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In neuroscience, the N100 or N1 is a large, negative-going evoked potential measured by electroencephalography (its equivalent in magnetoencephalography is the M100); it peaks in adults between 80 and 120 milliseconds after the onset of a stimulus, and distributed mostly over the fronto-central region of the scalp. It is elicited by any unpredictable stimulus in the absence of task demands. It is often referred to with the following P200 evoked potential as the "N100-P200" or "N1-P2" complex. While most research focuses on auditory stimuli, the N100 also occurs for visual (see visual N1, including an illustration), olfactory, heat, pain, balance, respiration blocking, and somatosensory stimuli.
The auditory N100 is generated by a network of neural populations in the primary and association auditory cortices in the superior temporal gyrus in Heschl's gyrus and planum temporale. It also could be generated in the frontal and motor areas. The area generating it is larger in the right hemisphere than the left.
The N100 is preattentive and involved in perception because its amplitude is strongly dependent upon such things as the rise time of the onset of a sound, its loudness, interstimulus interval with other sounds, and the comparative frequency of a sound as its amplitude increases in proportion to how much a sound differs in frequency from a preceding one. Neuromagnetic research has linked it further to perception by finding that the auditory cortex has a tonotopic organization to N100. However, it also shows a link to a person's arousal and selective attention. N100 disappears when a person controls the creation of auditory stimuli, such as their own voice.
There are three subtypes of adult auditory N100.
- N100b or vertex N100, peaking at 100 ms.
- T-complex N100a, largest at temporal electrodes at 75 ms
- T-complex N100c, follows N100a and peaks at about 130 ms. The two T-complex N100 evoked potentials are created by auditory association cortices in the superior temporal gyri.
The N100 is often known as the "auditory N100" because it is elicited by perception of auditory stimuli. Specifically, it has been found to be sensitive to things such as the predictability of an auditory stimulus, and special features of speech sounds such as voice onset time.
It occurs during both REM and NREM stages of sleep though its time is slightly delayed. During stage 2 NREM it seems responsible for the production of K-complexes. N100 is reduced following total sleep deprivation and this associates with an impaired ability to consolidate memories
The N100 depends upon unpredictability of stimulus: it is weaker when stimuli are repetitive, and stronger when they are random. When subjects are allowed to control stimuli, using a switch, the N100 may even disappear. This effect has been linked to intelligence, as the N100 attenuation for self-controlled stimuli occurs the most strongly (i.e., the N100 shrinks the most) in individuals who are also evaluated as having high intelligence. Indeed, researchers have found that in those with Down syndrome "the amplitude of the self-evoked response actually exceeded that of the machine-evoked potential". Being warned about an upcoming stimulus also reduces its N100.
The amplitude of N100 shows refractoriness upon repetition of a stimulus; in other words, it decreases at first upon repeated presentations of the stimulus, but after a short period of silence it returns to its previous level. Paradoxically, at short repetition the second N100 is enhanced both for sound and somatosensory stimuli.
Voice onset timeEdit
The difference between many consonants is their voice onset time (VOT), the interval between consonant release (onset) and the start of rhythmic vocal cord vibrations in the vowel. The voiced stop consonants /b/, /d/ and /g/ have a short VOT, and unvoiced stop consonants /p/, /t/ and /k/ long VOTs. The N100 plays a role in recognizing the difference and categorizing these sounds: speech stimuli with a short 0 to +30 ms voice onset time evoke a single N100 response but those with a longer (+30 ms and longer) evoked two N100 peaks and these are linked to the consonant release and vocal cord vibration onset.
Traditionally, 50 to 150 ms evoked potentials were considered too short to be influenced by top-down influences from the prefrontal cortex. However, it is now known that sensory input is processed by the occipital cortex by 56 ms and this is communicated to the dorsolateral frontal cortex where it arrives by 80 ms. Research also finds that the modulation effects upon N100 are affected by prefrontal cortex lesions. These higher-level areas create the attentive, repetition, and arousal modulations upon the sensory area processing reflected in N100.
Another top-down influence upon N100 has been suggested to be efference copies from a person's intended movements so that the stimulation that results from them are not processed. A person's own voice produces a reduced N100 as does the effect of a self-initiated compared to externally created perturbation upon balance.
Development in childrenEdit
The N100 is a slow-developing evoked potential. From one to four years of age, a positive evoked potential, P100, is the predominant peak. Older children start to develop a negative evoked potential at 200 ms that dominates evoked potentials until adolescence; this potential is identical to the adult N100 in scalp topography and elicitation, but with a much later onset. The magnetic M100 (measured by MEG rather than EEG is, likewise, less robust in children than in adults. An adult-like N100-P200 complex only develops after 10 years of age.
The various types of N100 mature at different times. Their maturation also varies with the side of the brain: N100a in the left hemisphere is mature before three years of age but this does not happen in the right hemisphere until seven or eight years of age.
The N100 may be used to test for abnormalities in the auditory system where verbal or behavioral responses cannot be used, such with individuals in coma; in such cases, it can help predict the probability of recovery. Another application is in assessing the optimal level of sedation in intensive critical care.
Many cognitive or other mental impairments are associated with changes in the N100 response, including the following:
- There is some evidence that the N100 is affected in those with dyslexia and specific language impairment.
- The sensory gating effect upon N100 with paired clicks is reduced in those in those with schizophrenia.
- In individuals with tinnitus, those with smaller N100 are less distressed than those with larger amplitudes.
- Migraine is associated with an increase rather than decrease in N100 amplitude with repetition of the high-intensity stimulation.
- headache sufferers also have more reactive N100 to somatosensory input than nonsufferers
Relationship to mismatch negativityEdit
The Mismatch negativity (MMN) is an evoked potential that occurs at roughly the same time as N100 in response to rare auditory events. It differs from the N100 in that:
- They are generated in different locations.
- The MMN occurs too late to be an N100.
- The MMN, unlike N100, may be elicited by stimulus omissions (i.e., not hearing a stimulus when you expect to hear one).
Though this suggests that they are separate processes, arguments have been made that this is not necessarily so and that they are created by the "relative activation of multiple cortical areas contributing to both of these 'components'".
Pauline A. Davis at Harvard University first recorded the wave peak now identified with N100. The present use of the N1 to describe this peak originates in 1966 and N100 later in the mid 1970s. The origin of the wave for a long time was unknown and only linked to the auditory cortex in 1970.
Due to magnetoencephalography, research is increasingly done upon M100, the magnetic counterpart of the electroencephalographic N100. Unlike electrical fields which face the high resistance of the skull and generate secondary or volume currents, magnetic fields which are orthogonal to them have a homogeneous permeability through the skull. This enables the location of sources generating fields that are tangent to the head surface with an accuracy of a few millimeters. New techniques, such as event-related beam-forming with magnetoencephalography, allow sufficiently accurate location of M100 sources to be clinically useful for preparing surgery upon the brain.
- ↑ PMID 7521558 (PMID 7521558)
- ↑ PMID 8753937 (PMID 8753937)
- ↑ 3.0 3.1 PMID 17533117 (PMID 17533117)
- ↑ PMID 15896482 (PMID 15896482)
- ↑ PMID 18719232 (PMID 18719232)
- ↑ 6.0 6.1 PMID 19081790 (PMID 19081790)
- ↑ 7.0 7.1 PMID 9562539 (PMID 9562539)
- ↑ PMID 11595143 (PMID 11595143)
- ↑ 9.0 9.1 9.2 PMID 3615753 (PMID 3615753)
- ↑ PMID 6939101 (PMID 6939101)
- ↑ PMID 14341718 (PMID 14341718)
- ↑ PMID 4162003 (PMID 4162003)
- ↑ PMID 5683660 (PMID 5683660)
- ↑ PMID 2446835 (PMID 2446835)
- ↑ PMID 7138998 (PMID 7138998)
- ↑ PMID 4730062 (PMID 4730062)
- ↑ 17.0 17.1 17.2 PMID 4711735 (PMID 4711735)
- ↑ 18.0 18.1 PMID 10770228 (PMID 10770228)
- ↑ PMID 8804056 (PMID 8804056&query_hl=14&itool=pubmed_docsum 8804056)
- ↑ PMID 8647042 (PMID 8647042)
- ↑ PMID 19340944 (PMID 19340944)
- ↑ PMID 6166459 (PMID 6166459)
- ↑ PMID 3615753 (PMID 3615753)
- ↑ PMID 7696592 (PMID 7696592)
- ↑ 25.0 25.1 25.2 PMID 16008770 (PMID 16008770)
- ↑ PMID 15238437 (PMID 15238437)
- ↑ PMID 10561410 (PMID 10561410)
- ↑ PMID 11797091 (PMID 11797091)
- ↑ PMID 7883451 (PMID 7883451)
- ↑ PMID 9654384 (PMID 9654384)
- ↑ PMID 14687881 (PMID 14687881)
- ↑ PMID 19422812 (PMID 19422812)
- ↑ PMID 11924892 (PMID 11924892)
- ↑ 34.0 34.1 PMID 10699397 (PMID 10699397)
- ↑ PMID 7797632 (PMID 7797632)
- ↑ PMID 1517407 (PMID 1517407)
- ↑ PMID 9390837 (PMID 9390837)
- ↑ PMID 10859413 (PMID 10859413)
- ↑ PMID 15326240 (PMID 15326240)
- ↑ PMID 15566595 (PMID 15566595)
- ↑ 41.0 41.1 PMID 17587643 (PMID 17587643)
- ↑ Shaul S. (2007). Evoked response potentials (ERPs) in the study of dyslexia: A review. pp. 51-91. In (Breznitz Z. Editor) Brain Research in Language. Springer ISBN 978-0-387-74979-2
- ↑ PMID 18836827 (PMID 18836827)
- ↑ PMID 8628490 (PMID 8628490)
- ↑ PMID 7595870 (PMID 7595870)
- ↑ PMID 6729458 (PMID 6729458)
- ↑ PMID 7774768 (PMID 7774768)
- ↑ PMID 7775056 (PMID 7775056)
- ↑ PMID 9715105 (PMID 9715105)
- ↑ PMID 16012601 (PMID 16012601)
- ↑ Davis PA. (1939). Effects of acoustic stimuli on the waking human brain. J Neurophysiol 2: 494-499 abstract
- ↑ PMID 5904525 (PMID 5904525)
- ↑ PMID 50170 (PMID 50170&query_hl=14&itool=pubmed_docsum 50170)
- ↑ PMID 4191187 (PMID 4191187&query_hl=14&itool=pubmed_docsum 4191187)
- ↑ Hämäläinen M, Hari R, Ilmoniemi RJ, Knuutila J. (1993). Magnetoencephalography-theory, instrumentation, and applications to noninvasive studies of the working human brain. Reviews of modern Physics. 65: 413-497. OCLC 197237696
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