214
|
6 Applications and Methods in Biosignal Processing
determines whether an action potential is triggered in the cell. If this is the case, the
action potential spreads from the dendrites along the axon and triggers the release of
neurotransmitters at the end of the axon (synapse) which are deposited there in ves-
icles. These neurotransmitters in turn react with the receptors of the next neuron and
control the cell membrane there (cf. chapter 3).
Stimulus propagation through a nerve cell occurs as the action potential advances
along the axon. If depolarization is triggered at one point, Na+ ions flow from the
environment outside the cell into the interior. This results in a local decrease in the
concentration of Na+ ions in the external cellular ambience, which is compensated by
diffusive ion currents from the environment. This, however, decreases the Na+ concen-
tration there, which briefly increases the transmembrane voltage above the threshold
voltage¹. By this the action potential is also triggered in the vicinity. However, this is
only possible in the area behind the the depolarization site. The area in front of the de-
polarization site is still in the refractory state at this point, because the action potential
has passed through there before. In the refractory phase the action potential cannot be
triggered again. Therefore, the action potential, and thus the electrical stimulus, con-
tinues in only one direction of the axon fiber. The speed of this process and thus the
conduction velocity is approx. 3 m/s. For neurons that excite skeletal muscles, how-
ever, this transmission speed would be too low, because due to the great length of the
connection between nerve center and muscle fiber of up to one meter, the reaction e.g.
to a dangerous situation would be too slow. In fact, in peripheral neurons that estab-
lish the connection to motor muscle units, a significantly higher conduction velocity
of up to 120 m/s is achieved. The peripheral neurons have a different structure com-
pared to brain neurons. The axon fiber is surrounded by Schwann cells, which prevent
the triggering of the action potential. The sheath is called myelin sheath. At intervals of
0.2 to 1.5 mm, the myelin sheath is interrupted by constrictions, the Ranvier constric-
tions. Only there can the action potential be triggered. Since, during depolarization
at a constriction, the cell-external compensatory currents extend to the next constric-
tion, the action potential jumps from one constriction to the next. This mechanism
significantly increases conduction velocity vs. brain neurons (cf. subsection 3.1.3).
The compensating currents along the axon fiber generate electric fields that
propagate in the neurons of the cerebral cortex to the surface of the skull surface.
The result is a potential difference between arbitrary locations on the scalp. The
overall potential distribution on the scalp results from the superposition of the po-
tentials of all active neurons and glial cells, with nearby cell regions making the
strongest contribution. A spatial potential distribution is created on the scalp that
varies in time with the activity of the cell regions involved. The voltage amplitude
measurable on the scalp is up to 100 μV. Recording by means of electrodes is called
1 The direction of the transmembrane voltage is from the cell interior to the -exterior. Thus, a lack of
positive ions in the cell exterior increases the transmembrane voltage.