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Neurotransmitters are endogenous chemicals acting as signaling molecules that enable neurotransmission. They are a type of chemical messenger which transmits signals across a chemical synapse from one neuron (nerve cell) to another 'target' neuron, to a muscle cell, or to a gland cell.[1] Neurotransmitters are released from synaptic vesicles in synapses into the synaptic cleft, where they are received by neurotransmitter receptors on the target cell. Many neurotransmitters are synthesized from simple and plentiful precursors such as amino acids, which are readily available and only require a small number of biosynthetic steps for conversion. Neurotransmitters are essential to the function of complex neural systems. The exact number of unique neurotransmitters in humans is unknown, but more than 200 have been identified.[2][3][4]


Synaptic vesicles containing neurotransmitters

Neurotransmitters are stored in synaptic vesicles, clustered close to the cell membrane at the axon terminal of the presynaptic neuron. Neurotransmitters are released into and diffuse across the synaptic cleft, where they bind to specific receptors on the membrane of the postsynaptic neuron.[5] Binding of neurotransmitters may influence the postsynaptic neuron in either an excitation or inhibitory way, depolarizing or repolarizing it respectively.

Most of the neurotransmitters are about the size of a single amino acid; however, some neurotransmitters may be the size of larger proteins or peptides. A released neurotransmitter is typically available in the synaptic cleft for a short time before it is metabolized by enzymes, pulled back into the presynaptic neuron through reuptake, or bound to a postsynaptic receptor. Nevertheless, short-term exposure of the receptor to a neurotransmitter is typically sufficient for causing a postsynaptic response by way of synaptic transmission.

Generally, a neurotransmitter is released at the presynaptic terminal in response to a threshold action potential or graded electrical potential in the presynaptic neuron. However, low level 'baseline' release also occurs without electrical stimulation.


Until the early 20th century, scientists assumed that the majority of synaptic communication in the brain was electrical. However, through histological examinations by Ramón y Cajal, a 20 to 40 nm gap between neurons, known today as the synaptic cleft, was discovered. The presence of such a gap suggested communication via chemical messengers traversing the synaptic cleft, and in 1921 German pharmacologist Otto Loewi confirmed that neurons can communicate by releasing chemicals. Through a series of experiments involving the vagus nerves of frogs, Loewi was able to manually slow the heart rate of frogs by controlling the amount of saline solution present around the vagus nerve. Upon completion of this experiment, Loewi asserted that sympathetic regulation of cardiac function can be mediated through changes in chemical concentrations. Furthermore, Otto Loewi is credited with discovering acetylcholine (ACh)--the first known neurotransmitter.[6]


There are four main criteria for identifying neurotransmitters:

  1. The chemical must be synthesized in the neuron or otherwise be present in it.
  2. When the neuron is active, the chemical must be released and produce a response in some targets.
  3. The same response must be obtained when the chemical is experimentally placed on the target.
  4. A mechanism must exist for removing the chemical from its site of activation after its work is done.

However, given advances in pharmacology, genetics, and chemical neuroanatomy, the term "neurotransmitter" can be applied to chemicals that:

  • Carry messages between neurons via influence on the postsynaptic membrane.
  • Have little or no effect on membrane voltage, but have a common carrying function such as changing the structure of the synapse.
  • Communicate by sending reverse-direction messages that affect the release or reuptake of transmitters.

The anatomical localization of neurotransmitters is typically determined using immunocytochemical techniques, which identify the location of either the transmitter substances themselves or of the enzymes that are involved in their synthesis. Immunocytochemical techniques have also revealed that many transmitters, particularly the neuropeptides, are co-localized, that is, a neuron may release more than one transmitter from its synaptic terminal.[7] Various techniques and experiments such as staining, stimulating, and collecting can be used to identify neurotransmitters throughout the central nervous system.[8]


There are many different ways to classify neurotransmitters. Dividing them into amino acids, peptides, and monoamines is sufficient for some classification purposes.[9]

Major neurotransmitters:

In addition, over 50 neuroactive peptides have been found, and new ones are discovered regularly.[] Many of these are co-released along with a small-molecule transmitter. Nevertheless, in some cases, a peptide is the primary transmitter at a synapse. Beta-Endorphin is a relatively well-known example of a peptide neurotransmitter because it engages in highly specific interactions with opioid receptors in the central nervous system.

Single ions (such as synaptically released zinc) are also considered neurotransmitters by some,[12] as well as some gaseous molecules such as nitric oxide (NO), carbon monoxide (CO), and hydrogen sulfide (H2S).[13] The gases are produced in the neural cytoplasm and are immediately diffused through the cell membrane into the extracellular fluid and into nearby cells to stimulate production of second messengers. Soluble gas neurotransmitters are difficult to study, as they act rapidly and are immediately broken down, existing for only a few seconds.

The most prevalent transmitter is glutamate, which is excitatory at well over 90% of the synapses in the human brain.[10] The next most prevalent is gamma-Aminobutyric Acid, or GABA, which is inhibitory at more than 90% of the synapses that do not use glutamate. Although other transmitters are used in fewer synapses, they may be very important functionally: the great majority of psychoactive drugs exert their effects by altering the actions of some neurotransmitter systems, often acting through transmitters other than glutamate or GABA. Addictive drugs such as cocaine and amphetamines exert their effects primarily on the dopamine system. The addictive opiate drugs exert their effects primarily as functional analogs of opioid peptides, which, in turn, regulate dopamine levels.

List of neurotransmitters, peptides, and gaseous signaling molecules

Category Name Abbreviation Metabotropic Ionotropic
Small: Amino acids (Arg) Arginine ?2-Adrenergic receptors, imidazoline receptors NMDA receptors
Small: Amino acids Aspartate Asp - NMDA receptors
Small: Amino acids Glutamate Glu Metabotropic glutamate receptors NMDA receptors, kainate receptors, AMPARs
Small: Amino acids Gamma-aminobutyric acid GABA GABAB receptors GABAA receptors, GABAA-? receptors
Small: Amino acids Glycine Gly - NMDA receptors, glycine receptors
Small: Amino acids D-serine Ser - NMDA receptors
Small: Acetylcholine Acetylcholine Ach Muscarinic acetylcholine receptors Nicotinic acetylcholine receptors
Small: Monoamine (Phe/Tyr) Dopamine DA Dopamine receptors, trace amine-associated receptor 1[14][15] -
Small: Monoamine (Phe/Tyr) Norepinephrine (noradrenaline) NE, NAd Adrenergic receptors -
Small: Monoamine (Phe/Tyr) Epinephrine (adrenaline) Epi, Ad Adrenergic receptors -
Small: Monoamine (Trp) Serotonin (5-hydroxytryptamine) 5-HT Serotonin receptors (all except 5-HT3) 5-HT3
Small: Monoamine (His) Histamine H Histamine receptors -
Small: Trace amine (Phe) Phenethylamine PEA Human trace amine-associated receptors: hTAAR1, hTAAR2 -
Small: Trace amine (Phe) N-methylphenethylamine NMPEA hTAAR1 |Small: Trace amine (Phe/Tyr) Tyramine TYR hTAAR1, hTAAR2 -
Small: Trace amine (Phe/Tyr) octopamine Oct hTAAR1 -
Small: Trace amine (Phe/Tyr) Synephrine Syn hTAAR1 -
Small: Trace amine (Trp) Tryptamine hTAAR1, various serotonin receptors -
Small: Trace amine (Trp) N-methyltryptamine NMT hTAAR1, various serotonin receptors -
Lipid Anandamide AEA Cannabinoid receptors -
Lipid 2-Arachidonoylglycerol 2-AG Cannabinoid receptors -
Lipid 2-Arachidonyl glyceryl ether 2-AGE Cannabinoid receptors -
Lipid N-Arachidonoyl dopamine NADA Cannabinoid receptors TRPV1
Lipid Virodhamine Cannabinoid receptors -
Small: Purine Adenosine Ado Adenosine receptors -
Small: Purine Adenosine triphosphate ATP P2Y receptors P2X receptors
Small: Purine Nicotinamide adenine dinucleotide ?-NAD P2Y receptors P2X receptors
Category Name Abbreviation Metabotropic Ionotropic
Bombesin-like peptides Bombesin BBR1-2-3 -
Bombesin-like peptide Gastrin releasing peptide GRP - -
Bombesin-like peptide Neuromedin B NMB Neuromedin B receptor -
Bradykinins Bradykinin B1, B2 -
Calcitonin/CGRP family Calcitonin Calcitonin receptor -
Calcitonin/CGRP family Calcitonin gene-related peptide CGRP CALCRL -
Corticotropin-releasing factors Corticotropin-releasing hormone CRH CRHR1 -
Corticotropin-releasing factors Urocortin CRHR1 -
Galanins Galanin GALR1, GALR2, GALR3 -
Galanins Galanin-like peptide GALR1, GALR2, GALR3 -
Gastrins Gastrin Cholecystokinin B receptor -
Gastrins Cholecystokinin CCK Cholecystokinin receptors -
Melanocortins Adrenocorticotropic hormone ACTH ACTH receptor -
Melanocortins Proopiomelanocortin POMC Melanocortin 4 receptor -
Melanocortins Melanocyte-stimulating hormones MSH Melanocortin receptors -
Neurohypophyseals Vasopressin AVP Vasopressin receptors -
Neurohypophyseals Oxytocin OT Oxytocin receptor -
Neurohypophyseals Neurophysin I - -
Neurohypophyseals Neurophysin II - -
Neuromedins Neuromedin U NmU NmUR1, NmUR2 -
Neuropeptide B/W Neuropeptide B NPB NPBW1, NPBW2 -
Neuropeptide B/W Neuropeptide S NPS Neuropeptide S receptors -
Neuropeptide Y Neuropeptide Y NY Neuropeptide Y receptors -
Neuropeptide Y Pancreatic polypeptide PP - -
Neuropeptide Y Peptide YY PYY - -
Opioids Enkephalins ?-Opioid receptor -
Opioids Dynorphins ?-Opioid receptor -
Opioids Neoendorphins ?-Opioid receptor -
Opioids Endorphins ?-Opioid receptors -
Opioids Endomorphins ?-Opioid receptors -
Opioids Morphine ?-Opioid receptors -
Opioids Nociceptin/orphanin FQ N/OFQ Nociceptin receptors -
Orexins Orexin A OX-A Orexin receptors -
Orexins Orexin B OX-B Orexin receptors -
RFamides Kisspeptin KiSS GPR54 -
RFamides Neuropeptide FF NPFF NPFF1, NPFF2 -
RFamides Prolactin-releasing peptide PrRP PrRPR -
RFamides Pyroglutamylated RFamide peptide QRFP GPR103 -
Secretins Secretin Secretin receptor -
Secretins Motilin Motilin receptor -
Secretins Glucagon Glucagon receptor -
Secretins Glucagon-like peptide-1 GLP-1 Glucagon-like peptide 1 receptor -
Secretins Glucagon-like peptide-2 GLP-2 Glucagon-like peptide 2 receptor -
Secretins Vasoactive intestinal peptide VIP Vasoactive intestinal peptide receptors -
Secretins Growth hormone-releasing hormone GHRH Growth hormone-releasing hormone receptor -
Secretins Pituitary adenylate cyclase-activating peptide PACAP ADCYAP1R1 -
Somatostatins Somatostatin Somatostatin receptors -
Tachykinins Neurokinin A - -
Tachykinins Neurokinin B - -
Tachykinins Substance P - -
Tachykinins Neuropeptide K - -
Other Agouti-related peptide AgRP Melanocortin receptor -
Other N-Acetylaspartylglutamate NAAG Metabotropic glutamate receptor 3 (mGluR3) -
Other Cocaine- and amphetamine-regulated transcript CART Unknown Gi/Go-coupled receptor[16] -
Other Gonadotropin-releasing hormone GnRH GnRHR -
Other Thyrotropin-releasing hormone TRH TRHR -
Other Melanin-concentrating hormone MCH MCHR 1,2 -
Category Name Abbreviation Metabotropic Ionotropic
Gaseous signaling molecule Nitric oxide NO Soluble guanylyl cyclase -
Gaseous signaling molecule Carbon monoxide CO - Heme bound to potassium channels
Gaseous signaling molecule Hydrogen sulfide H2S - -


Neurons form elaborate networks through which nerve impulses--action potentials--travel. Each neuron has as many as 15,000 connections with neighboring neurons.

Neurons do not touch each other (except in the case of an electrical synapse through a gap junction); instead, neurons interact at contact points called synapses: a junction within two nerve cells, consisting of a miniature gap within which impulses are carried by a neurotransmitter. A neuron transports its information by way of a nerve impulse called an action potential. When an action potential arrives at the synapse's presynaptic terminal button, it may stimulate the release of neurotransmitters. These neurotransmitters are released into the synaptic cleft to bind onto the receptors of the postsynaptic membrane and influence another cell, either in an inhibitory or excitatory way. The next neuron may be connected to many more neurons, and if the total of excitatory influences minus inhibitory influences is great enough, it will also "fire". That is to say, it will create a new action potential at its axon hillock, releasing neurotransmitters and passing on the information to yet another neighboring neuron.

Excitatory and inhibitory

A neurotransmitter can influence the function of a neuron through a remarkable number of mechanisms. In its direct actions in influencing a neuron's electrical excitability, however, a neurotransmitter acts in only one of two ways: excitatory or inhibitory. A neurotransmitter influences trans-membrane ion flow either to increase (excitatory) or to decrease (inhibitory) the probability that the cell with which it comes in contact will produce an action potential. Thus, despite the wide variety of synapses, they all convey messages of only these two types, and they are labeled as such. Type I synapses are excitatory in their actions, whereas type II synapses are inhibitory. Each type has a different appearance and is located on different parts of the neurons under its influence.

Type I (excitatory) synapses are typically located on the shafts or the spines of dendrites, whereas type II (inhibitory) synapses are typically located on a cell body. In addition, Type I synapses have round synaptic vesicles, whereas the vesicles of type II synapses are flattened. The material on the presynaptic and post-synaptic membranes is denser in a Type I synapse than it is in a type II, and the type I synaptic cleft is wider. Finally, the active zone on a Type I synapse is larger than that on a Type II synapse.

The different locations of type I and type II synapses divide a neuron into two zones: an excitatory dendritic tree and an inhibitory cell body. From an inhibitory perspective, excitation comes in over the dendrites and spreads to the axon hillock to trigger an action potential. If the message is to be stopped, it is best stopped by applying inhibition on the cell body, close to the axon hillock where the action potential originates. Another way to conceptualize excitatory-inhibitory interaction is to picture excitation overcoming inhibition. If the cell body is normally in an inhibited state, the only way to generate an action potential at the axon hillock is to reduce the cell body's inhibition. In this "open the gates" strategy, the excitatory message is like a racehorse ready to run down the track, but first, the inhibitory starting gate must be removed.[17]

Examples of important neurotransmitter actions

As explained above, the only direct action of a neurotransmitter is to activate a receptor. Therefore, the effects of a neurotransmitter system depend on the connections of the neurons that use the transmitter, and the chemical properties of the receptors that the transmitter binds to.

Here are a few examples of important neurotransmitter actions:

Brain neurotransmitter systems

Neurons expressing certain types of neurotransmitters sometimes form distinct systems, where activation of the system affects large volumes of the brain, called volume transmission. Major neurotransmitter systems include the noradrenaline (norepinephrine) system, the dopamine system, the serotonin system, and the cholinergic system, among others. Trace amines have a modulatory effect on neurotransmission in monoamine pathways (i.e., dopamine, norepinephrine, and serotonin pathways) throughout the brain via signaling through trace amine-associated receptor 1.[24][25] A brief comparison of these systems follows:

Neurotransmitter systems in the brain
System Pathway origin and projections Regulated cognitive processes and behaviors
Noradrenaline system
Noradrenergic pathways:
Dopamine system
Dopaminergic pathways:
  • Hypothalamospinal projection
Histamine system
Histaminergic pathways:
Serotonin system
Serotonergic pathways:

Caudal nuclei (CN):
Raphe magnus, raphe pallidus, and raphe obscurus

  • Caudal projections

Rostral nuclei (RN):
Nucleus linearis, dorsal raphe, medial raphe, and raphe pontis

  • Rostral projections
Acetylcholine system
Cholinergic pathways:

Forebrain cholinergic nuclei (FCN):
Nucleus basalis of Meynert, medial septal nucleus, and diagonal band

  • Forebrain nuclei projections

Brainstem cholinergic nuclei (BCN):
Pedunculopontine nucleus, laterodorsal tegmentum, medial habenula, and
parabigeminal nucleus

  • Brainstem nuclei projections

Drug effects

Understanding the effects of drugs on neurotransmitters comprises a significant portion of research initiatives in the field of neuroscience. Most neuroscientists involved in this field of research believe that such efforts may further advance our understanding of the circuits responsible for various neurological diseases and disorders, as well as ways to effectively treat and someday possibly prevent or cure such illnesses.[40][medical ]

Drugs can influence behavior by altering neurotransmitter activity. For instance, drugs can decrease the rate of synthesis of neurotransmitters by affecting the synthetic enzyme(s) for that neurotransmitter. When neurotransmitter syntheses are blocked, the amount of neurotransmitters available for release becomes substantially lower, resulting in a decrease in neurotransmitter activity. Some drugs block or stimulate the release of specific neurotransmitters. Alternatively, drugs can prevent neurotransmitter storage in synaptic vesicles by causing the synaptic vesicle membranes to leak. Drugs that prevent a neurotransmitter from binding to its receptor are called receptor antagonists. For example, drugs used to treat patients with schizophrenia such as haloperidol, chlorpromazine, and clozapine are antagonists at receptors in the brain for dopamine. Other drugs act by binding to a receptor and mimicking the normal neurotransmitter. Such drugs are called receptor agonists. An example of a receptor agonist is morphine, an opiate that mimics effects of the endogenous neurotransmitter ?-endorphin to relieve pain. Other drugs interfere with the deactivation of a neurotransmitter after it has been released, thereby prolonging the action of a neurotransmitter. This can be accomplished by blocking re-uptake or inhibiting degradative enzymes. Lastly, drugs can also prevent an action potential from occurring, blocking neuronal activity throughout the central and peripheral nervous system. Drugs such as tetrodotoxin that block neural activity are typically lethal.

Drugs targeting the neurotransmitter of major systems affect the whole system, which can explain the complexity of action of some drugs. Cocaine, for example, blocks the re-uptake of dopamine back into the presynaptic neuron, leaving the neurotransmitter molecules in the synaptic gap for an extended period of time. Since the dopamine remains in the synapse longer, the neurotransmitter continues to bind to the receptors on the postsynaptic neuron, eliciting a pleasurable emotional response. Physical addiction to cocaine may result from prolonged exposure to excess dopamine in the synapses, which leads to the downregulation of some post-synaptic receptors. After the effects of the drug wear off, an individual can become depressed due to decreased probability of the neurotransmitter binding to a receptor. Fluoxetine is a selective serotonin re-uptake inhibitor (SSRI), which blocks re-uptake of serotonin by the presynaptic cell which increases the amount of serotonin present at the synapse and furthermore allows it to remain there longer, providing potential for the effect of naturally released serotonin.[41]AMPT prevents the conversion of tyrosine to L-DOPA, the precursor to dopamine; reserpine prevents dopamine storage within vesicles; and deprenyl inhibits monoamine oxidase (MAO)-B and thus increases dopamine levels.

Drug-Neurotransmitter Interactions[42]
Drug Interacts with: Receptor Interaction: Type Effects
Botulinum Toxin (Botox) Acetylcholine - Antagonist Blocks acetylcholine release in PNS

Prevents muscle contractions

Black Widow Spider Venom Acetylcholine - Agonist Promotes acetylcholine release in PNS

Stimulates muscle contractions

Neostigmine Acetylcholine - - Interferes with acetylcholinerase activity

Increases effects of ACh at receptors

Used to treat myasthenia gravis

Nicotine Acetylcholine Nicotinic (skeletal muscle) Agonist Increases ACh activity

Increases attention

Reinforcing effects

d-tubocurarine Acetylcholine Nicotinic (skeletal muscle) Antagonist Decreases activity at receptor site
Curare Acetylcholine Nicotinic (skeletal muscle) Antagonist Decreases ACh activity

Prevents muscle contractions

Muscarine Acetylcholine Muscarinic (heart and smooth muscle) Agonist Increases ACh activity


Atropine Acetylcholine Muscarinic (heart and smooth muscle) Antagonist Blocks pupil constriction

Blocks saliva production

Scopolamine (Hyoscine) Acetylcholine Muscarinic (heart and smooth muscle) Antagonist Treats motion sickness and postoperative nausea and vomiting
AMPT Dopamine/norepinephrine - - Inactivates tyrosine hydroxylase and inhibits dopamine production
Reserpine Dopamine - - Prevents storage of dopamine and other monoamines in synaptic vesicles

Causes sedation and depression

Apomorphine Dopamine D2 Receptor (presynaptic autoreceptors/postsynaptic receptors) Antagonist (low dose)/Direct agonist (high dose) Low dose: blocks autoreceptors

High dose: stimulates postsynaptic receptors

Amphetamine Dopamine/norepinephrine - Indirect agonist Releases dopamine, noradrenaline, and serotonin

Blocks reuptake[24][25]

Methamphetamine Dopamine/norepinephrine - - Releases dopamine and noradrenaline

Blocks reuptake

Methylphenidate Dopamine - - Blocks reuptake

Enhances attention and impulse control in ADHD

Cocaine Dopamine - Indirect Agonist Blocks reuptake into presynapse

Blocks voltage-dependent sodium channels

Can be used as a topical anesthetic (eye drops)

Deprenyl Dopamine - Agonist Inhibits MAO-B

Prevents destruction of dopamine

Chlorpromazine Dopamine D2 Receptors Antagonist Blocks D2 receptors

Alleviates hallucinations

MPTP Dopamine - - Results in Parkinson like symptoms
PCPA Serotonin (5-HT) - Antagonist Disrupts serotonin synthesis by blocking the activity of tryptophan hydroxylase
Ondansetron Serotonin (5-HT) 5-HT3 receptors Antagonist Reduces side effects of chemotherapy and radiation

Reduces nausea and vomiting

Buspirone Serotonin (5-HT) 5-HT1A receptors Partial Agonist Treats symptoms of anxiety and depression
Fluoxetine Serotonin (5-HT) supports 5-HT reuptake SSRI Inhibits reuptake of serotonin

Treats depression, some anxiety disorders, and OCD[41] Common examples: Prozac and Sarafem

Fenfluramine Serotonin (5-HT) - - Causes release of serotonin

Inhibits reuptake of serotonin

Used as an appetite suppressant

Lysergic acid diethylamide Serotonin (5-HT) Post-synaptic 5-HT2A receptors Direct Agonist Produces visual perception distortions

Stimulates 5-HT2A receptors in forebrain

Methylenedioxymethamphetamine (MDMA) Serotonin (5-HT)/ norepinphrine - - Stimulates release of serotonin and norepinephrine and inhibits the reuptake

Causes excitatory and hallucinogenic effects

Strychnine Glycine - Antagonist Causes severe muscle spasms[43]
Diphenhydramine Histamine Crosses blood brain barrier to cause drowsiness
Tetrahydrocannabinol (THC) Endocannabinoids Cannabinoid (CB) receptors Agonist Produces analgesia and sedation

Increases appetite

Cognitive effects

Rimonabant Endocannabinoids Cannabinoid (CB) receptors Antagonist Suppresses appetite

Used in smoking cessation

MAFP Endocannabinoids - - Inhibits FAAH

Used in research to increase cannabinoid system activity

AM1172 Endocannabinoids - - Blocks cannabinoid reuptake

Used in research to increase cannabinoid system activity

Anandamide (endogenous) - Cannabinoid (CB) receptors; 5-HT3 receptors - Reduce nausea and vomiting
Caffeine Adenosine Adenosine receptors Antagonist Blocks adenosine receptors

Increases wakefulness

PCP Glutamate NMDA receptor Indirect Antagonist Blocks PCP binding site

Prevents calcium ions from entering neurons

Impairs learning

AP5 Glutamate NMDA receptor Antagonist Blocks glutamate binding site on NMDA receptor

Impairs synaptic plasticity and certain forms of learning

NMDA Glutamate NMDA receptor Agonist Used in research to study NMDA receptor

Ionotropic receptor

AMPA Glutamate AMPA receptor Agonist Used in research to study AMPA receptor

Ionotropic receptor

Ketamine Glutamate Kainate receptor Antagonist Used in research to study Kainate receptor

Induces trance-like state, helps with pain relief and sedation

Allyglycine GABA - - Inhibits GABA synthesis

Causes seizures

Muscimol GABA GABA receptor Agonist Causes sedation
Bicuculine GABA GABA receptor Antagonist Causes Seizures
Benzodiazepines GABA GABAA receptor Indirect agonists Anxiolytic, sedation, memory impairment, muscle relaxation
Barbiturates GABA GABAA receptor Indirect agonists Sedation, memory impairment, muscle relaxation
Alcohol GABA GABA receptor Indirect agonist Sedation, memory impairment, muscle relaxation
Picrotoxin GABA GABAA receptor Indirect antagonist High doses cause seizures
Tiagabine GABA - Antagonist GABA transporter antagonist

Increase availability of GABA

Reduces the likelihood of seizures

Moclobemide Norepinephrine - Agonist Blocks MAO-A to treat depression
Idazoxan Norepinephrine alpha-2 adrenergic autoreceptors Agonist Blocks alpha-2 autoreceptors

Used to study norepinephrine system

Fusaric acid Norepinephrine - - Inhibits activity of dopamine beta-hydroxylase which blocks the production of norepinephrine

Used to study norepinephrine system without affecting dopamine system

Opiates (Opium, morphine, heroin,and oxycodone) Opioids Opioid receptor[44] Agonists Analgesia, sedation, and reinforcing effects
Naloxone Opioids - Antagonist Reverses opiate intoxication or overdose symptoms (i.e. problems with breathing)


An agonist is a chemical capable of binding to a receptor, such as a neurotransmitter receptor, and initiating the same reaction typically produced by the binding of the endogenous substance.[45] An agonist of a neurotransmitter will thus initiate the same receptor response as the transmitter. In neurons, an agonist drug may activate neurotransmitter receptors either directly or indirectly. Direct-binding agonists can be further characterized as full agonists, partial agonists, inverse agonists.[][46]

Direct agonists act similar to a neurotransmitter by binding directly to its associated receptor site(s), which may be located on the presynaptic neuron or postsynaptic neuron, or both.[47] Typically, neurotransmitter receptors are located on the postsynaptic neuron, while neurotransmitter autoreceptors are located on the presynaptic neuron, as is the case for monoamine neurotransmitters;[24] in some cases, a neurotransmitter utilizes retrograde neurotransmission, a type of feedback signaling in neurons where the neurotransmitter is released postsynaptically and binds to target receptors located on the presynaptic neuron.[48][note 1]Nicotine, a compound found in tobacco, is a direct agonist of most nicotinic acetylcholine receptors, mainly located in cholinergic neurons.[44]Opiates, such as morphine, heroin, hydrocodone, oxycodone, codeine, and methadone, are ?-opioid receptor agonists; this action mediates their euphoriant and pain relieving properties.[44]

Indirect agonists increase the binding of neurotransmitters at their target receptors by stimulating the release or preventing the reuptake of neurotransmitters.[47] Some indirect agonists trigger neurotransmitter release and prevent neurotransmitter reuptake. Amphetamine, for example, is an indirect agonist of postsynaptic dopamine, norepinephrine, and serotonin receptors in each their respective neurons;[24][25] it produces both neurotransmitter release into the presynaptic neuron and subsequently the synaptic cleft and prevents their reuptake from the synaptic cleft by activating TAAR1, a presynaptic G protein-coupled receptor, and binding to a site on VMAT2, a type of monoamine transporter located on synaptic vesicles within monoamine neurons.[24][25]


An antagonist is a chemical that acts within the body to reduce the physiological activity of another chemical substance (as an opiate); especially one that opposes the action on the nervous system of a drug or a substance occurring naturally in the body by combining with and blocking its nervous receptor.[49]

There are two main types of antagonist: direct-acting Antagonist and indirect-acting Antagonists:

  1. Direct-acting antagonist- which takes up space present on receptors which are otherwise taken up by neurotransmitters themselves. This results in neurotransmitters being blocked from binding to the receptors. The most common is called Atropine.
  2. Indirect-acting antagonist- drugs that inhibit the release/production of neurotransmitters (e.g., Reserpine).

Drug antagonists

An antagonist drug is one that attaches (or binds) to a site called a receptor without activating that receptor to produce a biological response. It is therefore said to have no intrinsic activity. An antagonist may also be called a receptor "blocker" because they block the effect of an agonist at the site. The pharmacological effects of an antagonist, therefore, result in preventing the corresponding receptor site's agonists (e.g., drugs, hormones, neurotransmitters) from binding to and activating it. Antagonists may be "competitive" or "irreversible".

A competitive antagonist competes with an agonist for binding to the receptor. As the concentration of antagonist increases, the binding of the agonist is progressively inhibited, resulting in a decrease in the physiological response. High concentration of an antagonist can completely inhibit the response. This inhibition can be reversed, however, by an increase of the concentration of the agonist, since the agonist and antagonist compete for binding to the receptor. Competitive antagonists, therefore, can be characterized as shifting the dose-response relationship for the agonist to the right. In the presence of a competitive antagonist, it takes an increased concentration of the agonist to produce the same response observed in the absence of the antagonist.

An irreversible antagonist binds so strongly to the receptor as to render the receptor unavailable for binding to the agonist. Irreversible antagonists may even form covalent chemical bonds with the receptor. In either case, if the concentration of the irreversible antagonist is high enough, the number of unbound receptors remaining for agonist binding may be so low that even high concentrations of the agonist do not produce the maximum biological response.[50]


While intake of neurotransmitter precursors does increase neurotransmitter synthesis, evidence is mixed as to whether neurotransmitter release and postsynaptic receptor firing is increased. Even with increased neurotransmitter release, it is unclear whether this will result in a long-term increase in neurotransmitter signal strength, since the nervous system can adapt to changes such as increased neurotransmitter synthesis and may therefore maintain constant firing.[54][unreliable medical source?] Some neurotransmitters may have a role in depression and there is some evidence to suggest that intake of precursors of these neurotransmitters may be useful in the treatment of mild and moderate depression.[54][unreliable medical source?][55]

Catecholamine and trace amine precursors

L-DOPA, a precursor of dopamine that crosses the blood-brain barrier, is used in the treatment of Parkinson's disease. For depressed patients where low activity of the neurotransmitter norepinephrine is implicated, there is only little evidence for benefit of neurotransmitter precursor administration. L-phenylalanine and L-tyrosine are both precursors for dopamine, norepinephrine, and epinephrine. These conversions require vitamin B6, vitamin C, and S-adenosylmethionine. A few studies suggest potential antidepressant effects of L-phenylalanine and L-tyrosine, but there is much room for further research in this area.[54][unreliable medical source?]

Serotonin precursors

Administration of L-tryptophan, a precursor for serotonin, is seen to double the production of serotonin in the brain. It is significantly more effective than a placebo in the treatment of mild and moderate depression.[54][unreliable medical source?] This conversion requires vitamin C.[23]5-hydroxytryptophan (5-HTP), also a precursor for serotonin, is more effective than a placebo.[54][unreliable medical source?]

Diseases and disorders

Diseases and disorders may also affect specific neurotransmitter systems. The following are disorders involved in either an increase, decrease, or imbalance of certain neurotransmitters.


For example, problems in producing dopamine (mainly in the substantia nigra) can result in Parkinson's disease, a disorder that affects a person's ability to move as they want to, resulting in stiffness, tremors or shaking, and other symptoms. Some studies suggest that having too little or too much dopamine or problems using dopamine in the thinking and feeling regions of the brain may play a role in disorders like schizophrenia or attention deficit hyperactivity disorder (ADHD). Dopamine is also involved in addiction and drug use, as most recreational drugs cause an influx of dopamine in the brain (especially opioid and methamphetamines) that produces a pleasurable feeling, which is why users constantly crave drugs.


Similarly, after some research suggested that drugs that block the recycling, or reuptake, of serotonin seemed to help some people diagnosed with depression, it was theorized that people with depression might have lower-than-normal serotonin levels. Though widely popularized, this theory was not borne out in subsequent research.[56] Therefore, selective serotonin reuptake inhibitors (SSRIs) are used to increase the amounts of serotonin in synapses.


Furthermore, problems with producing or using glutamate have been suggestively and tentatively linked to many mental disorders, including autism, obsessive compulsive disorder (OCD), schizophrenia, and depression.[57] Having too much glutamate has been linked to neurological diseases such as Parkinson's disease, multiple sclerosis, Alzheimer's disease, stroke, and ALS (amyotrophic lateral sclerosis).[58]

CAPON Binds Nitric Oxide Synthase, Regulating NMDA Receptor-Mediated Glutamate Neurotransmission

Neurotransmitter imbalance

Generally, there are no scientifically established "norms" for appropriate levels or "balances" of different neurotransmitters. It is in most cases pragmatically impossible to even measure levels of neurotransmitters in a brain or body at any distinct moments in time. Neurotransmitters regulate each other's release, and weak consistent imbalances in this mutual regulation were linked to temperament in healthy people .[59][60][61][62][63] Strong imbalances or disruptions to neurotransmitter systems have been associated with many diseases and mental disorders. These include Parkinson's, depression, insomnia, Attention Deficit Hyperactivity Disorder (ADHD), anxiety, memory loss, dramatic changes in weight and addictions. Chronic physical or emotional stress can be a contributor to neurotransmitter system changes. Genetics also plays a role in neurotransmitter activities. Apart from recreational use, medications that directly and indirectly interact one or more transmitter or its receptor are commonly prescribed for psychiatric and psychological issues. Notably, drugs interacting with serotonin and norepinephrine are prescribed to patients with problems such as depression and anxiety--though the notion that there is much solid medical evidence to support such interventions has been widely criticized.[64] Studies shown that dopamine imbalance has an influence on multiple sclerosis and other neurological disorders.[65]

Elimination of neurotransmitters

A neurotransmitter must be broken down once it reaches the post-synaptic cell to prevent further excitatory or inhibitory signal transduction. This allows new signals to be produced from the adjacent nerve cells. When the neurotransmitter has been secreted into the synaptic cleft, it binds to specific receptors on the postsynaptic cell, thereby generating a postsynaptic electrical signal. The transmitter must then be removed rapidly to enable the postsynaptic cell to engage in another cycle of neurotransmitter release, binding, and signal generation. Neurotransmitters are terminated in three different ways:

  1. Diffusion - the neurotransmitter detaches from receptor, drifting out of the synaptic cleft, here it becomes absorbed by glial cells.
  2. Enzyme degradation - special chemicals called enzymes break it down. Usually, astrocytes absorb the excess neurotransmitters and pass them on to enzymes or pump them directly into the presynaptic neuron.
  3. Reuptake - re-absorption of a neurotransmitter into the neuron. Transporters, or membrane transport proteins, pump neurotransmitters from the synaptic cleft back into axon terminals (the presynaptic neuron) where they are stored.[66]

For example, 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 from their targeted synaptic junctions and are eliminated from the body via the kidneys, or destroyed in the liver. Each neurotransmitter has very specific degradation pathways at regulatory points, which may be targeted by the body's regulatory system or by recreational drugs.

See also


  1. ^ In the central nervous system, anandamide other endocannabinoids utilize retrograde neurotransmission, since their release is postsynaptic, while their target receptor, cannabinoid receptor 1 (CB1), is presynaptic.[48] The cannabis plant contains ?9-tetrahydrocannabinol, which is a direct agonist at CB1.[48]
  1. ^ GABA is a non-proteinogenic amino acid


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