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Our research has used quantitative trait loci (QTL)
localization to identify markers in the mouse genome that are significantly
associated with responsiveness to N2O
and have implicated the biological regulator nitric oxide (NO) as a critical
determinant of the analgesic mechanism of action of N2O.
Current research is elucidating the role of NO in the mechanism that
regulates neuronal release of opioid peptides.
We were also the first to demonstrate a specific anxiolytic effect of N2O
that was independent of its analgesic property and to show that this effect
is equivalent to the effect of benzodiazepines. N2O
and benzodiazepines produce parallel behavioral effects in various animal
models of experimental anxiety. Like the effects of chlordiazepoxide, the
effects of N2O
are antagonized by flumazenil, a benzodiazepine receptor blocker, and are
significantly attenuated in the presence of benzodiazepine tolerance.
Current research is localizing the neuroanatomical locations of the critical
enzymes in the signaling pathway, nitric oxide synthase, soluble guanylyl
cyclase and cyclic GMP-dependent protein kinase. These N2O
analgesia and anxiolysis studies utilize a combination of stereotaxic
neurosurgical, behavioral, pharmacological, neurochemical, microdialysis,
pharmacogenetic and molecular biology approaches.
Biographical Information
Raymond M. Quock, Professor, obtained his B.S.
degree in biology from the University of San Francisco in 1970 and his Ph.D.
in pharmacology from the University of Washington in 1974. He spent one year
as an instructor in pharmacology at the University of Washington (1974-75)
and the next four years as an assistant professor of pharmacology at the
University of Pacific School of Pharmacy in Stockton, California (1975-79).
Dr. Quock then worked at the Marquette University School of Dentistry in
Milwaukee, Wisconsin (1979-89), moving through the ranks of assistant
professor, associate professor and eventually to full professor. He also
held adjunct positions at the Medical College of Wisconsin and the V.A.
Medical Center. He then left Milwaukee for the University of Illinois
College of Medicine at Rockford (1989-98), where he was professor of
pharmacology and also adjunct professor of pharmacology in anesthesiology at
the University of Illinois College of Medicine in Chicago (1993-98). Dr.
Quock joined Washington State University as professor and chair of
pharmaceutical sciences in the College of Pharmacy in January 1999. He is a
member of both the Neuroscience and Pharmacology/Toxicology graduate
programs. After returning to teaching and research in 2002, he was
reappointed department chair in July 2007.
Recent Publications
S. Li, J.C. Doss, E.J. Hardee
and R.M. Quock. Involvement of cyclic GMP-dependent
protein kinase in nitrous oxide-induced anxiolytic-like behavior
in the mouse light/dark exploration test. Brain Research
1038(1):113-117 (2005)
E.D. Henry, Y. Ohgami, S. Li, E. Chung and R.M. Quock.
Correlation of inbred mouse sensitivity to nitrous oxide
antinociception with brain NOS activity following exposure to
nitrous oxide. Pharmacology, Biochemistry and Behavior
81(4):764-768 (2005)
R.M. Quock and L.K. Vaughn. Do general anesthetics
induce the neuronal release of endogenous opioid peptides? Life
Sciences 77(21):2603-2610 (2005)
M. Ishikawa, K. Abe, Y. Matsushita, I. Utsunomiya, R.M. Quock
and K. Taguchi. Involvement of brain PKC in nitrous
oxide-induced antinociception in mice. Neuroscience
140(1):227-223 (2006)
D.E. Emmanouil, Z. Papadopoulou-Daifoti, P.T. Hagihara, D.G.
Quock and R.M. Quock. Possible involvement of serotonin
in the anxiolytic effect of nitrous oxide in rodents. Pharmacology,
Biochemistry and Behavior 84(2):313–320 (2006)
E. Chung, B. Burke, A.J. Bieber, J.C. Doss, Y. Ohgami and R.M.
Quock. Dynorphin-mediated antinociceptive effects of l-arginine
and SIN-1 (an NO donor) in mice. Brain Research Bulletin
70(3):245–250 (2006)
L.K. Vaughn and R.M. Quock. Nitrous oxide and opioid
receptors. In: Willis, W.D. and R.F. Schmidt, eds.
Encyclopedia of Pain, pp. 1347-1349. Springer-Verlag,
Berlin Heidelberg New York (2007)
D.E. Emmanouil and R.M. Quock. Advances in understanding
the actions of nitrous oxide. Anesthesia Progress
54(1):9-18 (2007)
R.J. Pruhs, R.T. Peña and R.M. Quock. Antagonism of
phosphoramidon-induced antinociception in mice by
m-
but not
k-opioid
receptor blockers. Life Sciences 80(19):1817-1820 (2007)
Y. Matsushita, M. Ishikawa, K. Abe, I. Utsunomiya, K. Hoshi,
R.M. Quock and K. Taguchi. Protein kinase Cg
is a key enzyme in the development of tolerance to nitrous
oxide-induced antinociception in mice. Neuroscience (in
press)
D.E. Emmanouil, A.S. Dickens, R.W. Heckert, Y. Ohgami, E. Chung,
S. Han and R.M. Quock. Nitrous oxide-antinociception
is mediated by opioid receptors and nitric oxide in the
periaqueductal gray region of the brain. European
Neuropsychopharmacology (in press).
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