Assistant Professor, Biological Sciences
Cardiovascular disease is the leading cause of death in Americans. Even with successful resuscitation, long-term survivorship following cardiac arrest is poor. To date, no definitive treatment for the ischemia associated with stroke or cardiac arrest is available. The purpose of this study is to demonstrate the utility of a novel model for ischemia tolerance- the mammalian hibernator. Each winter season, hibernators likely experience approximately 15 natural periods of ischemia as they enter each torpor cycle.
Research
indicates that hibernators are inherently more tolerant to ischemia than are rats. The
comparison of mechanisms employed by hibernators to resist the effects of ischemia with
mechanisms implicated in ischemic injury incurred in rats may allow for the future
development of targeted therapies to promote survivorship in humans. In this study,
we will better define the onset, extent and duration of the ischemic insult in the context
of the natural rhythms of the hibernator as well as develop a manipulatable model for the
induction of ischemia that allows for direct comparison of responses in the ground squirrel
to those of the rat. Ultimately, this model will be utilized in the development of an NIH
RO1-sustainable program to identify the mechanisms of ischemia tolerance for later application
in human medicine.
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Progress report: Frank van Breukelen


