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Jeannette Vasquez Vivar, PhD
Professor; Vice Chair for Research in Biophysics; Associate Director, Redox Biology Program
Locations
- Biophysics
MFRC 6049
Contact Information
Education
Postdoctoral Fellow in Biochemistry, Instituto de Química, Universidade de São Paulo, Brazil, 1993-1996
PhD, Biochemistry, Universidade de São Paulo, Brazil, 1992
BS, Clinical Biochemistry, Universidad de Concepción Chile, 1988
BS, Biochemistry, Universidad de Concepción Chile, 1986
Biography
As a postdoctoral fellow, I investigated kinetics and mechanisms of free radical formation from reactions involving peroxynitrite and biomolecules, and later I discovered the role of tetrahydrobiopterin in the regulation of superoxide release from nitric oxide synthase. In 1998, I became a faculty member in the Department of Pathology at MCW, studying the endothelial nitric oxide synthase uncoupling in endothelial dysfunction. In 2001, I joined the faculty of the Department of Biophysics at MCW, where I continue my work on redox mechanisms of cardiovascular and fetal brain dysfunction.
Research Experience
- Antioxidants
- Arginine
- Ascorbic Acid
- Biomarkers
- Biopterin
- Blotting, Western
- Cerebral Palsy
- Electron Spin Resonance Spectroscopy
- Endothelial Cells
- Ethidium
- Free Radicals
- Free Radicals, Electron Paramagnetic Resonance Spin Trapping
Methodologies and Techniques
- Brain Diseases, Metabolic, Inborn
- Cells, Cultured
- Electron Spin Resonance Spectroscopy
- Energy Metabolism
- Fluorescent Dyes
- Folic Acid Antagonists
- HPLC, chromatography electrochemical, UV and fluorescence detection (Pterins, Neurotransmitters, Glutathione, 2-Hydroxyethidium)
- Kinetics
- NADP
- Oxygen Consumption
- Reactive Oxygen Species
- Spin Trapping
Leadership Positions
- Associate Director, Redox Biology Program
MCW Program / Core Facilities
- Redox Biology
Research Interests
My lab investigates cell-specific redox mechanisms disrupting normal cellular homeostasis. We focus on three different systems: fetal brain, heart, and endothelial cells. My research is supported by the National Institutes of Health.
Research Projects
Our project dealing with the fetal brain is supported by our discovery that a developmentally low tetrahydrobiopterin (BH4) cofactor in the fetal brain increases hypoxia-ischemia injury in specific brain regions and worsens motor disabilities in newborns. Our working hypothesis is that development of motor deficits can be explained by a two-hit model where transient low tetrahydrobiopterin represents an important vulnerability state of immature fetal brain neurons. In collaboration with the group of Dr. Tan (Wayne State University), we are testing the idea that BH4 is a critical neuronal developmental factor.
Our BH4 effects in cardiovascular health project examines the relationship between endothelial dysfunction and eNOS uncoupling in an animal model of atherosclerosis. While eNOS dysfunction is believed to be an important element promoting vascular dysfunction, it is yet unclear whether eNOS uncoupling controls a state of critical oxidant stress to promote disease. In this project we are examining the impact of BH4 in redox that could further support therapeutic effects in hypercholesterolemia. A second approach is to understand the role of BH4 in cardiomyocyte redox changes that could link BH4 deficiency with loss of function as could occur in heart failure.
Lab Members
James Woodcock, Research Technologist I