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Acute vibration training is gaining popularity as a modality for
sport, exercise and physical rehabilitation as it initiates a rapidly
and repeating eccentric-concentric action that evokes muscular work and
elevates metabolic rate (Rittweger et al., 2003).
Vibration exercise has taken on many different forms; custom built vibratory
devices have recently been constructed specifically for flexibility training
(Sands et al. , 2006),
while other vibration units have been attached to resistance training
equipment (Issurin and Tenenbaum, 1999)
and smaller units have been directly applied to muscle and tendon. Over
the past decade, two products have featured on the commercial market,
an electric powered vibrating dumbbell and the vibrating platform. There
are two types of vibrating platforms; the first produces vertical sinusoidal
vibrations (VV), which are transmitted to the body via the platform, the
second moves in a side-alternating motion (SV).
During vibration, the transference of energy occurs from the vibration
source to the whole body or body part, which causes reactive forces within
the body. These forces have the potential to be harmful, but also beneficial.
The human body is a spring-mass system where tendons and muscles act like
springs to store and release mechanical energy, where the stiffness and
mass of these body parts will determine the natural frequency (Rittweger,
2010).
Therefore, the body can acquire accumulated mechanical energy when the
vibration frequency of the device matches parallels with the resonance
frequency of the body (Rittweger, 2010).
This can be controlled by adjusting body position and changing muscle
stiffness (Mester et al., 2006)
where muscles have innate damping characteristics that can absorb energy
and generate heat (Wakeling et al., 2002).
The vibratory load is dependent on four variables: frequency (f), amplitude
(A), acceleration (a), and duration (t). The number of cycles of oscillation
determines the frequency (Hz); the amplitude refers to the maximal displacement
of the oscillatory motion (mm); the acceleration (m·s-2 or
g) determines the magnitude; and duration refers to the exposure time
(min or s). Low vibration frequency (5-45Hz) has been reported to increase
EMG activity, muscle force, and power (Bosco et al., 1999a;
1999b,
Cardinale and Lim, 2003;
Cochrane and Stannard, 2005;
Cochrane et al., 2010b;
Torvinen et al., 2002;
Stewart et al., 2009)
where excitatory responses of the muscle spindle are speculated to play
a role in enhancing muscle activation, involving a spinal reflex mechanism.
The muscle tuning response is another possible mechanism where the muscular
system damps the vibration stimuli to promote muscle activity that may
subsequently increase muscle function.
Additionally, the neural adaptations that occur from resistance and power
training have been purported to be similar to that of acute indirect vibration
(Bosco et al., 1998;
1999a;
1999b;
Cardinale and Bosco, 2003;
Delecluse et al., 2003).
Neural aspects, such as motor unit recruitment, synchronisation, and co-contraction
may be responsible for force and power increases following acute vibration.
Other mechanisms of vibration, such as a warm-up effect, where friction
between the vibrating tissues may raise muscle temperature (Issurin and
Tenenbaum, 1999),
coupled with a vibratory induced increase in blood flow (Kerschan-Schindl
et al., 2001)
may also contribute to enhancing muscle performance. To date, there has
been no direct attempt to identify which mechanism(s) may contribute to
the enhancement of neuromuscular performance. Therefore, this paper explores
and assesses the possible neural mechanism(s) of acute indirect vibration.
Methodology
A search was conducted using the following electronic databases: Medline,
PubMed, ISI Web of Knowledge and Scopus. Key search words included, vibration
and whole-body vibration; which were used in combination with spinal reflexes,
muscle tuning, neuromuscular (motor unit firing frequency, synchronisation,
intermuscular co-ordination) and central motor command. Articles were
checked for relevant content and were included based on the following
criteria: 1. published in English; 2. examined acute (single session)
vibration; 3. the participants were healthy and trained, 4. conference
abstracts and proceedings were excluded.
Types
of vibration
As mentioned previously there are many different methods of producing
acute vibration. Small vibratory units have been applied directly to the
muscle or tendon (Warman et al., 2002;
Jackson and Turner, 2003);
while larger custom-built vibratory units have been constructed for flexibility
training (Kinser et al., 2008;
Sands et al., 2006;
2008),
and resistance training to elicit vibration transmission through cables
of various machines (Issurin and Tenenbaum, 1999).
Over the last decade, two commercial forms of acute indirect vibration
are available for consumer use, the vibrating platform and vibrating dumbbell,
which produce vertical sinusoidal vibration. As stated earlier, two types
of vibrating platforms exist that involve standing and/or performing dynamic
and/or static exercises. One type of platform oscillates around a central
axis, where a crankshaft on each side of the platform translates to a
rotationalmotion of the electro- motor into a vertical displacement, inducing
a seesaw motion, of which the amplitude is either small closer to central
axis or larger near the edge of the platform (0-10 mm). The second commercial
machine has electro-motors that produce vertical synchronous vibration
where both legs vibrate as the platform moves predominately in the vertical
direction, which results in simultaneous and symmetrical movement of both
sides of the body during the vibration exposure. The foot placement of
this platform is independent of amplitude and has a pre-setting of two
ranges; 0- 2 mm or 4-6 mm. Commercially manufactured hand-held powered
vibrating dumbbells have also been developed to target the upper-body
where the central handle of the dumbbell rotates producing oscillatory
movements to the body.
Various vibration protocols have examined the purported neural mechanism(s),
through the investigation of different vibration equipment, varying vibration
frequencies, amplitudes and durations, various exercises and participant
types; all of the above could potentially influence the outcome measures.
Additionally, a difference exists in applying the vibration by direct
or indirect methods. Direct vibration is normally applied to muscle or
tendon at a high vibration frequency (100-150 Hz), at a small amplitude
(1-2 mm) for a short period of time (2-15 s), resulting in a transient
increase in muscle activity known as the tonic vibration reflex (Eklund
and Hagbarth, 1966).
However, indirect vibration typically uses a lower vibration frequency
(25-45 Hz), set at a high amplitude (2-10 mm) with longer duration time
of either continuous (3-5 min) or intermittent exposure (30-60 s), where
the vibration is applied through the feet (platform) or hands (cable or
dumbbell).
Even so, there is still a lack of prescriptive guidelines for vibration,
which makes it difficult to compare the various studies. The optimal vibration
frequency, amplitude, duration and the type of exercises to perform remains
equivocal due to inadequate validation of these variables. This aside,
some experiments have failed to include appropriate control and/or sham
conditions, giving uncertainty to the value of vibration. There is additional
concern over the potential difference in vibration transmission between
side-alternating (SV) and vertical (VV) vibration platforms. Earlier,
Rittweger et al., 2001
proposed a hypothesis that in SV, the feet alternate between up and down
positions, causing pelvis rotation and flexion of the spinal column, which
decreases vibration transmission to the head. To test this hypothesis
Abercromby et al., 2007b
compared SV and VV platforms at a set vibration frequency and amplitude
(f=30 Hz, A=4 mm) while performing slow dynamic squats (4s up and 4 s
down) from 10 to 35° knee flexion. They found that vibration transmitted
to the upper-body and head was 71 to 189% greater during VV than SV and
concluded that the pelvis damped the vibration energy more during SV than
the VV. However, a complete kinematic analysis of SV and VV conducted
over a larger range of knee angles across different vibration frequencies
and amplitudes are required to validate this claim.
In another study, the same authors (Abercromby et al., 2007a)
investigated muscle activity of SV and VV (f = 30 Hz, A = 4 mm). They
reported that during dynamic (from 10° to 35°of knee flexion, at a tempo
of 4 s up 4 s down) and static squatting (18.5° knee flexion) the lower
limb extensors (vastus lateralis and gastrocnemius) were activated significantly
more during SV than VV; and the activation of the tibialis anterior was
significantly greater during VV than SV. Therefore, it would be of interest
to conduct additional static squat experiments at a variety of fixed knee
angles and perform dynamic squats over a larger range of knee flexion
to identify if further differences in muscle activation exist between
VV and SV.
Spinal
reflexes
It is suggested that acute vibration may improve muscular performance
via neurogenic potentiation involving the spinal reflexes and muscle activation
(Cardinale and Bosco, 2003,
Rittweger et al., 2003).
The main evidence in supporting neurogenic potentiation is based on measurements
of the tonic vibration reflex (TVR). Previous studies have reported that
a vibration stimulus is capable of augmenting muscle spindle activity,
which causes an excitatory response in the primary endings of non-contracting
muscle (Burke et al., 1976;
Ribot-Ciscar et al., 1998).
As a result of direct vibration, an ensuing muscle contraction occurs
with reciprocal inhibition of its antagonists, which has been termed the
TVR (Eklund and Hagbarth, 1965;
1966;
Matthews, 1966).
This elicits an excitatory response of the muscle spindle Ia fibres (Burke
et al., 1976,
De Gail et al., 1966,
Roll et al., 1989),
which is mediated by monosynaptic and polysynaptic pathways (Matthews,
1966;
Romaiguere et al., 1991).
The excitability of the motoneurons innervating the antagonist muscles
are depressed by reciprocal inhibition (De Gail et al., 1966;
Lance et al., 1966),
and the monosynaptic stretch reflexes of the vibrated muscle are suppressed
during the vibration (De Gail et al., 1966;
Marsden et al., 1969).
Burke et al., 1976
found that when direct vibrations of 20-220 Hz (Table
1) were applied to a tendon of non-contracting muscle, the primary
endings responded more during high frequency vibration than secondary
endings, which corresponded to earlier findings from cat studies conducted
by Bianconi and van der Meulen (1963)
and Brown et al., 1967.
However, Burke et al. (1976)
also found that both primary and secondary endings respond by discharging
in synchrony to the vibration stimulus, which contradicts Bianconi et
al. (1963)
findings. The explanation for this discrepancy is that Bianconi et al.
(1963)
did not differentiate between endings that were unresponsive and those
capable of being activated from vibration.
When the vibratory stimulus is applied to an agonist muscle it causes
reciprocal inhibition of the antagonist motoneurons (Bishop, 1974);
but when vibration is applied simultaneously to the agonist and antagonist
muscles, the facilitatory effect of each muscle group is inhibited (Hagbarth,
1967).
However, when both muscles independently vibrate they show a strong TVR
(Bishop, 1974).
Vibration also causes suppression of the muscle's phasic stretch reflexes
(De Gail et al., 1966;
Marsden et al., 1969).
Arcangel et al., 1971
observed that during tendon vibration, the Achilles tendon reflex and
the Hoffmann response (H response) were suppressed, but in the post-vibratory
period the reflexes were potentiated, indicating that pre-synaptic inhibition
of the Ia afferent terminals occurred (Gillies et al., 1969).
Desmedt et al. (1978)
confirmed that motor unit recruitment was suppressed by the direct application
of high vibration amplitudes, which caused pre-synaptic inhibition of
Ia afferents.
According to Bishop, 1974,
four factors affect the TVR response: 1) the location of the vibration;
2) the excitability state of the CNS; 3) the initial length of muscle
i.e. pre-stretch; and 4) the vibration frequency and amplitude. Research
has suggested that the initial muscle length influences the strength of
the TVR where further lengthening of a muscle will induce a stronger TVR
(Bishop, 1974;(Eklund
and Hagbarth, 1966).
Vibration
amplitude can determine the amount of stretch occurring within the muscle.
Matthews, 1966
and Brown et al., 1967
reported that in decerebrated cats increasing the vibration amplitude
caused an increase in TVR, as this activated a larger number of muscle-spindle
endings and caused more ? motoneurons to be activated (Luo et al., 2005).
However, the range of amplitude, which caused augmentation, occurred between
25-150 ?m (Bishop, 1974).
Moran et al., 2007
argued that higher vibration amplitudes may only benefit sub-maximal contractions
and proposed that in maximal voluntary contractions the Ia afferent discharge
may reach a saturation threshold, where vibration is unable to cause further
increases in Ia afferent inflow. Supporting evidence is based on observations
that state, vibration can only increase maximal isometric contraction
force and EMG activity when fatigue is present in the intrafusal fibres
(Bongiovanni and Hagbarth, 1990)
or when ?-fibre are blocked (Hagbarth et al., 1986).
The Jendrassik manoeuvre is a procedure that involves contracting remote
muscles, normally of the upper-body (particularly the forearm and jaw
muscles) to induce a reflex response (Jendrassik, 1885).
A common method for eliciting a reflex is to grasp the hands and pull
them apart - this potentiates the stretch reflex and H-reflex (Delwaide
and Toulouse, 1980;
Dowman and Wolpaw, 1988).
Using a prototype vibration machine consisting of a motorised horizontal
leg press fitted with two electrically powered motors to the rear of the
foot plate; young (21.5y) and old (69.2y) participants were vibrated at
30 Hz (A = 1 mm), whilst performing the Jendrassik manoeuvre for four
minutes (Cochrane et al., 2008).
This involved pulling with both arms a dual handle load cell at 10% maximal
voluntary contraction while seated with their feet on the vibrating plate
of the leg press with the knees flexed at 70°. The authors reported that
superimposing the Jendrassik manoeuvre upon vibration enhanced metabolic
rate in both young (27.6%) and old (33%) groups, but there were no significant
differences between the groups (Table
1). Further, using a side-alternating vibration (SV) platform, acute
low frequency vibration (f = 6 Hz, A = 3.1 mm) produced a temporal association
between EMG activity and muscle contractile tissue displacement suggesting
that muscle lengthening may be a prerequisite to eliciting probable stretch
reflexes (Cochrane et al., 2009).
However, in a follow up study (Cochrane et al., 2010a)
reported that after five minutes of continuous acute indirect vibration
(f = 26 Hz, A = 6 mm, SV) there was minimal change in patellar tendon
reflex properties, but muscle twitch characteristics were potentiated
indicating that a greater myogenic response was present compared to a
neural-mediated effect of a reflex potentiation. Likewise, Hopkins et
al., 2008
found no effect on the patellar tendon reflex after intermittent (5 x
1 min bouts) vibration exposure (f = 26 Hz, A = 4 mm, SV). Other studies
have reported enhancement of the stretch reflex, for example, Melnyk et
al., 2008
initiated the stretch reflex in the hamstrings by inducing an anterior
tibial translation during standing; they also compared the reflex response
between two groups that performed either intermittent (2 x 1 min) vibration
(f=30 Hz, A= 4 mm, VV) or normal activity (control). The researchers found
post-vibration, that anterior tibial translation displacement decreased
with a corresponding increase in EMG of the hamstring short latency response.
The authors concluded that the effect of increased knee stability caused
reflex excitability. However, it is inconclusive whether the stretch reflex
was the causal factor in decreasing anterior tibial translation because
the control group did not perform the same protocol without vibration.
An earlier study reported an increase in the patellar tendon reflex immediately
following exhaustive squatting exercise with continuous vibration (f =
26 Hz, A = 12 mm, SV) and extra load (40% of body mass). The authors concluded
that ? motoneurons were augmented by the vibration, which recruited high-threshold
units and muscle fibres (Rittweger et al., 2003).
To date, only one study has confirmed that stretch reflexes were induced
during vibration (f = 5-30 Hz, A = 4 mm, SV) (Ritzmann et al., 2010).
This study measured the EMG activity of the soleus and medial gastrocnemius
muscles during different vibration frequencies in comparison to an evoked
stretch reflex of the same muscle groups using a custom-built ankle ergometer
and found that the EMG activity was identical between the vibration and
the evoked stretch reflex, indicating the existence of vibration-induced
reflexes.
Currently, two studies have examined the response of the H-reflex following
acute indirect vibration, both producing different results. Nishihira
et al., 2002
found that the H-reflex and H max/M max ratio was enhanced, suggesting
that motoneuron excitability was heightened; while Armstrong et al., 2008
found the H-reflex was suppressed (Table
1). The disagreement in these findings was most likely due to different
vibration and H-reflex protocols. Nishihira et al., 2002
used three sets of three minute vibration protocol (f = 25 Hz, A = not
reported, SV) where the H-reflex was activated from a seated position,
which differed to Armstrong et al., 2008
one minute duration performed on a VV platform (f = 40 Hz, A = 2-4 mm)
where the H-reflex was activated from a supine position. Major limitations
to the above studies were that both lacked a control group and both failed
to disclose the exact testing protocol of the H-reflex.
In summary, the proposed mechanism of acute indirect vibration causing
a response similar to that of TVR cannot be supported (Nordlund and Thorstensson,
2007).
TVR requires vibration to be directly applied to the muscle or tendon
at high vibration frequencies (>100 Hz), typically other vibration
methods such as, platforms and dumbbells are not directly applied to the
body and are subjected to lower frequencies (20-45 Hz) and longer exposure
times (>30s). Therefore, it is difficult to uphold the view that acute
indirect vibration may act through a spinal mechanism, such as TVR. However,
vibration may cause an indirect involvement of muscle spindles, where
other sensory inputs may influence gamma (?) motoneuron activity, causing
changes to spindle input (Gandevia, 2001).
Additionally, the evidence is inconclusive whether acute indirect vibration
potentiates stretch reflexes, this is due
to the different vibration protocols, applications and durations; therefore
it remains undetermined whether spinal reflexes are the causal mechanism.
Muscle
tuning
There is evidence to suggest that the body is capable of tuning its muscle
activity in order to reduce the vibrations that are passing through the
soft tissue that may produce a detrimental effect (Nigg, 1997).
The amount of muscle activity required is dependent on the level of vibration,
where maximal muscle activation can reduce or purge oscillations within
the tissues. Everyday activities such as walking, running and jumping
result in impact forces, from the collision of the heel with the ground,
producing vibrations of 10-20 Hz to the lower limbs (Wakeling and Nigg,
2001),
where an input signal from the impact force produces muscle activity or
'tuning' response to reduce soft tissue vibrations. This activation or
tuning supposedly occurs shortly before the heel strikes the ground (Nigg,
1997).
Consequently, muscle tuning relies on three components: i) the frequency
and amplitude of the input force, ii) the vibration resonance of the soft
tissue and iii) the level of muscle activity. To test the activation level
of additional muscles from vibrations, a hydraulic actuator was used to
mimic the force during running, by directly evoking vibrations onto the
sole of a foot using a range of vibration frequencies (10-65 Hz) (Wakeling
et al., 2002).
The study found that damping occurred in the lower limb soft tissues and
resonance reduction occurred at heel strike (Table
2). However, the natural frequency of the soft tissues did not change
and paralleled the frequency of the input. The mechanism of this response
remains unclear, but if damping does occur in soft-tissues, where resonance
is minimised at heel strike and the changes in frequency are a consequence
of altered muscle activity then energy absorbed by the muscle is likely
to involve cross-bridge cycling (Ettema and Huijing, 1994,
Wakeling et al., 2002).
Consequently, damping vibration will depend on the individual's neuromuscular
(muscle spindle) response, the sensitivity of joint and skin receptors,
the proportion of muscle fibre types and viscoelastic (stiffness) elements
(Bazzett-Jones et al., 2008).
Due to impact forces, there is a possibility of vibrations occurring in
soft tissues that have viscoelastic properties. Mechanical energy from
the vibration can be stored and returned from the elastic structures of
the muscle-tendon complex where the damping of vibrations may result in
a net dissipation of mechanical energy that can be absorbed by activated
muscle.
In summary, impact forces create vibrations in the foot where the vibrations
travel through the lower limb musculature. To prevent resonance, soft
tissues damp the vibrations, which cause sensory organs to send impulses
to the CNS to increase muscle activity and adjust joint stiffness. The
muscle tuning mechanism relies on the input force, the vibration response
of the tissue and the level of muscle activity, which can make it difficult
to analyse (Cardinale and Wakeling, 2005).
There are similarities between single repeated impact inputs and continuous
vibrations suggesting that the tissues minimise vibrations despite the
input force mode. However, the validation of the muscle tuning hypothesis
is dependent on developing further studies to determine the effect of
vibration amplitude on tissue response.
Neuromuscular
The increase in muscle force and power following acute indirect vibrations
are purported to be similar to resistance training (Bosco et al., 1998;
1999a;
1999b;
Cardinale and Bosco, 2003;
Delecluse et al., 2003).
According to Cardinale and Bosco, 2003,
resistance training and vibration place load on the neuromuscular system.
During resistance training, extra load is added to increase the influence
of gravity, in the form of barbells, dumbbells, rubber bands or manual
resistance. Resistance in terms of vibration is altered by adjusting vibration
frequency and/or amplitude, which increases the acceleration and force
placed on the body. Increasing the acceleration has the ability to modify
the neuromuscular aspects through neurogenic and myogenic factors. The
initial changes (1-3 weeks) due to resistance and power training are often
attributed to neural adaptations (Aagaard et al., 2002;
Gabriel et al., 2006;
Sale, 1988;
Staron et al., 1994).
However, protein synthesis, a precursor for hypertrophy can occur after
one resistance training session (Chesley et al., 1992),
changes in muscle size (hypertrophy) occur four to six weeks after training
commences (Kraemer et al., 2002).
Therefore, a closer examination of how acute indirect vibration may influence
neural responses of motor unit firing, motor unit synchronisation, inter-muscular
co-ordination is required.
Motor
unit firing frequency
Motor unit firing frequency refers to the number of impulses per second
that the muscle fibre of a motor unit receives from the motoneuron. The
force output of every motor unit can be varied by the firing frequency
from 10 to 60 impulses per second during sustained contractions (Sale,
2003).
However, in high speed movements firing rates of 60-120 impulses per second
are common during force production (Desmedt and Godaux, 1977).
Force production increases as a result of increased motor unit recruitment
and/or firing frequency. Therefore, when motor unit recruitment patterns
and firing frequency rates are optimized, a maximal contraction force
may occur. However, not all muscles exhibit the same characteristics;
firing frequency and recruitment may differ from muscle to muscle.
Rapid changes in motor unit firing frequency have been reported in both
young and older adults, after completing six weeks of resistance training
(Kamen and Knight, 2004).
The authors found that vastus lateralis motor unit firing frequency increased
by 15% and 49% in young and older adults, respectively during maximal
isometric knee extension. Likewise, Patten et al., 2001
reported that the firing frequency of the abductor digiti minimi was significantly
increased 48 hours after completing maximal isometric contractions. These
results indicate that early increases in force output due to resistance
training are partly caused by increased firing frequency. When high frequency
vibrations (150 Hz) were applied over the tendons of ankle dorsiflexor
muscles, Bongiovanni and Hagbarth, 1990
reported that the firing frequency in non-fatigued muscle did not change;
but the vibration caused an increase in force, EMG and firing frequency
during fatiguing isometric maximal voluntary contractions (Table
3). Similarly, Griffin et al., 2001
reported that the firing frequency increased when direct vibration was
applied to the distal tendon of the triceps brachii following a two minute
sustained 20% maximal voluntary contraction (MVC). The authors suggest
that during the isometric contraction muscle spindle activity declined
to support the motoneuron pool, and consequently firing frequency decreased.
However, muscle spindles are responsive to vibration, especially the Ia
afferents (Burke et al., 1976;
De Gail et al., 1966;
Roll et al., 1989),
which may prevent a decline in muscle spindle activity to support the
motoneuron pool (Griffin et al., 2001).
In summary, application of direct brief vibration (10-20 s) to fatigued
dorsiflexor muscles increased motor unit firing rate, enhanced EMG and
augmented maximal force (Bongiovanni and Hagbarth, 1990).
Likewise, motor unit firing frequency and isometric force increased in
fatigued arm muscles when short duration direct vibrations were applied
every 2s for 10s (Griffin et al., 2001)
suggesting that motor output facilitation occurs during brief vibratory
periods. However, current research has focused on direct vibration in
fatigued and non-fatigued muscle, the effects of acute indirect vibration
on the rate of motor unit firing frequency of non-fatigued muscle during
range vibration frequencies (25-45 Hz) and amplitudes (2-10 mm) are relatively
untested. Therefore, carefully well-designed studies with the appropriate
electrophysiological techniques are required to determine if motor unit
firing frequency plays a role in enhancing neuromuscular measures.
Motor
unit synchronisation
Motor unit synchronisation relies on the number of motor units firing
at any one time. Synchronisation occurs from branched inputs of pre-synaptic
neurons that produce a common synaptic input to increase the chance of
motoneurons discharging simultaneously (Fling et al., 2009).
Increased motor unit synchronisation is one explanation used to account
for the increase in force and power production following resistance training
(Gabriel et al., 2006,
Sale, 1988,
Semmler, 2002).
Milner-Brown et al., 1975
investigated the discharge rates of the first dorsal interosseous muscle
and found that synchronisation was greater in weightlifters than control
participants. However, synchronisation was estimated using an indirect
method of averaging surface EMG signal with respect to motor unit discharge,
which has since been challenged (Yue et al., 1995).
By using direct motor unit measurements, Semmler and Nordstrom, 1998
reported that resistance trained weightlifters produced a higher level
of synchronisation compared to highly skilled musicians, indicating that
synchronisation may be an adaptation of resistance training to enhance
force production. Yao et al., 2000
found that during motor unit synchronisation, EMG increased by 65-135%
with corresponding force fluctuations. Martin and Park, 1997
reported that when direct vibration was applied to finger and wrist muscles,
harmonic synchronisation decreased. However, sub-harmonic synchronisation
increased when vibration frequency increased from 40 to 200 Hz, where
high vibration frequency (>150 Hz) produced less motor unit synchronisation
(Table 4).
Following acute indirect vibration, an enhancement in
EMG, force, and power production provides evidence of improved motor unit
recruitment (Bosco et al., 1998;
1999a;
2000;
Cardinale and Bosco, 2003;
Delecluse et al., 2003).
However, according to Yue et al., 1995,
surface EMG is a poor indicator of motor unit synchronisation and caution
is required when interpreting results.
In summary, it has been well documented that direct vibration activates
the primary afferent endings of the motor spindles which activate the
? motoneurons to recruit previous inactive muscle fibres into contraction
(Bishop, 1974).
Future indirect vibration studies should focus on whether a greater number
of potential motor units are synchronised due to the transmission of vibration
from proximal to distal muscle groups. Further, it is there is a suggestion
that an optimal vibration frequency exists to increase motor unit synchronisation
and any vibration frequencies above this level may cause motor unit synchronisation
to decrease (Jackson and Turner, 2003;
Martin and Park, 1997).
It remains unclear to whether motor unit synchronisation occurs during
acute indirect vibration, as no studies have specifically assessed single
motor unit discharge.
Inter-muscular
co- ordination
Inter-muscular co-ordination is the interaction between muscle groups
during muscular activity. Contraction of the agonists may be associated
with simultaneous contraction of their antagonists (Sale, 1988).
Tyler and Hutton (1986)
reported antagonist co-contraction reduced agonist force production, indicated
by a decrease in muscle activity (EMG). When performing new and complex
tasks the co- contraction of antagonists through reciprocal inhibition
may impair agonist contraction (Sale, 1988).
However, through continual practice and training the level of co-contraction
may be reduced, which could allow for a greater activation of the agonists.
Carolan and Cafarelli, 1992
reported that after eight weeks of knee extensor resistance training,
force increased in the knee extensors with a reduction in antagonist (bicep
femoris) co-contraction, which was shown by a decrease in bicep femoris
EMG activity (Table 5).
It has been stated that acute indirect vibration causes neural changes
synonymous to that of resistance and power training (Bosco et al., 2000).
If true, an improvement in agonist activation and increased inhibition
of antagonist muscles should also exist. Evidence from acute direct vibration
studies suggest that an excitatory response of the muscle spindle occurs,
which activates the Ia afferents. These afferents in turn, excite the
? motoneurons of the homonymous muscle, which may uncouple the co-contraction
of agonist-antagonists (Eklund and Hagbarth, 1966).
Rothmuller and Cafarelli, 1995
have reported that antagonist co-contraction increased during fatigue
and vibration elicited a greater co-contraction than the control condition,
but the co-contraction did not change during
the fatigue of either condition.
Recently, Abercromby et al., 2007a
suggested that acute indirect vibration causes neuromuscular responses
that could be partly modulated by the co-contraction of the musculature
acting at the knee joint. A study conducted by Mischi and Cardinale, 2009,
investigated muscle activation and co-contraction of the biceps and triceps
brachii muscles during isometric exercise with and without vibration.
Using an electromagnetic actuator, mechanical sinusoidal vibrations generated
a frequency of 28 Hz, which was applied to the biceps and triceps brachii
for 15 s. They observed that co-contraction occurred at low levels of
muscle force (20% and 40% maximum sustained force) during elbow extension,
suggesting that co-contraction may serve to stabilise the joint, but it
does not modulate agonist force production (Table 5). The authors concluded that vibration could be a
viable option in the early stages of rehabilitation where low levels of
muscle force are required due to limited joint mobility.
In summary, Mischi and Cardinale, 2009
findings provide some new insights to the response of superimposing vibration
on agonist, antagonist and co-contraction of muscles. However, caution
is advised, as the study utilized a single vibration frequency (28 Hz)
with brief exposures to vibration and the recorded absence of amplitude
also limits the findings of the study. Therefore, further studies investigating
lower and upper limb vibration would assist in explaining the role that
intramuscular co-ordination has in vibration.
Central
motor command
Direct application of high frequency vibration on muscle and tendon activates
Ia afferent of the muscle spindles and to a lesser extent, the secondary
afferents and Ib afferents of the golgi tendon organ (Roll et al., 1989).
However, there is evidence to support the notion that cortical areas of
the brain receive and process proprioceptive information when direct high
frequency vibration is applied, which generates evoked cortical potentials
(Munte et al., 1996).
It appears that muscle afferent input to the cerebral cortex plays a role
in motor control (Wiesendanger and Miles, 1982);
30% of central motor drive is attributed to muscle afferent excitability
(Macefield et al., 1993).
Moreover, it has been reported that Ia afferent input has the ability
to excite the corticospinal pathway (Carson et al., 2004)
and activate the cortical motor areas (Lewis et al., 2001).
To examine the potential changes of the motor cortex, the transcranial
magnetic stimulation (TMS) method has been used to study the excitability
of the corticospinal system, as well as the intracortical inhibitory and
facilitatory processes. In brief, TMS delivers pulses to the motor cortex
through a double cone coil placed over the scalp. It has been reported
that motor-evoked potentials of TMS were enhanced when direct vibration
(f = 80 Hz) was applied to extensor carpi radialis muscle (Kossev et al.,
2001).
Researchers have also suggested anecdotally that acute indirect vibration
may influence the motor cortex to increase muscular performance (Cardinale
and Bosco, 2003).
Mileva et al., 2009
investigated the effects of acute indirect vibration (f = 30 Hz, A = 1.5mm,
VV) on corticospinal excitability and intracortical processes by studying
motor-evoked potentials in the tibialis anterior and soleus muscles in
response to TMS of the contralateral motor cortical leg area (Table 6). They found that acute indirect vibration
increased the tibialis anterior corticospinal excitability pathway, but
the intracortical facilitatory processing for the tibialis anterior was
reduced. However, no significant changes were evident in the corticospinal
excitability or intracortical facilitatory of the soleus. These findings
suggest that acute indirect vibration may stimulate the corticospinal
pathway; however, no performance measures were included with TMS.
In summary, there have been promising findings on vibration training and
central motor command. Studies both confirm and refute the concept that
direct and indirect vibration elicits a motor cortex response. Therefore,
extensive research is required in the area of indirect vibration training
to confirm that vibration causes an excitatory response in the motor cortex.
Future indirect vibration studies should focus on expanding vibration
platform research utilizing a range of vibration frequencies, amplitudes,
durations and postural positions. Further vibration work is also required
on the quadriceps and hamstrings to determine if acute indirect vibration
truly increases the excitability of the corticospinal pathway.
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