Q 7 Med 1996; 89:313-317 Commentary QJM The state of hypnosis: evidence and applications J. GRUZELIER From the Department of Psychiatry, Charing Cross and Westminster Medical School, London, UK Thoughtful clinicians have always believed that the alterations in brain function associated with hypnosis would one day come to be defined. This belief is inherent in the now outmoded concept 'hypnotic trance', and was encouraged by the sometimes uncontrolled observations of physical changes brought about by hypnosis. These have included relief from pain, anaesthesia, changes in the skin's allergen hypersensitivity response, reduction in the inflammatory responses to burns, control of the rate of blood coagulation and so forth. 1 " 4 The absence of proof of reliable alterations in brain activity from mid-century psychophysiological studies, however, gave backing to the psychosocial theories of imaginative participation and role-playing, which have dominated scientific thinking until recently. Over the past decade, advances have been made in delineating systematic changes associated with hypnosis. What is more, in the prehypnotic state, highsusceptibility hypnotic subjects have shown neurophysiological differentiation from those with low susceptibility. Whilst there is no doubt that in the clinical context a patient must be a willing participant in hypnosis, recent work suggests that to say that the influence of hypnosis on pain, blood coagulation, inflammatory responses, removal of warts, etc. is simply the result of role-playing or other psychosocial dynamics, is naive. This recent change in orientation of hypnosis theories is largely a consequence of more informed approaches to the complexities of brain systems, and greater rigour in the application of scientific methodology and experimental design. Individual differences in hypnosis susceptibility, glaringly obvious since the technique's discovery a century ago, have been of particular use here, as responder and nonresponder groups can be selected a priori. We can be thankful in this selection for the development of reliable and valid scales of hypnotic susceptibility such as those from Harvard and Stanford.5'6 The state and trait nature of hypnotic susceptibility7 means, however, that it is essential to establish the retest reliability of group assignment; in our studies we now do this on three occasions, including one that is concurrent with electrophysiological recording. During the late 1970s, when we began our neuropsychophysiological investigations, hemispheric specialization theories suggested striking parallels between hypnosis and right hemisphere functions. These functions included motor passivity, an emphasis on sensory images, slow and simple speech, and emotionally charged memories.8 Hypnosis was thought to enhance right hemispheric activity, and hypnotically susceptible subjects were thought to be characterized by a right hemispheric functional dominance or 'hemisphericity' in the baseline state.9 Our initial results led to the emergence of an altogether more complex picture. 10 ' 11 At first, we measured sympathetically-mediated eccrine sweat-gland activity, via electrodermal responses to a series of tones interspersed throughout the hypnotic induction. These responses were recorded bilaterally from the phalanges of the first and second fingers of each hand. There are strong limbic system influences on responses to simple sensory stimuli and their habituation. In hypnotized high-susceptibles, we found evidence of asymmetries in responses indicating dominance of right over left temporal-limbic influences, a finding in line with the laterality hypothesis. Further, in the baseline state, high-susceptibles showed asymmetry in the opposite direction, with left hemisphere dominance. Neither of these effects were seen in low-susceptibles, and the right hemisphere dominance was not seen in high- Address correspondence to Professor J. Gruzelier, Department of Psychiatry, Charing Cross and Westminster Medical School, St Dunstan's Road, London W6 8RF © Oxford University Press 1996 314 J. Gruzelier susceptibles in conditions without hypnosis which controlled for focussed attention or relaxation.11 These studies showed that whilst hypnosis produced an accentuation of right hemispheric influences, highsusceptibles in the prehypnosis state showed asymmetry favouring the left hemisphere, and hypnosis brought about a reversal of asymmetry. Highsusceptibles did not manifest right hemisphericity. The importance of the left hemisphere in hypnosis has been further highlighted by a series of studies of tactual discrimination, a task involving contralateral active touch pathways.10'12 In these experiments, subjects were blindfolded, and objects placed in each hand were identified tactually. Results confirmed that there was left-hemisphere dominance in high-susceptibles in the baseline state. With hypnosis, subjects displayed a decline in left hemisphere discriminations. These findings were in keeping with ideas of a lateralized inhibitory process in the left hemisphere. The salience of this for the hypnotic process was further emphasized by a correlation between the relative reduction in haptic processing speed and the magnitude of the susceptibility score monitored during the experiment, shown in Figure 1. In high-susceptibles, both the left hemisphere advantage in the baseline state, and the loss in hypnosis of this advantage, the magnitude of which correlated with the level of susceptibility reached, implied that left hemisphere dynamics were fundamental to the induction process. These findings, along with the enhancement of highright-sided activity with hypnosis in susceptibles, have been replicated in other measurement modalities including cortical evoked potentials, -10 EEG, and psychophysical and neuropsychological tasks.12"16 These studies have also highlighted the importance of anterior-posterior relations. In hypnosis there is an inhibition of frontal functions, more so on the left side than the right, and when the aim is to induce relaxation with hypnosis, there is an accentuation of posterior functions, greater in the right hemisphere. The importance of frontal inhibition in hypnosis is exemplified by recent neurophysiological evidence.17 Cortical evoked potentials were measured to rare tones presented amongst a series of identical but lower pitched frequent tones. The cortical evoked potentials of patients with frontal lobe lesions differentiate poorly between the classes of tones.18 This is reflected in the negative component at around 120 ms post stimulus, a component mirroring frontal attentional processes. We compared high- and lowsusceptibles prior to hypnosis and at an early and late stage of the induction. The differences in N120 amplitude between frequent and infrequent tones are shown in Figure 2. In high-susceptibles, the magnitude of the difference can be seen to decrease progressively from baseline to hypnosis, so that at the later stage of induction the N120 components were similar to those of frontal lobe patients. Note also that the opposite change in electrocortical activity is seen in low-susceptibles. They begin poorly, as would occur with inattention and distractibility, but improve with practice. This result raises another finding in our studies. Changes shown by low-susceptibles to instructions of hypnosis are often in the opposite direction to those found in high-susceptibles. The significance of 3 4 Hypnotic susceptibility Figure 1. The correlation between hypnotic susceptibility score and the slowing in right hand/left hemispheric processing time with hypnosis. The state of hypnosis 315 HIGH-SUSCEPTIBLES F4 LOW-SUSCEPTIBLES F4 Figure 2. Differences in microvolts between cortical evoked potentials for infrequent and frequent tones at baseline (B), at an early stage of hypnosis induction (H1), and at a later stage (H2). There is progressive loss of discriminability during hypnosis induction in high-susceptibles (top) and a progressive increase in discriminability in low-susceptibles. Measurements at central (Cz), frontal (Fz), and frontal left (F3) and right (F4) locations. See text for full description. these changes can be interpreted as antithetical to the induction of hypnosis. Firstly, instructions of hypnosis have lead to activation of the left hemisphere in low-susceptibles, with one experiment actually describing a reversal from right hemisphere activation prior to hypnosis.13'15 This left-sided activation contrasts with the inhibition of left-sided functions in high-susceptibles. Secondly, whereas highsusceptibles have shown fast habituation to irrelevant tones interspersed with the induction, 11 ' 19 lowsusceptibles have shown slower habituation. Slow habituation is a known accompaniment of anxiety.20 Consideration of the significance of the changes observed has lead to a neuropsychological translation of the induction procedure.21"23 The induction of hypnosis for a novice subject commonly begins with focussing attention on a small object. This will engage frontal supervisory attentional systems;24 focal attention underpinned by left-sided functions, and broad attention with right-sided systems. Once attention is engaged, the next step is to suggest that sustaining attention is tiring and that eyelids feel heavy, with the aim of producing eye closure. Accordingly once focal attention systems are engaged, the process of frontal inhibition is set in train. The shift of activation to the posterior, predomi- nantly right-sided functions begins, through emphasis on imagery, emotion, and simplified speech. The inhibition of frontal functions is compatible with the suspension of both reality testing and critical analysis of the instructions of hypnosis, and giving over the planning of behaviour to the therapist. Initial studies of other methods of inducing deep relaxation, such as floatation with restricted environmental stimulation, disclose that these methods fail to share the hypnosis properties of left-sided (frontal) inhibition. Right-sided functions, however, may be enhanced.11'25 Differentiation of hypnosis from states of physical relaxation has been demonstrated by having subjects ride a bicycle ergometer while hypnotized, 12 ' 26 a procedure which in our study produced evidence of right-sided enhancement and leftsided inhibition in haptic processing. This body of evidence of reproducible changes in brain function with hypnosis is currently being augmented with evidence from functional brain imaging procedures. These include EEG and metabolic measures.13'27"29 There is also a small body of knowledge accruing from intracranial recording.30"32 Evidence that hypnosis is, after all, a state of altered brain function will give new impetus to research on medical applications. This will encour- 316 J. Gruzelier age studies to verify important observations of organic changes and therapeutic benefits, many of which have awaited controlled investigations and replication. The work above offers markers of the depth of hypnosis, as well as insight into the processes that underlie low susceptibility, such as broadened instead of narrowed attention, or focussed attention without the ability to suspend reality testing. Applications of hypnosis to immunology (to mention just one medical field) now warrant a greater investment of effort. There is virtually unequivocal evidence that hypnosis can modulate inflammatory processes such as immediate and delayed skin hypersensitivity reactions to injections of histamine or tuberculin protein derivative. Pioneering work by Black and colleagues,1'33 has been replicated, 34 " 36 with one negative study.37 In children, increases in salivary IgA over baseline have been found with hypnosis. They were randomly assigned to two hypnosis groups which differed in imagery content or to a control group matched for staff interaction. Only when the imagery content involved specific suggestions to control salivary immunoglobulins was the effect of hypnosis observed, raising the importance of imagery content.38 Prophylactic influences on immunity have been claimed for hypnosis used to ease exam stress in medical students, as the more hypnotic relaxation was practised before exams, the higher were helper T-lymphocyte percentages (over baseline) during exam time. 39 While an alternative explanation may reside in personality factors associated with a greater enthusiasm for hypnosis in those that practised the most—a range of between 5 and 50 sessions, this does not necessarily diminish the importance of the result, or its basis in biological factors. We found in asymptomatic men at early stages of HIV-1 infection that there were prospective associations between EEG and neuropsychological profile on first testing and immune status (CD4 and CD8 counts) up to 30 months later.40 The neuropsychophysiological profiles associated with good and poor immune status have been associated with differences in personality and temperament.41'42 Consistent with this, a liveliness—listlessness dimension has been related to the hypersensitivity skin reaction.36 A landmark study in the field of cancer research further illustrates the involvement of hypnosis with immune functioning. Spiegel et al. 43 showed that in women with metastatic breast cancer, those that received hypnosis training for pain relief lived 18 months longer on average than the control group. As Walker44'45 concluded in a recent review, this evidence of increased longevity is preliminary; however, the efficacy of hypnosis in improving quality of life, alleviating pain and distress, and ameliorating the effects of chemotherapy is beyond doubt. The application of hypnosis to immunity is in its infancy, as it is with other medical applications outside of analgesia, childbirth and psychiatry. Applications that warrant closer scrutiny involve psoriasis,46 control of seizures47'48 neurological rehabilitation, 49 chronic fatigue syndrome,50 rheumatoid arthritis,51 reduction of the inflammatory response to burns4 and asthma52 to mention a few. Now that we are equipped with the seeds of neurophysiological validation, a new era in hypnosis research is just beginning. Undoubtedly the neurophysiological model requires further elucidation and refinement, but this can be expected to follow access to new brain-imaging facilities. We can now acknowledge that hypnosis is indeed a 'state' and redirect energies earlier spent on the 'state-nonstate' debate. We have gained neurophysiological insights about the induction of hypnosis, and in so doing have developed potential markers of stages in the induction process. Equipped with this knowledge we can proceed to investigate the therapeutic potential of a unique, safe and non-invasive psychological therapy. References 1. Black S. Inhibition of immediate-type hypersensitivity response by direct suggestion under hypnosis. Br MedJ 1963; 1:925-9. 2. Crasilneck HB, Hall JA. Physiological changes associated with hypnosis: A review of the literature since 1948. Int J Clin Exp Hypnosis 1959; 7:950. 3. Hilgard ER, Hilgard JR. Hypnosis in the relief of pain. Los Altos California, W Kauffman, 1983. 4. Patterson DR, Questad KA, Boltwood MD. Hypnotherapy as a treatment for pain in patients with burns: research and clinical considerations. J Burn Care Rehabil 1987; 8:263. 5. Shor RE, Orne EC. Harvard Croup Scale of Hypnotic Susceptibility, Form A. Palo Alto CA, Consulting Psychologists Press, 1962. 6. Weitzenhoffer AM, Hilgard ER. Stanford Hypnotic Susceptibility Scale, Forms A and B. Palo Alto CA, Consulting Psychologists Press, 1962. 7. Hilgard ER. Hypnotic susceptibility. New York Harcourt, Brace & World, 1965. 8. Galin D. Implications for Psychiatry of Left and Right Cerebral Specialisation. Arch Gen Psychiati974; 31:572-83. 9. Pedersen DL. Hypnosis and the right hemisphere. Proc Br Soc Med Dent Hypnosis 1984; 5:2-14. 10. Gruzelier JH, Brow TD, Perry A, Rhonder J, Thomas M. Hypnotic susceptibility: A lateral predisposition and altered cerebral asymmetry under hypnosis. Int) Psychophysiol 1984; 2:131-9. 11. Gruzelier jH, Brow TD. Psychophysiological evidence for a state theory of hypnosis and susceptibility. J Psychosom Res 1985; 29:287-302. 12. Cikurel K, Gruzelier J. The effect of an active-alert hypnotic induction on lateral asymmetry in haptic processing. Br J Exp Clin Hypnosis 1990; 7:17-25. 13. Crawford HJ, Gruzelier J. A midstream view of the The state of hypnosis neuropsychophysiology of hypnosis: Recent research and future directions. In Fromm W, Nash M, eds. Hypnosis; Research Developments and Perspectives, 3rd edn. New York, Guildford Press, 1992:227-66. 14. McCormack K, Cruzelier JH. Cerebral asymmetry and hypnosis: A signal detection analysis of divided visual field stimulation. J Abnorm Psychol 1993; 102:352-7. 15. Cruzelier JH, Warren K. Neuropsychological evidence of left frontal inhibition with hypnosis. Psychological Med 1993; 23:93-101. 16. Jutai J, Gruzelier JH, Golds J, Thomas M. Bilateral auditoryevoked potentials in conditions of hypnosis and focused attention. IntJ Psychophysiol \ 993; 15:167-76. 17. Cruzelier J, Cray M, Horn P. Cortical evoked potential evidence of frontal inhibitory influences of hypnosis in highly susceptible subjects. In preparation. 18. Knight RT, Hillyard SA, Woods DL, Neville HJ. The effects of frontal cortex lesions on event-related potentials during auditory selective attention. Electroencephalogr Clin Neurophysiol 1981; 52:571-82. 19. Gruzelier JH, Allison J, Conway A. A psychophysiological differentiation between hypnosis and the simulation of hypnosis. IntJ Psychophysiol WW; 6:331-8. 20. Gruzelier JH, Phelan M. Laterality-reversal in a lexical divided visual field task under stress. IntJ Psychophysiol 1991; 11:267-76. 21. Gruzelier JH. The neuropsychology of hypnosis. In Heap M, ed. Hypnosis: Current Clinical, Experimental and Forensic Practices. London, Croom Helm, 1988:68-76. 22. Cruzelier JH. Neuropsychological investigations of hypnosis: Cerebral laterality and beyond. In Van Dyck R, Spinhoven Ph, Van der Does AJW, eds. Hypnosis: Theory, Research and Clinical Practice. Free University Press, 1990:38-51. 23. Crawford HJ. Brain dynamics and hypnosis: Attentional and disattentional processes. IntJ Clin Exp Hypnosis 1994; 42:204-32. 24. Shallice T. Multiple levels of control processes. In Umilta C, Moscovitch M, eds. Attention and Performance, 15. Cambridge MA, MIT Press, 1994;945-65. 25. Raab J, Gruzelier J. A controlled investigation of right hemispheric processing enhancement after restricted environmental stimulation (REST) with flotation. Psychol Med 1994; 24:457-62. 317 32. Kropotov JD, Crawford HJ, Polyakov Yl. Somatosensory event-related potential changes to painful stimuli during hypnotic analgesia: Anterior cingulate cortex and anterior temporal cortex intracranial recordings in obsessive compulsives. IntJ Psychophysiol 1996; in press. 33. Black S, Friedman M. Adrenal function and the inhibition of allergic responses under hypnosis. BrMedJ 1965; 1:562-7. 34. Zachariae R, Bjerring P, Arendt-Nielsen L. Modulation of type I immediate and type IV delayed immonoreactivity using direct suggestion and guided imagery during hypnosis. Allergy 1989; 44:537-42. 35. Zachariae R, Bjerring P. The effect of hypnotically induced analgesia on flare reaction of cutaneous histamine prick test. Arch Dermatol Res 1990; 282:539-43. 36. Laidlaw TM, Booth RJ, Large RG. The variability of type I hypersensitivity reactions: the importance of mood. J Psychosom Res 1994; 38:51-61. 37. Locke SE, Ransil BJ, Covino NA, Toczydlowski J, Lohse CM, Dvorak HF, Arndt KA, Frankel FH. Failure of hypnotic suggestion to alter immune response to delayed-type hypersensitivity antigens. Ann N Y Acad 5c; 1987; 496:745-9. 38. Olness K, CulbertT, Uden D. Self-regulation of salivary immunoglobulin A by children. Pediatrics 1989; 3:66-71. 39. Kiecolt-Glaser JK, Glaser R, Strain EDC, Stout JC, Tarr KL, HollidayJE, Speicher CE. Modulation of cellular immunity in medical students. J Behav Med 1986; 9:5-21. 40. Gruzelier J, Burgess A, BaldewegT, Riccio M, Hawkins D, Stygall J, Catt S, Irving G, Catalan J. Longitudinal and prospective associations between neuropsychophysiological functions and immune status in HIV infection: a preliminary study. Submitted for publication. 41. Kang DH, Davidson RJ, Coe CL, Wheeler RE, Tomarken AJ, Ershler WB. Frontal brain asymmetry and immune function. Behav Neurosci 1991; 105:860-9. 42. Gruzelier J, Burgess A, Stygall J, Irving G, Raine A. Patterns of cerebral asymmetry and syndromes of schizotypal personality. Psychiat Res 1995; 56:71-9. 43. Spiegel D, Kraemer HC, Bloom JR, Gottheil E. Effect of psychological treatment on survival of patients with metastatic breast cancer. Lancet 1989; ii:288-91. 44. Walker LG. Hypnosis with cancer patients. Am) Prev Psychiat Neurol 1992; 3:42-9. 26. Banyai El, Hilgard ER. A comparison of active-alert hypnotic induction with traditional relaxation induction. J Abnorm Psychol 1976; 85:218-24. 45. Walker LG, Eremin O. Psychoneuroimmunology: A new fad or the fifth cancer treatment modality? AmJSurg 1995; 170:2-4. 27. De Benedittis G, Longostreui GP. Cerebral blood flow changes in hypnosis: A single photon emission computerized tomography (SPECT) study. Paper presented at the 4th Conference of the International Organisation of Psychophysiology, Prague, Czech Republic, 1988. 46. Frankel FH, Misch RC. Hypnosis in a case of long-standing psoriasis in a person with character problems. IntJ Clin Exp Hypnosis 1973; 21:121-30. 28. Crawford HJ, Gur RC, Skolnick B, Gur RE, Benson DM. Effects of hypnosis on regional cerebral blood flow during ischaemic pain with and without suggested hypnotic analgesia. IntJ Psychophysiol 1993; 15:181-95. 29. De Pascalis V, Perrone M. EEG asymmetry and heart-rate during experience of hypnotic analgesia in high and low hynotizables. IntJ Psychophysiol 1996; in press. 30. De Benedittis G, Sironi VA. Depth cerebral electrical activity in man during hypnosis. IntJ Clin Exp Hypnosis 1986; 34:63-70. 31. De Benedittis G, Sironi VA. Arousal effects of electrical deep brain stimulation in hypnosis. IntJ Clin Exp Hypnosis 1988; 36:96-106. 47. Williams DT, Spiegal H, Mostofsky Dl. Neurogenic and hysterical seizures in children and adolescents: differential diagnostic and therapeutic considerations. Am) Psychiat 1978; 135:82-6. 48. Williams DT, Gold A, Shrout P, Shaffer D, Adams D. The impact of psychiatric intervention on patients with uncontrolled seizures. J Ner Ment Dis 1979; 167:626-31. 49. Spiegel D, Chase RA. The treatment of contractures of the hand using self-hypnosis.; Hand Surg 1980; 5:428-32. 50. Gregg VH, Jones D. Hypnosis and the chronic fatigue syndrome: A case study. Contemp Hypnosis 1995; 12:87-91. 51. Baker GHB. Invited review psychological factors and immunity. J Psychosom Res 1987; 31:1 —10. 52. Moorefield CW. The use of hypnosis and behaviour therapy in asthma. Am) Clin Hypnosis 197'1; 13:162-8.
© Copyright 2026 Paperzz