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Vascular Medicine Institute
University of Pittsburgh
BST E1240
200 Lothrop Street
Pittsburgh, PA 15261
Phone: 412-383-5853
Fax: 412-648-5980

Christopher P. O'Donnell, PhD

 

chris odonnell

 

Chris O'Donnell, PhD

Executive Vice Chair for Academic Affairs, Department of Medicine

Professor of Medicine,
Division of Pulmonary, Allergy and Critical Care Medicine

E1152 BST
200 Lothrop Street
Pittsburgh, PA 15261

Phone: 412-648-9379
Email: odonnellcp@upmc.edu

   

Bio

Dr. O’Donnell received his undergraduate training at the University of Otago, New Zealand, graduating with First Class Honors in Physiology in 1984.  He was awarded a Commonwealth Scholarship for graduate training at the University of Cambridge, England, where he completed his Ph.D. in Physiology in 1988.  Dr. O’Donnell received an American Heart Association Fellowship to pursue post-doctoral training in the Physiology Department of the University of California, San Francisco from 1988-1991.   His first faculty appointment was at Johns Hopkins Medical School in 1991, where he was promoted from Instructor through to Associate Professor before leaving to join the University of Pittsburgh in July, 2004.  He is currently a tenured Professor in the Division of  Pulmonary, Allergy, and Critical Care Medicine (PACCM) as well as Professor of Cell Biology and Physiology, and has been continuously funded by the NIH since 1996.  He is a past Chairman of the NIH Respiratory Integrative Biology and Translational Research (RIBT) study section and Associate Editor for the journals Obesity and Journal of Applied Physiology.  Dr. O’Donnell plays a leading role in career development activities in PACCM, the Vascular Medicine Institute, and Cardiology, and is Co-Director on three T32s.

Academic and Research Interests

Dr. O’Donnell’s interests are in the pathophysiology of hypoxia and sleep apnea and its relationship to metabolic and cardiovascular dysfunction. His laboratory utilizes murine models of obesity and hypoxia using a variety of chronically instrumented inbred and transgenic mouse strains. In respiratory studies, he has established in the genetically obese ob/ob mouse that leptin deficiency leads to respiratory depression, and that leptin replacement can correct this respiratory depression independent of weight, food intake or metabolism. In metabolic studies, he has demonstrated that lean mice can exhibit insulin resistance and hyperlipidemia during exposure to intermittent hypoxia (simulating sleep apnea) as well as leading to a compensatory increase in pancreatic beta cell replication.  More recently he has shown that long-term exposure to sustained hypoxia (simulating altitude) can lead to compensatory increases in insulin sensitivity.  In cardiovascular studies, Dr. O’Donnell and colleagues have studied the impact of heart failure on disruption of sleep architecture, and examined how the upregulation of cardiac leptin signaling plays a crucial role in reducing morbidity and mortality in response to myocardial ischemia.  Finally, in collaboration with Dr. Bryan McVerry, Dr. O’Donnell is studying the mechanisms underlying the development of hyperglycemia in critical illness.

Figure 1

Figure 2

Dr. O’Donnell has developed the ability to record sleep (polysomongraphy) in mice and to score the sleep in real-time using the computer-generated algorithms shown above.  Using this real-time sleep assessment it is possible to expose mice to hypoxia only during sleep and restore the animals to normal room air breathing when they arouse or wake from sleep in response to the hypoxia.  As a result he can specifically model the sleep-induced hypoxia that occurs in patients experiencing obstructive sleep apnea, which is characterized by repetitive periods of airway obstruction and intermittent hypoxia during sleep.


We have developed techniques to perform the frequently sampled intravenous glucose tolerance test (FSIVGTT) in conscious unrestrained mice. After a rapid bolus of 1 g/kg of 50% dextrose, arterial blood samples are taken as rapidly as one minute intervals to measure blood glucose and plasma insulin.  The resulting glucose and insulin decay curves are mathematically modeled to give estimates of insulin sensitivity, non-insulin mediated glucose uptake, and insulin secretion.  We have validated the insulin sensitivity (Si) determined by the FSIVGTT with insulin sensitivity determined by the gold standard hyperinsulinemic euglycemic clamp in both lean mice (normal insulin sensitivity) and mice with diet-induced obesity (DIO; with impaired insulin sensitivity).
Figure 3

Chronic exposure to hyperglycemia is known to lead to a compensatory increase in pancreatic beta cell replication; a response can elevate circulating insulin levels and potentially lower blood glucose.  Dr. O’Donnell and colleagues in the Division of Endocrinology and Metabolism have now shown that exposure to intermittent hypoxia (IH) can also produce pancreatic beta cell replication at a rate comparable to hyperglycemia, but the combination of glucose and IH (Glu + IH) was no more effective than either hyperglycemia or hypoxia alone.  Since apoptosis (TUNEL (+) beta cells) was minimal during hypoxia it was concluded that IH leads to a compensatory increase in beta cell replication that mimics hyperglycemia.  This finding is somewhat counterintuitive to endocrinologists who make every effort to avoid hypoxic exposure of beta cells being prepared for transplantation into diabetic patients.  The O’Donnell laboratory is currently investigating the mechanisms through which IH can cause beta-cell proliferation and whether they share any common pathways with hyperglycemia-induced proliferation.

Figure 4

Leptin is a hormone primarily released from adipose tissue that has multiple systemic effects including suppressing appetite and increasing metabolism.  However, leptin is also produced in many tissues other than the central nervous system, which have their own leptin receptor/signal transduction pathways.  Dr. O’Donnell and colleagues in the Cardiovascular Institute have shown in mouse models of experimentally-induced heart failure that leptin deficiency leads to increased morbidity and mortality and that leptin administration can reverse this pathological phenotype.  Moreover, the experimentally-induced heart failure causes increased production of leptin in cardiac myocytes and the translocation of leptin receptors to the cell membrane of myocytes.  The figure above shows leptin receptors (red) in cardiac myocytes (green nuclei) in patients with heart failure (right panel) and control subjects without heart failure (left panel).  The same pattern of response was seen in human heart failure – activation of leptin signaling pathways in cardiac myocytes – as in the murine model of heart failure.  Dr. O’Donnell and colleagues are currently exploring the hypothesis that leptin may act as a metabolic switch in ischemic cardiac tissue to optimize the fuel source needed to maintain viability of the myocyte.


Key Publications

Davis, E.M., Locke, L.W.,  McDowell, A.L., Strollo, P.J., and O’Donnell, C.P.  Obesity accentuates circadian variability in breathing during sleep in mice, but does not predispose to apnea. Journal of Applied Physiology, 115(4):474-482, 2013.

Lee, E.J., Alonso, L.C., Stefanovski, D., Strollo, H., Romano, L.C., Zuo, B., Singamsetty, S., Yester, K.A., McGaffin, K.R., Garcia-Ocana, A., and O’Donnell, C.P.  Time-dependent changes in glucose and insulin regulation during intermittent hypoxia and continuous hypoxia.  European Journal of Applied Physiology, 113(2):467-78, 2013.

Alonso, L.C., Watanabe, Y., Stefanovski, D., Lee, E.J., Singamsetty, S., Romano, L.C., Zou, B., Garcia-Ocana, A., Bergman, R.N., and O’Donnell, C.P. Simultaneous measurement of insulin sensitivity, insulin secretion and the disposition index in conscious unhandled mice.  Obesity, 20(7):1403-1412, 2012.

McGaffin, K.R., W.G. Witham, K.A. Yester, L.C. Romano, R.M. O’Doherty, C.F. McTiernan, and C.P. O’Donnell. Cardiac specific leptin receptor deletion exacerbates ischemic heart failure in mice Cardiovas. Res. 89(1):60-71, 2011.

Ray, N.B., L. Durairaj, B.B. Chen, B.J. McVerry, A.J. Ryan, M. Donahoe, A.K. Waltenbaugh, , C.P. O'Donnell, F.C. Henderson, C.A. Etscheidt, D.M. McCoy, M. Agassandian, E.C. Hayes-Rowan, T.A. Coon, P.L. Butler, L. S.N. Gakhar, Mathur, J.C. Sieren, Y.Y. Tyurina, , V.E. Kagan, G. McLennan, R.K. Mallampalli. Dynamic regulation of cardiolipin by the lipid pump Atp8b1 determines severity of lung injury in experimental pneumonia.  Nature Medicine. 16(10):1120-1127, 2010.

McGaffin, K.R., C.K. Sun, J.J. Rager, L.C. Romano, B. Zou, M.A. Mathier, R.M. O’Doherty, C.F. McTiernan, C.P. O’Donnell.  Leptin signalling reduces the severity of cardiac dysfunction and remodelling after chronic ischaemic injury. Cardiovas. Res. 77(1):54-63,2008.

Yokoe, T., L.C. Alonso, L.C. Romano, T.C. Rosa, R.M. O’Doherty, A. Garcia-Ocana, K. Minoguchi, and C.P. O'Donnell.  Intermittent hypoxia reverses the diurnal glucose rhythm and causes pancreatic beta cell replication in mice. J. Physiol. 586:899-911, 2008.

Iiyori, N, L.C. Alonso, J. Li, M.H. Sanders, A. Garcia-Ocana, R.M. O’Doherty, V.Y. Polotsky, and C.P. O'Donnell.  Intermittent hypoxia causes insulin resistance in lean mice independent of autonomic activity.  Am. J. Resp. Crit. Care Med. 175:851-857, 2007.

Alonso, L.C., T. Yokoe, P. Zhang, D.K. Scott, S.K. Kim, C.P. O’Donnell, and A. Garcia-Ocana.  Glucose infusion in mice: a new model to induce beta-cell replication.  Diabetes. 56(7):1792-801, 2007.

Raju, S.V, M. Zheng, K.H. Schuleri, A.C. Phan, D. Bedja, R.M. Saraiva, O. Yiginer, K. Vandegaer, K.L. Gabrielson, C.P. O’Donnell, D.E. Berkowitz, L.A. Barouch, J.M. Hare. Activation of the cardiac ciliary neurotrophic factor receptor reverses left ventricular hypertrophy in leptin-deficient and leptin-resistant obesity.  P.N.A.S. 103(11):4222-4227, 2006.

Li, J. L.N. Thorne, N.M. Punjabi, C.K. Sun, A.R. Schwartz, P.L. Smith, R.L. Marino, A. Rodriguez, W.C. Hubbard, C.P. O’Donnell, and V.Y. Polotsky.  Intermittent hypoxia induces hyperlipidemia in lean mice Circ. Res.97:698-706, 2005.

Barouch, L.A., D.E. Berkowitz, R.W. Harrison, C.P. O’Donnell, and J.M. Hare. Disruption of leptin signaling contributes to cardiac hypertrophy independently of body weight in mice.  Circulation.  108:754-759, 2003.

Rubin, A.E, , V.Y. Polotsky, A. Balbir, J.A. Krishnan, A.R. Schwartz, P.L. Smith, R.S. Fitzgerald, C.G. Tankersley, M. Shirahata, C.P. O'Donnell.  Differences in sleep-induced hypoxia between A/J and DBA/2J mouse strains.  Am. J. Resp. Crit. Care Med. 168:1520-7, 2003.

Tagaito, Y., V.Y. Polotsky, M.J. Campen, J.A. Wilson, A., Balbir, P.L. Smith, A.R. Schwartz, and C.P. O'Donnell.  A model of sleep disordered breathing in the C57BL/6J mouse. J. Appl. Physiol. 91:2758-66, 2001.

Polotsky, V.Y., J.A. Wilson, A.S. Haines, M.T. Scharf, S.E. Soutiere, C.G. Tankersley, P.L. Smith, A.R. Schwartz, and C.P. O’Donnell.  The impact of insulin-dependent diabetes on ventilatory control in the mouse. Am. J. Respir. Crit. Care Med.  163:624-632, 2001.

O’Donnell, C.P.,  C.D. Schaub, A.S. Haines, C.G. Tankersley, A.R. Schwartz, and P.L. Smith. Leptin prevents respiratory depression in obesity.  Am J Respir Crit Care Med 159(5): 1477-1484, 1999.

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