SINTN Stanford Institute for Neuro-Innovation & Translational Neurosciences
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Rona Giffard

Academic Appointments

Key Documents

Contact Information

  • Academic Offices
    Personal Information
    Email Tel (650) 725-8482
    Alternate Contact
    William Magruder Research Administrator Tel Work (650) 725-5875

Professional Overview

Administrative Appointments

  • Vice-Chair for Research, Dept. of Anesthesia (1999 - present)

Honors and Awards

  • NIH Clinical Investigator Award, NIH (1990-1995)
  • Young Investigator Award, Foundation for Anesthesia Education and Research (1991-1992)
  • Ellen Weaver Award, Association for Women in Science, Northern California Chapters (1997)
  • Frontiers in Anesthesia Research Award, International Anesthesia Research Society (1998-2003)
  • AHA/Bugher Award, American Heart Association (2000-2004)
View all 6honors and awards of Rona Giffard

Professional Education

Ph.D.: Stanford University, Structural Biology
M.D.: Stanford University, Medicine

Postdoctoral Advisees

Robin WhiteXiaoxing Xiong

Scientific Focus

Current Research Interests

Brain injury from stroke, head trauma, and chronic neurologic degenerative diseases, is a major cause of morbidity and mortality. We are particularly interested in the cellular consequences of brain injury. To study this problem we work with primary cultures of neurons and astrocytes from mice in addition to employing rodent models of stroke. Current work focuses on: 1) the role of astrocytes in brain injury; 2) the interaction of neurons and glia during injury; 3) protection using heat shock protein and other protective proteins 4) changes in mitochondrial function and signaling in injury and ways to protect mitochondria; 5) the interaction of oxidative stress and inflammation in stroke; 6) computational modeling of cell death.

We use gene transfer techniques to express genes of interest in brain cells and intact brain and analyze ways in which these genes can provide protection. We use fluorescent probes for pH, intracellular calcium, ROS, mitochondrial membrane potential, glutathione, as well as morphologically evaluate outcome, and quantitate injury. We also use transgenic mice to analyze the effects of overexpression or loss of expression of specific genes on outcome from stroke. Mitochondria are central to both energy metabolism and the regulation of cell death. We study changes in mitochondria with stress. We are also interested in the interaction of oxidative stress and inflammation in stroke.

A new area for us is computational modeling of cell death and the effects of heat shock proteins. We are working on an ODE control model.

Publications

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