Martin Bienengraeber, PhD
Associate Professor of Anesthesiology, Pharmacology and Toxicology
Medical College of Wisconsin
8701 Watertown Plank Road
Milwaukee, WI 53226-0509
(414) 955-5690 | (414) 955-6507 (fax) | firstname.lastname@example.org
Mitochondria constitute the core of cellular energy metabolism as the site of the greatest ATP production. In addition, they play an important role in regulating ionic homeostasis of the cell. It has been suggested that mitochondrial dysfunction may be the major cause for tissue injury during cardiac ischemia and reperfusion. On the other hand, they present a valuable target for triggering protective mechanisms. Exposure of the heart to volatile anesthetics like isoflurane before or after an ischemic event helps to maintain cellular and mitochondrial function in the whole heart, in cardiomyocytes and in isolated mitochondria.
One of my research interests revolves around the role of mitochondria as triggers and effectors in protection of the heart from ischemia and stress. We use physiological, pharmacological and molecular techniques as well as proteomics to demonstrate quantifiable alterations in mitochondrial bioenergetics and protein expression during or after exposure to volatile anesthetics. We plan to apply our findings to target potentially protective proteins to mitochondria by overexpression, thereby increasing the cardiomyocytes' resistance against oxidative stress.
In other ongoing or just starting projects, we study the impact of near infrared light (670 nm) on the heart and mitochondria after ischemia. Exposure of the ischemic heart with this light at the time of reperfusion turns out to be protective, and mitochondria may play a crucial role in the mechanism behind this phenomenon. Projects are performed in collaboration with investigators from the Anesthesiology, the Pharmacology and Toxicology and the Physiology departments.