Neurotransmitters - Anatomy & Physiology

Nerve - © fig.cox.miami.edu 2008

Introduction

Neurotransmitters are chemicals that are used to relay, amplify and modulate signals between neurones and cells. They can be classified into two main groups; small-molecule transmitters (SMT) and neuropeptides. SMTs are synthesised within nerve terminals via enzymes that are produced within the cell body. Within most nerve junctions, the terminal membrane of the nerve contains numerous specific transport proteins that facilitate the transport of the majority of the SMTs back into the nerve terminal, effectively recycling the neurotransmitter. Neuropeptides are constructed of around 3 - 40 amio acid molecules that are synthesised within the cell body and are then transported to along the axon to the nerve terminal within vesicles running along microtubules. Neuropeptides are broken down by extracellular enzymes called peptidases once the neurotransmitter has been released. A small proportion of neuropeptides can bind to postsynaptic receptors in the nerve terminal membrane and can be taken up by endocytosis, although the degree of recycling of neuropeptides is lower than that of SMTs.

Types of neurotransmitter

Small-molecule Neurotransmitters

There are two major sub-groups of SMTs; amino acids and biogenic amines. All SMTs play an important role within the central nervous system with the exception of acetylcholine and norepinephrine which both are important within the peripheral nervous system.

Amino Acids

Amino acid glutamate is the most common excitatory SMT in the central nervous system whilst gamma-aminobutyric acid (GABA) is the most common inhibitory SMT. Other amino acid SMTs include aspartate and glycine.

Biogenic Amines

Biogenic amines are synthesised from only several types of amino acids and dependant on which amino acids are used in their formation depends on their classification. Biogenic amines that are derived from the amino acid tyrosine are classified as catecholamines and include the SMTs norepinephrine (NE) (noradrenaline), epinephrine (E) (adrenaline), melatonin and dopamine (DA). Adrenergic neurons release norepinephrine. The biogenic amine that is dervied from the amino acid tryptophane is called serotonin (5-HT) whilst the SMT derived from histidine is called histamine (HA). Serotonergic neurons release serotonin. Whilst these SMTs are primarily of importance in the central nervous system, norepinephrine is predominantly found in the peripheral nervous system.

Other SMTs

Other common SMTs include acetylcholine (ACh), ATP and nitric oxide (NO). Ach is the most common excitatory neurotransmitter in the peripheral nervous system. Cholinergic neurons release ACh and for example, are found in the neuromuscular junction. Adenosine triphosphate (ATP), as well as having many important intracellular functions, is an important neurotransmitter and also has an autocrine and paracrine function. ATP belongs to the Purines SMT group. All synaptic vesicles released by the terminal membrane of a nerve contain ATP as well as other neurotransmitters, although ATP can only function as a neurotransmitter in it's own right if the post-synpatic terminal membrane contains ATP receptors. These ATP receptors are referred to as purinergic receptors. A pre-synaptic nerve terminal or terminal membrane never releases multiple types of SMT in addition to ATP, although it is common that neuropeptides are released in addition to ATP and SMTs. Other SMTs within the purine group include Guanosine triphosphate (GTP) and their derivatives.

Although NO is a neurotransmitter, it's characteristics differ from those discussed above. NO relies on calcium ion activation of the enzyme nitric oxide synthase (NOS) which is found throughout the nervous system and is the enzyme that is responsible for catalysing NO from the amino acid L-arginine. NO has a very short half life and is highly reactive. It is able to pass easily through lipid membranes. What makes NO differ from the SMTs above is that is can be released in all directions rather than pre-synaptically as per the classical SMTs. Therefore NO is able to act as a signalling pathway for the post-synaptic neuron to affect the pre-synpatic neuron.

Neuropeptides

The neuropeptide group of neurotransmitters contain a wide range of molecules of which only the major transmitters are included below. These include; enkephalin, subtance P, LHRH, Vasopressin, cholecystokinin, VIP, endorphin, neurotensin, TRH, angiotensin-II, somatostatin and oxytocin. These neuropeptides have a wide range of effects throughout the nervous system. Many of these neuropeptides are released from nerve terminals but also as hormones from endocrine cells. Cholecystokinin is an example of a neuropeptide that acts as both a neuropeptide but also as a hormone.

Endorphins and enkephalins are both examples of opioids and act within neuronal synapses to reduce the sensation of pain and in humans, it has been shown that these neuropeptides also lead to a sense of euphoria. Both of these molecules belong to the same opioid category as morphine and heroin.

Other Types of Neurotransmitter

In many neuronal synapses, not only do the post-synaptic membranes contain receptors for neurotransmitters, they also contain ion channels. In many cases the neurotransmitter receptors and ion channels are directly linked giving rise to ionotropic receptors. When a neurotransmitter binds it's relevant receptor, this also may open affect the gating of adjacent ion channels, either opening or closing the channel. Ionotrophic receptors such as this are responsible for the fastest type of synaptic transmission. An example of an ionotrophic receptor is zinc which is synaptically released via this mechanism.

Other ion channel receptors also exist in which the ion channel is less well associated with the neurotransmitter receptors. This type of ion channel receptor are referred to as metabotrophic receptors and are affected indirectly via G-proteins or intracellular secondary messengers altering the status of the gate once an appropriate signal has been received. Despite relying on a intermediate messenger system, metabotrophic receptors can also propagate rapid signal transfers, although not as rapid as ionotrophic receptors.

Function

The release of excitatory neurotransmitters from the pre-synaptic membrane causes channels in the post-synaptic membrane to open and cause an increase in sodium ion concentration within the postsynaptic cell and a decrease in potassium ion concentration. This leads to a depolarisation of the postsynaptic cell, which is propagated further along the axon by an action potential (AP). For further information on action potential creation and propogation, please see Neurons_-_Anatomy_%26_Physiology#Nerve_Fibre|here]]. Inhibitory neurotransmitters cause hyperpolarization of the postsynaptic cell making it unable to generate an action potential.

Post-synaptic receptors determine the reaction of the neurotransmitter meaning that the same neurotransmitter may cause an excitatory effect on some membranes whilst exerting an inhibitory effect on others e.g ACH can be either excitatory to skeletal muscle cells or inhibitory to both smooth muscle and cardiac muscle.

Actions

This section will briefly outline the actions of most of the neurotransmitters introduced above. This will be done as per the groupings laid out above.

Small-Molecule Neurotransmitters

Biogenic Amines

Epinephrine is produced by the adrenal glands. It is primarily involved in an overall activation of the sympathetic nervous system and is involved in the management of stress. Norepinephrine is also produced by adrenal glands and is involved in the initiation and maintainence of conciousness within the sympathetic nervous system. Dopamine is involved in motivation as well as love and addiction. Serotonin is involved in emotions, conciousness, sleep and thermoregulation. Melatonin is responsible for the regulation of onset of sleep and also for seasonal changes in the body such as winter weight gain and mating seasons.

Other SMTs

The neuropeptide Acetylcholine (Ach) is primarily involved in skeletal muscle movement within the sympathetic nervous system and visceral movements as part of the parasympathetic nervous system.

Neuropeptides

|- | ATP | Timing mechanism of G proteins by displacement of ADP.

|- | GTP |Timing mechanism of G proteins by displacement of GDP.

|- | Vasopressin |Metabolic rate, metabolism.

|- | Somatostatin |Inhibits production of other hormones.

|- | Histamine | Gastric secretions increased, dilation of capillaries, constriction of bronchial smooth muscle and decreased blood pressure.

|- | Zinc |Release of neuropeptide Y.

|- | NO |Enlargement of genital organs leading to erection.

|- | CO |Sleep cycle.

|- | Glutamate | Exitatory, found in CNS.

|- | GABA | Inhibitory, found in CNS.

|- | Glycine | Spinal reflexes, motor. |}

Neurotransmitter systems

See somatic and autonomic nervous systems.

Degradation and elimination

• Acetylcholine is derived from Choline.
• Serotonin [5-Hydroxytryptamine (5-HT)] is derived from Tryptophan.
• GABA is derived from Glutamate.
• Histamine is derived from Histidine.
• Epinephrine, norepinephrine and dopamine are derived from Tyrosine.
• Adenosine is derived from ATP.
• Nitric oxide is derived from Arginine.

Neurotransmitters must be broken down once they reach the post-synaptic cell to end the excitatory or inhibitory signal and prevent over stimulation/perminent inhibition.

• e.g, ACH an excitatory neurotransmitter, is broken down by acetylcholinesterase (AchE).

• Choline is taken up and recycled by the pre-synaptic neuron to synthesize more ACH.

• Other neurotransmitters such as dopamine are able to diffuse away and are eliminated from the body via the kidneys, or destroyed in the liver.