John McNeill


About the Principal Investigator

John McNeil
E-mail: jmcneill@interchange.ubc.ca
Phone: 604-822-9373
   

Training

Degree: B.Sc. Pharmacy
Institution: University of Alberta
Period: 1960
   
Degree: M.Sc. Pharmacy
Institution: University of Alberta
Period: 1962
   
Degree: Ph.D. Pharmacology
Institution: University of Michigan
Period: 1967
   

Previous Positions

Position: Assistant Professor
Institution: Michigan State University
Period: 1967-1971
   
Position: Associate Professor and Chairman
Institution: Division of Pharmacology & Toxicology, UBC
Period: 1972-1975
   
Position: Professor
Institution: Faculty of Pharmaceutical Sciences
Period: 1975-2004
   
Position: Dean
Institution: Faculty of Pharmaceutical Sciences
Period: 1985-1996
   

Current Position

Position: Professor and Dean Emeritus
Period: 2004 - Present
   

Major Awards

Name: Fellow of the Canadian Academy of Health Sciences
Period: 2005
   
Name: Janssen-Ortho Pharmaceutical Research Award / Association of Faculties of Pharmacy of Canada
Period: 2004
   
Name: Killam Teaching Award (University of British Columbia)
Period: 2003
   
Name: Fellow of International Academy of Cardiovascular Sciences
Period: 2002
   
Name: Fellow of the Royal Society of Canada
Period: 2000
   
Name: Ken Bowman Research Award (International Academy of Cardiovascular Sciences)
Period: 1999
   
Name: Friend of Pharmacy (B.C. Pharmacy Association)
Period: 1997
   
Name: Outstanding Alumnus Award (University of Michigan)
Period: 1996
   
Name: Parke Davis Distinguished Lecturer (Ferris State University)
Period: 1996
   
Name: Killam Research Prize (University of B.C.)
Period: 1994
   
Name: MRC Visiting Professor, Queen's University
Period: 1992
   
Name: Jacob Biely Prize (University of B.C.)
Period: 1985
   
Name: McNeil Award (Association of Faculties of Pharmacy of Canada)
Period: 1983
   
Name: Upjohn Award (Pharmacological Society of Canada)
Period: 1983

 

About the Lab

Please Note: Dr. McNeill is no longer training new graduate students.

My research has centered on the effects of drugs on the heart. In particular, I have attempted to elucidate the biochemical mechanism of action of a number of drugs that produce a positive inotropic effect. In addition, I have been interested in the mechanisms of action of drugs that interact with cardio stimulant agonists to enhance or block their effects. These investigations have been at least partially successful in that I have contributed data leading to theories of drug action in the heart. We are also actively involved with studies on hypertension in animal models.

I have also investigated the effect of diabetes on the hearts of rats. Our investigations have revealed several biochemical, structural, functional and pharmacological differences in hearts from diabetic animals. We have also found ways of treating the diabetes and preventing the cardiac changes in addition to insulin treatment. More recently, our particular interest has been our discovery that vanadium containing compounds lower blood glucose and prevent the secondary complications of diabetes in diabetic rats. We have recently synthesized and patented several compounds which have potential to be therapeutic agents. The finding that vanadium deposits in bone has led us to investigate if vanadium has positive or negative effects on bone structure. In the past several years we have studied the positive effects of beta blockade on the diabetic heart.

We have developed rat animal models for the study of the metabolic syndrome, a syndrome characterized by hyperinsulinemia, insulin resistance and hypertension. We have shown that insulin-enhancing drugs will reduce all three of the above. These studies may lead to better treatments of hypertension by treating the root cause. We are currently studying how the syndrome increases blood pressure by examining changes in vasoactive factors such as endothelin and thromboxane (TXA2) and the effect of sex hormones.

Training Environment

My training philosophy had been to take good trainees and ground them in the science that we are investigating and then turn them loose. The reward is that I have learned from them and their successes, perhaps even more than I have managed to teach them.

Please Note: Dr. McNeill is no longer training new graduate students.

Projects

Diabetes produces deleterious changes in cardiac function in rats. There are significant alterations in cardiac metabolism, calcium handling and cell signaling that continue to be investigated. In addition, reactive oxygen species are increased in the diabetic state and contribute to the decrease in function. The cardiac muscle itself is damaged, a condition known as cardiomyopathy. Our lab is investigating both the pathology and potential treatments for the cardiomyopathy.

Our model of the metabolic syndrome is the Fructose Fed Rat. Feeding rats a high fructose diet results in insulin resistance and hypertension which appear to be related. Our work has shown an increase in activity of the sympathetic nervous system as well as in endothelin, angiotensin, thromboxane A2 and inflammatory factors. The presence of testosterone is also important in the development of the hypertension. We are attempting to understand these complex relationships as well as to investigate possible treatments.

I have also taught and had an interest in both therapeutic drugs and drugs of abuse, including alcohol. I have been recognized by the courts of British Columbia and elsewhere as an expert in these areas.

Selected Publications

Most Cited Paper

  • Heyliger CE, Tahiliani AG, McNeill JH. Effect of vanadate on elevated blood glucose and depressed cardiac performance of diabetic rats. Science 227:1474-1477, 1985.

Recent Papers (manuscripts)

  • Sharma V, Dhillon P, Parsons H, Allard MF, McNeill JH. Metoprolol represses PGC-1α-mediated carnitine palmitoyltransferase-1 ß expression in the diabetic heart. European Journal of Pharmacology 607:156-166, 2009.
  • Tran L, MacLeod KM, McNeill JH. Endothelin-1 modulates angiotensin II in the development of hypertension in fructose-fed rats. Mol Cell Biochem 325:89-97, 2009.
  • Tsai GY, Cui JZ, Syed H, Xia Z, Ozerdem U, McNeill JH, Matsubara JA. Effect of N-acetylcysteine on the early expression of inflammatory markers in the retina and plasma of diabetic rats. Clinical and Experimental Ophthalmology 37:223-231, 2009.
  • Nagareddy PR, McNeill JH, MacLeod KM. Chronic inhibition of inducible nitric oxide synthase ameliorates cardiovascular abnormalities in streptozotocin diabetic rats. Eur J Pharmacol 611:53-59, 2009.
  • Sharma V, Mustafa S, Patel N, Wambolt RF, Allard MF, McNeill JH. Stimulation of cardiac fatty acid oxidation by leptin is mediated by a nitric oxide/ p38 MAPK-dependent mechanism. Eur J Pharmacol 617:113-117, 2009.
  • Nagareddy PR, Soliman H, Lin G, Rajput PS, Kumar U, McNeill JH, MacLeod KM. Selective inhibition of protein kinase C ß2 attenuates inducible nitric oxide synthase-mediated cardiovascular abnormalities in streptozotocin-induced diabetic rats. Diabetes 58:2355-2364, 2009.
  • Nagareddy PR, Chow F, Hao L, Wang X, Nishimura T, MacLeod KM, McNeill JH, Fernandez-Patron C. Maintenance of adrenergic vascular tone by MMP-transactivation of the EGFR requires PI3K and mitochondrial ATP synthesis. Cardiovascular Research 84:368-377, 2009.
  • Tran L, MacLeod KM, McNeill JH. Chronic etanercept treatment prevents the development of hypertension in fructose-fed rats. Mol Cell Biochem 330:219-228 (doi 10.1007/s11010-009-0136-z), 2009.
  • Mustafa S, Vasudevan H, Yuen VG, McNeill JH. Renal expression of arachidonic acid metabolizing enzymes and RhoA/Rho kinases in fructose insulin resistant hypertensive rats. Mol Cell Biochem 333(1):203-209 (doi: 10.1007/s11010-009-0220-4), 2010.
  • Sharma V, Abraham T, So A, Allard MF, McNeill JH. Functional effects of protein kinases and peroxynitrite on cardiac carnitine palmitoyltransferase-1 in isolated mitochondria. Mol Cell Biochem 337:223-237 (doi:10.1007/s11010-009-0303-2), 2010.
  • Nagareddy PR, MacLeod KM, McNeill JH. GPCR agonist-induced transactivation of the EGFR upregulates MLC II expression and promotes hypertension in insulin resistant rats. Cardiovasc Res 87(1):177-186 (doi: 10.1093/cvr/cvq030), 2010.
  • Vasudevan H, Lau S, Jiang J, McNeill JH. Effects of insulin resistance and testosterone on the participation of cyclooxygenase isoforms in vascular reactivity. J Exper Pharmacol 2:169-179, 2010.
  • Sharma V, Sharma A, Saran V, Bernatchez PN, Allard MF, McNeill JH. ß-receptor antagonist treatment prevents activation of cell death signaling in the diabetic heart independent of its metabolic actions. Eur J Pharmacol 657:117-125 (doi:10.1016/j.ejphar.2011.01.044), 2011.
  • Sharma VJ, McNeill JH. Parallel effects of ß-adrenoceptor blockade on cardiac function and fatty acid oxidation in the diabetic hear t: Confronting the maze. World J Cardiol 3(9):281-302, 2011.

 

« Back



a place of mind, The University of British Columbia

Faculty of Pharmaceutical Sciences
2146 East Mall
Vancouver, BC, Canada V6T 1Z3
Tel (Dean’s Office): 604.822.2343

Emergency Procedures | Accessibility | Contact UBC | © Copyright The University of British Columbia