A neuron is a microscopic structure composed of three major parts namely cell body (soma), dendrites and axon. The cell body is the spherical part of the neuron that contains all the cellular organelles as a typical cell (except centriole). The plasma membrane covering the neuron is called neurilemma and the axon is axolemma. The repeatedly branched short fibres coming out of the cell body are called dendrites, which transmit impulses towards the cell body. The cell body and the dendrites contain cytoplasm and granulated endoplasmic reticulum called Nissl’s granules.

An axon is a long fibre that arises from a cone shaped area of the cell body called the Axon hillock and ends at the branched distal end. Axon hillock is the place where the nerve impulse is generated in the motor neurons. The axon of one-neuron branches and forms connections with many other neurons. An axon contains the same organelles found in the dendrites and cell body but lacks Nissl’s granules and Golgi apparatus.

The axon, particularly of peripheral nerves is surrounded by Schwann cells (a type of glial cell) to form myelin sheath, which act as an insulator. Myelin sheath is associated only with the axon; dendrites are always non-myelinated. Schwann cells are not continuous along

the axon; so there are gaps in the myelin sheath between adjacent Schwann cells. These gaps are called Nodes of Ranvier. Large myelinated nerve fibres conduct impulses rapidly, whereas non- myelinated fibres conduct impulses quite slowly (Figure 10.1).

The longest cells in the human body are the neurons. The longest axons in the human body, for example, are those of the sciatic nerve, which run from the base of the spine to the big toe of each foot. These single-cell fibers may extend a meter or even longer. The axons of the inter neurons in the CNS are the shortest.

Each branch at the distal end of the axon terminates into a bulb like structure called synaptic knob which possesses synaptic vesicles filled with neurotransmitters. The axon transmits nerve impulses away from the cell body to an inter neural space or to a neuro-muscular junction.

The neurons are divided into three types based on number of axon and dendrites they possess (Figure.10.2).

1. Multipolar neurons have many processes with one axon and two or more dendrites. They are mostly interneurons.

2.Bipolar neurons have two processes with one axon and one dendrite. These are found in the retina of the eye, inner ear and the olfactory area of the brain.

3. Unipolar neurons have a single short process and one axon. Unipolar neurons are located in the ganglia of cranial and spinal nerves.

This section deals with how the nerve impulses are produced and conducted in our body. Sensation felt in the sensory organs are carried by the nerve fibres in the form of electrical impulses. A nerve impulse is a series of electrical impulses, which travel along the nerve fibre. Inner to the axolemma, the cytoplasm contains the intracellular fluid (ICF) with large amounts of potassium and magnesium phosphate along with negatively charged proteins and other organic molecules.The extra cellular fluid (ECF) found outside the axolemma contains large amounts of sodium chloride, bicarbonates, nutrients and oxygen for the cell; and carbon dioxide and metabolic wastes released by the neuronal cells. The ECF and ICF (cytosol) contains negatively charged particles (anions) and positively charged particles (cations). These charged particles are involved in the conduction of impulses.

The neurons maintain an uneven distribution of various inorganic ions across their axolemma for transmission of impulses. This unequal distribution of ions establishes the membrane potential across the axolemma. The axolemma contains a variety of membrane proteins that act as ionic channels and regulates the movement of ions across the axolemma. (Shown in Table 10.1).

The transmission of impulse involves two main phases; Resting membrane potential and Action membrane potential.

Resting membrane Potential: The electrical potential difference across the plasma membrane of a resting neuron is called the resting potential during which the interior of the cell is negative due to greater efflux of K+ outside the cell than

Note: The charged particles have potential energy. The potential dif- ference is the measure of potential energy between two points which is measured in volts or millivolts.

Table 10.1 Ionic Channels in the Axolemma

Na+ influx into the cell. When the axon is not conducting any impulses i.e. in resting condition, the axon membrane is more permeable to K+ and less permeable to Na+ ions, whereas it remains impermeable to negatively charged protein ions.

Action Membrane Potential An action potential occurs when a neuron sends information down an axon, away from the cell body. It includes following phases, depolarization, repolarisation and hypo polarization.

Depolarization – Reversal of Polarity When a nerve fibre is stimulated, sodium voltage-gate opens and makes the axolemma permeable to Na+ ions; meanwhile the potassium voltage gate closes. As a result, the rate of flow of Na+ ions into the axoplasm exceeds the rate of flow of K+ ions to the outside fluid [ECF]. Therefore, the axolemma becomes positively charged inside and negatively charged outside. This reversal of electrical charge is called Depolarization.

During depolarization, when enough Na+ ions enter the cell, the action potential reaches a certain level, called threshold potential [-55mV]. The particular stimulus which is able to bring the membrane potential to threshold is called threshold stimulus.

The action potential occurs in response to a threshold stimulus but does not occur at subthreshold stimuli. This is called all or none principle. Due to the rapid influx of Na+ ions, the membrane potential shoots rapidly up to +45mV which is called the Spike potential.

Repolarisation [Falling Phase] When the membrane reaches the spike potential, the sodium voltage-gate closes and potassium voltage-gate opens. It checks influx of Na+ions and initiates the efflux of K+ions which lowers the number of positive ions within the cell. Thus, the potential falls back towards the resting potential. The reversal of membrane potential inside the axolemma to negative occurs due to the efflux of K+ ions. This is called Repolarisation.

Hyperpolarization If repolarization becomes more negative than the resting potential -70 mV to about -90 mV, it is called Hyperpolarization.

During this, K+ ion gates are more permeable to K+ even after reaching the threshold level as it closes slowly; hence called Lazy gates. The membrane potential returns to its original resting state when K+ ion channels close completely. During hyperpolarization the Na+ voltage gate remains closed (Figure 10.5).

Conduction Speed of a nerve impulse The conduction speed of a nerve impulse depends on the diameter of axon. The greater the axon’s diameter, the faster is the conduction. The myelinated axon conducts the impulse faster than the non-myelinated axon. The voltage-gated Na+ and K+ channels** are concentrated at the nodes of Ranvier. As a result, the impulse jumps node to node, rather than travelling the entire length of the nerve fibre. This mechanism of conduction is called Saltatory Conduction. Nerve impulses travel at the speed of 1-300 m/s.

The junction between two neurons is called a Synapse through which a nerve impulse is transmitted. The first neuron involved in the synapse forms the pre- synaptic neuron and the second neuron is the post-synaptic neuron. A small gap between the pre and postsynaptic membranes is called Synaptic Cleft that forms a structural gap and a functional bridge between neurons. The axon terminals contain synaptic vesicles filled with neurotransmitters. When an impulse [action potential] arrives at the axon terminals, it depolarizes the pre- synaptic membrane, opening the voltage gated calcium channels. Influx of calcium ions stimulates the synaptic vesicles towards the pre-synaptic membrane and fuses with it. In the neurilemma, the vesicles release their neurotransmitters into the synaptic cleft by exocytosis. The released neurotransmitters bind to their specific receptors on the post-synaptic membrane, responding to chemical signals. The entry of the ions can generate a new potential in the post-synaptic neuron, which may be either excitatory or inhibitory. Excitatory post-synaptic potential causes depolarization whereas inhibitory post-synaptic potential causes hyperpolarization of post-synaptic membrane (Figure 10.6).