Depression of human corticospinal excitability induced by magnetic theta-burst stimulation: evidence of rapid polarity-reversing metaplasticity.

Metaplasticity refers to the activity-dependent modification of the ability of synapses to undergo subsequent potentiation or depression, and is thought to maintain homeostasis of cortical excitability. Continuous magnetic theta-burst stimulation (cTBS; 50 Hz-bursts of 3 subthreshold magnetic stimuli repeated at 5 Hz) is a novel repetitive magnetic stimulation protocol used to model changes of synaptic efficacy in human motor cortex. Here we examined the influence of prior activity on the effects induced by cTBS. Without prior voluntary motor activation, application of cTBS for a duration of 20 s (cTBS300) facilitated subsequently evoked motor potentials (MEP) recorded from APB muscle. In contrast, MEP-size was depressed, when cTBS300 was preceded by voluntary activity of sufficient duration. Remarkably, even without prior voluntary activation, depression of MEP-size was induced when cTBS was extended over 40 s. These findings provide in vivo evidence for extremely rapid metaplasticity reversing potentiation of corticospinal excitability to depression. Polarity-reversing metaplasticity adds considerable complexity to the brain's response toward new experiences. Conditional dependence of cTBS-induced depression of corticospinal excitability on prior neuronal activation suggests that the TBS-model of synaptic plasticity may be closer to synaptic mechanisms than previously thought.

[1]  John C Rothwell,et al.  Effect of physiological activity on an NMDA-dependent form of cortical plasticity in human. , 2008, Cerebral cortex.

[2]  D. Linden,et al.  Ubiquitous Plasticity and Memory Storage , 2007, Neuron.

[3]  G. Turrigiano Homeostatic signaling: the positive side of negative feedback , 2007, Current Opinion in Neurobiology.

[4]  J. Rothwell,et al.  The after-effect of human theta burst stimulation is NMDA receptor dependent , 2007, Clinical Neurophysiology.

[5]  Z. Bashir,et al.  Long-term depression: multiple forms and implications for brain function , 2007, Trends in Neurosciences.

[6]  Juha Silvanto,et al.  Neural adaptation reveals state‐dependent effects of transcranial magnetic stimulation , 2007, The European journal of neuroscience.

[7]  P. Schwenkreis,et al.  Effekt von Theta Burst Stimulation über dem somatosensorischen Kortex bei gesunden Normalprobanden , 2007 .

[8]  J. C. Rothwell,et al.  Exploring Theta Burst Stimulation as an intervention to improve motor recovery in chronic stroke , 2007, Clinical Neurophysiology.

[9]  S. C. Gandevia,et al.  Theta burst stimulation does not reliably depress all regions of the human motor cortex , 2006, Clinical Neurophysiology.

[10]  Walter Senn,et al.  Repetitive TMS over the human oculomotor cortex: Comparison of 1-Hz and theta burst stimulation , 2006, Neuroscience Letters.

[11]  S. Gandevia,et al.  Decreased input to the motor cortex increases motor cortical excitability , 2006, Clinical Neurophysiology.

[12]  G. Davis Homeostatic control of neural activity: from phenomenology to molecular design. , 2006, Annual review of neuroscience.

[13]  T. Takano,et al.  Astrocytic Ca2+ signaling evoked by sensory stimulation in vivo , 2006, Nature Neuroscience.

[14]  Antonino Vallesi,et al.  Role of the prefrontal cortex in the foreperiod effect: TMS evidence for dual mechanisms in temporal preparation. , 2006, Cerebral cortex.

[15]  M. Poo,et al.  Visual stimuli–induced LTD of GABAergic synapses mediated by presynaptic NMDA receptors , 2006, Nature Neuroscience.

[16]  J. Rothwell,et al.  The role of dorsal premotor area in reaction task: comparing the “virtual lesion” effect of paired pulse or theta burst transcranial magnetic stimulation , 2005, Experimental Brain Research.

[17]  Y. Z. Huang,et al.  Theta‐burst repetitive transcranial magnetic stimulation suppresses specific excitatory circuits in the human motor cortex , 2005, The Journal of physiology.

[18]  Egidio D'Angelo,et al.  Intracellular Calcium Regulation by Burst Discharge Determines Bidirectional Long-Term Synaptic Plasticity at the Cerebellum Input Stage , 2005, The Journal of Neuroscience.

[19]  J. Rothwell,et al.  Theta Burst Stimulation of the Human Motor Cortex , 2005, Neuron.

[20]  M. Bear,et al.  LTP and LTD An Embarrassment of Riches , 2004, Neuron.

[21]  John C Rothwell,et al.  The effect of short-duration bursts of high-frequency, low-intensity transcranial magnetic stimulation on the human motor cortex , 2004, Clinical Neurophysiology.

[22]  J. Rothwell,et al.  Preconditioning of Low-Frequency Repetitive Transcranial Magnetic Stimulation with Transcranial Direct Current Stimulation: Evidence for Homeostatic Plasticity in the Human Motor Cortex , 2004, The Journal of Neuroscience.

[23]  D. Ruge,et al.  Learning Modifies Subsequent Induction of Long-Term Potentiation-Like and Long-Term Depression-Like Plasticity in Human Motor Cortex , 2004, The Journal of Neuroscience.

[24]  E. Wassermann,et al.  Priming Stimulation Enhances the Depressant Effect of Low-Frequency Repetitive Transcranial Magnetic Stimulation , 2003, The Journal of Neuroscience.

[25]  Y. Yoshimura,et al.  Two Forms of Synaptic Plasticity with Distinct Dependence on Age, Experience, and NMDA Receptor Subtype in Rat Visual Cortex , 2003, The Journal of Neuroscience.

[26]  L. Cohen,et al.  A temporally asymmetric Hebbian rule governing plasticity in the human motor cortex. , 2003, Journal of neurophysiology.

[27]  Wickliffe C Abraham,et al.  NMDA receptor‐mediated metaplasticity during the induction of long‐term depression by low‐frequency stimulation , 2002, The European journal of neuroscience.

[28]  Z. Bashir,et al.  Long-term depression: a cascade of induction and expression mechanisms , 2001, Progress in Neurobiology.

[29]  M. Sakurai,et al.  Differential induction of LTP and LTD is not determined solely by instantaneous calcium concentration: an essential involvement of a temporal factor , 2001, The European journal of neuroscience.

[30]  D Curran-Everett,et al.  Multiple comparisons: philosophies and illustrations. , 2000, American journal of physiology. Regulatory, integrative and comparative physiology.

[31]  S. Nelson,et al.  Hebb and homeostasis in neuronal plasticity , 2000, Current Opinion in Neurobiology.

[32]  A. Artola,et al.  Synaptic Activity Modulates the Induction of Bidirectional Synaptic Changes in Adult Mouse Hippocampus , 2000, The Journal of Neuroscience.

[33]  Á. Pascual-Leone,et al.  Transcranial magnetic stimulation: studying the brain-behaviour relationship by induction of 'virtual lesions'. , 1999, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[34]  J. Rothwell,et al.  Intracortical inhibition and facilitation in different representations of the human motor cortex. , 1998, Journal of neurophysiology.

[35]  W. Abraham,et al.  Metaplasticity: A new vista across the field of synaptic plasticity , 1997, Progress in Neurobiology.

[36]  M. Hallett,et al.  Depression of motor cortex excitability by low‐frequency transcranial magnetic stimulation , 1997, Neurology.

[37]  W. Singer,et al.  Calcium-induced long-term depression in the visual cortex of the rat in vitro. , 1996, Journal of neurophysiology.

[38]  M. Bear,et al.  Metaplasticity: the plasticity of synaptic plasticity , 1996, Trends in Neurosciences.

[39]  Hiroki Yasuda,et al.  Long-term depression in rat visual cortex is associated with a lower rise of postsynaptic calcium than long-term potentiation , 1996, Neuroscience Research.

[40]  B. Alger,et al.  GABAergic and developmental influences on homosynaptic LTD and depotentiation in rat hippocampus , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[41]  P. Stanton,et al.  Priming of homosynaptic long-term depression in hippocampus by previous synaptic activity. , 1993, Neuroreport.

[42]  W. Abraham,et al.  Priming of associative long-term depression in the dentate gyrus by θ frequency synaptic activity , 1992, Neuron.

[43]  Y. Yoshimura,et al.  Input-specific induction of long-term depression in Ca(2+)-chelated visual cortex neurons. , 1991, Neuroreport.

[44]  W. Singer,et al.  Different voltage-dependent thresholds for inducing long-term depression and long-term potentiation in slices of rat visual cortex , 1990, Nature.

[45]  Y. Yoshimura,et al.  Long-term depression but not potentiation is induced in Ca(2+)-chelated visual cortex neurons. , 1990, Neuroreport.

[46]  J. Lisman,et al.  A mechanism for the Hebb and the anti-Hebb processes underlying learning and memory. , 1989, Proceedings of the National Academy of Sciences of the United States of America.