2.6.2 Noninvasive Techniques to Evaluate the Neuro-myofascial Biology of Touch and Massage
Magnetic resonance spectroscopy (mrs) and fmri are powerful, noninvasive, non-radioactive techniques that may be used to evaluate the biology of manual therapies
46. These techniques are based on the mechanics and theory of nuclear magnetic resonance (nmr). Signals can be detected only from atomic nuclear species having the quantum mechanical property of spin. The 1H hydrogen atom is the most abundant of these. It provides the signal for routine mriscanning, which produces images using the contrast of water and fat. The mrs technique measures levels of particular chemical species within an acquired tissue volume. It is especially useful for evaluating the physiology of myofascial tissue.
Currently the nuclei of greatest interest are 1H, 13C, and 31P. Techniques that can be used to evaluate muscle physiology include
- 1H mrs of myoglobin to assess the intracellular partial pressure of oxygen (pO2),
- 31P mrs to assess metabolic capacity, and
- the combination of 31P chemical shift imaging to assess local metabolic demand (oxygen uptake:VO2).
Blood oxygenation level–dependent (BOLD) fmri can be used to image the neural correlates of touch and pain within the subcortical nuclei of the brain. This technique allows for indirect estimation of neural activity by detecting local hemodynamic changes, which are closely related to the integrated synaptic activity of nerve cells under physiologic circumstances
46–
48.
The pathways and neural centres involved in processing information from low-threshold mechanoreceptors of the skin, carried by fast-conducting myelinated afferent fibres, have been extensively investigated in nonhuman primates. Various cortical regions, including the anterior parietal cortex (primary somatosensory cortex), the lateral and posterior parietal cortices, and motor-related areas responding to mechanical stimuli have been identified
49. Humans appear to have an expanded somatosensory cortical network. Brain regions showing increased activity during vibrotactile input and tactile recognition extend beyond the parietal lobe to include portions of the frontal, cingulate, temporal, and insular cortices
50. Available evidence suggests that the central correlates of tactile stimuli vary according to their hedonic qualities. Pleasant touch induces greater activation in the medial orbitofrontal cortex than does more intense, but affectively neutral tactile stimuli
51. Additional areas activated by pleasant but not by neutral stimuli include a rostral portion of the midcingulate cortex and an area in or near the amygdala. These findings begin to identify parts of the limbic system that may underlie emotional, hormonal, and affiliative responses to skin contact.
The forebrain pain system partly overlaps structures involved in processing non-noxious input, but painful stimuli induce higher fmri signal increases than non-noxious stimuli do. A direct comparison between the cortical correlates of touch and pain using event-related fmri showed that, besides common activations in the contralateral postcentral gyrus and parietal operculum, pain is associated with stronger involvement of the contralateral midanterior insula, anterior portion of the midcingulate cortex, and dorsolateral prefrontal cortex
52,
53.
The autonomic responses to acute pain exposure usually habituate rapidly; the subjective ratings of pain remain high for more extended periods of time. Thus, systems involved in the autonomic response to painful stimulation—for example the hypothalamus and the brainstem—would be expected to attenuate the response to pain during prolonged stimulation. Areas in the brainstem are involved in the initial response to noxious stimulation, which is also characterized by an increased sympathetic response.
54 The perigenual anterior cingulate gyrus is a crucial location for integrating cognitive, emotional, and subconscious activities in the affective dimension of pain
55,
56. Pain-related modulation of fmri signals in other regions involved in reward and emotion circuitry, such as the nucleus accumbens–ventral striatum and the orbitofrontal cortex, has also been demonstrated
51. Evidence for amplified processing of mechanical stimuli in parietal, insular, and cingulate cortices has been obtained in patients with fibromyalgia, who show characteristically lowered pain thresholds. These studies have begun to shed light on the neural systems involved in central sensitization of nociceptive circuits in pathophysiologic conditions
57,
58.
The relative role of cognitive awareness versus subcortical modulation may be deciphered by using distraction and attention methodologies during an fmri examination
58–
63. Attentional effects may be exerted at various levels of the somatosensory system and involve activation of brainstem modulatory centres
62,
64.
In a study that employed covariation analysis, a functional interaction was found between the orbitofrontal cortex and perigenual anterior cingulate gyrus, the periaqueductal gray matter and posterior thalamus during pain stimulation and distraction, but not during pain stimulation
per se 61. Placebo-induced anticipation of pain relief treatment decreases brain activity in pain-related brain regions
65.
When evaluating the physical effect of massage, psychophysiologic techniques to discriminate between conscious attention and subconscious neurologic interaction are important. The brain networks underlying somatosensory perception are complex and highly distributed. A deeper understanding of perceptual-related and subconscious brain mechanisms therefore requires new approaches suited to investigate the spatial and temporal dynamics of activation in various brain regions and the functional interaction of those regions.
The development and application of refined tools for evaluating functional connectivity between neural populations will provide new insights into bottom-up and top-down mechanisms in somatosensory perception
53. Current evidence from fmri suggests that positive and negative tactile stimuli are both represented in the orbitofrontal cortex. The brain region in or near the amygdala is activated by pleasant touch. Most studies of the amygdala have tended to concentrate on its role in negative emotions, such as fear, but other imaging studies have found amygdala activation in response to affectively positive stimuli
51.
Therapeutic massage may transduce mechanical signals through skin sensation, proprioception, and non-noxious muscle perception
60. How this process translates into local electrophysiologic and chemical changes within muscle and fascia is not clear. Similarly, how therapeutic massage interacts with the central nervous system is not known, although some leads are emerging from research on touch. Preliminary physiologic investigations of muscle and the brain using nmrtechniques suggest that therapeutic massage may have distributed effects that can reduce various unpleasant symptoms.