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Department of Physiology and Biophysics


Email: physiology@rosalindfranklin.edu
Fax: 847.578.3265

Department of Physiology and Biophysics


Email: physiology@rosalindfranklin.edu
Fax: 847.578.3265

 
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Richard A. Hawkins, Ph.D.
Professor, Physiology and Biophysics

Scientific Resume || Biosketch || Hawkins Home

Richard A. Hawkins, Ph.D.
Professor, Physiology and Biophysics

Scientific Resume || Biosketch || Hawkins Home
 

 

Richard A. Hawkins, Ph.D.
Professor, Physiology and Biophysics


Phone: 847-578-3218
Fax:847-775-6510
E-mail:
Richard.Hawkins@rosalindfranklin.edu
Office number: 3.237C


 

Research Interests

We are invovled in two projects.

The first is the transport of essential nutrients across the blood-brain barrier using isolated cell constituents in vitro and autoradiography in vivo. Our focus has been on glucose and amino acid carriers in the constituent membranes of the blood-brain barrier, as well as those in intracellular pools. Both the luminal and abluminal membranes of endothelial cells, which constitute the blood-brain barrier, are isolated as vesicles, and various measurements made. We are testing the hypothesis that the distribution, ion dependency, and kinetics of transport proteins favor the delivery of glucose and essential amino acids to the brain, but prevent accumulation of nonessential amino acids that serve as neurotransmitters.

 

The second subject is hepatic encephalopathy, a significant cause of morbidity and mortality worldwide that is caused by elevated ammonia in circulation when blood bypasses the liver. The goal of our work is to test whether reducing the incorporation of ammonia into brain glutamine can mitigate the disease. The aims are to determine whether inhibiting brain glutamine synthetase activity can prevent hepatic encephalopathy and whether reduced glutamine synthetase activity can reverse already established hepatic encephalopathy.

 

 

Relevant Publications

Hawkins R.A., Viña. J. R., Darryl R. Peterson, D. R. O’Kane, R. , A. Mokashi, A. and Ian A. Simpson, I. A., Amino acid transport across each side of the blood-brain barrier. in Amino Acids in Nutrition and Health (J.P.F. D’Mello ed), CABI, Oxford 2011, In the Press.
Hawkins R.A.: The blood-brain barrier and glutamate. American Journal of Clinical Nutrition 90: 867S-874S, 2009.
Devraj K., Geguchadze R, Klinger M.E., Freeman W.M., Mokashi A., Hawkins R.A., and Simpson I.A. Improved membrane protein solubilization and clean-up for optimum two-dimensional electrophoresis utilizing GLUT-1 as a classic integral membrane protein. Journal of Neuroscience Methods. 184:119-23, 2009.
Hawkins R.A., Simpson I.A. Mokashi, A. and Viña, J.R.,: Pyroglutamate stimulates Na+-dependent amino-acid transport across the blood-brain barrier. FEBS letters 580: 4382-4386, 2006.
O’Kane R.L., Viña, J.R., Simpson, I.A., Zaragoza, R., Mokashi, A. and Hawkins, R.A.: Cationic amino acid transport across the blood-brain barrier is mediated exclusively by system y+. American Journal of Physiology, 291 :E412-419, 2006.
Hawkins, R.A., O’Kane, R.L., Simpson, I.A., and Viña, J.R.: Structure of the blood brain barrier and its role in transport of amino acids. Journal of Nutrition 136: 218S-226S, 2006.
Hawkins, R.A., Mokashi, A., Simpson I.A. An active transport system in the blood-brain barrier may reduce levodopa availability. Journal of Experimental Neurology, 195: 267-271, 2005.
O’Kane, R.L. Viña J.R., Simpson I.A. and Hawkins, R.A.: Na+-dependent neutral amino acid transporters (A, ASC and N) of the blood-brain barrier: mechanisms for neutral amino acid removal. American Journal of Physiology Endocrinology and Metabolism. . American Journal of Physiology, 287: E622-629, 2004.
O’Kane, R.L. and Hawkins, R.A.: A Na+-dependent carrier of large neutral amino acids exists at the abluminal membrane of the blood-brain barrier. American Journal of Physiology, 285:E1167-E1173. 2003
Hawkins, R.A., Peterson D.R. and Viña J.R. The complementary membranes forming the blood-brain barrier. IUBMB Life, 54:101-107, 2002.
Simpson I.A., Vannucci S.J., DeJoseph M.R., and Hawkins R.A. Glucose transporter asymmetries in the bovine blood-brain barrier Journal of Biological Chemistry, 20; 276(16):12725-9. 2001.
O’Kane, R.L., Martinez-Lopez, I., DeJoseph, M.R., Viña, J.R., Hawkins, R.A. Na+-dependent glutamate transporters (EAAT1, EAAT2, and EAAT3) of the blood-brain barrier. A Mechanism for glutamate removal. Journal of Biological Chemistry, 274:31891-31895, 1999.
Lee, W-J., Hawkins, R.A., Viña, J.R., and Peterson, D.R. Glutamine transport by the blood-brain barrier: a possible mechanism for nitrogen removal. American Journal of Physiology, 274: C1101-C1107, 1998.
Hawkins, P.A., DeJoseph, M.R. and Hawkins, R.A.: Diurnal rhythm returns to normal after elimination of portacaval shunting. American Journal of Physiology, 274:E426-E431, 1998.
Lee, W-J, Peterson, D.R., Sukowski, E.J. and Hawkins, R.A.: Glucose transport by isolated plasma membranes of the bovine blood-brain barrier. American Journal of Physiology, 272:C1552-C1557, 1997.
Hawkins, P.A., DeJoseph, M.R., Viña, J.R., and Hawkins, R.A.: Comparison of the metabolic disturbances caused by end-to-side and by side-to-side portacaval shunts. Journal of Applied Physiology, 80: 885-891, 1996.
Hawkins, P.A., DeJoseph, M.R. and Hawkins, R.A.: Eliminating metabolic abnormalities of portacaval shunting by restoring normal liver blood flow. American Journal of Physiology, 270: E1037-E1042, 1996.
Hawkins, P.A., DeJoseph, M.R. and Hawkins, R.A.: Reversal of portacaval shunting normalizes brain energy consumption in most brain structures. American Journal of Physiology, 271:E1015-E1020, 1996.

 

 
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