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Int J Yoga. 2011 Jan-Jun; 4(1): 3–6.
doi: 10.4103/0973-6131.78171
PMCID: PMC3099099
Neurohemodynamic correlates of ‘OM’ chanting: A pilot functional magnetic
resonance imaging study
Bangalore G Kalyani,Ganesan Venkatasubramanian,Rashmi Arasappa,Naren P Rao,Sunil V Kalmady,Rishikesh V
Behere,Hariprasad Rao,Mandapati K Vasudev, and Bangalore N Gangadhar
Department of Psychiatry, Advanced Center for Yoga, National Institute of Mental Health and Neurosciences, Bangalore – 560 029, India
Address for correspondence: Dr. B. N. Gangadhar, Department of Psychiatry, Advan ced Center for Yoga, National Institute of Mental Health
and Neurosciences, Bangalore – 560 029, India. E-mail: kalyanybg@yahoo.com
Copyright © International Journal of Yoga
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use,
distribution, and reproduction in any medium, provided the original work is properly ci ted.
Abstract
Background:
A sensation of vibration is experienced during audible ‘OM’ chanting. This has the potential for vagus
nerve stimulation through its auricular branches and the effects on the brain thereof. The
neurohemodynamic correlates of ‘OM’ chanting are yet to be explored.
Materials and Methods:
Using functional Magnetic Resonance Imaging (fMRI), the neurohemodynamic correlates of audible
‘OM’ chanting were examined in right-handed healthy volunteers (n=12; nine men). The ‘OM’ chanting
condition was compared with pronunciation of “ssss” as well as a rest state. fMRI analysis was done using
Statistical Parametric Mapping 5 (SPM5).
Results:
In this study, significant deactivation was observed bilaterally during ‘OM’ chanting in comparison to the
resting brain state in bilateral orbitofrontal, anterior cingulate, parahippocampal gyri, thalami and
hippocampi. The right amygdala too demonstrated significant deactivation. No significant activation was
observed during ‘OM’ chanting. In contrast, neither activation nor deactivation occurred in these brain
regions during the comparative task – namely the ‘ssss’ pronunciation condition.
Conclusion:
The neurohemodynamic correlates of ‘OM’ chanting indicate limbic deactivation. As similar observations
have been recorded with vagus nerve stimulation treatment used in depression and epilepsy, the study
findings argue for a potential role of this ‘OM’ chanting in clinical practice.
Keywords: Meditation, fMRI, ‘OM’ chanting, vagus nerve stimulation
INTRODUCTION
Vagal nerve stimulation (VNS) is used as treatment in depression and epilepsy.[1,2] A positron emission
tomography (PET) study[3] has shown decreased blood flow to limbic brain regions during direct
(cervical) VNS. Another functional magnetic resonance imaging (fMRI) study[4] has shown significant
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deactivation of limbic brain regions during transcutaneous VNS. In this procedure electrical stimulus is
applied over the inner part of the left tragus and hence the auricular branch of the vagus.
The use of ‘OM’ chanting for meditation is well known.[5] Effective ‘OM’ chanting is associated with the
experience of vibration sensation around the ears. It is expected that such a sensation is also transmitted
through the auricular branch of the vagus nerve. We therefore hypothesized that like transcutaneous
VNS, ‘OM’ chanting too produces limbic deactivation. Specifically, we predicted that ‘OM’ chanting would
evoke similar neurohemodynamic correlates, deactivation of the limbic brain regions, amygdala,
hippocampus, parahippocampal gyrus, insula, orbitofrontal and anterior cingulate cortices and
thalamus) as were found in the previous study.[4]
MATERIALS AND METHODS
Healthy volunteers (n=12; nine men) who were right-handed and were consenting to participate as
controls in an ongoing MRI research were approached. Two qualified psychiatrists independently
assessed these volunteers to exclude: 1) Psychiatric diagnosis, 2) family history of major psychiatric
disorder in first-degree relative, 3) pregnancy or post-partum, 4) co-morbid substance abuse or
dependence, 5) significant neurologic disorder, 6) any contraindication for MRI and, 7) left/mixed
handedness. The absence of psychiatric diagnosis was established using Mini International
Neuropsychiatric Interview Plus.[6] The age range of the subjects was 22-39 years (mean±SD=28±6
years). All were literate. Four of these had formal training in yoga including meditation and the rest were
naïve to this technique. The NIMHANS ethics committee had cleared the experimental protocol. In
addition to the consent that they had already given for the ongoing imaging study they were provided
with additional information about the present research (fMRI) and the need to be trained to chant ‘OM’
prior to the fMRI test. Written consent was obtained from all subjects for this study.
fMRI task
All the subjects were trained in ‘OM’ chanting by an experienced yoga teacher. The subjects were trained
to chant ‘OM’ without distress and interruption – the vowel (O) part of the ‘OM’ for 5 sec continuing into
the consonant (M) part of the ‘OM’ for the next 10 sec. While earlier electrophysiological studies used
mental ‘OM’ chanting, loud chanting of ‘OM’ was chosen in this study. This helped to objectively confirm
the task performance during fMRI as well as to provide the vibration sensation and stimulate vagus
nerves via the auricular branches thereof. The control condition was continuous production of ‘sssss….’
syllable for the same duration (15 sec). This was chosen to control for the expiratory act of chanting ‘OM’
but without the vibratory sensation around the ears. These practices were achieved in a supine posture.
They were familiarized with the same procedure while lying in the MRI console. Once they were
comfortable, the fMRI procedure was conducted. At the end of the task, one of the investigators
ascertained if the subjects experienced a vibration sensation while chanting ‘OM’ but not “ssss”.
The fMRI procedure had a block design. The fMRI experiment consisted of the following phases: 1) a
high-resolution structural brain scan was first performed; 2) this was followed by echoplanar imaging
(EPI) sequence in which blood oxygen level-dependent (BOLD) scans were performed. The EPI scans had
a repetition time (TR) of 3 sec. Two hundred EPI scans were performed over 10 min. These 10 min
consisted of 15-sec blocks of ‘OM’ and “ssss”. These blocks were interspersed with 15 sec of rest period.
Altogether there were 10 blocks of ‘OM’, 10 blocks of “ssss” and 20 blocks of rest Figure 1.
Image sequences
Imaging was done using 3 Tesla MRI scanner at NIMHANS. After the initial localization sequences, high-
resolution T -weighted, structural MR images of 1-mm slice thickness with no inter-slice gap were
obtained (TR=8.1 msec; TE=3.7 msec; matrix=256×256). This high-resolution structural image was
utilized for the purpose of localization of brain activation and also to rule out any gross brain abnormality
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in the study subjects. This was followed by a BOLD sensitive EPI sequence (TR=3000 msec; TE=35
msec; slice thickness=8 mm; number of slices=16; matrix=128×128). The total duration of EPI scans was
10 min. During the EPI scans, the subjects were cued to alternate among various states (i.e., ‘OM’, “ssss”
and “REST”) every 15 sec (as described above) through a MRI-compatible monitor display which was
synchronized with the image acquisition by e-prime software incorporated in eloquence fMRI hardware
setup.
Image analysis
fMRI analyses were carried out for all patients using Statistical Parametric Mapping 5 (SPM5)
(http://www.fil.ion.ucl.ac.uk/spm). Images were realigned, corrected for slice timing variations, spatially
normalized[7–9] and smoothened with a Gaussian kernel of 8-mm full-width-at-half-maximum. The
blocks were modeled by a canonical hemodynamic response function. SPM5 combines the General Linear
Model and Gaussian random field theory to draw statistical inferences from BOLD response data
regarding deviations from the null hypothesis in three-dimensional brain space. The voxel-wise fixed
effects analysis produced a statistical parametric map in the stereotactic space of the Montreal
Neurological Institute[10]. ‘OM’ as well as “ssss”-related BOLD-activation and de-activation, were
assessed using a subtraction paradigm by respectively contrasting with the “REST” condition. The BOLD
changes were examined specifically in the à priori regions-of-interest, namely the limbic brain regions
[amygdala, hippocampus, parahippocampal gyrus, insula, orbitofrontal and anterior cingulate cortices
and thalamus – the last three brain regions were examined because of their intricate connections with the
limbic brain]. For these à priori regions-of-interest masks were created using the WFU Pickatlas for SPM
analyses.[11] Significance corrections for multiple comparisons for the individual region-of-interest were
performed using a Family-wise Error Correction (FWE) [P<0.001].
RESULTS
Compared to rest condition the BOLD fMRI signals did not detect any significant brain activation during
‘OM’ chanting. However, significant deactivation was seen in the amygdala, anterior cingulate gyrus,
hippocampus, insula, orbitofrontal cortex, parahippocampal gyrus and thalamus during ‘OM’ chanting [
Table 1 and Figure 2]. The “ssss” task did not produce any significant activation/deactivation in any of
these brain regions. The coordinates of significant areas of deactivation were transformed from MNI
space[10] into the stereotactic space of Talairach and Tournoux.[12]
DISCUSSION
In this study, significant deactivation was observed bilaterally during ‘OM’ chanting in comparison to the
resting brain state in orbito-frontal, anterior cingulate, parahippocampal gyri thalami and hippocampi.
In addition the right amygdala demonstrated significant deactivation. No significant activation was
observed during ‘OM’ chanting. In contrast, neither activation nor deactivation occurred in these brain
regions during the comparative task – namely the ‘ssss’ condition.
Though there is no previous report on the effect of ‘OM’ chanting on brain hemodynamic responses, an
earlier study by Kraus et al.,[4] had examined the impact of transcutaneous VNS on BOLD changes using
fMRI. Because of the commonality of the vagus involvement (as hypothesized in the current study), we
compared our study observations with this earlier study.[4] Interestingly, our study findings are in tune
with this previous study; significant deactivation was observed in the amygdala, parahippocampal,
hippocampal brain regions. This suggests that neurophysiological effects of ‘OM’ chanting may be
mediated through the auricular branches of the vagal nerves. Using a different methodology (positron
emission tomography), other researchers[3] demonstrated reduced blood flow bilaterally in the
hippocampus, amygdala, and cingulate gyri following left cervical VNS in epilepsy patients. Similarly,
VNS treatment in depressed patients reduced regional cerebral blood flow in the amygdala, left
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hippocampus, left subgenual cingulate cortex, left and right ventral anterior cingulum, right thalamus
and brainstem as measured by single photon emission computed tomography.[13] Interestingly, these
regions become hyperactivated in patients with depressive disorder[14] for which VNS is used as therapy.
However, our observations to support VNS as the mechanism of ‘OM’ chanting are preliminary and
further studies are required to support our hypothesis.
Alternatively, ‘OM’ chanting may have been a cue to relaxation. As meditation is shown to activate
structures involved in relaxation response, namely cingulate cortex, dorsolateral, prefrontal and parietal
cortices, hippocampus and temporal lobes,[15] the confounding effect of relaxation could not be ruled
out.
In summary, the hemodynamic correlates of ‘OM’ chanting indicate limbic deactivation. Since similar
observations have been recorded with VNS treatment used in depression and epilepsy, the clinical
significance of ‘OM’ chanting merits further research.
Acknowledgments
This study was supported by the Innovative Young Biotechnologist Award grant to Dr. G.
Venkatasubramanian awarded by the Department of Biotechnology, Government of India.
Footnotes
Source of Support: Nil
Conflict of Interest: None declared
REFERENCES
1. Nahas Z, Marangell LB, Husain MM, Rush AJ, Sackeim HA, Lisanby SH, et al. Two-year outcome of
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stimulation. Epilepsia. 2004;45:1064–70.[PubMed: 15329071]
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temporal brain structures and mood enhancing effect by transcutaneous vagus nerve stimulation. J
Neural Transm. 2007;114:1485–93.[PubMed: 17564758]
5. Kumar S, Nagendra H, Manjunath N, Naveen K, Telles S. Meditation on ‘OM’: Relevance from ancient
texts and contemporary science. Int J Yoga. 2010;3:2–5. [PMCID: PMC2952121][PubMed: 20948894]
6. Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, Weiller E, et al. The Mini-International
Neuropsychiatric Interview (M.I.N.I.): The development and validation of a structured diagnostic
psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. 1998;59:22–33. quiz 4-57.
[PubMed: 9881538]
7. Friston K, Ashburner J, Frith CD, Poline JB, Heather JD, Frackowiak RS. Spatial registration and
normalization of images. 1995
8. Venkatasubramanian G, Hunter MD, Wilkinson ID, Spence S. Expanding the response space in
chronic schizophrenia: The role of left prefrontal cortex. NeuroImage. 2005;25:952–7.
[PubMed: 15808995]
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9. Venkatasubramanian G, Spence SA. Schneiderian first rank symptoms are associated with right
parietal hyperactivation: A replication utilising fMRI. Am J Psychiatry. 2005;162:1545.
10. Evans A, Collins DL, Mills SR, Brown RD, Kelly RL, Peters TM. 3D statistical neuroanatomical
models from 305 MRI volumes. IEEE Nucl Sci Symp Med Imag Conf Proc. 1993;108:1877–8.
11. Maldjian J, Laurienti PJ, Kraft RA, Burdette JH. An automated method for neuroanatomic and
cytoarchitectonic atlas-based interrogation of FMRI data sets. Neuroimage. 2003;19:1233–9.
[PubMed: 12880848]
12. Talairach P, Tournoux JA. A Stereotactic Co-Planar Atlas of the Human Brain. Thieme. 1988
13. Zobel A, Joe A, Freymann N, Clusmann H, Schramm J, Reinhardt M, et al. Changes in regional
cerebral blood flow by therapeutic vagus nerve stimulation in depression: An exploratory approach.
Psychiatry Res. 2005;139:165–79.[PubMed: 16043331]
14. Malhi GS, Lagopoulos J, Ward PB, Kumari V, Mitchell PB, Parker GB, et al. Cognitive generation of
affect in bipolar depression: An fMRI study. Eur J Neurosci. 2004;19:741–54.[PubMed: 14984424]
15. Lazar SW, Bush G, Gollub RL, Fricchione GL, Khalsa G, Benson H. Functional brain mapping of the
relaxation response and meditation. Neuroreport. 2000;11:1581–5.[PubMed: 10841380]
Figures and Tables
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Figure 1
Shows one cycle of REST-‘OM’-REST-ssss; 10 such cycles were performed by each subject during the
fMRI scan
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Table 1
Brain regions with significant deactivation during ‘OM’ condition in comparison with “REST” condition
Brain region X Y Z T FWE-p
Right amygdala 24 -10 -08 5.2 <0.001
Left anterior cingulate gyrus -02 45 -02 10.2 <0.001
Right anterior cingulate gyrus 12 49 -01 9.8 <0.001
Left hippocampus -32 -18 -11 6.5 <0.001
Right hippocampus 30 -31 -05 4.6 <0.001
Left insula -28 19 -06 6.5 <0.001
Right insula 38 15 -06 4.9 <0.001
Left orbitofrontal cortex -28 29 -08 6.6 <0.001
Right orbitofrontal cortex 30 29 -08 7.3 <0.001
Left parahippocampal gyrus -30 -20 -21 5.1 <0.001
Right parahippocampal gyrus 32 -28 -22 5.0 <0.001
Left thalamus -14 -05 13 6.6 <0.001
Right thalamus 16 -07 11 6.2 <0.001
X, Y, Z Talairach coordinates of peak activation
Family-wise error corrected ‘P’ value
** *
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Figure 2
Compared to REST, ‘OM’ chanting produced deactivation of thalami (A) and limbic structures - anterior
cingulum (B), hippocampi (C), insula (D) and parahippocampi (E); Whereas control condition ‘ssss’
produced no deactivation in any of these regions (F). The color bar represents the T scores given in the
table
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