The
plasma (cell)
membrane of neurons, like all other cells, has an unequal distribution
of ions and electrical charges between the two sides of the membrane. The
outside of the membrane has a positive charge, inside has a negative charge.
This charge difference is a resting potential and is measured in millivolts.
Passage of ions across the cell membrane passes the electrical charge along
the cell. The voltage potential is -65mV (millivolts) of a cell at rest (resting
potential). Resting potential results from differences between sodium
and potassium positively charged ions and negatively charged ions in the
cytoplasm. Sodium ions are more concentrated outside the membrane, while
potassium ions are more concentrated inside the membrane. This imbalance is
maintained by the active transport of ions to reset the membrane known as
the sodium potassium pump. The
sodium-potassium pump maintains this unequal concentration by
actively transporting ions against their concentration gradients.

Neurons
send messages through an electrochemical process. This means that chemicals
result in an electrical signal. Chemicals in the body are
"electrically-charged" - when they have an electrical charge, they are
called "ions". The important ions in the nervous system are sodium and
potassium (both have 1 positive charge, +), calcium (has 2 positive charges,
++) and chloride (has a negative charge, -). There are also some negatively
charged protein molecules. It is also important to remember that nerve cells
are surrounded by a membrane that allows some ions to pass through while it
blocks the passage of other ions. This type of membrane is called
semi-permeable.
Changed polarity of the membrane, the
action potential, results in propagation of the nerve impulse along the
membrane. An action potential is a temporary reversal of the electrical
potential along the membrane for a few milliseconds. Sodium gates and
potassium gates open in the membrane to allow their respective ions to
cross. Sodium and potassium ions reverse positions by passing through
membrane protein channel gates that can be opened or closed to control ion
passage. Sodium crosses first. At the height of the membrane potential
reversal, potassium channels open to allow potassium ions to pass to the
outside of the membrane. Potassium crosses second, resulting in changed
ionic distributions, which must be reset by the continuously running
sodium-potassium pump. Eventually enough potassium ions pass to the outside
to restore the membrane charges to those of the original resting
potential. The cell begins then to pump the ions back to their original sides
of the membrane.
The action potential begins at one spot on the membrane, but spreads to
adjacent areas of the membrane, propagating the message along the length of
the cell membrane. After passage of the action potential, there is a brief
period, the refractory period, during which the membrane cannot be
stimulated. This prevents the message from being transmitted backward along
the membrane.
- At rest the outside of the membrane is more
positive than the inside.
- Sodium moves inside the cell causing an action
potential, the influx of positive sodium ions makes the inside of the
membrane more positive than the outside.
- Potassium ions flow out of the cell, restoring the
resting potential net charges.
- Sodium ions are pumped out of the cell and
potassium ions are pumped into the cell, restoring the original
distribution of ions.
The
junction between a nerve cell and another cell is called a
synapse. Messages travel within the neuron as an electrical action
potential. The space between two cells is known as the
synaptic cleft. To cross the synaptic cleft requires the actions of
neurotransmitters. Neurotransmitters are stored in small
synaptic vessicles clustered at the tip of the axon.

Arrival of the action potential causes some of the
vesicles to move to the end of the axon and discharge their contents into
the synaptic cleft. Released neurotransmitters diffuse across the cleft, and
bind to receptors on the other cell's membrane, causing ion channels on that
cell to open. Some neurotransmitters cause an action potential, others are
inhibitory.
Neurotransmitters tend to be small molecules, some
are even hormones. The time for neurotransmitter action is between 0,5 and 1
millisecond (that's one-thousandth of a second). Neurotransmitters are
either destroyed by specific enzymes in the synaptic cleft, diffuse out of
the cleft, or are reabsorbed by the cell. More than 30 organic molecules are
thought to act as neurotransmitters. The neurotransmitters cross the cleft,
binding to receptor molecules on the next cell, prompting transmission of
the message along that cell's membrane.
Acetylcholine is an example of a neurotransmitter, as is
norepinephrine, although each acts in different responses. Once in the
cleft, neurotransmitters are active for only a short time.
Enzymes in the cleft inactivate the neurotransmitters. Inactivated
neurotransmitters are taken back into the axon and recycled.
Diseases that affect the function of signal transmission can have serious
consequences. Parkinson's disease
has a deficiency of the neurotransmitter dopamine. Progressive death of
brain cells increases this deficit, causing tremors, rigidity and unstable
posture. L-dopa is a chemical related to dopamine that eases some of the
symptoms (by acting as a substitute neurotransmitter) but cannot reverse the
progression of the disease.
The bacterium Clostridium tetani produces a toxin that prevents the release
of GABA. GABA is important in control of skeletal muscles. Without this
control chemical, regulation of muscle contraction is lost; it can be fatal
when it effects the muscles used in breathing.
Clostridium botulinum produces a toxin found in improperly canned foods.
This toxin causes the progressive relaxation of muscles, and can be fatal. A
wide range of drugs also operate in the synapses: cocaine, LSD, caffeine,
and insecticides.

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