Documenti di Didattica
Documenti di Professioni
Documenti di Cultura
Department of Psychology, Bowling Green State University, 1001 East Wooster Street,
Bowling Green, OH 43403, e-mail:
Published online: 09 Jan 2014.
To cite this article: Jaak Panksepp (1999) Emotions as Viewed by Psychoanalysis and Neuroscience: An Exercise in
Consilience, Neuropsychoanalysis: An Interdisciplinary Journal for Psychoanalysis and the Neurosciences, 1:1, 15-38, DOI:
10.1080/15294145.1999.10773241
To link to this article: http://dx.doi.org/10.1080/15294145.1999.10773241
15
16
Jaak Panksepp
17
PRIORITIZATION OF VARIABLES
IN THE STUDY OF EMOTIONS
5r---------------------.
en
z
CJ
i=
c(
::E 2
1 FEELINGS
COGN.
AUTON.
FACIAL
VOCAL
EMOTIONAL ATTRIBUTES
Figure 1. Average ( SEM) opinions of 40 psychology graduate and undergraduate students requested to prioritize the following five major attributes of emotions from least important (rating of 1) to most important
(rating of 5). The options were listed in the following order: Facial Expressions, Vocal Expressions, Feeling States, Cognitive Changes and Autonomic Changes, with an open space for any other options, which was never
used. Although Feeling States had the highest overall rating, Cognitive and
Autonomic Changes were not far behind. However, these results are not
representative for the population at large. When 10 music majors were
asked the same questions, the ratings were more clearly skewed for Feeling
State (mean 4.6) compared to Cognitive Changes (mean 2.9) (p<.01). In
contrast, the response generated by 10 philosophy students was essentially
just the opposite (p< .05) To evaluate the lower strataes of society, of 35
drivers incarcerated for drinking and driving, 30 listed Feeling State as
the most important attribute of emotions. In sum, most people probably
believe that Feeling States are the most important attributes of emotions,
but this opinion is not necessarily shared by highly cognitivized individuals
and/or those who have been exposed to the intellectual biases that are
traditional in psychology.
18
Jaak Panksepp
cerebral rationalizations, but it has yet to deal effectively with the basic biological nature of affective
feelings.
By trying to cover all aspects, while disregarding
the most troublesome and essential attributes of emotions (i.e., the nature of subjective states), modern psychological theories of emotions often do not provide
the necessary analytic simplifications that can yield
robust empirical evaluations of key issues. Although
Freud's view was also quite broad, encompassing most
of the now well-accepted attributes of emotions, he
did take a harder stance on the primacy of emotional
feelings. I respect the fact that he placed affect-the
pleasure-unpleasure principle-at the center of his
scheme. This can still be deemed courageously controversial, but in my estimation, it is the correct point of
view. Without such functions, we cannot even make
computers truly intelligent (Clark, 1997), and humans
seem to lose a lot of their common sense when emotional systems are damaged (Damasio, 1994; Picard,
1997). Without emotions we would probably be little
more than the zombies of philosophical renown (Harnad, 1994).
Of course, id functions need to be subdivided and
taxonomized more extensively than Freud was able to
do. Such deep functional issues must be clarified
through conjoint psychological and brain research,
and it should be more widely recognized that animal
work is absolutely essential to resolve the fine details
of the underlying systems with adequate clarity. Because of the lack of any credible methodology or database, Freud had remarkably little to say about the deep
nature of the id-based foundation for his system of
thought. He devoted his efforts to discussing the higher
psychological processes-how ego and superego functions are molded through experience. My own work
for the past quarter of a century has been based on the
supposition that it will be through the neuroanatomical
and neurochemical clarification of the various id energies of the mammalian brain that our understanding
of the fundamental nature of the basic forms of human
emotional experience and behavioral control must be
based. I work from the premise that the id energies
evolved long ago and remain homologous in all of our
close evolutionary relatives. This is not a view shared
by many of my colleagues, especially when it comes
to the importance of internal feeling, which cannot be
directly observed, in the governance of animal behavior.
Even though emotional systems, as all brain systems, have changed during speciation as a result of
selective pressures, it is reasonable to assume that di-
19
Accordingly, the issue of affective experience in
other animals is gradually becoming a scientifically
workable problem. Now that we are recognizing the
deep homologies that exist in the (1) anatomical structure; (2) neurophysiological dynamics; and (3) neurochemical coding of brain processes across all
mammalian species, we have the opportunity to validate many of the findings and conclusions derived
from animal behavior and brain research with subjective reports derived from human research. Although,
informative correspondences can be achieved at all
those levels of analysis, the most useful ones are
bound to emerge from a study of the neurochemical
coding of behavior. Young Dr. Freud realized this in
the 1890s when he discussed the pleasure and unpleasure of "sexual release" in his "Project," and speculated that' 'a suspicion forces itself on us that in both
instances the endogenous stimuli consist of chemical
products, of which there may be a considerable number" (Freud, 1950, p. 321). Also, as Solms and Nersessian note in their sixth footnote, the elderly Freud
still held out the hope that: "The future may teach us
to exercise a direct influence, by means of particular
chemical substances, on the amounts of energy and
their distribution in the mental apparatus" (1940, p.
182). And he followed that with a statement which
remains as true now as it was then: "It may be that
there are still undreamt-of-possibilities of therapy" --especially since the day is approaching when we
will be able to pharmacologically modulate specific
neuropeptide-based emotional systems of the brain.
Even with the currently splendid, but still quite limited, stockpile of accepted pharmacological tools for
human research-from amphetamines to Viagra, so to
speak-we can initiate many experimental inquiries
that may highlight the causal underpinnings of id energies in humans. Credible predictions can be derived
from the many studies that have already been done in
other species.
Although considerably less useful for deriving
causal connections, neurophysiological and neuroanatomical correspondences also help highlight affective
homologies within human and animal brains. Localized brain stimulation has yielded remarkable correspondences (Panksepp, 1985), and more recently,
noninvasive stimulation of the cortical surfaces with
rapid transcranial magnetic stimulation (rTMS)
(George, Kettner, Kimbrell, Steedman, and Post,
1996) is providing a powerful way to analyze the role
of higher cerebral domains. Neuroanatomical correlates of emotional processing can now be achieved
with various modern modes of brain imaging (George
20
et aI., 1996; Lane, Reiman, Bradley, Lang, Ahern, Davidson, and Schwartz, 1997).
Unfortunately, many of these correlative techniques, which detect changes of activity in cerebral
canopies more readily than subcortical trunk lines,
tend to promote and reinforce corticocentric views of
emotional systems. This has led to a neglect, during
the current era, of the many subcortical systems that
are absolutely essential for the basic emotions to be
generated within the brain. In fact, it remains possible
that cortical inhibition of lower processes actually suppresses the conscious experience of affect in humans,
leading to the internalization or "binding" of emotional energies as Freud discussed extensively. In any
event, most of Freud's theorizing was also devoted to
the higher cognitive levels where the basic instinctual
energies are dealt with by various emotion-regulatory
mechanisms including repression, projection, reaction
formation, and so on (issues that are almost impossible to address in animal research except to the extent
that different memory processes can be shown to govern emotional output). My personal view is that the
shared subcortical heritage, from which the various id
energies emerge across mammalian species, provides
an essential and solid foundation for understanding
the nature of affective processes as well as higher emotion-regulating functions of the brain. Unfortunately,
these central state controls can only be monitored, at
present, with indirect behavioral measures.
Although Freud did not take any clear positions
on the brain organization of emotionality, I find it
intriguing how closely so many of his ideas, as outlined by Solms and Nersessian, mesh with my own.
Most importantly, in putting affect at the heart of his
analysis, he recognized that the assignment of value
to behavioral and higher psychological processes was
the key function of emotions. Freud did not equivocate
on the issue that still plagues most neuroscientists interested in the problem of emotions. Freud recognized
that affect registers the importance of salient world
events, and thereby, permeates the higher conscious
functions of the brain-mind. He also viewed affect as
arising from fundamental biological mechanisms (presumably brain circuits), which guide instinctual action
tendencies. The affect programs of the brain that have
now been revealed are probably the immediate infrastructures of such processes (Panksepp, 1998a). At the
heart of these systems there are a variety of chemical
codes (largely neuropeptidergic) that may eventually
permit powerful new modes of psychiatric intervention, and new ways to evaluate how feelings are con-
Jaak Panksepp
structed in the human brain. These findings can now
enrich psychoanalytic thought.
21
many direct and indirect influences such as the strong
two-way connections with frontal executive areas of
the brain and widespread influences on sensory cortices through the extended reticular and thalamic activating systems (ERTAS) conceptualized by Newman
and Baars (1993). I believe that various emotional systems create affective experiences by interacting with
such an extended ego structure. The resting level of
reverberation within this system is an epicenter (homeostatic settling point) upon which the various basic
pleasures and unpleasures of life may be predicated.
Because of the centrality of such a value coding
system for everything an animal does, I disagree with
the widespread assumption among behavioral neuroscientists that feelings may be causally inefficacious
epiphenomena within the human brain. Even though
unconscious processes are obviously much vaster in
the brain than conscious ones, the denial of affective
consciousness in animals is certainly a dubious and
potentially nefarious point of view. It will not serve
our neuroscience well, in the long run, to make wrongheaded choices about such matters. Such points of
view compromise the ability of neuroscience to establish better relations with the social sciences and humanities, as well as the everyday society in which our
work is embedded. In any event, I believe that the
neural grounding of the virtual body of the SELF is
such that it can interrelate external stimuli (simple
perceptions) and internal values (emotional states)
with a coherent and stable motor representation of the
body (a basic action system). In this scheme, feelings
may ultimately reflect the various types of action
readiness that permeate the extended neurodynamics
of the SELF. In other words, the distinct, primal feeling states may simply reflect the natural types of neurodynamics (resonances) that can exist within the
animate core of our being.
The anatomy of the underlying neural structures
are congruent with the view that the centromedial
brain stem contains essential ingredients for organismic coherence and action readiness (Figure 2). (1) The
PAG contains a massive convergence of many distinct
emotional systems which are strongly connected to
spinal sensory and motor systems. (2) The overlying
colliculi contain a massive convergence of most of the
major external sensory systems. (3) Nestled between
them there exist motor maps that can yield coherent
bodily movements, especially of the orienting and simple rhythmic locomotor varieties. I assume that this
primal SELF anchors organisms as coherent, feeling
creatures with a basic form of self-identity, but also,
the widespread neural connections of the primitive
Jaak Panksepp
22
A //
/
CINGULA TE
"" \
"',SC
\....
BASAL FOREBRAIN
'\--I
'\
TEMPORAl. l.OBE
AMYGDALA
"
CONVERGENCE OF SOMATIC
INFORMATION IN THE
SUPERIOR COLLICULUS
PANIC
FEAR
SELF, especially directed toward frontal cortical areas, may provide various forms of affective arousal
and coherence throughout the neuroaxis. Also, as indicated, it has strong connections to the ERTAS which
has been postulated to be the staging ground for a
generalized work-station of sensory consciousness
(Baars, 1996; Newman, 1997), whereby perceptions
can become imbued with affect. With such an extended neural entity, it is easy to imagine how emotional and motivational values could percolate
throughout the neuroaxis, and how it may be the foundation for higher forms of consciousness, and its various satisfactions and discontents. All that is required is
strong modulation of ascending ERTAS components
(including cholinergic and catecholaminergic) from
the PAG/SELF system, and such neural connections
have been demonstrated. The wide neural extents of
these systems permit abundant types of emotional expression-from passionate addictions and fixations to
repressions and rationalizations-to be constructed
from raw feelings. In this view, the essence of affective
feelings arises from various basic emotional operating
23
unlearned sensorimotor integrative abilities of ancient,
subcortical regions of the brain that can establish various types of neurodynamic feeling states within the
brain.
We can be certain that there is much more affective information encapsulated in the brain (via extended, "modular" circuits) than could have been
anticipated when Freud was pursuing his synthesis.
Simply consider the fact that there are ludic circuits
in the mammalian brain which generate joyous social
engagement (i.e., play and laughter). Freud barely anticipated such id/ego functions in his Jokes and Their
Relation to the Unconscious (1905). At present, the
infrastructure of the PLAY system includes the reticular nuclei of the posterior thalamus and centromedial
brain stem. Indeed, ludic urges may reflect one of the
earliest coherent manifestations of ego functions that
emerged from the neural evolution of the primitive
SELF. This is suggested by the dramatically assertive
way in which organisms spontaneously throw themselves into playful activities when such brain systems
are active (Panksepp, 1993). How these systems control psychological and neural maturation should be an
interesting chapter in brain research (Panksepp,
1998b).
From my vantage, Freud did not adequately recognize the existence of emotional systems devoted to
distinct social processes. Although he gave abundant
attention to sexuality, perhaps rather too creatively,
he failed to acknowledge the probable existence of
basic instinctual systems for maternal devotion (tenderness), social attachment (lovingness), separation
distress (sadness), and playfulness (joyfulness), all of
which are heavily represented in midline thalamic and
limbic cortices (frontal, anterior cingulate, and insular
areas) (Panksepp, 1998a). Of course, later generations
of psychoanalytic thought developed some of these
themes under the rubric of "object relations," but
much of this was discussed in the context of derivative
rather than basic emotional processes. We can now
hypothesize that it is through the auspices of the various basic social-emotional systems that such psychodynamics emerge. Indeed, the types of self-serving
cognitive patterns and deceptive tendencies promoted
by exigencies of reproductive success are vaster than
anyone could have imagined in Freud's day (Zahavi
and Zahavi, 1997). How higher social emotions (presumably superego functions), such as envy, guilt, jealousy, and shame emerge from these systems will be a
fascinating chapter of neuropsychology, that has received some attention from psychoanalytically oriented investigators (Lewis, 1988). The refinement of
24
Jaak Panksepp
the overarousal of these brain areas (Schwartz, Stoessel, Baxter, Martin, and Phelps, 1996).
It will be most interesting to conceptualize how
the more subtle defenses may be constructed in the
brain. They probably are not simply the straightforward associative processes that have been the stock in
trade for behaviorists, but may include various forms
of internally mediated implicit learning, including
condensations, displacements, projections, and transferences. For instance, as Freud also explicitly emphasized, excessive early experiences with certain
negative emotional states may promote different routes
of self-organization within the hierarchical processes
that control behavior (Mascolo and Griffin, 1998).
There is little relevant research, except for the fact that
certain experiences can sensitize emotional responses
(Rosen and Schulkin, 1998), perhaps by promoting
the ability of higher functions to trigger subcortical
emotional systems, a process that has been conceptualized as an increase in "limbic permeability" (Adamec, 1991, 1993). From this perspective, the
supposition that many psychiatric ailments may reflect
imbalances within and among the activities of the basic emotional systems, deserves more attention (Panksepp, 1988). In any event, the aim of therapy should
be to establish more harmonious emotional resonances
within the primitive neural infrastructures, and it now
seems that psychopharmaceuticals are most efficacious in achieving such results. However, systematic
evaluation of the long-term benefits of nontraditional
approaches ranging from rTMS to music and other
somatic therapies need to be considered by those who
wish to entrain beneficial brain rhythms and thereby
indirectly change behavioral patterns by inducing positive mood states. It would be most interesting to determine how affective id energies might be recruited for
therapeutic change when free-association therapies are
combined with such modalities. In general, psychoanalytic approaches need to develop stronger relations to
all of the somatic approaches that are known to modify
moods (Thayer, 1989; Parkinson, Tottersdell, Briner,
and Reynolds, 1996).
A key empirical issue at the present time is the
clarification of the manner in which the various affective states are represented within the brain. Most
likely the answer is "widely," but one of the least
likely places is the neocortex. This is not to say that
cortical processing is not massively affected by emotions. To document this, one need only analyze how
heavily the cortex is aroused during emotional episodes using techniques ranging from EEG to cFos expression. If you simply allow animals to play or force
25
VASOPRESSIN/OXYTOCIN
(Functions: AVP promotes male-typical persistence:
Oxytocin, female-type nurturance and aeceptance)
CORTICOTROPHIN
RELEASING FACTOR
CHOLECYSTOKININ
(Functions: Regulation of emotional systems:
feeding, sex, exploration, anxiety, and pain)
Figure 3. Cartoon parasaggital rat brain representations of four neuropeptide systems that are important in various positive emotions (left side)
and various negative emotions (right side). Anatomical designations are:
LC-Iocus coeruleus; DB-dorsal noradrenergic bundle; VB-ventral
noradrenergic bundle; CN-Caudate nucleus; AC-anterior commmissure; OB-olfactory bulb; CTX-eortex; BF-basal forebrain; HC-hippocampus; TH-thalamus; SC-superior colliculus; IC-inferior
colliculus; CC-eorpus callosum; POA-preoptic area; VTA-ventral tegmental area. Small circles in the cortex indicate dispersion of local interneurons. The figure is adapted, with permission, from Panksepp
(1998a), courtesy of Oxford University Press.
26
PAG may be essential for creating feeling states which
are then broadcast widely in the brain. If so, a key to
understanding the nature of feelings is the identification of the various neurodynamic and neurochemical
correlates that accompany the various types of feeling,
and the evaluation of their causal roles through parallel
lines of manipulative research. Such lines of inquiry
have barely been initiated (for summary, see Panksepp, in press).
This should make the study of affective processes
a primary goal for both psychology and neuroscience,
but it is understandable why progress has been so slow
on the most basic issues-we cannot visualize the
spontaneous and long-term internal neurodynamics of
the brain as readily as we can image how the brain
responds to events in the world. Being human, we
prefer to look where the light is brightest, so we often
focus on rapid onset emotional responses to conditioned stimuli, where affect clearly cannot be the primary mediator of the observed behavior (LeDoux,
1996).
Historically, the hope was that emotions could be
explained by focusing on the autonomically induced
cognitive commotion that accompanies emotional
arousal (e.g., leading to the James-Lange,
Schacter-Singer, cognitive-attributional traditions).
Some also hoped that we could ignore the likelihood
that there were specific brain mechanisms that were
evolutionarily designed to instigate and coordinate affective responses. The same bias is still evident in
modern emotion research, both psychological and neuroscientific, with more effort devoted to peripheral autonomic and cognitive issues than the lowest common
denominators in the brain. I suspect that a clarification
of the core brain issues (i.e., the pathways and neurochemistries for the instinctual id energies) will be essential for establishing a substantive foundation for
psychoanalytic thought, even though the other levels
of analysis may be more important for developing new
ideas of how emotions become "bound," potentially
yielding various defense mechanisms.
Although a definitive answer to the question
posed by Solms and Nersessian, "what are affects a
perception of," cannot yet be provided, relevant empirical work can now be conducted, even in the social
realm (Panksepp, Nelson, and Bekkedal, 1997). There
are bound to be some surprises-for instance neuropeptides such as GLP-l (Glucagon Like Peptide-I)
and urocortin that are thought to control feeding behavior, may do so only indirectly by modulating emotional processes (Panksepp and Bekkedal, 1997a).
While many levels of the neuroaxis surely provide
Jaak Panksepp
important ingredients for fully resolved affective responses, the integrity of the higher functions is bound
to be more dependent on the integrity of the lower
functions than vice versa. Accordingly, I strongly urge
investigators to devote more research to brain zones
like centromedial areas of the mesencephalon and the
reticular nuclei of the thalamus where emotional values and external events are first coordinated with a
coherent map of the body and exteroceptively triggered perceptions. These may be critical brain zones
where id and ego processes begin their massively entangled battle for primacy that reverberates through
all subsequent levels of neural development of each
individual and species. This is where the various "energies" of the anima emerge. With each layer of development, there are new opportunities for the
emergence of defenses, displacement activities, and
neural sensitizations that will be most difficult to disentangle.
'Ii 1600
c
~ 1400
0
C")
1200
(/)
1000
a.
...
.... ~......
-0....
......0- .....
---e-
VEHICLE
0'
...'"
0
.....,.. ..... '0.
.......0. ...
"0- '0.
>
a
Q)
0)
......0- . 0
800
600
CD
>
ct
400
200
TIME (Hrs.)
27
of these possible connections can be asserted with assurance, except to note that one of the major functions
of the neocortex (especially the frontal cortex), in its
role of processing exteroceptive information, is to inhibit more impulsive subcortical processes.
As suggested by Solms and Nersessian, a provocative way to make the distinction between the "quantitative" and "qualitative" aspects of affective life
may be to focus on the generalized systems (e.g., NE,
5-HT and ACh) shared by all of the discrete functional
systems of the brain which contribute substantially to
a quantitative dimension of affect while the more specific neuromodulators, like many of the neuropeptide
systems, are more influential in establishing the qualitative differences among affects. This seems highly
promising. However, it is unlikely that neuroscientific
investigators would be eager to relate the nonspecific
components to a vague, hydraulic concept like
"drive," for they already have more specific descriptions of how these systems operate in the brain. For
instance, NE controls how efficiently the cortex processes information by increasing the effects of incoming signals as compared to background noise; 5-HT
tends to diminish the impact of information on the
cortex; and ACh focuses attentional resources. All of
these generalized functions interact with a host of specific brain systems for discrete types of information
processing (both exteroceptive-cognitive and interoceptive-emotional), which necessitates that we study
their various localized effects only under the most exacting experimental conditions.
Periodically there has been a desire to relate these
systems to specific affects, especially fear, but the data
remain most consistent with the existence of broad and
nonspecific affective as well a cognitive informationprocessing effects. Although these systems act globally, if one restricts focus to limited areas of the brain,
they may appear to have distinct qualitative effects on
emotional memories within very specific brain circuits
such as the FEAR circuits of the amygdala (McGaugh,
Cahill, and Roozendaal, 1996). However, it may well
be that normally such effects are not seen within the
brain except when FEAR systems have already been
aroused by other, more specific stimuli. For the time
being we must remain cautious in reaching any definitive conclusions, since it is certainly possible that a
great deal more qualitative specificity may emerge
through the overall circuit neurodynamics, as well as
the effects of the remarkably diverse types of receptor
subpopulations that aminergic transmitters act upon.
The possibility that a single chemical system can
have both qualitative and quantitative consequences is
28
also a reasonable conceptual alternative. This is especially evident for glutamatergic transmission in the
brain. Glutamate appears to operate directly in practically every cognitive and affective process that has
been studied in animals. Along with some other excitatory amino acids, it appears to construct the skeletal
form of every thought and emotion of which the brain
is capable. This is evidenced by the large number of
emotional responses-from anger to fear to separation-distress-that can be activated by glutamatergic
stimulation of different brain areas. However, it would
seem that most of these fundamental potentialities are
not manifested until instigating stimuli arouse more
specific emotion control systems such as the various
neuropeptide circuits. The way I would envision this
process is that once a neuropeptidergic command influence is aroused in the brain (both at synaptic sites
of interaction as well as in more nonspecific broadcasting via paracrine transmissions), the selected glutamatergic response within a subset of available
response elements may carry the functional message
forward both in qualitative and quantitative terms.
Meanwhile, its metabolically related cousin
gamma-aminobutyric acid (GABA), the most prolific
inhibitory transmitter of the brain, exerts local inhibitory controls over these same neuropsychological and
behavioral potentials. Thus, one can envision glutamate as controlling both quantitative and qualitative
excitatory components of each emotional response,
while GABA can do the same, by controlling the inhibitory components of such responses, both in functionally restricted circuits as well as broader brain
networks that mediate supportive psychological processes. No doubt, tonic activity in all of these systems
might also contribute to a general concept like
"drive" for it is known that brains with low GABA
are very excitable, tending toward epileptic activity,
while facilitation of glutamatergic activity also promotes epileptic arousal. Conversely, if we markedly
reduce glutamate activity and increase GABAergic activity (as can be done with sedatives ranging from
alcohol to barbiturates), organisms become unconscious. In sum, a variety of generalized brain influences as well as the arousal of specific emotional
systems contribute to overall affective integration in
the brain.
Freud did anticipate that the neurochemical control of affective states could eventually become a reality. The rise of biological psychiatry has amply
confirmed this prediction, and thereby diminished the
influence of psychoanalysis. But we are now on the
verge of a second great revolution of biological psy-
Jaak Panksepp
chiatry-one that may allow us to harness specific
neuropeptidergic emotional controls within the brain.
Such a revolution may eventually help reopen the
doors to certain psychoanalytic concepts. However,
none of those findings may be able to breathe life into
Freud's generalized concept of "drive." It is simply
too broad and imprecise for any compelling neuroscience treatment. The hydraulic concept of drives building up that was so popular in Freud's day now appears
to be misleading in so many ways, even though it is
not difficult to imagine how such metaphoric entities
may correspond to the intensity of excitatory inputs
to central integrative systems such as the SELF. Unfortunately, there are too many distinct influences to subsume them under a single concept, except perhaps as
a general class-identifier. Ultimately Freud's drive
concept probably reflected the way higher conceptmediating areas of the brain seek to create order from
the complexities of subcortical neurodynamics. It is
reminiscent of the arousal axis in current dimensional
theories of emotions (Lang, 1995), which may also
simply be another broad, higher order abstraction that
has no unidimensional representation within the subcortical dynamics of emotional systems.
Also, it is worth noting that the term has been
used in too many ways in the history of psychology
to be resurrected as a major explanatory concept in
any system. The traditional utilization of the "drive"
concept in psychology fell into disfavor when it was
realized that it was intrinsically ambiguous and might
be devoid of explanatory power (Bolles, 1975). In my
own recent overview of emotions and motivations
(Panksepp, 1998b), the "drive" concept was relegated
to those specific regulatory motivational functions
such as hunger, thirst, and thermoregulation, where
specific interoreceptive detector elements have been
identified in medial strata of the diencephalon. One
could also employ the drive concept for transmitters
such as dopamine (DA) that help regulate generalized
appetitive arousal functions (which I have conceptualized as a SEEKING function), but it should be noted
that such circuits do not directly up-regulate other energetic affective behaviors such as playfulness and
fear. Thus it seems conceptually fuzzy to label such
systems as general behavioral arousal or facilitation
systems as some have done. We should avoid talking
about these systems as if they "energize" every behavior or provide an infrastructure for an omnibus
"positive affect" system of the brain. Of course, seeking an optimal conceptual structure that does not do
injustice to the underlying complexities, remains a
29
increasing its activity only modestly to highly stressful
stimuli. One could propose that NE and DA arousal
and 5-HT quiescence promote drive, while catecholaminergic quiescence and 5-HT arousal tend to reduce
the overall perceived feeling of drive tension.
However, for all this to be a useful exercise, it
should provide some explanatory power for existing
observations concerning the normal human psyche.
There simply is not sufficient data at that level to proceed very far. Indeed, carefully conducted studies that
specifically modify these systems are just becoming
available, and so far the results generally indicate that
global affective-personality tendencies can be
changed in predicted directions. For instance, increasing 5-HT in the normal human brain reduces negative
affect and increases social cooperation without influencing positive affect (Knutson et aI., 1998). Thus, we
can be confident that affect intensity can certainly be
linked to the synaptic levels of such neurochemical
activities, but I expect that the qualitative aspects of
affective feelings do emerge largely from other, concurrently aroused, neuropeptide systems. In any event,
the database remains too meager to proceed confidently much farther on such fragile limbs of speculation.
30
wise-arises from brain matter, and how such processes are intermeshed with the long-term regulation
of behavior. There is no question that a great deal of
emotional behavior, usually the rapid-reflexive variety, requires no precipitous arousal of affective consciousness in order for emotional behaviors to be
initiated (LeDoux, 1996), but we may be seriously
amiss in our judgment if we believe longer-term emotional processes do not control future behaviors. And
in that trailing role, affective states are not just epiphenomena; they surely have longer-term regulatory effects on future behavioral outputs. In other words,
internally experienced emotional feelings may be seen
as long-term modulatory influences which figure most
heavily in the planning of behaviors and the more deliberate selection of future actions, rather than in the
mere emission of eruptive emotional acts (which is
only one component, and a transient one, of the overall
emotional response). In the same way, in young people
thoughts may more commonly follow impulsive actions than precede them. In other words, most conscious brain activity, affective as well as cognitive,
is not simply devoted to generating behavior, but for
dwelling on future behavioral strategies. In their longterm regulatory role, affective states can create inner
turmoil and conflict in people's lives leading them to
seek assistance (therapy) or to indulge in psychological and behavioral diversions (fixations, sublimations,
and displacement behaviors of various kinds).
It is probably fair to say, that for humans, more
theorizing has been devoted to the sensory-appraisal
side of the affective integration than to the motor side.
I believe that more effort should now be devoted to
the motor side, recognizing that mind is typically embodied in actions. This may sound like a perplexing
assertion, since behavioral neuroscience has in fact
expended most of its resources on analyzing explicit
motor processes. In clarification, I would suggest that
in situations where explicit actions are inhibited by
learned social-display rules, many motor responses of
the nervous system continue to be reflected in various
bodily tensions, small twitches, postures, gestures as
well as many other local bodily effects, from autonomic to hormonal. These small motor responses
should figure as heavily in our analysis of affective
states of consciousness as the grosser forms of action
readiness that are typically manifested in the varieties
of instinctual motor actions that characterize the eruptive emotional states of animals. Indeed, psychoanalysis is better positioned than most other disciplines to
try to analyze these small but powerful outputs that
seem to reflect a battle between the various id energies
Jaak Panksepp
and ego controls, but verbal approaches may need to
be supplemented with ethological analysis of both
gross and subtle neuromuscular tendencies. The nervous twitches of facial muscles and gaze aversions
may eventually allow us to read a person's affective
state more accurately than what they say, especially
if it turns out, as some lines of research suggest, that
the speech functions of the left hemisphere evolved as
much for lying and deception as for straightforward
communication.
Freud recognized such issues in his concept of
"bound" affective energy, and in this context, Solms
and Nersessian encourage us to conceptualize how
voluntary-instrumental actions emerge developmentally from the more primitive affective actions of the
nervous system. A simple and straightforward answer
to this may be that changes in internal affective states,
as they relate to both implicit and explicit motor actions, probably reinforce the preceding behavior patterns. Emotional states may constitute the major
reinforcers for the development of long-term behavior
patterns. An underutilized but complementary approach to the problem may be to search for the neural
instantiation of certain emotional affects more within
the motor organization of the brain rather than among
neural systems that are closely related to the afferent
side (which may contribute more to the classical motivational rewards, as in the pleasures of gustatory and
other bodily sensations).
It is widely recognized by embryologists that motor competence emerges in the nervous system earlier
than sensory guidance, suggesting its primacy in brain
evolution. For instance, in the chick embryo, we observe coherent whole-body motor movements before
they are capable of being modulated by sensory inputs
(Provine, 1980; Oppenheim, 1991). This primacy of
the motor system should be of considerable interest
for those who wish to clarify affective consciousness,
and Damasio (1994) has emphasized the role of the
whole body in affective experience. However, rather
than focusing on the material body (which is obviously
important for harvesting all manner of sensory and
reafferent impressions), I suspect that it is the neurosymbolic representations of the' 'virtual body" of the
SELF within fairly low levels of the brain that will
give us the greatest leverage in understanding the fundamental nature of affect within the brain.
The distinct resonances of emotional systems on
such a "virtual body" may yield emotion specific neurodynamics, which are broadcast widely in the brain,
thereby constituting the very essence of emotional
feeling. As feelings are transmitted through the brain,
31
freeing patients from dwelling on certain negative life
events. These individuals could still exhibit practically
all forms of simple emotional arousal, but they would
not become entrapped in such episodes. Across the
years, it has become clear that other higher limbic
areas serve similar roles for other affective processes
(Figure 2). For instance, social-affective issues, which
characterize depression and obsessive--compulsive
disorders, find a focus of cogitation within anterior
cingulate areas (Drevets et aI., 1997; Mayberg et al.
1997). Anxious and angry thoughts probably find executive domains in lateral and medial temporal lobe/
amygdala zones, respectively, even though frontal areas are not without influence (Gloor, 1990).
There are reasons to suspect that the primary excitant for all such cogitations is glutamate, and the
main inhibitor is GABA, with a more general upward
and downward tuning of information processing in
these areas exerted by NE and 5-HT, respectively, and
ACh helping construct an attentional searchlight
which is directly under the control of the emotional
SELF. Individual neuropeptides apparently bring restricted parts of the widely distributed affect control
mechanisms to bear on specific types of life problems.
A detailed understanding of how so many systems
work together, and how they construct the abstract
neurodynamics of higher psychological processes, remains a great challenge for all of the mind sciences.
Conclusion
It is a daunting task to build solid linkages between
psychoanalytic ideas derived from clinical observations, especially ones that have not been adequately
subjected to standard modes of scientific validation,
and the incredibly rich empirical findings of modern
neuroscience, which have typically been harvested in
the most austere spirit of logical positivism. Regrettably, modern neuroscience has not been adept at conceptualizing how the internal neurodynamics of the
brain weave psychological realities by blending evolutionarily provided abilities with neurodynamic symbolizations of ongoing world events. This is
understandable; to accept the potential existence of
hidden functions, neuroscience would have to drop its
ultrapositivistic veil. It will not do so until the data
massively and unambiguously mandate acceptance of
a deeper integrative reality-complexity behind the surface appearances that we can directly measure. In my
estimation, compelling evidence for this has long been
available for both humans and related animals, but the
32
Jaak Panksepp
in various eruptive emotional outbursts. However, the
volcano of active mood states can continue to smolder
even when such short-lasting emotional eruptions are
not evident. In humans, higher ego and superego functions can keep these eruptive forces from being expressed outwardly, but much less so inwardly.
Freud was among the first to probe into these
darker areas of the human psyche, and he sought to
untangle, at a conceptual level, how such functions
might generally be organized and internalized within
the psyche. Our concern here is to discuss whether his
insights can be linked credibly to modern neuroscience. I believe many can. But will such exercises provide new avenues of thought that can promote the
maturation of functional neuroscience and psychoanalysis? We must wait and see. There is much to gain
and little to lose in pursuing such endeavors, especially
if the work remains empirically focused.
I believe the "great intermediate net" of the
brain can only be disentangled if global psychodynamic and molecular and systems neuroscience approaches can be brought to bear on problems of mutual
interest. To bring this to pass, psychoanalysts will
have to invest more intensely in the study of experimental manipulations, especially psychopharmacological ones, where human verbal reports of internal
experiences and dynamics are studied after systematically induced transient changes in the arousability in
specific brain systems. We finally have a great many
experimental tools to pursue such studies well. Psychoanalysis has carefully nurtured a listening approach that can minimize the use of loaded questions
and other demand characteristics. Unfortunately, the
transcription and content analysis of free associations
is a tedious and a tricky business, but computerized
transcription techniques can now be implemented.
Such approaches should be supplemented with spectral analyses and electronic processing of the acoustic
data, as well as the development of new qualitative
tools to systematically probe the psyche.
But for all this to be useful, we must encourage
individuals to speak rather directly and systematically
about their internal experiences, perhaps in controlled
settings where the experimenter-therapist is not in the
physical presence of the person being studied. We
must cultivate a greater willingness to ask appropriate
questions concerning the affective changes that various individuals experience in various situations. There
may also need to be some careful personality descriptions and perhaps selection of individuals for such
studies. At times it may be essential to have wellprimed, cooperative individuals who are willing to try
33
Indeed, opiate antagonists have provided such effects in the treatment of autistic symptoms (Kolmen,
Feldman, Handen, and Janosky, 1997). In our experience with this medication in the treatment of autism
(Panksepp, Lensing, Leboyer, and Bouvard, 1991;
Bouvard et aI., 1995), modest benefits have been evident in about half the children, especially the highfunctioning ones. I am especially fond of insight provided by a highly self-centered and emotionally aloof
17-year-old teenager who had good language skills.
On naltrexone, she became more sensitive and concerned with the feelings of her parents, but when asked
what had changed inside her, she seemed perplexed
and answered that nothing had changed within her.
Only the world had changed from her point of
view-other people were simply behaving differently.
And perhaps they were, through subtle interactions,
that arose from her increased intimacy with their lives.
This, of course, is the great dilemma of the subjective phenomenological view. Our affects are value
constructions of the brain, and our emotional systems
are designed in such a way as to project our feelings
into the world. We are not just angry; we are typically
angry with someone who seems hateful. We are not
just in love, but we love someone who seems lovable.
We are not just emotionally moved by the music we
enjoy, but the emotions actually appear to flow directly
from the music. Even as we recognize that the information triggering the feelings is encapsulated within
the well-interpreted musical score, the resulting mood
changes arise from the dynamic responses of our
brains. Recently, Fried and colleagues (Fried, Wilson,
MacDonald, and Behnke, 1998) stimulated the human
prefrontal cortex and provoked feelings of hilarity in
humans with nothing special having happened in the
environment, and these feeling were also projected
outwards. During the brain stimulation, everything the
individual focused on seemed funny.
In short, our brains are designed to project affect
(as well as perceptions, of course) back into the world,
and even our animal subjects seem to imbue neutral
environmental events with affective salience for they
exhibit contextual conditioning remarkably easily.
This is the way the brain generates its highly adaptive
illusions of emotional realities, and that may also be
why behavioral scientists are so timid in trying to deal
forthrightly with such brain processes. After all, by
accepting the probable existence of emotional feelings
in other creatures, we may only be studying our own
anthropomorphistic tendencies, rather than the functional competencies of other animals. However, the
available data, taken together, do suggest that we are
34
not deluding ourselves, for a neurochemical understanding of the brain mechanisms that generate the
affective behavioral tendencies in other animals can
predict many of our own feelings (Panksepp, 1998a).
Similar types of correspondence maps cannot be generated for thoughts. Thus, in the restricted arena of
basic emotions and motivations, careful, scientifically
advised anthropomorphism is a viable preliminary
strategy for identifying which types of value-encoding
processes exist in other brains. Through a detailed
study of the underlying neural mechanisms in animals,
we can now achieve a general understanding of how
homologous neural processes operate in our own
minds. Now we need to figure out how the animal
brain actually generates affect, but that work is still
proceeding remarkably slowly, partially because of
the conceptual blinders that behavioral neuroscience
has imposed on itself and the resulting research funding policies.
In pursuing parallel phenomenological studies of
subjective emotional experiences in humans, we are
confronted by one enormous obstacle: The speaking
hemisphere appears to be a master of confabulation
and deception in its appointed role of verbally communicating with others in the world (LeDoux, 1985). Social desirability factors appear to be much more
important to the left hemisphere than to the emotionally deeper and more sincere, right hemisphere. This
hemispheric specialization of emotional values was
strikingly evident in a recent study by Ross, Homan,
and Buck (1994), where individuals changed their
heartfelt emotional confessions toward more superficial~avalier directions when their right hemispheres
were selectively anesthetized.
What problems does this pose for future psychoanalytic work? Would subjects coming to participate
in a study be more left-hemisphere oriented, focusing
their psychological resources toward sustaining a high
level of social desirability? If so, would they be less
likely to reveal their deeper emotional feelings? If the
left hemisphere is, in fact, an expert at emotional repression (i.e., having a preference for an alexithymic
communication style, especially in males), research
would have to try to work past that barrier. This is
where the psychoanalytic tradition may be a special
blessing to empirical pursuits in the area. Testing situations where individuals are willing to confide their
inner lives may help us see, more clearly, the deeper
feelings that reside beyond the surface veneer of social
desirability. Indeed, one could imagine that such studies could eventually be used to effectively probe, with
Jaak Panksepp
full client feedback, which types of psychotropic medications might have optimal effects for which patients.
In closing, I would again reemphasize that it is
unlikely that neuroscientific findings will match up
precisely with psychoanalytic concepts. Also, the levels of complexity already revealed at the neuroscience
level, mostly derived from animal brain research, are
so vast that no one can have confidence in relating
them to human psychodynamics that arise from the
immeasurably complex interactions of many neural
systems. Still, there is an incredibly rich neuroscientific database from which we can derive testable ideas,
and after preclinical testing, the best concepts should
eventually be taken to psychoanalytic laboratories.
Obviously, most of the basic knowledge concerning human emotions remains to be collected. We do
not yet understand the natural time-courses of emotional episodes (even though some progress is being
made, e.g., Potegal, Kosorok, and Davidson, 1996).
We know little about how various emotions interact;
few have tried to characterize the real oscillatory neurodynamics of the affective states (using not only electronic technologies but various depth psychological
approaches). A great deal of careful behavioral, psychological, and psychoanalytic work is needed to answer such questions, but ultimately, our explanations
for many human feelings must be based on our understanding of the neural processes that control homologous processes in related animals.
In pursuing such lines of inquiry, we should be
under no illusion that neuroscience has progressed farther toward a substantive understanding of emotional
processes than it actually has. Within the grand edifice
of modern neuroscience, the study of emotions remains little more than a cottage industry, even though
leaders in the field are recognizing that "the study of
emotion is enjoying a renaissance" (Hyman, 1998, p.
417). Still, to get support for such work, it is best not
to mention that you are interested in understanding
emotions, especially in animals. Feel free to highlight
learning or any variety of other accepted brain mechanisms, but please, please do not mention that you are
interested in understanding the fundamental nature of
affective experiences.
The majority of neuroscientists (and hence peerreview panels) still believe such questions are outside
the purview of standard science. This is most perplexing, for we can be certain that a great deal of brain
activity is devoted to creating the affective infrastructure upon which our cognitive abilities are built. Psychoanalysis has recognized that fact, and the
systematic study of human affective experience is one
35
Neuroscience can be of great assistance to psychoanalysis and all the other social sciences, by providing
the foundational knowledge that is essential for us to
explain how minds exist. Progress will be made
largely by those who recognize that mind is a bodily
function of the brain and are willing to do the hard
scientific work.
As the predictive gap between neural and psychological processes narrows through the development of
conciliatory frameworks, the "explanatory gap" will
no longer be as intimidating as it used to be. Of course,
the critical ingredient for all modes of thought will be
their ability to generate predictions that can be supported or disconfirmed by generally accepted scientific
methodologies. For psychoanalysis a critical challenge
will be the extent to which it can refresh Freudian
theory, which now has an unpalatable and distinctly
post-Victorian flavor for many, into a modern and dynamic mode of thought that continues to be rejuvenated by the accumulating evidence. That, I believe,
is the goal of this new journal and, I hope, its many
future contributors.
References
Adamec, R. E. (1991), Partial kindling of the ventral hippocampus: Identification of changes in limbic physiology
which accompany changes in feline aggression and defense. Physiol. & Behav., 49:443-453.
- - - (1993), Lasting effects of FG-7142 on anxiety, aggression and limbic physiology in the cat. J. Psychopharmaco!., 7:232-248.
Adolphs, R., Tranel, D., & Damasio, A. R. (1998), The
human amygdala in social judgment. Nature,
393:470-474.
Baars, B. 1. (1996), Understanding subjectivity: Global
workspace theory and the resurrection of the observing
self. J. Consciousness Studies, 3:211-216.
Baram, T. Z., Koutsoukos, Y., Schultz, L., & Rivier, J.
(1996), The effect of "Astressin," a novel antagonist of
corticotropin releasing hormone (CRR), on CRR-induced seizures in the infant rat: Comparison with two
other antagonists. Mol. Psychiatry, 1:223-226.
Baron-Cohen, S. (1997), Mindblindness: An Essay on Autism and Theory of Mind. Cambridge, MA: MIT Press.
Berridge, K. C. (in press), Pleasure, pain, desire, and dread:
Biopsychological pieces and relations. In: Understanding Quality of Life: Scientific Understanding of Enjoyment and Suffering, ed. D. Kahneman, E. Diener, & N.
Schwarz. New York: Russell Sage Foundation.
Bilder, R., Ed. (1998), Centennial of Freud's Project for a
Scientific Psychology. New York: New York Academy
of Sciences.
Jaak Panksepp
36
Psychobiol., 24:211-218.
Depue, R. A., & Collins, P. F. (in press), Neurobiology of
the structure of personality: Dopamine, facilitation of
incentive motivation, and extraversion. Behav. & Brain
Sciences.
Devinsky, 0., Morrell, M. J., & Vogt, B. A. (1995), Contributions of anterior cingulate cortex to behaviour.
Brain, 118:279-306.
Drevets, W. C., Price, J. L., Simpson, J. R., Jr., Todd, R.
D., Rich, T., Vannier, M., & Raichle, M. E. (1997), Subgenual prefrontal cortex abnormalities in mood disorders. Nature, 386:824-827.
Freud, S. (1905), Jokes and Their Relation to the Unconscious. Standard Edition, 8. London: Hogarth Press,
1958.
- - - (1940), The Technique of Psycho-Analysis. Standard Edition, 23: 172-182. London: Hogarth Press, 1964.
- - - (1950), Project for a Scientific Psychology. Standard Edition, 1:281-391. London: Hogarth Press, 1966.
Fried, I., Wilson, C. L., MacDonald, K. A., & Behnke, E.
J. (1998), Electrical current stimulates laughter. Nature, 391 :650.
George, M. S., Kettner, T. A., Kimbrell, T. A., Steedman,
J. M., & Post, R. M. (1996), What functional imaging
has revealed about the brain basis of mood and emotion.
In: Advances in Biological Psychiatry, Vol. 2, ed. J.
Panksepp. Greenwich, CT: JAI Press, pp. 63-114.
Gloor, P. (1990), Experiential phenomena of temporal lobe
epilepsy. Facts and hypotheses. Brain, 113: 1673-1694.
Griffiths, P. E. (1997), What Emotions Really Are: The
Problem of Psychological Categories. Chicago: University of Chicago Press.
Harkness, K. L., & Tucker, D. M. (in press), Motivation of
neural plasticity: Neural mechanisms in the self-organi-
Nature, 393:417--418.
Kelso, J. A. (1995), Dynamic Patterns: The Self-Organization ofBrain and Behavior. Cambridge, MA: MIT Press.
Knutson, B., Wolkowitz, O. M., Cole, S. W., Chan, T.,
Moore, E. A., Johnson, R. C., Terpstra, J., Turner, R.
A., & Reus, V. I. (1998), Selective alteration of personality and social behavior by serotonergic intervention.
gist, 50:372-385.
Leak, & Christopher, S. B. (1982), Freudian psychoanalysis
and sociobiology. Amer. Psychologist, 37:313-322.
LeDoux, J. E. (1985), Brain, mind, and language. In: Brain
and Mind, ed. D. A. Oakley. London: Methuen, pp.
197-216.
- - - (1996), The Emotional Brain: The Mysterious Underpinnings of Emotional Life. New York: Simon &
Schuster.
Lewis, H. B. (1988), The role of shame in symptom formation. In: Emotions and Psychopathology, ed. M.
Clynes & J. Panksepp. New York: Plenum, pp. 95-106.
MacLean, P. D. (1990), The Triune Brain in Evolution: Role
in Paleocerebral Functions. New York: Plenum.
Macmillan, M. (1997), Freud Evaluated, rev. ed. Cambridge, MA: MIT Press.
Mascolo, M. F., & Griffin, S., Eds. (1998), What Develops
in Emotional Development? New York: Plenum Press.
Mayberg, H. S., Brannan, S. K., Mahurin, R. K., Jerabek,
P. A., Brickman, J. S., Tekell, J. L., Silva, J. A.,
McGinnis, S., Glass, T. G., Martin, C. C., & Fox, P.
T. (1997), Cingulate function in depression: A potential
predictor of treatment response.
Neuroreport,
8:1057-1061.
McGaugh, J. L., Cahill, L., & Roozendaal, B. (1996),
Involvement of the amygdala in memory storage: Interaction with other brain systems. Proc. U.S. Nat. Acad. Sci.,
93: 13508-13514.
Miller, H. L., Delgado, P. L., Salomon, R. M., Berman, R.,
Krystal, J. H., Heninger, G. R., & Charney, D. S. (1996),
37
- - - (1998b), The quest for long-term health and happiness: To play or not to play, that is the question. Psycholog. Inq., 9:56-65.
- - - (in press), On measuring the neurodynamics of
emotions: An evolutionary-neurodevelopmental view.
In: Emotion, Self-Organization, and Development, ed.
M. D. Lewis & I. Granic. New York: Cambridge Universities Press.
- - - Abbott, B. B. (1990), Modulation of separation distress by a-MSH. Peptides, 11 :647-653.
- - - Bekkedal, M. (1997a), Neuropeptides and the varieties of anxiety in the brain. Giorn. Ita!' Psicopat.,
1:18-27.
- - - - - - (1997b), The affective cerebral consequences of music: Happy vs sad effects on the EEG and
clinical implications. Internat. J. Arts Med., 5: 18-27.
- - - Burgdorf, J. (1998), Laughing rats? Playful tickling
arouses 50KHz ultrasonic chirping in rats. Soc. Neurosci.
Abstr., 24:691.
- - - Lensing, P., Leboyer, M., & Bouvard, M. (1991),
Naltrexone and other potential new pharmacological
treatments of autism. Brain Dysfunction, 4:281-300.
- - - Nelson, E., & Bekkedal, M. (1997), Brain systems
for the mediation of social separation-distress and socialreward. Evolutionary antecedents and neuropeptide intermediaries. NY Acad. Sci., 807:78-100.
- - Siviy, S. M., & Normansell, L. A. (1985), Brain
opioids and social emotions. In: The Psychobiology of
Attachment and Separation, ed. M. Reite & T. Fields.
New York: Academic Press, pp. 3-49.
- - - Yates, G., Ikemoto & Nelson, E. (1991), Simple
ethological models of depression: Social-isolation induced "despair" in chicks and mice. In: Animal Models
in Psychopharmacology, ed. B. Oliver & J. Moss. Holland: Duphar, pp. 161-181.
Paradiso, S., Robinson, R. G., Andreasen, N. C., Downhill,
J. E., & Davidson, R. J. (1997), Emotional activation of
limbic circuitry in elderly normal subjects in a PET
study. Amer. J. Psychiatry, 154:384-389.
Parkinson, B., Totterdell, P., Briner, R. B., & Reynolds, S.
(1996), Changing Moods: The Psychology of Mood and
Mood Regulation. London: Addison Wesley Longman.
Picard, R. W. (1997), Affective Computing. Cambridge,
MA: MIT Press.
Potegal, M., Kosorok, M. R., & Davidson, R. J. (1996), The
time course of angry behavior in the temper tantrums of
young children. Ann. NY Acad. Sci., 794:1:31-45.
Provine, R. R. (1980), Development of between-limb movement synchronization in the chick embryo. Develop. Psychobiol., 13:151-163.
Rosen, J. B., & Schulkin, J. (1998), From normal fear to
pathological anxiety. Psycholog. Rev., 105:325-350.
Ross, E. D., Homan, R. W., & Buck, R. (1994), Differential
hemispheric lateralization of primary and social emotions. Neuropsychiatry, Neuropsychol. & Behav. Neurol., 7:1-19.
Antonio R. Damasio
38
Ryff, C. D., & Singer, B. (1998), The contours of positive
human health. Psycholog. Inq., 9:1-28.
Schore, A. N. (1994), Affect Regulation and the Origin of
the Self: The Neurobiology of Emotional Development.
Hillsdale, NJ: Lawrence Erlbaum.
- - - (1997), A century after Freud's project: Is a rapprochement between psychoanalysis and neurobiology
at hand? J. Amer. Psychoanal. Assn., 45:807-840.
Schwartz, J. M., Stoessel, P. W., Baxter, L. R., Martin, K.
M., & Phelps, M. E. (1996), Systematic changes in cerebral glucose metabolic rate after successful behavior
modification treatment of obsessive-compulsive disorder. Arch. Gen. Psychiatry, 53:109-113.
Scoville, W. B., & Bettis, D. B. (1977), Results of orbital
undercutting today: A personal series. In: Neurosurgical
Treatment in Psychiatry, Pain and Epilepsy, ed. W. H.
Sweet, S. Obrador, & J. G. Martin-Rodriguez. Baltimore:
University Park Press, pp. 189-202.
Siegel, A., Schubert, K. L., & Shaikh, M. B. (1997), Neurotransmitters regulating defensive rage behavior in the cat.
Neurosci. & Biobehav. Rev., 21:733-742.
Solms, M. (1996), Was sind Affekte? Psyche, 50:485-522.
- - - (1997), The Neuropsychology of Dreams: A Clinico-Anatomical Study. Hillsdale, NJ: Lawrence Erlbaum.
Thayer, R. E. (1989), The Biopsychology of Mood and
Arousal. New York: Oxford University Press.
Wilson, E. O. (1998), Consilience: The Unity ofKnowledge.
New York: Knopf/Random House.
Zahavi, A., & Zahavi, A. (1997), The Handicap Principle:
A Missing Piece of Darwin's Puzzle. New York: Oxford
University Press.
Jaak Panksepp
Department of Psychology
Bowling Green State University
1001 East Wooster Street
Bowling Green, OB 43403
e-mail: jpankse@bgnet.bgsu.edu