Ionic and molecular basis of nerve fiber action potential, comparison of AP and PSP
Action potencial(excitement) arises from a change in resting equilibrium(change of polarization) on the membrane. This change is caused by spreading voltage that changes activity of voltage-gated ion channels.
The principle of action potential formation[edit | edit source]
The excitation occurs in place, where outbalance the voltage-gated channels. These channels follows the rule-all or nothing. It means that excitement will only occur when there is sufficient stimulus, which is called threshold stimulus( the most often about 5-15 mV higher than value of resting membrane potential). At this value the voltage-gated Na+ channels are opened. Sodium ions then can go in intracelular space according to concentration gradient and electric gradient. Interior side of membrane becomes more positive than outer side of membrane. This condition is called depolarization. In case, when outer side of membran is more electronegative than interior side of membrane we talk about transpolarization. Along with sodium channels are opened slowly the kalium channels, whose opening is delayed. Opening of this channels reaches a maximum at closure of sodium channels. Due to the flow of K+ ions along the direction of concentration gradient, the polarity begins to come back to original values and we are talking about repolarization. In case of deepening the original membrane potencial we use the term hyperpolarization. Accomplisment of original values of resting membrane potencial is conditioned by activity of Na+/K+ ATPase, which overpumps ionts againts concentration gradient.
Refractory phase[edit | edit source]
Condition, when is not possible to stimulate the nervous cell so that action potential occurse. Refractory phase can be relative which means that we are able to evoke an action potential with suprathreshold stimulus. Refractory phase can be also absolute which means that we are able to evoke an actional potential with none stimulus.
Conduction of excitement[edit | edit source]
Actional potential is spreading without decrement, which means that it is not losing intensity. It is caused by emergence of local stream. Local streams arise above place, where the ion distribution occurred. As a result of the creation of these streams is depolarization of membrane in the adjacent fiber section. Local streams speed up the conduction of excitement. In case of extension of fiber( e.g isolation by myelin sheath) occurs to effect local streams in next section, which is isolated, so it is faster than unmyelinated. It is called saltatory conduction of actional potential.
Actional potential of different tissues[edit | edit source]
Actional potential wich is descibed above applies to all capable cells of generating an excitation. This general pattern is describing general model at nervous cell. At different cells it differs in e.g value of treshold, duration, ion channels etc.
Effects of Calemia[edit | edit source]
Calemia is value of K+ ECT. Higher surface of K+ ECT(hyperkalemia) slightly depolarizes the membrane, because concentration gradient for K+ is limited so i tis not possible full repolarization after depolarization. The cell is not excitable. It could be also call as calium depresion. Irritation during hypercalemia is increased at first but after are blocked the voltage-gated channels and excitment is reduced(higher than 5,3 mmol/l)→shortening of actional potential. The voltage reaches to thresholds more easily.
Hypocalemia(less than 3,7 mmol/l) occures hyperpolarization→extension of actional potential. Neuron come up to threshold harder.
Comparison of AP and PSP[edit | edit source]
Basics differents between AP an PSP are circumstances. AP arises according to rule everything or nothing. PSP is directly proportional to the quant of poured out neurotransmiters. They are different in voltage and duration.
| Parameter | AP | PSP |
| meaning | Transmission of excitement whithout quality changeover long distances | Processing, connection of individual PSP and decision whether AP should be created |
| behaviour | Everything or nothing | Continuous, it can have various values |
| amplitude | About 100mV | About 1-10 mV |
| duration | About 10-40 ms | About 1-5 ms |
| Ion channels | Voltage-gated | chemical |
| Permeability for | Na+, K+-fast channels | K+-leak channels |
| location | axons | Postsynaptic membrane |
| spreading | Without decrement | With dekrement, the signal strength decreases |
Literature[edit | edit source]
- KITTNAR, Otomar. Lékařská fyziologie. 1. edition. Grada, 2011. 790 pp. ISBN 978-80-247-3068-4.
- MYSLIVEČEK, Jaromír. Základy neurověd. 2. edition. TRITON, 2009. 390 pp. ISBN 978-80-7387-088-1.
- TROJAN, Stanislav. Lékařská fyziologie. 4. edition. Grada, 2003. 772 pp. ISBN 80-247-0512-5.
