THE winner of the 2005 American Society of Anesthesiologists Excellence in Research Award is David S. Warner, M.D., Professor of Anesthesiology, Neurobiology, and Surgery at Duke University Medical Center, Durham, North Carolina. Although Dr. Warner’s achievements are internationally recognized across a broad spectrum of highly competitive fields such as neurobiology, neurology, neuroanesthesiology, stroke physiology, and biochemistry, ironically, his contributions to these areas may be “off the radar screen” for some practicing anesthesiologists. Perhaps this is because Dr. Warner is an individual with quiet dignity, one who does not need to trumpet his accomplishments. The quality of Dr. Warner’s scientific accomplishments speak for themselves and have changed medicine.

David Warner is a Midwesterner, born, raised, and educated in the heartland of the United States. Born in Evanston, Illinois, on July 20, 1953, David was raised in Oshkosh, Wisconsin, and completed college with a B.A. degree in psychology from the University of Wisconsin, Madison, Wisconsin, in 1976. His first scientific article resulted from a senior research project investigating interactions between acoustic and auditory perception. David stayed in Wisconsin for medical school, graduating from the University of Wisconsin-Madison with the M.D. degree in 1980. He then moved to another part of the Midwest, The University of Iowa, Iowa City, Iowa, to pursue an interest in clinical neuroscience as a neurosurgery resident. During a required anesthesia rotation in his surgery residency, David realized that his true passion in medicine was anesthesia, so he switched careers to start an anesthesiology residency at The University of Iowa and never looked back. Because of his background in psychology and neurosurgery, not surprisingly, David found his clinical base in neuroanesthesiology. Soon after completion of his anesthesiology residency in 1984, to pursue further training in basic mechanisms underlying neuroprotection, David moved to Sweden to spend a year in the Laboratory of Experimental Brain Research at the University of Lund. His mentor, Bo K. Siesjö, M.D, Ph.D., offered him exposure to world-class neuroscience in the study of pathologic brain energy metabolism. David then returned to the faculty in the Department of Anesthesia at The University of Iowa, where he worked closely with Michael M. Todd, M.D., from 1987 to 1994 under the leadership of department chair John H. Tinker, M.D. Initially supported by the Foundation for Anesthesia Education and Research, David rapidly developed his own National Institutes of Health (NIH)–funded line of scientific investigation, continued fruitful collaborations with Mike Todd, and administered the University of Iowa Anesthesiology research training grant. In 1992, David became director of the Division of Neuroanesthesiology in the Department of Anesthesia at The University of Iowa College of Medicine, a testament to his clinical and teaching skills in addition to research prowess. In February 1994, Dr. Warner moved his laboratory and some of his staff to Durham, North Carolina, where he become Professor of Anesthesiology, Neurobiology, and Surgery in the Department of Anesthesiology at Duke University Medical Center and is currently Vice-Chairman for Academic Development and Director of the Multidisciplinary Neuroprotection Laboratories.

Dr. Warner is one of the world’s most respected neuroanesthesiologists, whether viewed from inside anesthesiology or “outside” from neurology, physiology, or biochemistry perspectives. With his focus on mechanisms of stroke and brain protection, Dr. Warner is often the speaker of choice at international meetings on brain protection; in fact, some international societies have chosen their meeting dates around Dr. Warner’s availability. Taking after his mentor, Mike Todd, David has built multidisciplinary teams of investigators across fields such as anesthesiology, neurology, biochemistry, neuroradiology, pediatrics, neurosurgery, cell biology, and neurobiology. He asks probing questions, and then uses a range of tools at the cutting edge of medical research to answer these questions. As a result, his publications use a range of approaches, including rat and transgenic mouse outcome models of central nervous system (CNS) injury, hippocampal slices, tissue culture, magnetic resonance imaging, and biochemical and genetic analyses. He is frequently called upon by investigators from many disciplines to perform sophisticated protocols of neurologic injury analysis on their transgenic/knockout mice. David has successfully recruited outstanding scientists from all over the world to synergize in creating a unique neuroscience brain protection group covering almost an entire floor of one of the research buildings in Duke University Medical Center; this group now includes six principle investigators exemplified by a neuroradiologist who runs an on-site animal magnetic resonance imaging facility, a biochemist focusing on endoplasmic reticulum responses to brain injury, neurologists and anesthesiologists using various animal models to explore acute CNS injury, a pediatric anesthesiologist exploring mechanisms of fetal brain injury, and David’s own group, focusing on mechanisms of neuroprotection by anesthetics and antioxidants. Dr. Warner has been consistently funded by the NIH (multiple R01 grants) during his entire career and has served on NIH (National Institute of General Medical Science–sponsored) study sections focused on evaluating pharmacology and anesthesiology training grants. In addition to his major laboratory efforts, clinically, David has been instrumental in the safe introduction of several drugs into neuroanesthesia practice and has served as the Physician Protocol Monitor for the NIH-funded multinational Intraoperative Hypothermia for Aneurysm Surgery Trial. In the laboratory, his work has focused primarily on development of valid rodent (rat and mouse) outcome models of brain and spinal cord ischemia/trauma, perinatal hypoxia–ischemia, and subarachnoid hemorrhage. His most significant contributions relate to effects of anesthetic agents on outcome from these injuries, genomic contributions to ischemic/traumatic outcome, role of hyperglycemia in ischemic brain injury, contribution of extracellular reactive oxygen species to neural tissue demise, and mechanisms of cerebral vasospasm. These studies are briefly described below.

One can divide David’s research career into two periods: The University of Iowa period and the Duke University period. In his initial career in Iowa, David’s key findings included identifying unique patterns of cerebral blood flow distribution for different anesthetic agents and interrelationships with metabolic rate,1–4effects of anesthetics on patient responses to craniotomy,5,6identification of N -methyl-d-aspartate receptor glycine recognition site as a valid target for ischemic neuroprotection,7–9identification of the importance of osmotic pressure in defining effects of intravenous volume expanders on brain water content in models of CNS injury,10–13defining additive interactions of ester–ester and ester–amide local anesthetic combinations in producing CNS toxicity,14and discovering efficacy of insulin in reducing diabetes-induced hyperglycemia-augmented ischemic brain injury.15Also during this period, David performed an elegant set of experiments introducing comparison of anesthetics to the awake state (rather than an alternative anesthetic state) when assessing for neuroprotection.16,17These studies provided a more appropriate frame of reference in discerning drug efficacy and also introduced the importance of brain temperature regulation in defining efficacy of anesthetics. During the next (Duke) phase of David’s career, key findings to date have included defining the importance of apolipoprotein E alleles in outcome from CNS injury, including influences on oxidative stress and neuroinflammation,18–21identifying major neuroprotection by volatile anesthetics against global cerebral ischemia independent of effects on systemic stress,22,23identifying the γ-aminobutyric acid type A receptor as a prominent site of volatile anesthetic action in providing ischemic neuroprotection,24discovering that extracellular superoxide dismutase is a critical factor in defining outcome from acute CNS injury,25–27identifying delayed and profound neuroprotection from metalloporphyrin catalytic antioxidants,28–30leading introduction of remifentanil into neuroanesthesia practice,31–33defining the role of P50 in hypothermic neuroprotection,34inventing and advancing models of CNS injury in mice allowing study of transgenic strains,35–37defining postoperative nausea and vomiting epidemiology and treatment efficacy in patients undergoing craniotomy,38–40and discovering efficacy of β-hydroxy-β-methylglutaryl-CoA reductase inhibitors (statins) in treatment of subarachnoid hemorrhage-induced cerebral vasospasm.41,42Dr. Warner has published more than 180 original manuscripts in prestigious journals such as Neuroscience , Journal of Neuroscience , Journal of Biology and Chemistry , Stroke , Journal of Cerebral Blood Flow Metabolism , Anesthesiology, Anesthesia & Analgesia , Critical Care Medicine , Annals of Neurology , Neurosurgery , and Journal of Neurosurgery .

In addition to research, David has also played a major role in research training and fellow/faculty development. He is principal investigator on Duke’s NIH-funded institutional research training grant, having written the original grant and successfully leading several competitive renewals. In his own laboratory, more than 60 individuals have been trained, ranging from high school students to postdoctoral research fellows, with about a 50–50 balance between American citizens and international fellows. More than 80% of these trainees remain in academic practice. Many have established their own laboratories in the United States, Europe, and Asia and have obtained competitive peer-reviewed funding to support their ongoing work. Many have been supported in their training by competitive funding mechanisms (Foundation for Anesthesia Education and Research, International Anesthesia Research Society, American Heart Association, NIH) and have won national or international prizes for their research. Dr. Warner also serves as the Vice-Chair for Academic Development in a department of 75 faculty members, having specific responsibilities for programmatic academic development of junior faculty. He can often be found late at night reviewing fellow and junior faculty grant applications; no one is more dedicated to the training of future academicians in our specialty than David. In addition to his research advancements, Dr. Warner’s career and responsibilities in the anesthesiology community are exemplary. He is a past president of the Society for Neurosurgical Anesthesia and Critical Care. Dr. Warner has been a very active and dedicated section editor for Anesthesia & Analgesia , organizing experts to review articles from a cross-section of anesthesiology as well as having particular emphasis on reviewing neuroscience studies. He is also on numerous other editorial boards including Journal of Anesthesia , Neurocritical Care , Journal of Neurosurgical Anesthesia , and Anesthesiology. Many have benefited from Dr. Warner’s thoughtful review of their research manuscripts and grants, through his insightful comments and his ability to hone in quickly on key strengths and weaknesses. David has also served as an American Board of Anesthesiology oral board examiner.

In spite of his notoriety and recognition, Dr. Warner is a very down-to-earth teacher and researcher and a warm human being. He guides residents through anesthesia for craniotomy surgery and teaches the essentials of safe human neuroanesthesiology. He leads by example in his research laboratory, working harder than his research fellows. He consistently helps fellows learn to write clear and cogent research manuscripts and grants. No one is a more passionate believer in the academic enterprise. Dr. Warner’s work with research trainees in their career development stems from his strong belief that physician–scientists are critical in integrating basic science and clinical medicine. He is certainly deserving of the 2005 American Society of Anesthesiologists Excellence in Research Award.

Hansen T, Warner D, Todd M, Vust L, Trawick D: Distribution of cerebral blood flow during halothane versus isoflurane anesthesia in rats. Anesthesiology 1988; 69:332–7
Hansen T, Warner D, Todd M, Vust L, Trawick D: The role of cerebral metabolism in determining the local cerebral blood flow effects of volatile anesthetics: Evidence for persistent flow-metabolism coupling. J Cereb Blood Flow Metab 1989; 9:323–8
Hansen T, Warner D, Todd M, Vust L, Trawick D: Effects of nitrous oxide and volatile anesthetics on cerebral blood flow. Br J Anaesth 1989; 63:290–5
Reasoner D, Warner D, Todd M, Strauss D, McAllister A: Effects of nitrous oxide on cerebral metabolic rate in isoflurane anaesthetized rats. Br J Anaesth 1990; 65:210–5
From R, Warner D, Todd M, Sokoll M: Anesthesia for craniotomy: A double-blind comparison of alfentanil, fentanyl, and sufentanil. Anesthesiology 1990; 73:896–904
Todd M, Warner D, Sokoll M, Maktabi M, Hindman B, Scamman F, Kirchner J: A prospective, comparative trial of three anesthetics for supratentorial craniotomy: Fentanyl/propofol, isoflurane/N2O, and fentanyl/N2O. Anesthesiology 1993; 78:1005–20
Pearlstein R, Massey G, Beirne J, Warner D: Neuroprotective effects of NMDA receptor glycine recognition site antagonist: Dependence on glycine concentration. J Neurochem 1998; 70:2012–9
Takaoka S, Bart R, Pearlstein R, Warner D, Brinkhous A: Neuroprotective effect of the glycine recognition site antagonist ACEA-1021 persists when brain temperature is controlled. J Cereb Blood Flow Metab 1997; 17:161–7
Warner D, Martin H, Ludwig P, McAllister P: In vivo models of cerebral ischemia: effects of parenterally administered NMDA receptor glycine site antagonists. J Cereb Blood Flow Metab 1995; 15:188–96
Hansen T, Warner D, Traynelis V, Todd M: Plasma osmolality and brain water content in a rat glioma model. Neurosurgery 1994; 34:505–11
Kaieda R, Takaoka S, Cook L, Warner D: Acute effects of changing plasma osmolality and colloid oncotic pressure on brain edema formation after cryogenic injury. Neurosurgery 1989; 24:671–8
Kaieda R, Takaoka S, Warner D: Prolonged reductions in colloid oncotic pressure does not increase brain edema following cryogenic injury in rabbits. Anesthesiology 1989; 71:554–60
Warner D, Boehland L: The effects of iso-osmolal hemodilution on post-ischemic brain water content in the rat. Anesthesiology 1988; 68:86–91
Spiegel D, Warner D, Dexter F, Baker M, Todd M: CNS toxicity of local anesthetic mixtures in the rat. Anesth Analg 1992; 75:922–8
Warner D, Gionet T, Todd M, McAllister A: Insulin-induced normoglycemia improves ischemic outcome in hyperglycemic rats. Stroke 1992; 23:1775–81
Warner D, Ludwig P, Pearlstein R, Brinkhous A: Halothane reduces focal ischemic injury in the rat when brain temperature is controlled. Anesthesiology 1995; 82:1237–45
Warner D, McFarlane C, Todd M, Ludwig P, McAllister A: Sevoflurane and halothane reduce focal ischemic brain damage in the rat: Possible influence on thermoregulation. Anesthesiology 1993; 79:985–92
Laskowitz D, Sheng H, Bart R, Joyner A, Roses A, Warner D: Apolipoprotein E deficient mice have increased susceptibility to focal ischemia. J Cereb Blood Flow Metab 1997; 17:753–8
Lee Y, Kudo M, Massey G, Laskowitz D, Warner D, Pearlstein R: Protective effects of apolipoprotein E on H2O2toxicity in primary neuronal cell culture. Neurochem Int 2004; 44:107–18
Lynch J, Pineda J, Morgan D, Zhang L, Warner D, Benveniste H, Laskowitz D: Apolipoprotein E affects the CNS response to injury and the development of cerebral edema. Ann Neurol 2002; 51:113–7
Sheng H, Laskowitz D, Bennett E, Schmechel D, Bart R, Pearlstein R, Roses A, Warner D: Isoform specific effects of human apolipoprotein E on focal ischemic outcome in transgenic mice. J Cereb Blood Flow Metab 1998; 18:361–6
Mackensen G, Nellgard B, Miura Y, Dexter F, Pearlstein R, Warner D: Sympathetic blockade masks positive effect of isoflurane on histologic outcome from near-complete ischemia in the rat. Anesthesiology 1999; 90:873–81
Miura Y, Grocott H, Bart R, Pearlstein R, Dexter F, Warner D: Differential effects of anesthetic agents on outcome from near complete, but not incomplete, global ischemia in the rat. Anesthesiology 1998; 89:391–400
Bickler P, Warner D, Strattman G, Schuyler J: GABA receptors contribute to isoflurane neuroprotection in organotypic hippocampal cultures. Anesth Analg 2003; 97:564–71
Sheng H, Bart R, Oury T, Pearlstein R, Crapo J, Warner D: Mice overexpressing extracellular superoxide dismutase have increased resistance to focal cerebral ischemia. Neuroscience 1999; 88:185–91
Sheng H, Brody T, Pearlstein R, Crapo J, Warner D: Extracellular superoxide dismutase deficient mice have increased sensitivity to focal cerebral ischemia. Neurosci Lett 1999; 267:13–7
Pineda J, Aono M, Sheng H, Lynch J, Wellons J, Laskowitz D, Pearlstein R, Bowler R, Crapo J, Warner D: Extracellular superoxide dismutase over expression improves outcome from closed head injury in the mouse. J Neurotrauma 2001; 18:625–34
Mackensen G, Patel M, Sheng H, Calvi C, Batinic-Haberle I, Dan B, Fridovich I, Crapo J, Pearlstein R, Warner D: Neuroprotection from delayed post-ischemic administration of a metalloporphyrin catalytic antioxidant. J Neurosci 2001; 21:4582–92
Sheng H, Enghild J, Bowler R, Patel M, Batinic-Haberle I, Calvi C, Day B, Pearlstein R, Crapo J, Warner D: Effects of metalloporphyrin catalytic antioxidants in experimental brain ischemia. Free Rad Biol Med 2002; 33:947–61
Sheng H, Spasojevic I, Warner D, Batinic-Haberle I: Mouse spinal cord compression injury is ameliorated by intrathecal cationic manganese (III) porphyrin catalytic antioxidant therapy. Neurosci Lett 2004; 366:220–5
Balakrishnan G, Raudzens P, Samra S, Song K, Boening J, Bosek V, Jamerson B, Warner D: Safety and efficacy of remifentanil versus fentanyl in patients undergoing surgery for intracranial mass lesions. Anesth Analg 2000; 91:163–9
Guy J, Hindman B, Baker K, Borel C, Maktabi M, Ostapkovich N, Kirchner J, Todd M, Fogarty-Mark P, Yancy V, Sokall M, McAllister A, Roland C, Young W, Warner D: A comparative study of remifentanil and fentanyl in patients undergoing craniotomy for supratentorial space occupying lesions. Anesthesiology 1997; 86:514–24
Warner D, Hindman B, Takaoka S, Sawin P, Kirchner J, Roland C, Jamerson B: Intracranial pressure effects of remifentanil versus alfentanil in patients undergoing supratentorial craniotomy. Anesthesiology 1996; 86:514–24
Wainwright M, Sato Y, Mackensen G, Steffen R, Pearlstein R, Warner D: Hypothermic neuroprotection is not reversed by RSR13-induced increase in P50 during transient focal cerebral ischemia in the rat. Am J Physiol Heart Circ Physiol 2002; 282:H1863–70
Parra A, McGirt M, Sheng H, Laskowitz D, Pearlstein R, Warner D: Murine model of aneurysmal subarachnoid hemorrhage associated cerebral vasospasm: Methodological analysis. Neurol Res 2002; 24:510–6
Sheng H, Wang H, Homi H, Spasojevic I, Batinic-Haberle I, Pearlstein R, Warner D: A no laminectomy spinal cord compression injury model in mice. J Neurotrauma 2004; 21:595–604
Wellons J, Sheng H, Laskowitz D, Mackensen G, Pearlstein R, Warner D: A comparison of strain-related susceptibility in two murine recovery models of global cerebral ischemia. Brain Res 2000; 868:13–21
Fabling J, Gan T, El-Moalem H, Warner D, Borel C: A randomized, double-blinded comparison of ondansetron versus placebo for the prevention of nausea and vomiting after infratentorial craniotomy. J Neurosurg Anesth 2002; 14:102–7
Fabling J, Gan T, Guy J, Borel C, Warner D: Postoperative nausea and vomiting: a retrospective analysis in patients undergoing elective craniotomy. J Neurosurg Anesth 1997; 9:308–12
Fabling J, Gan T, Guy J, El-Moalem H, Molaisoodum T, Warner D, Borel C: A randomized, double-blind comparison of ondansetron, droperidol and placebo for prevention of post-operative nausea and vomiting after supratentorial craniotomy. Anesth Analg 2000; 91:358–61
Lynch JR, Wang H, McGirt MJ, Floyd J, Freidman AH, Coon AL, Blessing R, Alexander MJ, Graffagnino C, Warner DS, Laskowitz DT: Simvastatin reduces vasospasm after aneurysmal subarachnoid hemorrhage: Results of a pilot randomized clinical trial. Stroke 2005; 36:1989–91
McGirt M, Lynch J, Parra A, Sheng H, Pearlstein R, Laskowitz D, Pelligrino D, Warner D: Simvastatin increases endothelial nitric oxide synthase and ameliorates cerebral vasospasm resulting from subarachnoid hemorrhage. Stroke 2002; 23:2950–6