Mike Fallon, M.D.
Professor of Medicine
Phone: 205-975-5676
E-mail: mfallon@uab.edu
Dr. Fallon's research interests focus on understanding the pathogenesis of vascular alterations in chronic liver disease. A major investigative effort in his laboratory is directed to characterizing endothelial cell dysfunction in the pulmonary vasculature in cirrhosis, changes that result in vasodilatation and the hepatopulmonary syndrome. His clinical research interests include the diagnosis and therapy of the hepatopulmonary syndrome and the prevention and treatment of complications of chronic liver disease. In recent studies, he is investigating the role of intestinal macrophages in the loss of mucosal integrity and paracellular function that accompanies cirrhosis and results in bacterial translocation .
1. Fallon, M.B., Mennone, A. and Anderson, J.M. Altered expression and immunolocalization of the tight junction protein ZO-1 after common bile duct ligation. Am. J. Physiol. (Cell Physiol. 33):C1439-47, 1993.
2. Fallon, M.B., Nathanson, M.H., Mennone, A., Saez, J. and Anderson, J.M. Altered expression and function of hepatocyte gap junctions following common bile duct ligation. Am. J. Physiol. (Cell Physiol. 37):C1186-94, 1995.
3. Fallon, M.B., Gorelick, F.S., Anderson, J.M., Mennone, A., Saluja, A. and Steer, M. Effect of cerulein hyperstimulation on the paracellular barrier of rat exocrine pancreas. Gastroenterology. 108:1863-72, 1995.
4. Fallon, M.B., Abrams, G.A., Hou, Z. and Luo, B. Common bile duct ligation in the rate: A model of intrapulmonary vascodilatation and the hepatopulmonary syndrome. Am. J. Physiol. 272 (Gastrointest.. Liver Physiol. 35): G779-84, 1997.
5. Fallon, M.B., Abrams, G.A., Lou, B. Hou, Z., Dai, J. and Ku, D.D. The role of endothelial nitric oxide synthase in the pathogenesis of a rat model of hepatopulmonary syndrome. Gastroenterology. 113:606-14, 1997.
6. Luo, B., Abrams, G.A. and Fallon, M.B. Endothelin-1 in the rate bile duct ligation model of hepatopulmonary syndrome: correlation with pulmonary dysfunction. J. Hepatol. 29:571-8, 1998.
7. Zhang, M., Luo, B., Chen, S. and Fallon, M.B. Endothelin-1 stimulation of endothelial nitric oxide synthase. A pathogenetic mechanism in experimental hepatopulmonary syndrome. Am. J. Physiol. 277 (Gastrointest. Liver Physiol.) G944-53, 1999.
8. Zhang, J., Ling, Y., Luo, B., Tang, L., Stockard, C.R., Grizzle, W.E. and Fallon, M.B. Analysis of heme oxygenase-1 and nitric oxide synthase alterations in experimental hepatopulmonary syndrome. Gastroenterology 125:1441-51, 2003.
9. Luo, B., Tang, L., Wang, Z., Zhang, J., Ling, Y., Feng, W., Sun, J.Z., Stockard, C.R., Frost, A.R., Chen, Y.F., Grizzle, W.E. and Fallon, M.B. Cholangiocyte endothelin 1 and transforming growth factor beta1 production in rat experimental hepatopulmonary syndrome. Gastroenterology. 129:682-95, 2005.
10.Tang, L., Luo, B., Patel, R.P., Ling, Y., Zhang, J. and Fallon, M.B. Modulation of pulmonary endothelial endothelin B receptor expression and signaling: implications for experimental hepatopulmonary syndrome. Am. J. Physiol. 292:L1467-72, 2007.