Christopher Pawela, PhD
Assistant Professor of Anesthesiology, Biomedical Engineering, and Biophysics
Christopher Pawela, PhD
Department of Anesthesiology
Medical College of Wisconsin
8701 Watertown Plank Road
Milwaukee, WI 53226
(414) 955-5626 office
(414) 955-6507 fax
Faculty Collaboration Database Profile
Dr. Pawela received his BS degree in Bacteriology and MS degree in Chemistry from the University of Wisconsin. In 2008, he was awarded a PhD in Biophysics from the Medical College of Wisconsin. He joined the MCW faculty immediately upon graduation and joined the Department of Anesthesiology in 2015. Dr. Pawela has a secondary appointment in the MCW Department of Biophysics. His research interests are in the areas of neurovascular coupling, brain connectivity, neural plasticity and cerebrovascular structure/function. Dr. Pawela is the founding co-editor-in-chief of the scientific journal, Brain Connectivity, and is the chair of the executive committee for the Society for Brain Connectivity which organizes a biennial scientific conference.
- BS, Microbiology, University of Wisconsin - Madison
- MS, Chemistry, University of Wisconsin - Madison
- PhD, Biophysics, Medical College of Wisconsin
- Brain connectivity
- Neural plasticity
- Cerebrovascular structure and function
- Neurovascular coupling
My laboratory focuses on identifying reorganizational changes in brain associated with injury and disease. Our expertise is in magnetic resonance imaging (MRI) methodologies. However, we also use other modalities such as electrophysiology, optical coherence tomography (OCT), laser Doppler, animal behavior testing, and optogenetics to complement our MRI results. Our projects are generally initiated in a preclinical animal model with possible concurrent studies in human subjects. I am the founding co-editor-in-chief of the scientific journal, Brain Connectivity, and I am also on the executive committee for the Society for Brain Connectivity which organizes a biennial scientific conference. There are three ongoing projects in my laboratory.
Hypertension and Neurovascular Coupling
My laboratory is funded through an NIH grant titled: “FMRI studies of cerebrovascular structure and function in low-renin hypertension.” Chronic hypertension causes reduced vascular function, reduced blood flow, damaged cerebral autoregulation, and is a known risk factor for ischemic stroke and vascular-associated cognitive decline. Blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) is sensitive to changes in cerebrovascular hemodynamic function. Preliminary rodent fMRI data demonstrate a diminished cerebrovascular BOLD hyperemic response to sensory stimulation in salt-induced hypertensive Dahl Salt-Sensitive (SS) rats, a widely-used animal model of low-renin hypertension. Clinically, salt-induced low-renin hypertension accounts for 25% of all essential hypertensive patients, but 75% in African Americans.
Our data suggests that neurovascular coupling is impaired in low-renin salt-induced hypertension. Mechanistically, we hypothesize that salt-sensitive hypertension leads to vessel endothelium dysfunction through damage by oxidative stress. Free radicals reduce the bioavailability of nitric oxide, a key factor in neurovascular coupling. Our research has three goals: 1) Characterize the neurovascular uncoupling in salt-induced hypertension. 2) Define the sensitivity and selectivity of the brain BOLD fMRI signal to chronic hypertension. 3) Determine the influence of the SS Renin gene allele on phenotypic differences in the BOLD signal in salt-induced hypertension. This collaborative project includes investigators in the MCW Physiology Department.
Brain Reorganization following Peripheral Nerve Injury
This project is funded through a VA grant titled: “Persisting functional CNS changes following peripheral nerve repair” and is a cooperative effort with my MCW Anesthesiology colleague, Dr. Quinn Hogan MD. Peripheral nerve injuries are a common consequence of trauma and often result in a poor prognosis with complications such as abnormal sensation, motor function loss, pain, and depression. Our laboratory and others have shown that brain reorganization occurs immediately after a nerve is damaged or transected.
The reorganizational process (or neuroplasticity) post-injury/repair is dynamic and persists even after surgical repair and a subsequent recovery period. We hypothesize that a portion of the neuroplasticity following injury is maladaptive and accounts for some of the individual variability in outcomes post-repair within the same nerve(s)/level of injury. Our laboratory is developing methods to track brain reorganization post-injury/repair and strategies to target this process therapeutically. Our overall goal is to improve outcomes for these debilitating injuries where few new treatment strategies have been introduced clinically in the last 40 years.
Brain Connectivity Mechanisms
The biological mechanism(s) that generate the BOLD fMRI signal and drive BOLD signal low-frequency fluctuations leading to correlations between brain regions is unclear after many years of scholarship. FMRI methodologies are being explored as biomarkers of neurological and psychiatric diseases and the number of studies using these techniques is growing exponentially. Understanding the nature of these signals is key to the utility of these imaging methods as potential biomarkers. My laboratory is carrying out fundamental studies in preclinical animal models using multi-modal imaging techniques to explore the BOLD fMRI signal mechanism. We are using evolving methods such as optogenetics and concurrent MR/electrophysiology experiments to study neurovascular coupling at high spatial and temporal resolution. Our goal is to discover essential knowledge about the BOLD fMRI signal which will lead to further refinement of the imaging methodology and enhance stability with clinical application of fMRI as a potential biomarker for neurological and psychiatric diseases.