Neural mechanisms involved in the functional linking of motor cortical points

We sought to understand the basic neural processes involved in the functional linking of motor cortical points. We asked which of the two basic neural mechanisms, excitation or inhibition, is required to functionally link motor cortical points. In the ketamineanaesthetized cat, a microstimulation electrode was positioned at a point (control point) that was identified by the following three characteristics of the EMG responses: the muscle(s) activated at threshold, any additional muscles recruited by supra-threshold stimulation, and their relative latency. A second distinct point (test point) producing activation of a muscle at a different joint was then identified. At this test cortical point the GABAA receptor antagonist bicuculline was ejected iontophoretically, while stimulating the control point near threshold. A combined response was elicited consisting of the response normally elicited at the control point plus that elicited at the test point. Thus, an artificial muscle synergy was produced following disinhibition of the test point. This was never the case when glutamate was ejected at the test point, even when supra-threshold stimuli were used at the control point. Therefore, simply increasing the excitability of a cortical point was not sufficient to release the muscle(s) represented at that point into a muscle synergy. Kynurenate, a broadly acting excitatory amino acid receptor antagonist, ejected at the bicuculline point reversed the effect of bicuculline. This shows that the release phenomenon was mediated synaptically and was not due to spread of the stimulating current. We suggest that release from inhibition may be one of the neural mechanisms involved in functionally linking motor cortical points. This functional linking may be part of the ensemble of motor cortical mechanisms involved in recruitment of muscle synergies.

[1]  C. Capaday,et al.  Intracortical connections between motor cortical zones controlling antagonistic muscles in the cat: a combined anatomical and physiological study , 1998, Experimental Brain Research.

[2]  J. Donoghue,et al.  Shared neural substrates controlling hand movements in human motor cortex. , 1995, Science.

[3]  P. Ashby,et al.  Inhibition in the human motor cortex is reduced just before a voluntary contraction , 1999, Neurology.

[4]  P. Lalley,et al.  Microiontophoresis and Pressure Ejection , 1999 .

[5]  T. Freund,et al.  GABA-containing neurons in the septum control inhibitory interneurons in the hippocampus , 1988, Nature.

[6]  P. Somogyi,et al.  Differentially Interconnected Networks of GABAergic Interneurons in the Visual Cortex of the Cat , 1998, The Journal of Neuroscience.

[7]  P. Cheney,et al.  Consistent Features in the Forelimb Representation of Primary Motor Cortex in Rhesus Macaques , 2001, The Journal of Neuroscience.

[8]  J. Donoghue,et al.  Static and dynamic organization of motor cortex. , 1997, Advances in neurology.

[9]  KM Jacobs,et al.  Reshaping the cortical motor map by unmasking latent intracortical connections , 1991, Science.

[10]  I. Kaufman The Cerebral Cortex of Man: A Clinical Study of Localization of Function , 1951 .

[11]  A. Arnold,et al.  Spinal branching of corticospinal axons in the cat , 1976, Experimental Brain Research.

[12]  鯨井 隆 Corticocortical inhibition in human motor cortex , 1994 .

[13]  C. Sherrington,et al.  OBSERVATIONS ON THE EXCITABLE CORTEX OF THE CHIMPANZEE, ORANG‐UTAN, AND GORILLA , 1917 .

[14]  Charles Capaday,et al.  Integrated motor cortical control of task-related muscles during pointing in humans. , 2002, Journal of neurophysiology.

[15]  T. Drew,et al.  Electromyographic responses evoked in muscles of the forelimb by intracortical stimulation in the cat. , 1985, The Journal of physiology.

[16]  Liisa A. Tremere,et al.  Expansion of receptive fields in raccoon somatosensory cortex in vivo by GABAA receptor antagonism: implications for cortical reorganization , 2001, Experimental Brain Research.

[17]  C. Capaday,et al.  Quantitative evidence for multiple widespread representations of individual muscles in the cat motor cortex , 2001, Neuroscience Letters.

[18]  J. Donoghue,et al.  Organization of the forelimb area in squirrel monkey motor cortex: representation of digit, wrist, and elbow muscles , 2004, Experimental Brain Research.

[19]  L. Acsády,et al.  Different populations of vasoactive intestinal polypeptide-immunoreactive interneurons are specialized to control pyramidal cells or interneurons in the hippocampus , 1996, Neuroscience.

[20]  A Keller,et al.  Intrinsic connections between representation zones in the cat motor cortex. , 1993, Neuroreport.

[21]  B. Alstermark,et al.  Motoneuronal projection pattern of single C3-C4 propriospinal neurones. , 1996, Canadian journal of physiology and pharmacology.

[22]  M. Schieber,et al.  How somatotopic is the motor cortex hand area? , 1993, Science.

[23]  V. Amassian,et al.  Some positive effects of transcranial magnetic stimulation. , 1995, Advances in neurology.

[24]  P. Cheney,et al.  Corticomotoneuronal postspike effects in shoulder, elbow, wrist, digit, and intrinsic hand muscles during a reach and prehension task. , 1998, Journal of neurophysiology.

[25]  I. Mody,et al.  Modulation of decay kinetics and frequency of GABAA receptor-mediated spontaneous inhibitory postsynaptic currents in hippocampal neurons , 1992, Neuroscience.

[26]  E. G. Jones,et al.  Relationship of intrinsic connections to forelimb movement representations in monkey motor cortex: a correlative anatomic and physiological study. , 1991, Journal of neurophysiology.

[27]  J Tanji,et al.  Input organization of distal and proximal forelimb areas in the monkey primary motor cortex: A retrograde double labeling study , 1993, The Journal of comparative neurology.