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NASA Scientific and Technical Aerospace Reports

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meeting or exceeding their caloric intake goals. In conclusion, we are making good progress toward completion of this study.<br />

DTIC<br />

Aerobes; Circulation; Diets; Estrogens; Exercise Physiology; Females; Menstruation; Physical Exercise<br />

20040073768 Wright State Univ., Dayton, OH<br />

Low Level Chemical Toxicity: Relevance to Chemical Agent Defense<br />

Morris, Mariana; Jul. 2003; 134 pp.; In English<br />

Contract(s)/Grant(s): DAMD17-00-C-0020<br />

Report No.(s): AD-A422716; No Copyright; Avail: CASI; A07, Hardcopy<br />

A multidisciplinary project is underway to study the influence of low-level exposure to chemicals to which military<br />

personnel had contact during the Persian Gulf War. The research group includes investigator with expertise in neuroscience,<br />

molecular biology, enzymology, cardiovascular physiology <strong>and</strong> neuropharmacology. The overall objectives is to study the<br />

effect of chemical exposure from the single cell/gene level to the whole animal <strong>and</strong> ending with the human condition. Results<br />

include but are not limited to: proteomic changes have been identified that are different between pyridostigmine bromide <strong>and</strong><br />

physostigmine; spectral analysis has showed dramatic alterations in heart rate variability <strong>and</strong> baroreflex index in mice<br />

challenged with stress <strong>and</strong>/or pyridostigmine; sarin <strong>and</strong> noise stress <strong>and</strong> also pyridostigmine bromide <strong>and</strong> DEET with noise<br />

stress induce significant decreases in electron transfer rates compared to noise stress alone, factors have been identified which<br />

will increase the reliability of correlations between enzymatic analyses <strong>and</strong> abnormal or disease states; modest gene expression<br />

changes have been determined using Mann-Whitney tests after eliminating those genes with expression levels that appear to<br />

represent inactive genes.<br />

DTIC<br />

Chemical Defense; Chemical Warfare<br />

20040073772 Minnesota Univ., Minneapolis, MN<br />

Metabolizing Enzyme 1 Polymorphisms <strong>and</strong> Prognosis Among Women Treated with Breast Cancer<br />

Sweeney, Carol; Oct. 2003; 7 pp.; In English<br />

Contract(s)/Grant(s): DAMD17-01-1-0128<br />

Report No.(s): AD-A422722; No Copyright; Avail: CASI; A02, Hardcopy<br />

This study will use archived tissue <strong>and</strong> data to examine survival of women treated for breast cancer in relation to inherited<br />

polymorphisms of drug metabolizing enzymes. During year 1, we completed compilation of tumor registry data for eligible<br />

subjects (Task 1 of the approved Statement of Work) <strong>and</strong> study start-up tasks, including IRB review, hiring study staff, creating<br />

data collection forms, establishing a study database, <strong>and</strong> training study staff on data collection procedures. Collection of tissue<br />

samples (Task 2 of the approved Statement of Work) has proceeded during year 2, including obtaining pathology slides <strong>and</strong><br />

blocks, review of slides by the study pathologist, <strong>and</strong> abstracting information from pathology reports into the study database.<br />

As described in the statement of work, data collection tasks will continue into years 2 <strong>and</strong> 3, 50 no reportable scientific results<br />

are available at the end of year 2.<br />

DTIC<br />

Cancer; Enzymes; Females; Mammary Gl<strong>and</strong>s; Metabolism; Polymorphism; Prognosis; Tissues (Biology)<br />

20040073784 Virginia Univ., Charlottesville, VA<br />

Increasing Oxygen Consumption During Shock<br />

Gainer, John L.; May 4, 2004; 9 pp.; In English<br />

Contract(s)/Grant(s): N00014-95-1-0213<br />

Report No.(s): AD-A422762; No Copyright; Avail: CASI; A02, Hardcopy<br />

Whole-body oxygen consumption is decreased after hemorrhage. Typical methods for increasing oxygen consumption<br />

have involved increasing the blood oxygen concentration using enriched oxygen gases, hemoglobins <strong>and</strong> fluorocarbon<br />

compounds; however, clinical trials involving these have not been totally successful. Increasing the oxygen concentration<br />

increases its diffusion rate through blood plasma; however, an alternative method would be to increase the diffusion coefficient<br />

of oxygen itself. This was shown to be possible using a naturally- occurring compound called crocetin. Crocetin also increased<br />

whole-body oxygen consumption in hemorrhaged rats <strong>and</strong> resulted in an increased survival rate. However, this occurred over<br />

a relatively small concentration range. Thus, trans sodium crocetinate (TSC) was developed, which also increases oxygen<br />

consumption in rats after hemorrhage <strong>and</strong> increases survival. TSC has also been shown to increase blood pressure <strong>and</strong> to<br />

172

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