
Budget Start
2000-08-01
Budget End
2001-06-30
Support Year
1
Fiscal Year
2000
Total Cost
$204,000
Indirect Cost
Name
Marquette University
Department
Other Basic Sciences
Type
Schools of Allied Health Profes
DUNS #
046929621
City
Milwaukee
State
WI
Country
United States
Zip Code
53201
Lobner, Doug; Liot, Geraldine (2004) Role of MAPK/ERK in neurotrophin-4 potentiation of necrotic neuronal death. Neurochem Res 29:2303-9
David, Alexis; Lobner, Doug (2004) In vitro cytotoxicity of orthodontic archwires in cortical cell cultures. Eur J Orthod 26:421-6
Hanson, Mark; Lobner, Doug (2004) In vitro neuronal cytotoxicity of latex and nonlatex orthodontic elastics. Am J Orthod Dentofacial Orthop 126:65-70
Lobner, Doug; Golner, Susan; Hjelmhaug, Julie (2003) Neurotrophic factor effects on oxidative stress-induced neuronal death. Neurochem Res 28:749-56
Asrari, Mahshid; Lobner, Doug (2003) In vitro neurotoxic evaluation of root-end-filling materials. J Endod 29:743-6
Lobner, D; Asrari, M (2003) Neurotoxicity of dental amalgam is mediated by zinc. J Dent Res 82:243-6
Lobner, Doug (2002) Saturation of neuroprotective effects of adenosine in cortical culture. Neuroreport 13:2075-8
Lobner, Doug; Ali, Carine (2002) Mechanisms of bFGF and NT-4 potentiation of necrotic neuronal death. Brain Res 954:42-50