Numerous studies have produced results which indicate that the cell membrane is an important site of cell damage from ionizing irradiation. The cell membranes are a major target for radiation induced free radicals. Development of effective therapeutic strategies to treat ionizing radiation injuries (""""""""radiation burns"""""""") continues to be an important medical research objective. Most radioprotectant strategies are based on free radical scavengers which are effective if administered before the exposure. We have found that poloxamer 188, a biocompatible non-ionic surfactant, applied ten minutes after radiation exposure induces sealing of membranes permeabilized by intense gamma irradiation (appendix I). In addition, we have demonstrated that poloxaner 188 and similar molecules, are capable of sealing electroporated and thermally permeabilized cell plasma membranes, resulting in restoration of cell viability (appendices ll & III). We propose to quantify the dose response relationship between gamma irradiation exposure and altered plasma membrane transport properties; determine the efficacy of selected surfactant agents on membrane and viability after irradiation of isolated adult skeletal muscle fibers; investigate the effects of isolated irradiation membrane sealing on the kinetics of apoptosis and necrosis in proliferating cells; and examine the therapeutic efficacy of these surfactants for prevention of skeletal muscle necrosis in situ. The major goals of this project are to quantitatively describe the effect of irradiation on plasma membrane transport properties and determine if surfactant based cell membrane repair strategies can be effective in preventing tissue necrosis following toxic level exposure to ionizing irradiation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM053113-03
Application #
2459658
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1995-08-01
Project End
1999-07-31
Budget Start
1997-08-01
Budget End
1998-07-31
Support Year
3
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Chicago
Department
Surgery
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Soneru, Alexander P; Beckett, Michael A; Weichselbaum, Ralph R et al. (2011) Mg ATP and antioxidants augment the radioprotective effect of surfactant copolymers. Health Phys 101:731-8
Matthews 2nd, Kenneth L; Aarsvold, John N; Mintzer, Robert A et al. (2006) Tc-99m pyrophosphate imaging of poloxamer-treated electroporated skeletal muscle in an in vivo rat model. Burns 32:755-64
Greenebaum, Ben; Blossfield, Katie; Hannig, Jurgen et al. (2004) Poloxamer 188 prevents acute necrosis of adult skeletal muscle cells following high-dose irradiation. Burns 30:539-47
Bier, Martin; Chen, Wei; Gowrishankar, T R et al. (2002) Resealing dynamics of a cell membrane after electroporation. Phys Rev E Stat Nonlin Soft Matter Phys 66:062905
Maskarinec, Stacey A; Hannig, Jurgen; Lee, Raphael C et al. (2002) Direct observation of poloxamer 188 insertion into lipid monolayers. Biophys J 82:1453-9
Lee, R C; Zhang, D; Hannig, J (2000) Biophysical injury mechanisms in electrical shock trauma. Annu Rev Biomed Eng 2:477-509
Hannig, J; Zhang, D; Canaday, D J et al. (2000) Surfactant sealing of membranes permeabilized by ionizing radiation. Radiat Res 154:171-7
Terry, M A; Hannig, J; Carrillo, C S et al. (1999) Oxidative cell membrane alteration. Evidence for surfactant-mediated sealing. Ann N Y Acad Sci 888:274-84
Hannig, J; Yu, J; Beckett, M et al. (1999) Poloxamine 1107 sealing of radiopermeabilized erythrocyte membranes. Int J Radiat Biol 75:379-85
Lee, R C (1997) Injury by electrical forces: pathophysiology, manifestations, and therapy. Curr Probl Surg 34:677-764

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