We know that transmission of signals from nerve to muscle is affected by acetylcholine or neurotransmitter substance. similarly neuron to neuron transmission is also achieved by acetylcholine. In addition to acetylcholine There are several other by chemical that function as neuro transmitter. A limited number have already been identify and news one are being identified.

A chemical can be called a neurotransmitters in a given tissue only if its fulfill certain conditions like:
- When applied to the postsynaptic membrane it should be able to produce the same effect as does presynaptic stimulation.
- It should also be released by the presynaptic membrane
- Its action should be blocked by the same agent that block neural transmission.
The neurotransmitter are either drived:
i) From amino acid tyrosine, which includes dopamine ‚norepinephrine (also called noradrenaline), epinephrine (also called adrenaline )and serotonin.
ii) From neuropeptides which include neurotransmitter endorphins and enkephalins , that reduce pain perception. Therefore, these are also called natural opiates (morphine like substance ).
The neurons that are involved in pain reception have receptor molecules to which internal opiates attach so that the pain receptor are inhibited from releasing their own transmitter substance (substance P )on two neurones in the pain perception centres.Thus the relay of information to the brain is blocked. the pain killing the effectiveness of endorphins is similar to that of morphine.
Neurotransmitter have three mechanism of action ‚namely ionotropic, metabotropic and modulatory.

- Ionotropic mechanism of action : Includes the opening of specific ionic Gates in the plasma membrane . Glutamate, GABA and acetylcholine are all ionotropic and so bind to their respective and ionotropic receptors.Glutamate is excitatory as it opens Na+ gates ‚leading to de polarization. GABA opens the Cl (chloride ion) gates, thereby allowing the movement of Cl ion into neuron and leading to hyper polarization hence it is inhibitory. Acetylcholine is ionotropic and excitatory at nicotinic synapses (acetylcholine. Has two types of receptor one thats responds to nicotine and called nictin receptor and another type known as muscarinic receptor that responds to muscarine , a drug obtained from certain types of mushrooms) , including the opening of Na+ gates . These ionotropic effects are rapid (occuring typically within 10 milliseconds after neurotransmitter release( and lasts for a short period from 1 to 20 miliseconds.
- Metabotropic Mechanisms : of actin is more complicated involving a sequence of metabolic reactions. These effects typically involve a ” second messenger ” , molecule taht May open or close an ion gate,After the production of proteins or alter the structure of the postsynaptic cell.The biogenic amine epinephrine is a metabotropic transmitter that binds to the metabotropic receptor of the plasma membrane. The effects are much lower to occur ( 30 millisecond after neurotransmitter release )are longer lasting ( up to several seconds in duration).
- Neuro modulator mechanism of action : Involves neuro modulator which are peptide molecules (shot protein) whose function lie somewhere between that of a neurotransmitter and a hormone.Neuro modulator may influence and number of neurons in the region of release including the neuron releasing them. Neurotransmitter acts by prolonging or limiting the effects of a neuro modulators. Most neurons synthesize and release both neurotransmitter and neuro modulators . this combination supports a broader range of effects.
Neurons do not always function in the way they should. things can go wrong in a deadly way if the synaptic cleft is occupied by chemical that interfere with neurotransmission.