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Course of Study for which scanned: Introduction to Psychology 2
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ISBN (of book) or ISSN (of journal): 9780495601500
Publication Title (Books or journal): Sensation and Perception
Journal year or volume number:
Article/Chapter Title: 14: The Cutaneous Senses
Page numbers: 343-349
Name of Author (or visual creator, if an image) : Goldstein, E.B.
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pain. They include subcortical structures, such as the hypothalamus the amygdala, and the thalamus, and areasin
the cortex, including the somatosensorycortex, the insula
(an area deep in the cortex between the parietal and temporal regions), the anterior cingulate cortex (ACC),and the
prefrontal cortex (Chapman, 1995; Derbyshire et al., 1997;
Price, 2000; Rainville, 2002). All of the brain regions that
are involved in pain perception, taken together, have been
Representation
of the Sensory
and Affective
Components
of Pain
The definition of
pain on page343 states that pain is "an unpleasant sensory
and emotional experience."This referenceto both sensory
and emotional experiencereflects the multimodal nature
of pain, which is illustrated by how people describe pain.
When people describe their pain with words like throbbing,
prickly)hot,or dull, they are referring to the sensory component of pain. When they use words like torturing, annoying,
frightful, or sickening,they are referring to the affective (or
emotional) component of pain (Melzack, 1999).
Evidencethat thesetwo components of pain are served
by different areasof the brain is provided by an experimentby
R. K. Hofbauer and coworkers(2001),in which participants
were presented with potentially painful stimuli and were
asked to rate (1) subjective pain intensity (the sensorycomponent of pain) and (2) the unpleasantnessof the pain (the
affective component of pain). Hofbauer and coworkersmeasured brain activity using PET,as participants respondedto
pain induced by immersing their hands in hot water.
What makes this experiment particularly interesting
is that Hofbauer and coworkers not only asked their participants to rate both the sensoryand affective components
of their pain, but they also used hypnotic suggestionto decreaseor increaseeach of these components. Figure 14.27a
shows that presenting suggestions to decreaseor increase
subjective
intensitychanged the participants' ratings of both
subjective intensity (left pair of bars) and unpleasantness
(right pair of bars). These changes were accompanied by
changesin activity in 51, the primary somatosensoryreceivmg area.
Figure 14.27b shows that presenting suggestions to
decreaseor increase the unpleasantness
of the pain did not
Pain
347
.
.
Suggestion:
.
.
Decrease intensity
Increase intensity
Suggestion:
Decrease unpleasantness
Increase unpleasantness
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Ratings
(a) Hypnotic suggestion: change
intensity of pain
Ratings
(b) Hypnotic suggestion: change
unpleasantness of pain
affect ratings of subjective intensity (left bars), but did affect ratings of unpleasantness (right bars). These changes
were accompanied by changes in activity in the anterior
cingulate cortex (ACC), but not in S1. From these results
Hofbauer concluded the ACC is important for determining
unpleasantnessand that unpleasantnesscan change even
when the intensity of pain remains the same. Many other
experiments have confirmed the importance of the ACC in
determining the affective component of pain, and also that
different structures in the brain serve different aspects of
pain perception (Rainville, 2002).
Chemicals
in the Brain
Another important development in our understanding of the relationship between
brain activity and pain perception is the discovery of a link
betweenchemicalscalled opioids and pain perception. This
can be traced back to researchthat began in the 1970son
opiate drugs, such as opium and heroin, which have been
used since the dawn of recorded history to reduce pain and
induce feelings of euphoria.
By the 1970s,researchershad discoveredthat the opiate
drugs act on receptorsin the brain that respond to stimulation by molecules with specific structures. The importance
of the molecule's structure for exciting these "opiate receptors" explains why injecting a drug called naloxone into a
person who has overdosedon heroin can almost immediately revivethe victim. Becausenaloxone'sstructure is similar to heroin's, it blocks the action of heroin by attaching
itself to receptor sites usually occupied by heroin (Figure
14.28a).
Why are there opiate receptor sites in the brain? After
all, they certainly have been present since long before people started taking heroin. Researchersconcluded that there
must be naturally occurring substancesin the body that
act on these sites, and in 1975 neurotransmitters were discoveredthat act on the samereceptorsthat are activated by
opium and heroin. One group of these transmitt~rs are the
pain-reducing endorphins.
348
(a)
..
(b)
...
Less pain
Increases pain
by blocking
endorphins
(c)
349