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John Gruzelier
Abstract
Introduction
This article provides a review of experiments,thematicallyrather than chronologi-
cally structured,that were carried out in the Charing Crosslaboratory of Cognitive
Neurosciencewith the aim of understandingthe neuropsychophysiological basisof
hypnosis.Hypnosiswas defined operationallyon the basisof the traditional relax-
ation procedure,which beganwith eyefixation, suggestions of relaxationand eye clo-
sure,and wasfollowed by imageryassociated with deeprelaxationand a dream.This
was applied in all experimentsexceptone where the active-alertprocedure(B6nyai
and Hilgard,I976) wascompared.During the inductionthere were behaviouralchal-
lengesto assessdepth of hypnosis,and at the end questionsabout memory for the
induction,a post hypnotic suggestionand subjectiveratings.The purposewas to
unravel someof the changesin brain activity that accompanythe hypnotic induction
in both high and low susceptibleindividuals,and featuresthat may differentiatethem
in the baselinestate.
4 Gruzelier
The history of localizing neurophysiologicalmechanismsin hypnosisbegan by
likening hypnosisto sleep.Pavlovdemonstratedthe existenceof hypnosisin his con-
ditionedreflex studiesin dogsand attributedthis to a partial and spreadinginhibition
of the cortex, lessextensivethan occursin sleep,though Heidenhainhad reasoned
earlier that more than the cortex was involved becauseanimalsdid not behaveas if
they were decorticate(Windholz,1996).Although sleepbecamean increasinglypop-
ular analogy,to date electroencephalographic (EEG) studieshavenot found similari
ties betweenhypnosisand sleep(for a review seeCrawford and Gruzelier,1992).At
the sametime sleepcanbe inducedby instructionsof hypnosis,but conventionalpro-
ceduresstop short of sleepinduction.Hernandez-Peon (1977)proposedthat hypnosis
wascloserto wakefulnessthan sleep,involving alterationsin both consciousness and
executivefunctions, which he localized to the midbrain, pons and medulla.
Nevertheless, dependingon the nature of the induction,dream-likefeaturesare close
to the hypnoticexperienceof many high susceptibles.
Recordingsfrom intracranial electrodesin epileptic patients have disclosedthe
importanceof limbic structuresin hypnosis.Craiselneck,McCranie and Jenkins
(1956)reportedanecdotallythat hypnosiswasterminatedeachtime the hippocampus
was electricallystimulated.De Benedittisand Sironi (1986)demonstratedin a high
hypnotizable that there was a reduction in interictal focal abnormalities in the hip-
pocampusduring hypnosisand an increasein alpha activity.In a secondpatient they
concludedthat hypnosiswas associatedwith functional inhibition of the amygdala,
becausestimulationof the amygdalaarousedthe patient from hypnosisunlike stimu-
lation of the adjacentand reciprocallyconnectedhippocampus.Electricalactivity in
the amygdalabecamesynchronizedwith hypnosiswhereasactivity in the hippocam-
pus becamedesynchronized (De Benedittisand Sironi,1988).
In the 1960sparallelswere drawn betweenhypnosisand right hemisphericpro-
cessingand high hypnotic susceptibleswere assumedto be characterizedby right
hemisphericity.This point of view has been popularizedand has been found to be
important in the clinical useof hypnosis(Pedersen,1984).Aside from evidencefrom
cognitivestudieswith putative hemispherespecifictasks,there were also neuropsy-
chophysiologicalmeasureswhich took into account brain anatomy such as EEG,
dichotic listening and conjugatelateral eye movements(Crawford and Gruzelier,
1,992).Experimental evidencewas, however,conflictual,but the methodologiesof
many studieswere questionable(Gruzelier, 1988).Methods of inducing hypnosis
were various and often poorly described.Often there was a failure to distinguish
betweenhigh and low susceptiblesor to attribute changesin low susceptiblesthat
were absentin high susceptibles to the hypnotic process.Seldomwas evidencecited
of test-retestreliability, or of replication,or of validationof hypnoticlevel during the
experimentalprocedure.
In integratingthe resultsof a decadeago a three-stageworking model of the
inductionprocesswasproposed(Gruzelier,1988,1990).
StageI: The initial instructionsof fixating on a small object and listeningto the
hypnostist'svoice waspositedto involve an attentionalnetwork includingthalam-
ocorticalsystemsand parietofrontalconnectionswith engagementof a left ante-
rior focusedattention control system.This underpins the focused,selective
attentioninherentin fixation and listeningto the hypnotist'svoice,processes that
together require left hemisphericfrontotemporal processing.
StageII: The first stageis then replacedby eye closure,suggestions of fatigue at
continued fixation, and tirednesstogether with deep relaxation.This sets in
Neurophysiologyof hypnosis 5
motion frontolimbic inhibitory processesunderpinningthe suspensionof reality
testing and critical evaluation,and the handing over of executiveand planning
functionsto the hypnotist;the 'letting go' componentof the hypnoticinduction.
. StageIII: The third stageinvolvesinstructionsof relaxed,passiveimageryleading
to a redistributionof functionalactivity and an augmentationof posteriorcortical
activity,particularlyof the right hemispherein high susceptibles.Simplifyingthe
verbal contentof the inductionmessagemay alsofacilitateright hemisphericpro-
cessing,as does emphasizingpast experienceand emotion. In contrast,low sus-
ceptiblesfail to show engagementof left frontal attentionalcontrol mechanisms,
or if there is focal attentional engagement,low susceptiblesfail to undergo the
inhibitory, letting go process.This working model will serve to structurethe
review of findings.Here emphasiswill be placedon the cognitiveneuroscience of
hypnosis;implicationsfor socio-cognitiveapproacheswill be found in a commen-
tary (Gruzelier,1998)on a theoreticalpaperby Wagstaff(1998).
TONESALONE HYPNOSIS
WITHTONES
AFTER
INDUCTION
t2
10
R
4 8
IONESALONE TONESWITH
AFITRSTORY STORY
e
0
4 8 12 16 4 8 t216
Patients
Students
Increase
in Habituation
q ?
ia 3 -
'E-
0
o 9
o
O
L
o
L
SameHabituation
2 o
Decrease
in Habituation
0 2 t 4 6 8 1 0
Susceptibil
ity Score
arousability and attentional engagement and these did not vary with susceptibility.
Turning to the relaxation condition, this was insufficient to change either habituation
(see also Teasdale, 1972) or sensitization, so that the facilitation of habituation could
not be explained away as a function of relaxation. At the same time some compo-
nents of arousal reduction were associated with hypnosis. This was shown by fewer
Neurophysiologyof hypnosis 7
non-specificresponsesduring hypnosisboth in the first half and secondhalf of the
hypnotic induction as well as by reductionsin tonic levels of skin conductance.
However, one high susceptiblehad levels of skin conductancetwo standarddevia-
tions abovethe control group mean,indicatingthat a reductionin tonic arousalis not
a necessarypart of the hypnotic processas will be confirmedlater in an experiment
with the active-alertinductionprocedure.
The facilitation of habituation with hypnosiswas replicated in an experiment
designedto compare hypnosiswith simulating hypnoslsin medium/high hypnotiz-
ables(Gruzelier et al., 1988).Subjectswere examinedfirst in a baselinesessionand
then assignedwith the Barber SuggestibilityScale(Barber, 1969)to the simulatoror
hypnosisgroups matchedfor suggestibility,electrodermalreactivity and sex.
Hypnotic susceptibilitywasmonitoredthroughoutthe secondsessionasin the former
experiment.Levels of susceptibilityall fell within the moderate to high range. As
before, rate of habituation was faster with hypnosisin the susceptiblesubjects
whereasin simulatorshabituationwas slower.Simulatorswere more arousedduring
the inductionprior to presentationof the tones(p <0.005)but subsequentlythere was
no differencein the number of non-specificelectrodermalresponses.Support was
found for reports that simulatorsare characlerizedby exaggeratedcompliance
(Williamsenet al., 1965;Hilgard et al., 1978),for in compliancewith instructionby
the hypnotistto forget about the tones,all but one simulatingsubjectclaimedat the
end of the sessionnot to have heard the tones,whereasall but one in the hypnosis
group admittedto hearingthe tones.
Neuroanatomicallythe influenceon electrodermalorienting and habituationwas
compatiblewith the evidenceof De Benedittisand Sironi (1988)arisingfrom record-
ings of intracranialelectricalactivity. They found that hypnosisinvolved functional
inhibition of the amygdalaand activation of the hippocampus.The amygdalahas
been shown to exert mainly excitatoryinfluenceson orienting activity whereasthe
inhibitory action of the hippocampusfacilitatesthe habituationof the orienting
responsewith stimulus repetition (Gruzelier and Venables, 1972;Pribram and
McGuinness ,I975).
HIGHSUSCEPTIBLES
lH1
[f H2
LOWSUSCEPTIBLES
tr--t R
IH1
t--1 H)
-to.@
Site: Cz
-4.@
high susceptibles
-6.08
a,Ba
a z-gs
4.SS
pre-hgpnos is
[i | | iieconds
Figure 4. Error detection and error evaluation waves in medium/high susceptiblesin hypnosis
and pre-hypnosis baseline.
Neurophysiologyof hypnosis 11
Left anterior inhibition
Someevidencehassuggestedthat the anterior inhibition may be laterally asymmetrical
and biasedtowardsthe left hemisphere.This was disclosedby measuringright and left
hemisphereprocessingtimes in dextral subjectswith a haptic object sorting task com-
paringleft and right hands(Gruzelieret al., 1984).This wasplannedinitially to validate
asymmetriesdisclosedby the bilateral monitoring of electrodermalorienting and habit-
uationprocesses describedin the next section;in the haptictaskthe mediationof hemi-
sphericinfluencesis unambiguouslycontralateral.Subjectssorted objectsby classwith
each hand separatelywhile blindfolded.Hand order was counterbalanced and there
was control for movement time. The task was done prior to hypnosisand again after
the hypnotic induction, with susceptibilitymonitored through the experiment.As
shown in Figure 5 high susceptiblesshowedan increasein right hand processingtimes
with hypnosiswhile there was no changein their left hand times, nor were there bilat-
eral changesin low susceptibles.The increasein the processingtimes of the right hand
(indexingthe left hemisphere)correlatedpositivelywith the hypnotic susceptibility
score.We replicated the slowing of left hemisphericprocessingwith hypnosisin high
susceptiblesin contrastto low susceptiblesin a follow-up experimentwith middle aged
subjects,which was performed away from the laboratory and which included a non-
hypnosiscontrol group, (Gruzelier et al., 1984).The combiningof both experiment
samplesdisclosedevidenceof a left hemisphericpreferencein high susceptiblesat base-
line ashad beenshownin the electrodermalstudyoutlinedin the next section.
Left-sidedinhibition of somatosensory functionswas replicatedfurther by exam-
ining haptic processingwith an active-qlertinduction (Cikurel and Gruzelier, 1990).
Following B6nyai and Hilgard (1976)subjectspedalleda stationaryexercisebicycle
againsta load and with instructionsof mental alertnessin the hypnotic induction.
Dextral subjectswere selectedwith the Barber scaleto form groupsof high and
medium susceptibles.Each subjectparticipated in two sessions,one involving the
conventionalrelaxation induction and the other the active-alertinduction. In both
conditionsa baselinemeasurewas obtained either while seatedor while pedalling.
Sessionorder was counterbalancedand in each sessionhypnotic susceptibilitywas
monitored to validate the group designationand to compare the induction proce-
dures,which in the event producedsimilar influenceson susceptibility(r = 0.79,
(J
20
o)
3
q)
E
IE
,a
C
c,
(J
o
o-
L
ro
post pre
Hypnos
is
Figure 5. Haptic processing times for right and left hands for pre-hypnosis baseline and with
hypnosis in high (left figure) and low (right figure) susceptibles.
12 Gruzelier
p <0.001).As in previousexperimentsthere was a hypnosisx hand interaction such
that for the group as a whole there was a slowing of right hand processingtimes
with hypnosisand no changewith the left hand. Subdivision of the subjectsinto
high and medium groups showed that whereasboth groups sharedthe right hand
slowing with hypnosis,the left hand of high susceptiblesgave faster sorting times
with hypnosis,whereasin medium susceptiblesthere was a bilateral slowingof pro-
cessing.Comparinginduction procedures,the active-alertinduction sharedwith the
conventionalprocedure the slowing of left hemisphericprocessingbut the active-
alert induction was solely responsiblefor the improvement in right hemispheric
processing.
Lateralized anterior inhibitory functions were examined further with a small bat-
tery of neuropsychological tasks(Gruzelierand Warten, 1993).Theseincludedword
and categoryfluency, which are both left hemispheretaskswith word fluency left
frontal and categoryfluencyleft temporal.Designfluencywasincludedto index right
anterior processing.Left and right hand finger tapping was included to examine
motor and pre-motor functions.Dextral subjectswere first selectedwith the Barber
scaleand divided into high and low susceptibilitygroups.Susceptibilitylevel was also
monitored throughout the experiment.The influence of hypnosison word fluency
differedsubstantivelybetweenthe groups.While low susceptibles showedan increase
in fluency from the pre-hypnosisbaselinewith hypnosis,high susceptibles showeda
decrease.While the groupsdid not differ at baselinein word fluency (althoughthere
was a mean advantageto high susceptibles) with hypnosisthere was a highly signifi-
cant differencebetweenthem. The semanticcategorytest showedsimilar mean
changesbut did not disclosesignificanteffects.Theseresultsare contrastedin Figure
6. With designfluency both groupsshowedan improvement with hypnosiswhereasin
finger tappingonly the low susceptibles showedimprovementin finger tapping- the
high susceptiblesshowedan impairment.The word versuscategoryfluency effects
have now been replicatedin the Finnishstudy mentionedabove(Kallio et al., 1998),
which has brought togetherin one investigationoppositechangesin susceptibleand
unsusceptiblesubjects,first in vigilance performanceinvolving a thalamo-cortical
(parieto-frontal)attentionalnetwork mentionedabove and secondin word genera-
tion involving the left prefrontal cortex.
Categoryfluency
,< unsusceptible
suscePtible
pre-hypnosis hypnosis
Figure 6. Word fluency for letters and categoriesin high and low susceptiblesin pre-hypnosis
baselineand with hypnosis.
Neurophysiologyof hypnosis 13
Patternsof correlationsbetweenthe fluency taskssupportedan inhibitory influ-
ence of hypnosiscentring on the left anterior word fluency performance.First, the
three fluency tests did not correlate at baselineimplying an independenceof func-
tion. Second,correlationsbetween baselineand hypnosisconditions were signifi-
cant for categoryfluency and designfluency but not for word fluency,in support of
the word fluency test alone being altered by hypnosis.In contrast,significantcorre-
lations were obtainedwith hypnosisbetweenword fluency and both designfluency
and categoryfluency, but not between designand categoryfluency. This could be
interpreted as showingthat an underlyingprocesssuch as distributedinhibition
was most at work with word fluency, and while centring on left anterior processes
was also having some impact on design and categoryfluency which involved right
anterior and left temporal processingrespectively.Correlations also showed that
the significantrelation betweenleft and right hand finger tapping dexterity before
hypnosiswas reducedwith hypnosisin keepingwith a tendencytowards lateral
dissociation.
Anterior disconnectionwith hypnosisin susceptiblesubjectswas recently dis-
closedby Kaiser in an unpublishedexperimentinvolving EEG topographicalmap-
ping with a 32 electrodeanay in which we examinedregionalconnectivitywith EEG
coherence.EEG coherence,a putative measureof connectivity,was examined
betweenbipolar pairs of electrodes.This discloseda significanthypnosisx group x
conditioninteractionin high alphaactivity,as shownin Figure 7. In high susceptibles
with hypnosisthere was a reductionin connectivitywithin the left prefrontalregion-
specificallybetweenleft lateral (FP1and F7) and medial (F3 and FTCI) placements-
whereasthe oppositeeffect,namelyan increasein connectivitywasfound in low sus-
ceptibles.In baselinethere was also a highly significantdifferencebetweensuscepti-
bility groupsin the direction of greaterleft anterior connectivityin high rather than
low susceptibles.
o I
a
I
o I
o
c-l -I-
I
?
O
I
I prehypnotic
I
I hypnotio
hish
hypnoticsusceptibility
Figure 7. Left anterior EEG coherencein baselineand hypnosisfor medium/high and low sus-
ceptibles(high short distancecoherencerepresentslow connectivityand vice versa).
1,4 Gruzelier
Importantly the coherenceresult did not generalizeto all bandsbut wasrestricted
to high alpha activity.This representsan EEG band that relatesto cognitiveas dis-
tinct from connativeprocessing,variouslydescribedas indexinghigh workload, sus-
tained motor control and long-termmemory (Mecklinger and Bosel, 1989;Sterman
eI a1.,7994; Klimesche,1996;Burgessand Gruzelier,1998).The importanceof selec-
tivity in narrow band EEG power has also been demonstratedby our differentiating
hypnosisfrom baselinein high and low susceptibles(Williamsand Gruzelier,1998).
Summary
action of hypnosiswas shown
Further evidenceof a selectivityof neurophysiological
throughexaminationof anteriorinhibitory influences:
Right-sided processing
I BLE
SUSCEPT UNSUSCEPTIELE
_Len
-3.0 -3.0
-1., -7.'
Log.
Log. Amplltude
Amplitude
-4.0
l0
l0
Irial
Trlal
-3.0 -3.0
-).5 -3.'
109. Log.
AmDlitude Amplitude
-4.0
l0 l0
Trial Irial
LHem. .
xigtt
---.--- RHem. )
.a.'"'' -.-.... LHem. .
.,"'' Medium
nHem. l
fr;;;':'il:L--
Conclusion
Acknowledgements
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