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The basic similarities between the nervous and the endocrine systems are that they provide the body with methods to communicate with its internal and external ...
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The ability to respond to stimuli is a fundamental characteristic of living organisms. Organisms with a central nervous system (CNS) are well adapted to cope with changes in the external environment and within the body. The nervous system has three distinct functions:
One remarkable feature is the speed of the response which is virtually instantaneous.
The central nervous system is composed of specialised cells called nerve cells or neurones. These cells are bound together by connective tissue to form nerve fibres. These neurones are stimulated by changes in their environment to transmit information to and from the central nervous system. This is done by a series of electrical impulses passing along the length of a neurone.
There are three types of neurones. Their main functions are:
The specific function of each type of neurone are summarised below:
Name of neurone Stimulated by^ Transmits impulse to
Motor neurone Another neurone, relay or sensory neurone To an organ e.g. heart or a gland
Relay neurone Another relay neurone or sensory neurone Another relay neurone or motor neurone
Sensory neurone
A receptor e.g. neurones in the skin or rods and cones in the eye A relay neurone or a motor neuron
The electrical impulses can only travel in one direction in a neurone. Motor neurones are sometimes called effector neurones since they produce a physical response to stimulation.
The neurone in general contains a cell body with a nucleus that controls the activity of the cell. The cytoplasm within the cell is extended to produce dendrons. Each dendron has a number of long fine structures called dendrites. These dendrites are stimulated by electrical impulses from other neurones. The information is then passed to the cell body.
The axon is the long thin section of the neurone, which can be up to a metre long. This is formed by a single extension of the cell body cytoplasm. The axon always transmits impulses away from the cell body.
Axons end in a series of synaptic knobs. These structures stimulate other nerves or a target organ, in which case a physical response happens (e.g. an arm to move or to close the eye lid). Another important feature is Schwann cells. These cells are found along the length of the axon. Schwann cells wrap around the axon with small gaps between each cell. Neurones with Schwann cells are called myelinated neurones. These cells act as an electrical insulator and speed up transmission of
impulses. There are neurones that are unmyelinated ; they transmit impulses more slowly than myelinated neurones.
All living cells maintain an (electrical) potential difference across the cell membrane, i.e. maintain a difference in the electrical field inside and outside the cell membrane. This is called the membrane potential. Neurones have the ability to change their membrane potential.
Under normal conditions (no stimulation) the membrane of a neurone has a negative charge (-ve), compared to its surroundings. This is known as the resting potential.
The resting potential depends on the concentration of four ions within the cell:
The concentrations of potassium and carboxylate ions are high inside the cell while the concentration of sodium and chloride ions is higher outside the cell. In the resting phase, the axon membrane allows K+^ ions to pass through it more freely than the other ions.
The K+^ ion diffuse out rapidly this makes the environment inside the cell slightly negative since there are fewer positive ions.
Eventually a balance between the number of K +^ ions entering and leaving the cell is achieved. This movement of K+^ ions creates the resting potential. When a membrane is in this condition it is said to be polarised.
When a neurone is stimulated the electrical potential of its cell membrane is altered, it is depolarised. Depolarisation changes the permeability of the membrane towards sodium ions at the site of the stimulation causing a sudden influx of sodium ions into the axon. Now the overall charge inside the cell is more positive. This is known as the action potential.
An animation showing the propagation of the action potential can be viewed on: http://www3.uah.es/farmamol/Public/Animaciones/actionp.html
When enough sodium ions have entered, creating a positive charge inside the axon, the membrane permeability towards sodium ions decreases significantly in favour of the potassium ions again.
This flow of potassium ions continues until the resting potential is achieved, that is the concentration of the ions, is restored in this region of the axon and the membrane is re-polarised.
As the concentration is restored in the first section, the polarisation of an adjacent section of the membrane is depolarised. The ion transfer reaction is repeated.
These reactions are localised , they start at the first stimulation point on the axon. The first reaction starts a wave of localised ion transfer reactions. These reactions propagate a series of action potentials followed by resting potentials repeated at regular intervals along. In this way electrical or nerve impulses are transported along the whole length of the axon by the movement of ions between the axon and its external environment.
is released into the gap. The empty vesicles return to the cytoplasm. The acetylcholine diffuses across the synaptic cleft and fuses with the receptor molecules at the surface of the post-synaptic membrane.
The attachment of the neurotransmitter depolarises the membrane altering its permeability in favour of sodium ions, Na+^. This flow of Na+^ ions into the post-synaptic neurone creates a new localised ion transfer reaction - a new action potential.
As soon as acetylcholine depolarises the post-synaptic membrane , it must be removed from its surface to allow for the transmission of another impulse. This is achieved with assistance of water and a suitable biological enzyme. The acetylcholine molecule is hydrolysed by water.
This reaction breaks the acetylcholine to make two products. An ethanoate ion CH 3 COO -^ , combines chemically with the H +^ from the water to produce ethanoic acid, CH 3 COOH.
The hydroxyl ion OH -^ portion from the water, combines chemically to the remaining portion of the molecule producing choline, HOCH 2 CH 2 N +^ (CH 3 ) 3.
These products are released by the receptor molecules. They diffuse across the cleft and back into the pre-synaptic neurone where they recombine to form acetylcholine. These molecules are stored in the synaptic vesicles for future use. A lot of energy is required for the recombination process that is provided by the many mitochondria present.
Successive nerve impulse transmissions build up on the post-synaptic membrane until enough depolarisation has taken place and an action potential is generated. The impulse is then transported by the propagation of action potentials along the length of this neurone to another neurone or to a target organ.
Discovering the chemical structure of neurotransmitters has given chemists an understanding of the action of drugs and poisons on the nervous system. There are many drugs that are known to influence the functioning of synaptic transmissions. An example is nicotine found in tobacco products. Nicotine is only one of 3500 different compounds found in tobacco smoke.
Nicotine
Nicotine is part of a group of nitrogen-containing chemicals called alkaloids. Alkaloids have hydrocarbon-based skeletons, i.e. they contain mainly carbon and hydrogen atoms and are found in plants. Examples of other alkaloids are caffeine, morphine and cocaine.
Nicotine mimics the action of neurotransmitter chemicals like acetylcholine. Both molecules are based on hydrocarbon skeletons but the important fact about these structures is that they contain a nitrogen atom with a positive charge. This makes the structures very reactive in the part of the molecule that has the charge. Acetylcholine receptors on post-synaptic membranes will accept nicotine because it has a similar arrangement of is atoms and similar charge on the nitrogen atom.
When tobacco is burned, small droplets of tar containing nicotine are inhaled and find their way to the lungs and eventually to the alveoli or air sacs. Nicotine is a weak base (pH 8.5); its pH is adjusted when it enters the airway to match the pH of body fluids (pH 7.4).
It is rapidly absorbed through the fine membrane of the air sac and the mouth into the bloodstream. From this point nicotine is distributed very quickly throughout the body, taking about eight seconds to reach the brain. In the brain it creates a burst of activity amongst the acetylcholine receptors to give a feeling of pleasure.
The initial concentration of nicotine is high after one inhalation. It takes about 45 minutes for this concentration to be reduced by half. At low concentrations it acts as a stimulant at higher levels it acts as an inhibitor, i.e. it will prevent neurone stimulation.
When nicotine is bound to the postsynaptic receptor, it depolarises the membrane triggering the influx of sodium ions from surrounding tissues. This initiates a wave of action potentials as before.
However nicotine is not removed by hydrolysis so the stimulation is maintained, i.e. the flow of ions is maintained and other nerve transmissions cannot get through. However eventually nicotine is broken down mainly in the liver by oxidation , in a number of stages with the assistance of enzymes.
This over-stimulation happens at all axons exposed to nicotine and it has an effect on all organs and functions. One adverse effect of the over-stimulation of nerve fibres is the constriction of blood vessels, at the same time stimulating the heart making it beat faster and increasing the blood pressure.
As the level of nicotine falls the affected neurones have a chance to recover. However it is likely that long-term use of nicotine is likely to result will result in chronic illness or death as there will always be permanent tissue as well as nerve damage.