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International Handbook of Clinical Hypnosis - E-Lib FK UWKS

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NEUROPSYCHOPHYSIOLOGY OF HYPNOSIS 69<br />

will permit us to understand how hypnotic analgesia affects both cortical and<br />

subcortical processes.For instance, the ®rst fMRI study Crawford et al., 1998;<br />

Crawford, Horton, Harrington, Hirsh-Downs, Fox, Daugherty & Downs, 2000) that<br />

examined hypnotic analgesia in highly hypnotizable individuals showed dramatic<br />

activation shifts between attend and hypnotic analgesia in response to noxious<br />

stimuli presented to the left middle ®nger.In the cingulate cortex, there was<br />

bilateral or right hemisphere activation during attend, whereas in hypnotic analgesia<br />

only left hemisphere activation remained.Among other ®ndings, we also<br />

observed reductions <strong>of</strong> insular and shifts in thalamic activity during hypnotic<br />

analgesia.<br />

Human pain responses have been successfully studied through the analysis <strong>of</strong><br />

brain somatosensory event-related potentials SEPs).Hypnotically suggested analgesia<br />

results in signi®cant decreases in the later SEP components 100 msec or<br />

later after stimulus) at certain scalp leads using painful electrical e.g., Crawford,<br />

1994a; Crawford, Clarke & Kitner-Triolo, 1996; De Pascalis, Crawford & Marucci,<br />

1992; Meszaros, BaÂnyai & Greguss, 1978; Spiegel, Bierre & Rootenberg, 1989;<br />

but see Meier, Klucken, Soyka & Bromm, 1993), laser heat e.g., Arendt-Nielsen,<br />

Zachariae & Bjerring, 1990; Zacharie & Bjerring, 1994) or tooth pulp Sharav &<br />

Tal, 1989) stimulation.Earlier studies, <strong>of</strong>ten plagued by methodological ¯aws,<br />

provide mixed evidence for reviews, see Crawford & Gruzelier, 1992; Spiegel,<br />

Bierre & Rootenberg, 1989).<br />

Multiple intracranial electrodes temporarily implanted in the anterior cingulate<br />

cortex, amygdala, temporal cortex and parietal cortex <strong>of</strong> two patients undergoing<br />

evaluation and treatment <strong>of</strong> obsessive-compulsive disorder permitted Kropotov,<br />

Crawford & Polyakov 1997) to conduct a unique evaluation <strong>of</strong> pain processes.We<br />

investigated changes in SEPs accompanying electrical stimulations to the right ®nger<br />

during conditions <strong>of</strong> attention and hypnotically suggested analgesia.Only in the<br />

hypnotically responsive patient was reduced pain perception during suggested<br />

hypnotic analgesia accompanied by a signi®cant reduction <strong>of</strong> the positive SEP<br />

component within the range <strong>of</strong> 120±140 msec.In the left anterior temporal cortex, a<br />

signi®cant enhancement <strong>of</strong> the negative SEP component in the range <strong>of</strong> 210±<br />

260 msec was observed.Enhancement <strong>of</strong> the N200 component is thought to be<br />

indicative <strong>of</strong> increased active and controlled inhibitory processing.No signi®cant<br />

changes were observed at the amygdala or at Fz.Rainville, Duncan, Price, Carrier<br />

and Bushnell 1997), using hypnotically suggested reduction <strong>of</strong> affective but sensory<br />

pain to cold pressor pain during PET recordings, reported a relationship between the<br />

degree <strong>of</strong> affective pain experienced and activation <strong>of</strong> the anterior cingulate cortex.<br />

Considered together, Crawford et al.1998), Kropotov et al.1997) and Rainville et<br />

al.1997) demonstrate changes in the activation <strong>of</strong> the anterior cingulate during<br />

hypnotic analgesia, a region known to show increased activation during attention to<br />

pain e.g., Bromm & Chen, 1995; Jones et al., 1991; Talbot et al., 1991).<br />

In our laboratory, we evaluated SEPs in two populations: a) normal college<br />

undergraduates who were either low or `virtuoso' highs, the latter <strong>of</strong> whom could

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