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Edgar E. Coons, Jr.
Psychology
Brain mechanisms of reward
As an undergraduate at Colorado College and later in the Yale
University School of Music, I prepared for a career in music
composition and theory. In this pursuit, I became interested in the
question of what impact the temporal form of a composition can have on
the feelings of an audience. Clearly, the ability to perceive and
react to temporal form rests on the ability to store the history of
events in memory and to interact this history with brain mechanisms
governing emotions. I realized that I had to turn to psychology and
neurophysiology in order to profitably explore the question of form
and feeling.
One thing led to another, and now, many years later, I am a
professor of physiological psychology running a laboratory devoted to
studying drive and hedonic mechanisms in the brain and how they
interact. While a graduate student in Neal E. Miller's lab at Yale, I
discovered stimulation-bound feeding in rats implanted with electrodes
in the lateral hypothalamus. Subsequently, my students and I have
continued to examine the relationships between a "hunger'' system that
is apparently involved and systems subserving reward, pain, and
anxiety. What has become evident is that the same hypothalamic
stimulation that elicits eating not only ameliorates anxiety and pain
but also increases the attractiveness of otherwise unpalatable
foods. Opioid and anxiolytic transmitters are implicated. Apparently,
some mechanism is involved that adjudicates between the risks of
eating, such as attacks from predators or illness from food poisoning,
and the risks of starving as a result of avoiding such dangers.
In the process of making these investigations, my lab has also
parametrically varied interpulse interval, amplitude, and
conditioning-to-test-pulse interval of brain stimulation to ascertain
the synaptic and axonal characteristics of the neurons mediating
feeding, reward, and pain. In effect, I've taken my interests in
studying the relationship between compositional form and audience
reaction down to the neural level where cells are presented with
electrical pulses in various patterns to study the effects these
engender in the sense of reward, hunger, anxiety, and pain felt by the
whole audience of cells we call the organism.
E-mail: ted@psych.nyu.edu
Representative Publications
Coons, E. E., Schupf, N., and Ungerleider, L. G. (1976). Uses of
double-pulse stimulation behaviorally to infer refractoriness,
summation, convergence, and transmitter characteristics of
hypothalamic reward systems. Journal of Comparative and Physiological
Psychology 90, 317-342.
Coons, E. E., and White, H. A. (1977). Tonic properties of
orosensation and the modulation of intracranial self-stimulation: The
CNS weighting of external and internal factors governing reward. In
Tonic Functions of Afferent Systems, eds. Wenzel, B., and Ziegler,
P. (Annals of the New York Academy of Sciences 290, 158-179).
Carr, K. D., and Coons, E. E. (1982). Rats self-administer
nonrewarding brain stimulation to ameliorate aversion. Science 215,
1516-1517.
Porrino, L. J., Coons, E. E., and MacGregor, B. (1983). Two types
of medial hypothalamic inhibition of lateral hypothalamic
reward. Brain Research 277, 269-282.
Simson, P. E., and Coons, E. E. (1989). Lateral hypothalamic
stimulation can augment or attenuate Nucleus Gigantocellularis escape:
Evidence for appetite-associated aversion amelioration. Behavioral
Neuroscience 103, 612-620.
Carden, S. E., and Coons, E. E. (1989). Diazepam modulates lateral
hypothalamic self-stimulation but not stimulation-escape in
rats. Brain Research 483, 327-334.
Miserendino, M. J. D., and Coons, E. E. (1989). Hedonic
interactions of medial prefrontal cortex and Nucleus Reticularis
Gigantocellularis. Brain Research 483, 233-250.
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