Evidence indicating that meditation leads to an increase in alpha rhythms
(slow, high amplitude brain waves extending to anterior channels and
ranging in frequency from eight to thirteen cycles per second) is extensive. The following studies, using many types of meditation, with subject
groups of one to more than fifty including beginners and Zen masters,
reach that conclusion: Delmonte (1984f), Daniels and Fernhall (1984),
Stigsby et al. (1981), Lehrer et al. (1980), Wachsmuth et al. (1980),
West (1980a), Dostalek et al. (1979), Corby et al. (1978), Pelletier and Peper (1977b), Elson et al. (1977), Kasamatsu et al. (1957), Kras
(1977), Fenwick et al. (1977), Glueck and Stroebel (1975), Tebecis (1975),
Williams and West (1975), Woolfolk (1975), Banquet
(1972, 1973),
Vassiliadis (1973), Benson et al. (1971c), Wallace et al. (1971c), Akishige (1970), Wallace (1970), Kasamatsu and Hirai (1963, 1966, 1969a, 1969b),
Kamiya (1968, 1969b), Anand et al. (1961a), Hirai (1960), Hirai (1959), Bagchi and Wenger (1957), and Das and Gastaut (1955) [see also
the EEG research review of Echenhofer and Coombs (1987)].
In contrast, some studies report a decrease in alpha activity during
meditation. See Jacobs and Luber (1989), Warrenburg et al. (1980),
and Tebecis (1975). A possible explanation may be found in differences
in the initial level of relaxation of subjects.
Gayten (1978) examined the EEGs of
tai chi practitioners (a form of moving meditation) using a Medi-Log Ambulatory Monitor and did not find
brain-wave patterns similar to those of meditators. After reviewing
their own and other studies, Jevning and O'Halloran (1984) concluded
that various TM-correlated changes persisted after the cessation of
TM practice, particularly EEG changes of the kind reported in the studies
we have listed here.
Sim and Tsoi (1992) investigated the
effects of three centrally acting drugs (naloxone, diazepam, and flumazenil) on the significant increase
in the intermediate alpha frequency of the EEG that accompanied meditation
in an experienced meditator. They found no significant changes, which
would indicate that the EEG correlates of meditation are not causally
related to the rise or fall of endogenous opioid peptides or benzodiazepinelike
substances in the brain.
A characteristic brainwave pattern of long-term meditators includes
strong bursts of frontally dominant theta rhythms (five to seven cycles
per second), during which meditators report peaceful, drifting, and
generally pleasant experiences with intact self-awareness. The following
studies have reported this pattern: Jacobs and Luber (1989), Delmonte
(1984f), West (1979a), Hebert and Lehmann (1977), Elson et al. (1977),
Pelletier and Peper (1977b), Fenwick et al. (1977), Banquet and Sailhan (1977), Ghista et al. (1976), Levine (1976), Tebecis (1975), Glueck and Stroebel (1984), Krahne and Tenoli (1975), Hirai (1974), Banquet
(1972, 1973), Wallace and Benson (1972), Wallace et al. (1971b), Wallace (1971), Kasamatsu and Hirai (1963, 1966), Anand et al. (1961b), and
Bagchi and Wenger (1958).
During deep meditation, experienced subjects sometimes exhibit bursts
of high-frequency beta waves (twenty to forty cycles per second). This
sudden autonomic activation is often associated by the meditator with
an approach of yogic ecstasy or a state of intense concentration; and
it is usually accompanied by an acceleration of heart rate. The following
studies have reported beta activity: West (1980a, Peper and Ancoli
(1979), West (1979a, Corby et al. (1978), Fenwick et al. (1977), Banquet (1973), Kasamatsu and Hirai (1963, 1966), Anand et al. (1961a), and
Das and Gastaut (1955). Surwillo and Hobson (1978)
recorded the EEGs of six Protestant adults during prayer to discover whether the pattern was slower than during
rest. They did not find any evidence of EEGs slowing during prayer,
and in fact found the opposite in the majority of subjects. The authors
speculated that this phenomenon was similar to that observed in experienced
meditators during deep meditation.
EEG synchronization/coherence with respect to the distribution of alpha
activity between the four anatomically distinct regions of the brain-left,
right, anterior, and posterior-may indicate the effectiveness
of meditation. It has been positively correlated with creativity (Orme-Johnson
et al. 1977b). Such neural ordering has been reported in the following
studies: Jevning and O'Halloran (1984), Badawi et al. (1984), Orme-Johnson
and Haynes (1981), Dillbeck and Bronson (1981), Dillbeck et al. (1981a),
Glueck and Stroebel (1978), Corby et al. (1978), Bennett and Trinder
(1977), Orme-Johnson (1977a), Morse et al. (1977), Hebert and Lehmann
(1977), Westcott (1977), Haynes et al. (1977), Ferguson and Gowan (1976),
Davidson (1976), Levine (1976), Ferguson (1975), Glueck and Stroebel (1975), Banquet and Sailhan (1974), Banquet (1973 and 1972), Wallace et al. (1971c), Wallace (1971), Anand et al. 1961a), and Das and Gastaut (1955).
Whether meditation produces a heightened awareness that resists habituation
is a significant question, we feel, because many traditional teachings
maintain that it does. The Sanskrit anuraga, or constant freshness
of perception, for example, is said to be a primary result of yoga;
Zen Buddhist teachers describe the freedom from "perceptual averaging"
that zazen and right living lead to; and Taoist stories accentuate the
spontaneity of each moment for those who are wise in the way of the
Tao. Such teachings are supported by most modern meditation studies,
though a few experiments have failed to replicate their findings. Some
religious ecstatics, however, become so absorbed in trance that they
inhibit or entirely suppress their responses to the outer world. Early
studies by Bagchi and Wenger compared yogis and Zen masters in this
regard, and appeared to show significant differences in EEG response
between the two kinds of meditation. The yogis they studied habituated
to repeated stimuli more rapidly and completely than Zen masters, leading
Bagchi and Wenger to speculate that the two types of discipline produced
different spiritual resultseither inner absorption or heightened
awareness of the outer world. The following studies report that meditation
leads to a heightened perceptual awareness, in which the EEGs remain
responsive to repeated stimuli such as clicks or light flashes instead
of habituating to them: Delmonte (1984b), McEvoy et al. (1980), Davidson
(1976), Williams and West (1975, Hirai (1974), Wada and Hamm (1974),
Banquet (1973), Orme-Johnson (1973), Gellhorn and Kiely (1972), Naranjo
and Ornstein (1971), Wallace et al. (1971b), Wallace (1971), Akishige 1970), Kasamatsu and Hirai (1963, 1966), Anand et al. (1961a), and
Bagchi and Wenger (1957).
Other studies, however, failed to replicate this finding. Heide (1986)
compared seventeen TM meditators and seventeen controls and found no
significant differences between groups in the rate of habituation of
alpha blocking. Becker and Shapiro (1981) used three groups of Zen,
yoga, and TM meditators with five to seven years of experience, and
two groups of controls. They found that EEG alpha suppression in response
to repeated stimuli did not differ among the five groups. West (1980a)
concluded that too few systematic studies of habituation have been made
to reach a solid conclusion. Barwood et al. (1978) tested auditory-evoked
potentials of eight experienced meditators before, during, and after
meditation, and also during light sleep, and found no consistent changes
between baseline and meditating or meditating and sleep auditory-evoked
potentials.
Traditional teachers did not have electroencephalographs to study cortical
activity, but the findings in modern studies that meditators achieve
various kinds of control over specific kinds of brain function conform
to the tenet of many contemplative literatures that self-awareness brings
self-mastery. As various kinds of functioning are brought to consciousness,
their integration can be more deliberately guided, according to most
traditional teachings. Several modern studies seem to show that meditators
do indeed acquire control of specific brain functions.
Delmonte (1984b) concluded that meditation practice may begin with
left-hemisphere activity, which then gives way to functioning characteristics
of the right hemisphere, while both left- and right-hemisphere activity
are largely inhibited or suspended in advanced meditation.
Pagano and Frumkin (1977) reported strong evidence that meditation
enhances functioning in the right hemisphere, with cumulative effects
among experienced meditators. Prince (1978) suggested that meditation
may inhibit the left hemisphere somewhat, shifting the focus of consciousness
to the right hemisphere. Bennett and Trinder (1977) reported that TM
meditators had greater flexibility in shifting from one brain hemisphere
to the other. Davidson and Goleman (1977) suggested that during periods
of intense concentration in meditation, sensory information may become
attenuated below the level of the cortex. Earlier, Davidson (1976)
reported that during mystical experience cerebral function is dominated
by the right hemisphere. Goleman (1976a) stated that meditators showed
a significantly increased cortical excitation during meditation and
a simultaneous limbic inhibition that delinked the cortex and limbic
systems. He also reported that Gurdjieff meditators' brains showed
cortical specificity, or the ability to turn on those areas of the brain
necessary to the task at hand while leaving the irrelevant areas inactive.
Schwartz (1975) stated that meditation practices can lead to heightened
cortical arousability plus decreased limbic arousability, so that perception
is heightened and emotion is simultaneously reduced, which he described
as a "skilled response."
Others reporting cortical specificity of response are Warrenburg (1979),
Hirai (1974), Banquet (1973), and Orme-Johnson (1973).
Persinger (1984) stated that transient, focal, epilepticlike electrical
changes in the temporal lobe, without convulsions, have been hypothesized
to be primary correlates of religious experiences. He investigated
two cases of this kind. The first involved the occurrence of a delta-wave
dominant electrical seizure for about ten seconds, from the temporal
lobe only, of a TM teacher during a peak experience. The second involved
the occurrence of spikes, within the temporal lobe only, during protracted
intermittent episodes of glossalalia by a member of a Pentecostal sect. Persinger concluded that religious experiences are natural correlates
of temporal-lobe transients that can be detected by routine EEG measures.
Researchers have analyzed EEG differences between meditators and those
in stages of sleep, hypnosis, and other self-regulation strategies.
Brown et al. (1977-78) were not able to differentiate between EEG data
during meditation, sleep, and therapeutic touch healing states. Fenwick et al. (1977)
found that EEG results showed TM to be a method of holding the meditators' level of consciousness at stage "onset" sleep.
He found no evidence to suggest that TM produced a hypometabolic state
beyond that produced by muscle relaxation, nor support for the idea
that TM is a fourth stage of consciousness. Pagano et al. (1976) studied
the EEGs of five experienced meditators, and found appreciable amounts
of sleep stages two, three, and four during meditation. Otis (1974)
found during a posttreatment testing session that twenty-three Transcendental
Meditators displayed significantly more sleep-stage-one activity than
they had in a premeditation rest period, and significantly more sleep
than controls. Rao (1965) described meditation as a form of autohypnotism
parallel to the state of hypnotic trance or hypnotic sleep. On the
other hand, those who have found the EEGs of meditators to be distinct
include West (1979a), Wachsmuth (1978), Patey et al. (1977), Dash and
Alexander (1977), Banquet and Sailhan (1974), Wallace and Benson (1972),
Wallace et al. (1971b), Wallace (1971), Kasamatsu and Hirai (1966),
Onda (1967), Anand et al. (1961a), and Bagchi and Wenger (1957).
A few researchers have looked at EEG results in terms of the ergotropic/trophotropic
model developed by Gellhorn [see Gellhorn and Kiely (1972).] Davidson
(1976) stated that mystical states may be experienced during either
ergotropic (excited) or trophotropic (relaxed) conditions. He suggested
that the whirling dances of Sufis and the violent abdominal contractions
of Ishiguro Zen monks induce ergotropic conditions, whereas TM and other
forms of sitting meditation elicit trophotropic reactions. Sargant
(1974) speculated that trophotropic states may occur in the midst of
an ergotropically induced experience. Gellhorn and Kiely (1972) observed
that physiological changes in meditation are due to a shift in the ergotropic/trophotropic
balance in the trophotropic directiona good strategy for improving
mental health. Their model was criticized by Mills and Campbell (1974),
because it ignored differences in meditation techniques, left out certain
evidence of alpha-blocking differences between yoga and Zen, and provided
an ambiguous interpretation of trophotropic/ergotropic effects on the
orienting reflex. Emerson (1972) concluded that the religion of the
meditator determines the way in which his EEG pattern will change during
the course of meditation. Fisher (1971) stated that the mystic may switch
between extreme ergotropic and extreme trophotropic forms of mystical
experience, a rebound from ecstatic rapture to yogic samadhi in response
to intense ergotropic excitation. Das and Gastaut (1955) characterized
the mystical state of yogic ecstacy as predominantly ergotropic, where
no effect on the EEG pattern as a result of external stimuli was noticed.
Strict comparisons between traditional understandings of bodily change
in contemplative practice and modern studies of meditation's effect
on blood chemistry are uncertain at best, though the finding in some
studies that meditation lowers adrenal hormones, lactates, and cholesterol
seems to confirm the repeated discovery that spiritual practice reduces
stress and anxiety. This area of research is not as well developed,
though, as other areas of meditation research. Only more investigation
will reveal the intricate relationships of blood chemistry in contemplative
activity.
Meditation generally produces psychological results opposite from those
of stress, yet researchers have been puzzled by the fact that stress-induced
adrenal hormone levels do not fall consistently in the blood of meditators. Benson (1983a)
studied nineteen subjects who practiced the relaxation response technique twice daily for thirty days. He found increased
norepinephrine levels without any increase in heart rate or blood pressure,
and concluded that the relaxation response technique reduces central
nervous system responsivity to norepinephrine. Or norepinephrine levels
rise because less is used up by tissues that ordinarily respond to it.
Benson (1989) concluded that reduced norepinephrine end-organ responsivity
may be the mechanism through which physiologic changes persist after
the elicitation of the relaxation response [see also Morrell (1985)].
Mills et al. (1990) measured functional lymphocyte beta-andrenergic
receptors and found lower levels in TM meditators supporting Benson's
hypothesis. Engle (1983), commenting on Benson's work, agreed that
the relaxation response is a useful technique to modify physiological
functions, but that little is understood about the mechanisms that mediate
its effect. Earlier, Hoffman et al. (1982) assessed sympathetic nervous
system activity in experimental subjects practicing the relaxation response
and in control subjects, all of whom were exposed to graded orthostatic
and isometric stress during monthly hospital visits. They found higher
concentrations of norepinephrine for experimental subjects and no changes
for controls [see the follow-up study by Morrell and Hollandsworth (1986)
that supports this conclusion].
Sudsuang et al. (1991) reported decreased cortisol levels measured
after meditation in inexperienced meditators. Michaels et al. (1979)
studied eight TM meditators and eight controls, and found that cortisol
decreased progressively for both groups, aldosterone did not change
for either group, and renin increased by 14% for the meditation group,
thereby not supporting the hypothesis that TM induces a unique state
characterized by decreased sympathetic activity or release from stress.
However, since cortisol concentrations varied more widely for controls
than for meditators during the experiment, Michaels concluded that meditators
may be less responsive to acute stress. Lang et al. (1979), in a study
of ten advanced meditators with over four years of experience and ten
meditators with over two years of experience, found that catecholamine
levels were higher in advanced meditators during the experiment, and
concluded that meditation enhances sympathetic activity. Michaels et
al. (1976) measured plasma epinephrine and norepinephrine in twelve
meditators before, during, and after meditation, and in a control group
matched for sex and age who rested instead of meditating, and obtained
the same results for both groups, thereby concluding that TM does not
reduce stress and the activity of the sympathetic nervous system. Bevan
et al. (1976) found significant decreases in plasma and urinary-free
cortisol during TM, the effect being cumulative with increased meditation
experience. However, no significant effects on catecholamine excretion
were noted. He concluded that TM produces an acute and chronic reduction
in trophotropic anterior hypothalamic activity but little effect on
ergotropic posterior hypothalamic function, and that the mechanisms
underlying the practice are not a simple counterpart of the fight-or-flight
response.
Other researchers, however, have reported decreases in adrenal hormones
during meditation. Werner et al. (1986) evaluated eleven subjects before
and during a three-year period after starting the TM-Sidhi program.
They found a progressive decrease in serum TSH, growth hormone, and
prolactin levels, with no consistent change in cortisol, T4, or T3. Stone and DeLeo (1976)
measured plasma dopamine-B-hydroxylase as an index of sympathetic nervous system activity in a six-month controlled
trial of simple word meditation in hypertension patients. They noted
significant reductions of plasma D-B-H, which was positively correlated
with significant reductions of blood pressure. Schildkraut et al.
(1990) found a possible common mechanism of action for the drug alprazolam
(a triazolobenzodiazepine with antianxiety and antidepressant as well
as antipanic effects) and elicitation of the relaxation response that
involves decreased catecholamine output. Bujatti and Riederer (1976)
found a significant decrease of the catecholamine metabolite VMA (vanillicmandelic
acid) in meditators. This decrease was associated with a reciprocal
increase of the serotonin metabolite 5-HIAA, which supports, as a feedback
necessity, the rest-and-fulfillment response versus fight and flight. Loliger (1991) also reported an increase in 5-HIAA during the practice
of TM and the TM-Sidhi program.
Several studies have found decreased cortisol levels in meditators
versus controls with the level of effect increasing with duration of
meditation practice. See Ahuja et al. (1981), Jevning et al. (1978a,
1978d), Udupa et al. (1975), and Jevning et al. (1975).
Jevning and O'Halloran (1984) stated
that adrenocortical activity may be the one parameter sufficient to determine the relationship between
TM and sleep, since cortisol secretion is not apparently related to
sleep. They reviewed the literature, particularly Jevning, Wilson,
and Davidson's study (1978), and concluded that it is unlikely that
TM can be the same as sleep, or accounted for as unstylized rest/relaxation,
since sharp declines of up to 25% in cortisol during meditation for
long-term meditators was measured, whereas insignificant declines were
noted in short-term meditators, and no changes were noted in the rest/relaxation
control group.
Androgen levels are a well-established correlate of the response to
acute stress, and are possibly of adrenocortical origin. Jevning and Wilson (1978) studied
testosterone concentration changes during TM and during rest among a group of fifteen TM practitioners with three to
five years of experience and a group of fifteen controls. The controls
were restudied as practitioners after three to four months of practice.
No change in testosterone concentration was found during either rest
or TM. Cooper et al. (1985) studied ten experienced Transcendental
Meditators and found no clear evidence that meditation suppressed stress-related
hormones [see the comments of Davis (1986)].
The serum level of the adrenal androgen, dehydroepiandrosterone sulfate
(DHEA-S), is closely correlated with age in humans and has also been
associated with measures of health and stress. Levels of DHEA-S decrease
with age, stress, and illness. Glaser et al. (1992) found generally
higher levels of DHEA-S in TM meditators versus controls suggesting
greater health and adaptability for meditators.
Hill (1990) studied ten meditators to investigate the acute autonomic
effects of Transcendental Meditation and found that both divisions of
the autonomic nervous system are attenuated. The results also provide
preliminary evidence to support the hypothesis that TM is associated
with acutely reduced hypothalamic and peripheral serotonergic activity.
Werner et al. (1986), in a study of eleven subjects in the TM-Sidhi
program found decreased TSH, growth hormone, and prolactin levels and
no consistent change in cortisol, T3 or T4. Jevning and Wilson (1977)
found in a study of TM practitioners that T3, T4 and insulin levels
did not change during meditation, but that TSH levels declined dramatically.
Decreased TSH, along with stable thyroid hormone levels, may suggest
change of the set point for feedback control of TSH secretion during
TM and is consistent with primarily neural modulation of TSH secretion. The stability of T3, T4 and insulin make it unlikely that these hormones
regulate the acute metabolic changes associated with the meditative
state.
Sudsuang et al. (1991) reported increased serum protein levels after
six weeks of meditation and speculated that cortisol reduction during
meditation practice may be related to an increase in total protein because
of reduction of gluconeogenesis and increased total protein synthesis
by the liver.
There is some evidence that amino acid metabolism is related to mental
states, since alteration of plasma amino acid levels has been correlated
with various forms of behavior. Jevning et al. (1977b) measured thirteen
plasma neutral and acidic amino acids in twenty-eight subjects, thirteen
of whom were controls and fifteen of whom had practiced TM twice daily
for three to five years, and found that phenylalanine concentration
increased by 23% during TM practice with no change during control relaxation.
No significant changes were noted for the other twelve amino acids studied.
Jevning speculated that since the liver is the principal utilizer of
phenylalanine hydroxylase, reduced blood flow to the liver during meditation
[see Jevning (1978c)] might be the cause of increased phenylalanine
levels. He also suggested that the brain might utilize less phenylalanine
during meditation.
Werner et al. (1986) evaluated the endocrine changes of eleven subjects
before and over a three-year period after starting the TM-Sidhi program.
A progressive decrease in serum thyroid stimulating hormone (TSH), growth
hormone, and prolactin levels occurred over the three years, while no
consistent change in cortisol, total thyroxine, or triiodothyronine
was observed. Jevning, Wilson, and Vanderlaan (1978b) studied the concentrations
of plasma prolactin and growth hormone before, during, and after forty
minutes of TM. Twenty-four subjects were studied, including a group
of twelve who had regularly practiced TM for three to five years and
a group of twelve who had been regular practitioners for three to four
months. The short-term practitioner group was studied as controls before,
during, and after a forty-minute eyes-closed rest period. Prolactin
concentration began to increase toward the end or after meditation in
both groups of practitioners, with levels continuing to increase in
the post-TM period. The increases were not correlated with sleep occurrence.
Prolactin levels were stable in controls throughout the experiment. Growth hormone concentration was unchanged in both TM and rest groups.
Bevan et al. (1979) studied the short-term endocrine changes of five
experienced meditators before, during, and after a thirty-minute period
of meditation; and restudied the same group under the same experimental
conditions, except that instead of meditating they read and talked quietly
among themselves. A comparable group of five previously unstudied meditators
were examined under the same nonmeditation conditions to offset the
"second-experience" effect. A significant 38% reduction in
serum hGH occurred during TM. The hGH fall commenced before the onset
of meditation and appeared to be a response to anticipation of meditation.
Serum hGH concentrations after TM rebounded to 50% above premeditation
values. There was no change in the same subjects during a comparable
nonmeditation experimental period, and the absence of hGH changes was
not due to a second-experience effect. The experienced meditators showed
slight decreases in prolactin and cortisol during meditation, which
were not statistically significant. There were no statistically significant
changes in thyroxine, triiodothyronine, reverse triiodothyronine, hemoglobi,
packed cell volume, or total serum protein during the experimental period.
High blood lactate concentrations have been associated with anxiety
and high blood pressure, and the infusion of lactate in the blood has
been found to produce symptoms of anxiety. The following studies have
reported significant declines of up to 33% in blood lactate during meditation,
and a rate of decline nearly four times faster than the rate of decrease
among people resting or in a premeditation period: Bagga et al. (1981),
Jevning et al. (1978c), Jevning and Wilson (1977), Benson (1975), Benson
et al. (1973a, 1973b), Orme-Johnson (1973), Wallace and Benson (1972),
Wallace et al. (1971a), and Wallace (1971).
Other studies have not confirmed a drop in lactate concentrations during
meditation. Michaels et al. (1979) studied the plasma concentration
of lactates of eight TM meditators before, during, and after twenty
to thirty minutes of meditation, and of eight controls who rested quietly.
Their failure to observe a change in lactate was consistent with their
previously published report (Michaels et al.,1976).
Parulkar et al. (1974) studied twelve TM practitioners and found the
following average decreases: white blood cell count before TM, 7,100,
after TM, 6,813; eosinophil count before TM, 638, after TM, 460; and
lymphocyte count before TM, 2,855, after TM, 2,781.
Jevning et al. (1983) studied thirty-two TM instructors with at least
six years of meditation experience. They found a marked decline of whole
blood metabolism during TM, which was accounted for mostly by a decline
of red cell glycolite rate. This was correlated with decreased plasma
lactate concentration and with relaxation as indicated by electrodermal
response.
Chronic sympathetic nervous system overactivity has been implicated
as a factor capable of elevating and maintaining high serum cholesterol
levels independent of dietary measures. Bagga et al. (1981) studied
forty female medical students who practiced TM and yoga, and reported
that their average serum cholesterol decreased from 196.3 mg/dl to 164.7
mg/dl. Cooper and Aygen (1979) measured serum cholesterol levels at
the beginning and end of an eleven-month period for twelve hypercholesterolemic
subjects who practiced TM. Eleven hypercholesterolemic controls who
did not practice the technique were similarly followed for thirteen
months. Paired comparisons showed a significant reduction in fasting
serum cholesterol levels for those subjects who practiced meditation. The cholesterol mg per 100 ml for the meditation group was 254 at the
start and 225 at the end of the period, and for the control group it
was 259 at the start and 254 at the end of the period.