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Allan W. Jones , Ph.D.

Professor
JonesA@missouri.edu

Research Interests
My research program currently focuses on mechanisms of membrane regulation and vascular smooth muscle function leading to abnormalities associated with hyper- lipidemia as well as adaptative echanisms during exercise training. We are studying mechanisms of adenosine transport and adenosine regulation of smooth muscle responses to acute metabolic depression in porcine coronary arteries. These studies have shown a novel mechanism by which smooth muscle generated adenosine has an autocoid function during an ischemic response. Mechanisms being pursued relate to adenosine interaction with receptors and subsequent cellular events causing relaxation; as well as adenosine interaction with a target enzyme, AMP kinase, which in turn regulates both cell metabolism and functional responses. We have observed that exercise training may alter the sensitivity of vascular smooth muscle in the porcine coronary arteries especially in males. Gender studies have also been initiated. These studies involve close collaboration with
members of a program project team on exercise physiology, the Center for Gender Physiology and Environmental Adaptation, and the Center for Diabetes and Cardiovascular Health. Methods utilize microfluorometry of calcium probes, digital image analyses, patch clamp techniques, radio isotopes fluxes, contractile responses, phosphor-image analyses, and biochemical and immuno-measures of AMP kinase.

Professional Background

  • Received Ph.D., Department of Physiology, University of Pennsylvania, 1965
  • Postdoctoral study, Department of Pharmacology, Oxford University
  • Joined Department in 1972
  • Named James O. Davis Professor in Cardiovascular Research
  • Chair of the Department of Physiology in 1983-2002
  • Interim Chair, Department of Medical Pharmacology and Physiology 2002-
  • Interim Director, Center for Diabetes and Cardiovascular Health, 2002
  • Associate Director of the Dalton Cardiovascular Research Center
  • Elected member of societies including: The American Physiological Society,
  • American Society for Pharmacology and Experimental Therapeutics, and Council for High Blood Pressure Research
  • Past chair of the Experimental Cardiovascular Sciences Study Section of the National Institutes of Health (NIH)
  • Research program has been continuously funded for 28 years
  • A National MERIT awardee of the NIH

Selected Publications

  • Jones AW, Magliola L, Waters CB, Rubin LJ.  Endothelin-1 activates phospholipases and channels at similar concentrations in porcine coronary arteries.  Am J Physiol 1998; 274:C1583-C1591.
  • Magliola L, Jones AW .  Calcium-tension relationship in mesenteric arteries from normotensive and aldosterone hypertensive rats.  J Vasc Res 1999; 36:404-414.
  • Jones AW, Rubin L, Magliola L.  Endothlin-1 sensitivity of procine coronary arteries is reduced by exercise training and is gender dependent. J Appl Physiol 1999;87:1172-1177.
  • Rubin LJ, Johnson LR, D'halla AK, Magliola L, Laughlin MH, Jones AW.  Selective transport of adenosine into porcine coronary smooth muscle.  Am J Physiol 2000; 279:H1397-H1410.
  • Dhalla AK, Dodam J, Jones AW, Rubin, LJ.  Characterization of an NBTI-sensitive equilibrative nucleoside transporter in vascular smooth muscle.  J Mol Cell Cardiol 2001; 33:1143-1154.
  • Laughlin MH, Schrage W, McAllister R, Garverick HA, Jones AW .  Interaction of gender and exercise training:  vasomotor reactivity of porcine skeletal muscle arteries. J Appl Physiol 2001; 90:216-227.

Methodology/Techniques


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