Tactile-dependant corticomotor facilitation is influenced by discrimination performance in seniors
© Master and Tremblay; licensee BioMed Central Ltd. 2010
Received: 4 January 2010
Accepted: 5 March 2010
Published: 5 March 2010
Active contraction leads to facilitation of motor responses evoked by transcranial magnetic stimulation (TMS). In small hand muscles, motor facilitation is known to be also influenced by the nature of the task. Recently, we showed that corticomotor facilitation was selectively enhanced when young participants actively discriminated tactile symbols with the tip of their index or little finger. This tactile-dependant motor facilitation reflected, for the large part, attentional influences associated with performing tactile discrimination, since execution of a concomitant distraction task abolished facilitation. In the present report, we extend these observations to examine the influence of age on the ability to produce extra motor facilitation when the hand is used for sensory exploration.
Corticomotor excitability was tested in 16 healthy seniors (58-83 years) while they actively moved their right index finger over a surface under two task conditions. In the tactile discrimination (TD) condition, participants attended to the spatial location of two tactile symbols on the explored surface, while in the non discrimination (ND) condition, participants simply moved their finger over a blank surface. Changes in amplitude, in latency and in the silent period (SP) duration were measured from recordings of motor evoked potentials (MEP) in the right first dorsal interosseous muscle in response to TMS of the left motor cortex.
Healthy seniors exhibited widely varying levels of performance with the TD task, older age being associated with lower accuracy and vice-versa. Large inter-individual variations were also observed in terms of tactile-specific corticomotor facilitation. Regrouping seniors into higher (n = 6) and lower performance groups (n = 10) revealed a significant task by performance interaction. This latter interaction reflected differences between higher and lower performance groups; tactile-related facilitation being observed mainly in the former group. Latency measurements and SP durations were not affected by task conditions.
The present findings provide further insights into the factors influencing task-dependant changes in corticomotor excitability in the context of aging. Our results, in particular, highlight the importance of adjusting task demands and controlling for attention when attempting to elicit task-specific motor facilitation in older persons engaged in fine manual actions. Such information could be critical in the future for planning interventions to re-educate or maintain hand function in the presence of neurological impairments.
In everyday life, we often rely on our sense of touch when it comes to appreciating object and surface properties, as when searching for keys inside the pocket. Such a task typically engages the finger in fine exploratory movements to detect specific tactile features, which can then lead to fast object recognition . While trivial in appearance, tactile discrimination (TD) tasks have been shown to engage a large cortical network involving primary and secondary motor and sensory areas, as well as, associative regions of the frontal and parietal lobes [2–5]. Recently , we investigated task-dependant changes in corticomotor excitability with transcranial magnetic stimulation (TMS) when young adults actively moved their index or little finger over a surface. Our results showed a large selective enhancement in corticomotor excitability when participants discriminated between surface features, as opposed to simply moving the finger over a blank surface. Further to this, we showed that such tactile-dependant extra facilitation was largely abolished when participants performed a concurrent distraction task. This suggested that task influences, linked with the increased attentional demands associated with tactile sensing, were primarily responsible for the observed extra facilitation.
In the present report, we attempted to extend those observations on tactile-dependant increase in corticomotor excitability to healthy seniors to investigate whether age-related alterations in sensorimotor capacities and cognitive functions would affect the ability to produce motor facilitation in the context of active finger movements. Previous reports in this regard have produced mixed results. For instance, D'Esposito et al.  examined task-dependant changes in motor cortical activation using functional magnetic resonance imaging (fMRI) and reported an age-related decrease both in the number of subjects showing detectable activation and in the volume of activation during performance of a button press task. This suggested a decline with age in the ability to activate the motor cortex during simple finger movement execution. The fact that older subjects also displayed higher levels of background noise might have affected the results, however. The issue of age-related differences in motor activation was further examined by McConnell et al.  who combined TMS with fMRI to measure motor cortical activity induced either by volitional movement or by direct stimulation using TMS. Their results revealed no differences in haemodynamic responses with age for both voluntary-induced and TMS-induced finger movements, indicating a preserved capacity to drive the corticomotor system in normal aging. Similar results were reported by Sale and Semmler  who examined right-left differences in corticomotor excitability in young and old adults. Their results showed that older adults had preserved MEP responses in the right hand, although MEP amplitude tended to be reduced in the left hand. No such bilateral difference was found in young adults. Interestingly, they observed that performance of a complex hand action (using gardening shears, as opposed to a simple action) produced large MEP facilitation in the right hand of old adults, whereas no such facilitation could be elicited in the left hand. The authors attributed this asymmetry in the older group to a lifetime preferential use of the dominant hand in executing fine motor tasks.
Using a different task paradigm, Leonard and Tremblay  showed recently that older adults were capable of producing corticomotor facilitation in their dominant hand in the context of overt and covert action execution, i.e. during observation, imagination and imitation of a complex hand action (scissoring action). This preserved capacity for motor facilitation in older adults was however less specific than that seen in young adults in terms of muscle selectivity; older adults showing facilitation in both the task and non-task relevant muscles. This loss in selectivity was thought to reflect compensatory mechanisms in older adults whereby performance of simple motor actions often leads to extra activation in areas that are not normally recruited in younger subjects, such as the pre-supplementary motor area, pre-dorsal premotor area, rostral cingulate, and prefrontal cortex [11–14]. For Heuninckx et al. , such a wide activation extending to associative areas of the cortex reflected the need for older adults to exert greater cognitive control over on-going actions to maintain performance at the desired level [see also ]. This penetration of cognition into motor control with age raises the issue of resource allocation when task demands are increased, given the expected decline in selective attention and working memory with aging [16, 17]. With limited resources, older participants might be particularly challenged when hand movements require fine control such as when the finger is used to explore tactile features for recognition. As stated earlier, in the present report, we attempted to address this issue using TMS to measure task-dependant corticomotor facilitation elicited in a demanding task paradigm wherein participants had to actively move their index finger at a prescribed speed over a surface with or without constraints for tactile sensing at the fingertip.
The Institutional Review Ethics Board approved the study procedure in accordance with the principles of the Declaration of Helsinki and informed consent was obtained before the experimental session. All assessments were performed in a controlled laboratory environment. Each participant received an honorarium for his or her participation.
The methods and procedures have been detailed previously in our report [see ] in young adults, where we used the same experimental paradigm as in the present experiment. Briefly, corticomotor facilitation was tested in a group of healthy seniors (8 female, 8 male; mean age: 68.0 years, range: 58-83 years, 15 right-handers) using a Magstim 200 stimulator (Magstim Co. Dyfed, UK) connected to a figure-eight coil (70 mm loop diameter). Before testing participants were screened for contra-indications to TMS and for the presence of sensory neuropathies using a graduated Rydel-Seiffer tuning fork [18, 19]. Corticomotor excitability was determined by monitoring changes in the amplitude and latency of motor evoked potentials recorded in the first dorsal interosseous (FDI) using surface electrodes (10 mm diameter, Ag-AgCl). We intended initially, as in our previous study in young adults, to include observations on adductor digiti minimi, but this turned out to be impossible because most participants could not perform the task properly with the little finger. Electromyographic (EMG) signals were amplified and filtered (5 Hz to 5 kHz) using a polygraph amplifier (RMP-6004, Nihon-Kohden Corp.) and stored on computer (digitized @ 1 kHz, BNC-2090, National Instrument Corp.) for off-line analyses.
A paired-samples t-test was performed on background EMG levels (% MVC) recorded during the two tasks, TD and ND. As suggested by Nielsen  and Schmidt et al. , MEP amplitudes were log-transformed to get a normal distribution (Shapiro-Wilk P > 0.1). Repeated measures analyses of variance (ANOVAs) were then performed on the dependent variables of MEP log-amplitude, MEP latency, and SP duration with task condition (TD, ND) as the repeated factor and discrimination performance as the between-subjects factor. The latter factor was entered into the ANOVA as a dichotomized variable (high vs. low) after examining the distribution of individual performance values with respect to age (see Results). The level of significance was set at P < 0.05. All tests were performed using SPSS software version 17.0 for Windows™ (Chicago, IL, USA). Figures were prepared using GraphPad Prism version 5.02 for Windows (GraphPad Software, San Diego California USA, http://www.graphpad.com). All values are reported as mean ± 1 SD.
In the present report, we extend our previous observations on task-specific motor facilitation in young adults  to healthy seniors. In this respect, our results reveal important differences between our former observations in young adults and the way seniors responded to increasing task demands in the context of this experiment. First, seniors tended to show much larger variability in terms of their ability to cope with increasing task demands, i.e. from simple auditory paced rhythmic finger movements to rhythmic finger movement combined with tactile sensing. Second, age greatly influenced task performance, which in turn, affected levels of MEP facilitation.
The issue of greater variability in behavioural and neurophysiological responses with advancing age is a common theme in aging studies. In the present study, participants in the older age group tended to exhibit lower performance with accompanying low or absent MEP facilitation under the TD condition, when compared to younger seniors. In our previous work on tactile sensation and aging, we observed a similar pattern of results with more variable performance and greater decline in tactile acuity being observed for individuals over 75 years [22, 23]. Such variability was also observed in a TMS study by Peinemann et al.  looking at levels of intra-cortical inhibition (ICI) and intra-cortical facilitation (ICF) elicited in older adults in response to paired pulse stimulation. They noticed, much like in the present study, a differential pattern of modulation in a subgroup of older participants aged >60 years, where the expected increase in ICF was actually replaced by a decline. An increase in MEP amplitude variability with age was also reported by Pitcher et al , when examining variations in MEP size with increasing TMS intensities (i.e., stimulus-response curve). Interestingly, they found that the age-related difference in stimulus-response profiles, reflecting the strength of corticospinal projections, was evident only in older female subjects but not in male subjects; again illustrating the inherent variability associated with aging. Thus, it is not uncommon in aging studies to find subsets of participants exhibiting different patterns of responses, as we found in the present study.
Before addressing the issue as to why certain participants showed task-specific facilitation, while others did not, it is important to ascertain that motor over-activity was not a factor in limiting the ability to produce corticomotor facilitation. This question is critical since seniors tend to show compensatory activity and higher activation levels in both motor and non motor areas of the cortex even when executing simple finger movements [11–14, 26, 27]. This possibility is unlikely, however, given that no participants actually showed signs of MEP saturation under the TD task condition. In fact, MEP's were actually reduced in amplitude in all but two of the participants who failed to show extra facilitation with tactile sensing. The fact that the finger movements in the two tasks were associated with relatively low levels of background EMG activity likely contributed to limit the level of motor activation, associated with the finger movements. In fact, our observations of task-related MEP facilitation with tactile sensing in seniors fit with the recent findings of Van Impe et al.  who measured cortical activation during a hand-foot coordination task in older adults. Their results showed that, although age was associated with activation of a larger brain network, this activation reflected increased attentional deployment to enhance somatosensory processing and integration rather than increased motor cortical activity. Thus, other factors, besides motor over-activity, likely contributed to the variations observed in MEP amplitude under the two task conditions in our group of seniors.
We have already mentioned that performance in the tactile task largely influenced MEP facilitation in our group of seniors. In fact, the present results show that the degree of task-specific facilitation was linked with the actual perceptual performance of seniors in discriminating the tactile symbols; a higher performance being associated with large MEP facilitation, while a lower performance was not. In many respects, the present results are reminiscent of our previous findings in young adults, where high performance (mean, 84% correct) was associated with substantial tactile-related MEP facilitation (mean relative increase, 45%), while the same facilitation was abolished when attention was diverted away from the tactile inputs by performance of a concurrent cognitive task. Together, these observations strongly suggest that the observed task-related corticomotor facilitation seen during tactile sensing is central in origin, reflecting enhanced excitability mediated by top-down attentional mechanisms acting on the motor cortex to facilitate task performance. This idea is further supported by recent findings showing a participation of anterior motor cortical area 4 in complex somatosensory processing , highlighting the importance of finely tuned central motor control during the execution of tactile exploratory tasks.
In light of these observations, the inverse association between age and task performance can be explained, in the case of older seniors, by a difficulty in attending to the tactile stimuli as the finger moved over the surface. The converse can be said for younger seniors, where effective coping with task demands likely allowed them to selectively attend to the tactile symbols as the index finger moved, resulting in higher discrimination performance and MEP facilitation during tactile sensing. However, it is still possible that a greater degree of peripheral decline in tactile sensibility in older seniors might have affected their ability to sense the tactile spatial features when touching the stimuli. Two arguments mitigate this possibility, however. First, all participants were screened for the presence of sensory deficits at the outset of the study using validated vibratory thresholds as an index of tactile sensation. Second, the spatial dimensions of the tactile symbols (3.2 mm radius, 0.18 mm relief) were in the range of easily detectable spatial stimuli, even for individuals advanced in age . In fact, the great majority of participants experienced no difficulties in discriminating between the two tactile symbols in the familiarization period before formal testing. It seems more likely, as we suggested above, that ineffective coping mechanisms in the context of multiple task demands was responsible for the poor performance in older seniors. Such an explanation would be consistent with observations suggesting that deficits in top-down modulation mechanisms are critical in leading to cognitive decline in normal aging; older adults being particularly impaired in their ability to selectively suppress task-irrelevant information . As recently shown by Gazzeley et al , such an inability seems to result from excessive attention towards distracting stimuli early in the sensory encoding process, resulting in lower processing speed and decreased performance (i.e., longer response time and lower accuracy). In the context of our TD task, the sound of metronome ticks in the background could have drawn too much attention on the part of certain older seniors to the detriment of the tactile information arising from contact with the symbols; leading to low discrimination performance and inefficient task-related corticomotor facilitation.
The deficit in top-down modulation with age is thought to correspond to changes in the frontal and parietal lobes and the resulting decreased connectivity of the anterior-to-posterior network, in particular the frontal associative areas and the motor cortex [32, 33]. In support of this argument, Rowe  showed recently that cortical connectivity between the contralateral premotor and prefrontal cortices was impaired during an externally paced randomized button-pressing task in seniors. Indeed, the anterior-to-posterior network would have been important for the TD task, given that it is involved in haptic sensing [34–36] and attention to action . A recent review of the literature on somatosensory-motor interactions by Bressler  supports the idea that attentional mechanisms are part of the large-scale, synchronized cortical network controlling motor activity, and can mediate the critical relationship between the somatosensory and motor cortices.
The present results are based on a relatively small sample of healthy seniors, which might not be representative of the elderly population in general. In addition, the degree of difficulty associated with the TD task proved to be very challenging for some seniors. It would be important for future studies investigating task-related motor facilitation in older adults to control for the degree of task difficulty, providing some adjustments when necessary, to account for the increased variability generally observed in this population in terms of perceptual performance.
In conclusion, the present findings provide further insights into the factors influencing tactile-dependant changes in corticomotor excitability, in the context of aging. Our results, in particular, highlight the importance of adjusting task demands and modulating attentional influences at the individual level to elicit proper task-specific facilitation when older persons are engaged in fine motor actions. Such information could be critical in the future for planning interventions to re-educate hand function in the presence of neurological impairments.
The authors wish to thank all participants for their time and patience during testing. Special thanks to Francisca Avila-Ramirez and Catherine Lebel for their help with data collection. Part of this work served as a partial fulfillment for a research practicum in experimental psychology by Sabah Master. François Tremblay is supported by NSERC (Canada).
- Jones LA: The assessment of hand function: a critical review of techniques. J Hand Surg Am. 1989, 14a: 221-228. 10.1016/0363-5023(89)90010-5.View ArticleGoogle Scholar
- Deibert E, Kraut M, Kremen S, Hart J: Neural pathways in tactile object recognition. Neurology. 1999, 52: 1413-1417.View ArticlePubMedGoogle Scholar
- Bodegård A, Geyer S, Grefkes C, Zilles K, Roland PE: Hierarchical Processing of Tactile Shape in the Human Brain. Neuron. 2001, 31: 317-328. 10.1016/S0896-6273(01)00362-2.View ArticlePubMedGoogle Scholar
- Stoeckel MC, Weder B, Binkofski F, Buccino G, Shah NJ, Seitz RJ: A fronto-parietal circuit for tactile object discrimination: an event-related fMRI study. Neuroimage. 2003, 19: 1103-1114. 10.1016/S1053-8119(03)00182-4.View ArticlePubMedGoogle Scholar
- Miquee A, Xerri C, Rainville C, Anton JL, Nazarian B, Roth M, Zennou-Azogui Y: Neuronal substrates of haptic shape encoding and matching: a functional magnetic resonance imaging study. Neuroscience. 2008, 152: 29-39. 10.1016/j.neuroscience.2007.12.021.View ArticlePubMedGoogle Scholar
- Master S, Tremblay F: Task-specific increase in corticomotor excitability during tactile discrimination. Exp Brain Res. 2009, 194: 163-172. 10.1007/s00221-008-1679-z.View ArticlePubMedGoogle Scholar
- D'Esposito M, Zarahn E, Aguirre GK, Rypma B: The effect of normal aging on the coupling of neural activity to the bold hemodynamic response. Neuroimage. 1999, 10: 6-14. 10.1006/nimg.1999.0444.View ArticlePubMedGoogle Scholar
- McConnell KA, Bohning DE, Nahas Z, Shastri A, Teneback C, Lorberbaum JP, Lomarev MP, Vincent DJ, George MS: BOLD fMRI response to direct stimulation (transcranial magnetic stimulation) of the motor cortex shows no decline with age. J Neural Transm. 2003, 110: 495-507. 10.1007/s00702-002-0804-6.View ArticlePubMedGoogle Scholar
- Sale MV, Semmler JG: Age-related differences in corticospinal control during functional isometric contractions in left and right hands. J Appl Physiol. 2005, 99: 1483-1493. 10.1152/japplphysiol.00371.2005.View ArticlePubMedGoogle Scholar
- Leonard G, Tremblay F: Corticomotor facilitation associated with observation, imagery and imitation of hand actions: a comparative study in young and old adults. Exp Brain Res. 2007, 177: 167-175. 10.1007/s00221-006-0657-6.View ArticlePubMedGoogle Scholar
- Heuninckx S, Wenderoth N, Debaere F, Peeters R, Swinnen SP: Neural basis of aging: the penetration of cognition into action control. J Neurosci. 2005, 25: 6787-6796. 10.1523/JNEUROSCI.1263-05.2005.View ArticlePubMedGoogle Scholar
- Hutchinson S, Kobayashi M, Horkan CM, Pascual-Leone A, Alexander MP, Schlaug G: Age-related differences in movement representation. Neuroimage. 2002, 17: 1720-1728. 10.1006/nimg.2002.1309.View ArticlePubMedGoogle Scholar
- Ward NS: Compensatory mechanisms in the aging motor system. Ageing Res Rev. 2006, 5: 239-254. 10.1016/j.arr.2006.04.003.View ArticlePubMedGoogle Scholar
- Mattay VS, Fera F, Tessitore A, Hariri AR, Das S, Callicott JH, Weinberger DR: Neurophysiological correlates of age-related changes in human motor function. Neurology. 2002, 58: 630-635.View ArticlePubMedGoogle Scholar
- De Serres SJ, Fang NZ: The accuracy of perception of a pinch grip force in older adults. Can J Physiol Pharmacol. 2004, 82: 693-701. 10.1139/y04-085.View ArticlePubMedGoogle Scholar
- Scialfa CT: The role of sensory factors in cognitive aging research. Can J Exp Psychol. 2002, 56: 153-163.View ArticlePubMedGoogle Scholar
- Iachini T, Poderico C, Ruggiero G, Iavarone A: Age differences in mental scanning of locomotor maps. Disabil Rehabil. 2005, 27: 741-752. 10.1080/09638280400014782.View ArticlePubMedGoogle Scholar
- Kastenbauer T, Sauseng S, Brath H, Abrahamian H, Irsigler K: The value of the Rydel-Seiffer tuning fork as a predictor of diabetic polyneuropathy compared with a neurothesiometer. Diabet Med. 2004, 21: 563-567. 10.1111/j.1464-5491.2004.01205.x.View ArticlePubMedGoogle Scholar
- Pestronk A, Florence J, Levine T, Al-Lozi MT, Lopate G, Miller T, Ramneantu I, Waheed W, Stambuk M: Sensory exam with a quantitative tuning fork: rapid, sensitive and predictive of SNAP amplitude. Neurology. 2004, 62: 461-464.View ArticlePubMedGoogle Scholar
- Nielsen JF: Logarithmic distribution of amplitudes of compound muscle action potentials evoked by transcranial magnetic stimulation. J Clin Neurophysiol. 1996, 13: 423-434. 10.1097/00004691-199609000-00005.View ArticlePubMedGoogle Scholar
- Schmidt S, Cichy RM, Kraft A, Brocke J, Irlbacher K, Brandt SA: An initial transient-state and reliable measures of corticospinal excitability in TMS studies. Clin Neurophysiol. 2009, 120: 987-993. 10.1016/j.clinph.2009.02.164.View ArticlePubMedGoogle Scholar
- Tremblay F, Backman A, Cuenco A, Vant K, Wassef MA: Assessment of spatial acuity at the fingertip with grating (JVP) domes: validity for use in an elderly population. Somatosens Mot Res. 2000, 17: 61-66. 10.1080/08990220070300.View ArticleGoogle Scholar
- Tremblay F, Wong K, Sanderson R, Cote L: Tactile spatial acuity in elderly persons: assessment with grating domes and relationship with manual dexterity. Somatosens Mot Res. 2003, 20: 127-132. 10.1080/0899022031000105154.View ArticlePubMedGoogle Scholar
- Peinemann A, Lehner C, Conrad B, Siebner HR: Age-related decrease in paired-pulse intracortical inhibition in the human primary motor cortex. Neurosci Lett. 2001, 313: 33-36. 10.1016/S0304-3940(01)02239-X.View ArticlePubMedGoogle Scholar
- Pitcher JB, Ogston KM, Miles TS: Age and sex differences in human motor cortex input-output characteristics. J Physiol. 2003, 546: 605-613. 10.1113/jphysiol.2002.029454.PubMed CentralView ArticlePubMedGoogle Scholar
- Talelli P, Ewas A, Waddingham W, Rothwell JC, Ward NS: Neural correlates of age-related changes in cortical neurophysiology. Neuroimage. 2008, 40: 1772-1781. 10.1016/j.neuroimage.2008.01.039.PubMed CentralView ArticlePubMedGoogle Scholar
- Rowe JB, Siebner H, Filipovic SR, Cordivari C, Gerschlager W, Rothwell J, Frackowiak R: Aging is associated with contrasting changes in local and distant cortical connectivity in the human motor system. Neuroimage. 2006, 32: 747-760. 10.1016/j.neuroimage.2006.03.061.View ArticlePubMedGoogle Scholar
- Van Impe A, Coxon JP, Goble DJ, Wenderoth N, Swinnen SP: Ipsilateral coordination at preferred rate: Effects of age, body side and task complexity. Neuroimage. 2009, 47: 1854-1862. 10.1016/j.neuroimage.2009.06.027.View ArticlePubMedGoogle Scholar
- Terumitsu M, Ikeda K, Kwee IL, Nakada T: Participation of primary motor cortex area 4a in complex sensory processing: 3.0-T fMRI study. Neuroreport. 2009, 20: 679-683. 10.1097/WNR.0b013e32832a1820.View ArticlePubMedGoogle Scholar
- Gazzaley A, D'Esposito M: Top-down modulation and normal aging. Ann N Y Acad Sci. 2007, 1097: 67-83. 10.1196/annals.1379.010.View ArticlePubMedGoogle Scholar
- Gazzaley A, Clapp W, Kelley J, McEvoy K, Knight RT, D'Esposito M: Age-related top-down suppression deficit in the early stages of cortical visual memory processing. Proc Natl Acad Sci USA. 2008, 105: 13122-13126. 10.1073/pnas.0806074105.PubMed CentralView ArticlePubMedGoogle Scholar
- Langley LK, Fuentes LJ, Vivas AB, Bagne AG: Differential age effects on attention-based inhibition: Inhibitory tagging and inhibition of return. Psychol Aging. 2005, 20: 356-360. 10.1037/0882-79188.8.131.526.View ArticlePubMedGoogle Scholar
- Poliakoff E, Ashworth S, Lowe C, Spence C: Vision and touch in ageing: Crossmodal selective attention and visuotactile spatial interactions. Neuropsychologia. 2006, 44: 507-517. 10.1016/j.neuropsychologia.2005.07.004.View ArticlePubMedGoogle Scholar
- Stoesz MR, Zhang M, Weisser VD, Prather SC, Mao H, Sathian K: Neural networks active during tactile form perception: common and differential activity during macrospatial and microspatial tasks. Int J Psychophysiol. 2003, 50: 41-49. 10.1016/S0167-8760(03)00123-5.View ArticlePubMedGoogle Scholar
- Harada T, Saito DN, Kashikura K, Sato T, Yonekura Y, Honda M, Sadato N: Asymmetrical neural substrates of tactile discrimination in humans: a functional magnetic resonance imaging study. J Neurosci. 2004, 24: 7524-7530. 10.1523/JNEUROSCI.1395-04.2004.View ArticlePubMedGoogle Scholar
- Dum RP, Strick PL: Motor areas in the frontal lobe of the primate. Physiol Behav. 2002, 77: 677-682. 10.1016/S0031-9384(02)00929-0.View ArticlePubMedGoogle Scholar
- Rowe J, Friston K, Frackowiak R, Passingham R: Attention to action: specific modulation of corticocortical interactions in humans. Neuroimage. 2002, 17: 988-998. 10.1016/S1053-8119(02)91156-0.View ArticlePubMedGoogle Scholar
- Bressler SL: The sensory component of tonic motor control. Clin Neurophysiol. 2009, 120: 1035-1036. 10.1016/j.clinph.2009.03.017.View ArticlePubMedGoogle Scholar
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