In neurology, the Bereitschaftspotential or BP (German for "readiness potential"), also called the pre-motor potential or readiness potential (RP), is a measure of activity in the motor cortex and supplementary motor area of the brain leading up to voluntary muscle movement. The BP is a manifestation of cortical contribution to the pre-motor planning of volitional movement. It was first recorded and reported in 1964 by Hans Helmut Kornhuber and Lüder Deecke at the University of Freiburg in Germany. In 1965 the full publication appeared after many control experiments. [1]
In the spring of 1964 Hans Helmut Kornhuber (then docent and chief physician at the department of neurology, head Professor Richard Jung, university hospital Freiburg im Breisgau) and Lüder Deecke (his doctoral student) went for lunch to the 'Gasthaus zum Schwanen' at the foot of the Schlossberg hill in Freiburg. Sitting alone in the beautiful garden they discussed their frustration with the passive brain research prevailing worldwide and their desire to investigate self-initiated action of the brain and the will. Consequently, they decided to look for cerebral potentials in man related to volitional acts and to take voluntary movement as their research paradigm. [2]
The possibility to do research on electrical brain potentials preceding voluntary movements came with the advent of the 'computer of average transients' (CAT computer), invented by Manfred Clynes, the first still simple instrument available at that time in the Freiburg laboratory. In the electroencephalogram (EEG) little is to be seen preceding actions, except of an inconstant diminution of the α- (or μ-) rhythm. The young researchers stored the electroencephalogram and electromyogram of self-initiated movements (fast finger flexions) on tape and analyzed the cerebral potentials preceding movements time-reversed with the start of the movement as the trigger, literally turning the tape over for analysis since they had no reversal playback or programmable computer. A potential preceding human voluntary movement was discovered and published in the same year. [3] After detailed investigation and control experiments such as passive finger movements the Citation Classic with the term Bereitschaftspotential was published. [2]
The BP is ten to hundred times smaller than the α-rhythm of the EEG; only by averaging, relating the electrical potentials to the onset of the movement it becomes apparent. Figure shows the typical slow shifts of the cortical DC potential, called Bereitschaftspotential, preceding volitional, rapid flexions of the right index finger. The vertical line indicates the instant of triggering t = 0 (first activity in the EMG of the agonist muscle). Recording positions are left precentral (L prec, C3), right precentral (R prec, C4), mid-parietal (Pz); these are unipolar recordings with linked ears as reference. The difference between the BP in C3 and in C4 is displayed in the lowest graph (L/R prec). Superimposed are the results of eight experiments as obtained in the same subject (B.L.) on different days. see Deecke, L.; Grözinger, B.; Kornhuber H.H. (1976)
Note that the BP has two components, the early one (BP1) lasting from about −1.2 to −0.5; the late component (BP2) from −0.5 to shortly before 0 sec. [4] The pre-motion positivity is even smaller, and the motor-potential which starts about fifty to sixty milliseconds before the onset of movement and has its maximum over the contralateral precentral hand area is still smaller. Thus, it takes great care to see these potentials: exact triggering by the real onset of movement is important, which is especially difficult preceding speech movements. Furthermore, artifacts due to head-, eye-, lid-, mouth-movements and respiration have to be eliminated before averaging because such artifacts may be of a magnitude which makes it difficult to render them negligible even after hundreds of sweeps. [5] In the case of eye movements eye muscle potentials have to be distinguished from cerebral potentials. In some cases animal experiments were necessary to clarify the origin of potentials such as the R-wave. Therefore, it took many years until some of the other laboratories were able to confirm the details of Kornhuber & Deecke's results. In addition to the finger or eye movements as mentioned above, the BP has been recorded accompanying willful movements of the wrist, arm, shoulder, hip, knee, foot and toes. It was also recorded prior to speaking, writing and also swallowing. [6]
The magnetoencephalographic (MEG) equivalent of the Bereitschaftspotential (BP), 'Bereitschafts(magnetic)field' (BF), or readiness field (RF) was first recorded in Hal Weinberg's laboratory at Simon Fraser University Burnaby B.C. Canada in 1982. [7] It was confirmed that the early component, BP 1 or BF1, respectively was generated by the supplementary motor area (SMA), including the pre-SMA, while the late component, BP2 or BF2, was generated by the primary motor area, MI[ citation needed ].
A very similar event-related potential (ERP) component had earlier been discovered by the British neurophysiologist William Grey Walter in 1962 and published in 1964. It is the contingent negative variation (CNV). [8] [9] The CNV also composes two waves; the initial wave (i.e., O wave) and the terminal wave (i.e., E wave). The terminal CNV has similar characteristics as the BP and many researchers have claimed that the BP and the terminal CNV are the same component. [10] At least there is a consensus that both indicate a preparation of the brain for a following behavior. [11]
The Bereitschaftspotential was received with great interest by the scientific community, as reflected by Sir John Eccles's comment: "There is a delightful parallel between these impressively simple experiments and the experiments of Galileo Galilei who investigated the laws of motion of the universe with metal balls on an inclined plane". [12] The interest was even greater in psychology and philosophy because volition is traditionally associated with human freedom (cf. Kornhuber 1984). [13] The spirit of the time, however, was hostile to freedom in those years; it was believed that freedom is an illusion. The tradition of behaviourism and Freudism was deterministic. While will and volition were frequently leading concepts in psychological research papers before and after the first world war and even during the second war, after the end of the second world war this declined, and by the mid-sixties these key words completely disappeared and were abolished in the thesaurus of the American Psychological Association. [14] The BP is an electrical sign of participation of the supplementary motor area (SMA) prior to volitional movement, which starts activity prior to the primary motor area. [15] The BP has precipitated a worldwide discussion about free will (cf. the closing chapter in the book "The Bereitschaftspotential"). [16]
As said above, the activity of the SMA generates the early component of the Bereitschaftspotential (BP1 or BP early). [17] The SMA has the starting function of the movement or action. The role of the SMA was further substantiated by Cunnington et al. 2003, [18] showing that SMA proper and pre-SMA are active prior to volitional movement or action, as well as the cingulate motor area (CMA). This is now called ‘anterior mid-cingulate cortex (aMCC)’. Recently it has been shown by integrating simultaneously acquired EEG and fMRI that SMA and aMCC have strong reciprocal connections that act to sustain each other’s activity, and that this interaction is mediated during movement preparation according to the Bereitschaftspotential amplitude. [19]
EEGs and EMGs are used in combination with Bayesian inference to construct Bayesian networks which attempt to predict general patterns of Motor Intent Neuron Action Potentials firing. Researchers attempting to develop non-intrusive brain–computer interfaces are interested in this, as are system analysis, operations research, and epistemology (e.g. the Smith predictor has been suggested in the discussion).[ further explanation needed ]
In a series of neuroscience of free will experiments in the 1980s, Benjamin Libet studied the relationship between conscious experience of volition and the BP e.g. [20] and found that the BP started about 0.35 sec earlier than the subject's reported conscious awareness that "now he or she feels the desire to make a movement." Libet concludes that we have no free will in the initiation of our movements; though, since subjects were able to prevent intended movement at the last moment, we do have the ability to veto these actions ("free won't").
These studies have provoked widespread debate. [21] [22]
In 2016, a group around John-Dylan Haynes in Berlin (Germany) determined the time window after the BP in which an intended motion could possibly be cancelled upon command. [23] The authors tested whether human volunteers could win a "duel" against a BCI (brain–computer interface) designed to predict their movements in real-time from observations of their EEG activity (the BP). They aimed to determine the exact time at which cancellation (veto) of movements was not possible anymore (the point of no return). The computer was trained to predict by means of the BP when a proband would move. The point of no return was at 200 ms before the movement. However, even after that, when a pedal was already set in motion, the subjects were able to reschedule their action by not completing the already started behavior. The authors pointed out in their report that cancellation of self-initiated movements had already been reported by Libet in 1985. Thus, the new achievement was a more precise determination of the point of no return.
An interesting use of the Bereitschaftspotential is in brain–computer interface (BCI) applications; this signal feature can be identified from scalp recording (even from single-trial measurements) and interpreted for various uses, for example control of computer displays or control of peripheral motor units in spinal cord injuries. [24] The most important BCI application is the 'mental' steering of artificial limbs in amputees.
Magnetoencephalography (MEG) is a functional neuroimaging technique for mapping brain activity by recording magnetic fields produced by electrical currents occurring naturally in the brain, using very sensitive magnetometers. Arrays of SQUIDs are currently the most common magnetometer, while the SERF magnetometer is being investigated for future machines. Applications of MEG include basic research into perceptual and cognitive brain processes, localizing regions affected by pathology before surgical removal, determining the function of various parts of the brain, and neurofeedback. This can be applied in a clinical setting to find locations of abnormalities as well as in an experimental setting to simply measure brain activity.
An event-related potential (ERP) is the measured brain response that is the direct result of a specific sensory, cognitive, or motor event. More formally, it is any stereotyped electrophysiological response to a stimulus. The study of the brain in this way provides a noninvasive means of evaluating brain functioning.
The motor cortex is the region of the cerebral cortex involved in the planning, control, and execution of voluntary movements. The motor cortex is an area of the frontal lobe located in the posterior precentral gyrus immediately anterior to the central sulcus.
A K-complex is a waveform that may be seen on an electroencephalogram (EEG). It occurs during stage 2 NREM sleep. It is the "largest event in healthy human EEG". They are more frequent in the first sleep cycles.
Benjamin Libet was an American neuroscientist who was a pioneer in the field of human consciousness. Libet was a researcher in the physiology department of the University of California, San Francisco. In 2003, he was the first recipient of the Virtual Nobel Prize in Psychology from the University of Klagenfurt, "for his pioneering achievements in the experimental investigation of consciousness, initiation of action, and free will".
Beta waves, or beta rhythm, are a type of neural oscillations (brainwave) in the brain with a frequency range of between 12.5 and 30 Hz. Beta waves can be split into three sections: Low Beta Waves ; Beta Waves ; and High Beta Waves. Beta states are the states associated with normal waking consciousness.
Neural oscillations, or brainwaves, are rhythmic or repetitive patterns of neural activity in the central nervous system. Neural tissue can generate oscillatory activity in many ways, driven either by mechanisms within individual neurons or by interactions between neurons. In individual neurons, oscillations can appear either as oscillations in membrane potential or as rhythmic patterns of action potentials, which then produce oscillatory activation of post-synaptic neurons. At the level of neural ensembles, synchronized activity of large numbers of neurons can give rise to macroscopic oscillations, which can be observed in an electroencephalogram. Oscillatory activity in groups of neurons generally arises from feedback connections between the neurons that result in the synchronization of their firing patterns. The interaction between neurons can give rise to oscillations at a different frequency than the firing frequency of individual neurons. A well-known example of macroscopic neural oscillations is alpha activity.
Theta waves generate the theta rhythm, a neural oscillation in the brain that underlies various aspects of cognition and behavior, including learning, memory, and spatial navigation in many animals. It can be recorded using various electrophysiological methods, such as electroencephalogram (EEG), recorded either from inside the brain or from electrodes attached to the scalp.
The supplementary motor area (SMA) is a part of the motor cortex of primates that contributes to the control of movement. It is located on the midline surface of the hemisphere just in front of the primary motor cortex leg representation. In monkeys the SMA contains a rough map of the body. In humans the body map is not apparent. Neurons in the SMA project directly to the spinal cord and may play a role in the direct control of movement. Possible functions attributed to the SMA include the postural stabilization of the body, the coordination of both sides of the body such as during bimanual action, the control of movements that are internally generated rather than triggered by sensory events, and the control of sequences of movements. All of these proposed functions remain hypotheses. The precise role or roles of the SMA is not yet known.
Premovement neuronal activity in neurophysiological literature refers to neuronal modulations that alter the rate at which neurons fire before a subject produces movement. Through experimentation with multiple animals, predominantly monkeys, it has been shown that several regions of the brain are particularly active and involved in initiation and preparation of movement. Two specific membrane potentials, the bereitschaftspotential, or the BP, and contingent negative variation, or the CNV, play a pivotal role in premovement neuronal activity. Both have been shown to be directly involved in planning and initiating movement. Multiple factors are involved with premovement neuronal activity including motor preparation, inhibition of motor response, programming of the target of movement, closed-looped and open-looped tasks, instructed delay periods, short-lead and long-lead changes, and mirror motor neurons.
The contingent negative variation (CNV) is a negative slow surface potential, as measured by electroencephalography (EEG), that occurs during the period between a warning stimulus or signal and an imperative ("go") stimulus. The CNV was one of the first event-related potential (ERP) components to be described. The CNV component was first described by W. Grey Walter and colleagues in an article published in Nature in 1964. The importance of this finding was that it was one of the first studies which showed that consistent patterns of the amplitude of electric responses could be obtained from the large background noise which occurs in EEG recordings and that this activity could be related to a cognitive process such as expectancy.
In neuroscience, the lateralized readiness potential (LRP) is an event-related brain potential, or increase in electrical activity at the surface of the brain, that is thought to reflect the preparation of motor activity on a certain side of the body; in other words, it is a spike in the electrical activity of the brain that happens when a person gets ready to move one arm, leg, or foot. It is a special form of bereitschaftspotential. LRPs are recorded using electroencephalography (EEG) and have numerous applications in cognitive neuroscience.
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Neuroscience of free will, a part of neurophilosophy, is the study of topics related to free will using neuroscience and the analysis of how findings from such studies may impact the free will debate.
Error-related negativity (ERN), sometimes referred to as the Ne, is a component of an event-related potential (ERP). ERPs are electrical activity in the brain as measured through electroencephalography (EEG) and time-locked to an external event or a response. A robust ERN component is observed after errors are committed during various choice tasks, even when the participant is not explicitly aware of making the error; however, in the case of unconscious errors the ERN is reduced. An ERN is also observed when non-human primates commit errors.
Lüder Deecke in Lohe-Rickelshof, Germany is a German Austrian neurologist, neuroscientist, teacher and physician whose scientific discoveries have influenced brain research and the treatment and rehabilitation of neurological disorders.
Self-agency, also known as the phenomenal will, is the sense that actions are self-generated. Scientist Benjamin Libet was the first to study it, concluding that brain activity predicts the action before one even has conscious awareness of his or her intention to act upon that action. Daniel Wegner later defined the three criteria of self-agency: priority, exclusivity, and consistency.
Hans Helmut Kornhuber was a German neurologist and neurophysiologist.
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