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Monoamine neurotransmitter

From Wikipedia, the free encyclopedia

Dopamine
Norepinephrine
Serotonin

Monoamine neurotransmitters are neurotransmitters and neuromodulators that contain one amino group connected to an aromatic ring by a two-carbon chain (such as -CH2-CH2-). Examples are dopamine, norepinephrine and serotonin.

All monoamines are derived from aromatic amino acids like phenylalanine, tyrosine, and tryptophan by the action of aromatic amino acid decarboxylase enzymes. They are deactivated in the body by the enzymes known as monoamine oxidases which clip off the amine group.

Monoaminergic systems, i.e., the networks of neurons that use monoamine neurotransmitters, are involved in the regulation of processes such as emotion, arousal, and certain types of memory. It has also been found that monoamine neurotransmitters play an important role in the secretion and production of neurotrophin-3 by astrocytes, a chemical which maintains neuron integrity and provides neurons with trophic support.[1]

Drugs used to increase or reduce the effect of monoamine neurotransmitters are used to treat patients with psychiatric and neurological disorders, including depression, anxiety, schizophrenia and Parkinson's disease.[2]

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  • Types of neurotransmitters | Nervous system physiology | NCLEX-RN | Khan Academy
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Transcription

Voiceover: In this video I want to talk about the different types of neurotransmitters. Neurotransmitters are molecules that communicate information between neurons and their target cells and chemical synapses. There may be hundreds of different types of neurotransmitters and they can be categorized in a number of different ways, but probably the most common as to divide them up by their molecular structure into amino acids, peptides, monoamines and others. I'm gonna mention a bunch of chemistry terms next. Don't worry about them if you don't know them but if you are interested there are many great videos on these topics on the Khan Academy. The first category of neurotransmitters I'm gonna represent with these three neurotransmitters right here and this category is the amino acids. Amino acid neurotransmitters. Amino acids. That's these three right here. Amino acids have an amino group, this guy right here and they have a carboxylic acid group. This part right here. There are lots of different types of amino acids but just a few of them function as neurotransmitters in the nervous system. The next category of neurotransmitters I'm gonna represent with this one right here and these are the peptides. Peptide neurotransmitters and I'll just have this one representative here. Peptides are actually polymers or chains of amino acids. A bunch of these amino acids get strung together in these chains, these polymers and we call them peptides. Peptides are much larger molecules than all the other types of neurotransmitters. Sometimes people divide up neurotransmitters just into peptides and they lump together all the other neurotransmitters and call them small molecule neurotransmitters. The neurotransmitters in this row will represent our next big category which are the monomines. Monoamine neurotransmitters, monoamines. That's this whole row. I've picked out five representative neurotransmitters for the monoamines. These are also sometimes called biogenic amines. Either monoamines or biogenic amines. The monoamines are organic molecules with an amino group here and here and here, here and here connected to an aromatic group here, here, here, here and here. The amino group and aromatic group are connected by a two carbon chain, this part here and here and here, here and here. Some of the monoamines, these three. Draw little stars next to these three, are also called by a different name and that name, and let me draw a little star. That name is the catecholamines. Catecholamines. Catecholamines are a subgroup of the monoamines and the catecholamines have a catachol group which is this part right here which has a benzine, this ring and two hydroxyl groups. Here's one hydroxyl group and here's another hydroxyl group. This catechol group, all the catecholamines have this group these three right here. There are many other types of neurotransmitters that are not amino acids or monoamines or peptides and this neurotransmitter right here is gonna be the representative for that. I'll just call this category other. These are the other molecular types of neurotransmitters. Now I'm gonna introduce some important neurotransmitters in these different groups and I'm gonna mention some of their functions. Don't worry too much about their functions right now because they do so many different things in different parts of the nervous system that we'll come back to all of that in other videos. I just want to briefly introduce the different important neurotransmitters in each of these classes. Starting with the amino acids. Important amino acid neurotransmitters are this one which is called glutamate. Glutamate. This one which is called gamma-aminobutryic acid which pretty much everybody just shortens to GABA. G-A-B-A for gamma-aminobutryic acid. This one which is glycine. Glycine. Glutamate is the most common excitatory neurotransmitter of the nervous system. Let me just draw a big plus sign above glutamate here because most of the time in the nervous system when a neuron is releasing a neurotransmitter that it's exciting its target cell most of the time that neurotransmitter is glutamate because it usually causes depolarization of target cells so that it excites them. GABA and glycine are the most common inhibitory neurotransmitters of the nervous system. Let me just write some big minus signs above GABA and glycine because they usually cause hyper polarization of target cells and inhibit those target cells. GABA is the most common inhibitory neurotransmitter in the brain while glycine is the most common inhibitory neurotransmitter in the spinal cord, so that the amino acid neurotransmitters are really involved in most functions of the nervous system. Pretty much if you think of anything the nervous system is doing at some point in the chains and networks of neurons glutamate, GABA and/or glycine are probably involved in moving information through those networks. There are many important monoamine neurotransmitters but I'm just gonna mention these five that are arguably the most important. The first one here is serotonin. Serotonin. The next one here is histamine. Histamine. The next one is called dopamine. Dopamine. Then this one is epinephrine. Epinephrine. Right next to epinephrine is its close cousin norepinephrine. Norepinephrine. All five of these are monoamine neurotransmitters but these three dopamine, epinephrine and norepinephrine are also called catecholamines. The monoamines play a lot of different functions in the nervous system and in particular a lot of functions of the brain including big things like consciousness, inattention and cognition or thinking, and emotions or us having feelings. Norepinephrine is also released by some autonomic neurons in the peripheral nervous system. Many disorders of the nervous system involve abnormalities of these monoamine neurotransmitters systems, and many drugs that people commonly take affect the monoamine neurotransmitters. There are many important peptide neurotransmitters including a group of peptide neurotransmitters called the opioids. Opioids. The opioids are a group within the bigger group of the peptide neurotransmitters. This one is one example of an opioid. This is endorphin. Endorphin. The peptide neurotransmitters play a role in many functions of the nervous system but the opioids in particular play a big role in our perception of pain. A number of pain medications affect the opioid neurotransmitters. Last but definitely not least are the other neurotransmitters. Usually when there's an other category of anything that means it's not very important but in the case of neurotransmitters there are some really important neurotransmitters that are not amino acids, monoamines or peptides. For example, this neurotransmitter right here is called acetylcholine. Acetylcholine. Acetylcholine is definitely one of our most important neurotransmitters. It does a number of functions in the central nervous system, and then in the peripheral nervous system it's released by most neurons in the autonomic nervous system. Let me just right ANS for autonomic nervous system and it's released by neurons called motor neurons that synapse on skeletal muscle and tell our skeletal muscle to contract to make us move. Again, don't worry too much about these functions because in other videos we'll go more into the structure and the function of the nervous system and talk about specific neurotransmitter pathways. I just wanted to introduce the different types of neurotransmitters here and start to give you a feel for the huge variety of functions all these different neurotransmitters have in the nervous system.

Examples

Biosynthetic pathways for catecholamines and trace amines in the human brain[3][4][5]
The image above contains clickable links
Phenethylaminergic trace amines and the catecholamines are derivatives of L-phenylalanine.
Classical monoamines
Trace amines

Specific transporter proteins called monoamine transporters that transport monoamines in or out of a cell exist. These are the dopamine transporter (DAT), serotonin transporter (SERT), and the norepinephrine transporter (NET) in the outer cell membrane and the vesicular monoamine transporter (VMAT1 and VMAT2) in the membrane of intracellular vesicles.[citation needed]

After release into the synaptic cleft, monoamine neurotransmitter action is ended by reuptake into the presynaptic terminal. There, they can be repackaged into synaptic vesicles or degraded by the enzyme monoamine oxidase (MAO), which is a target of monoamine oxidase inhibitors, a class of antidepressants.[citation needed]

Evolution

A phylogenetic tree showing how a number of monoamine receptors are related to each other.

Monoamine neurotransmitter systems occur in virtually all vertebrates, where the evolvability of these systems has served to promote the adaptability of vertebrate species to different environments.[12][13]

A recent computational investigation of genetic origins shows that the earliest development of monoamines occurred 650 million years ago and that the appearance of these chemicals, necessary for active or participatory awareness and engagement with the environment, coincides with the emergence of bilaterian or “mirror” body in the midst of (or perhaps in some sense catalytic of?) the Cambrian Explosion.[14]

See also

References

  1. ^ Mele T, Čarman-Kržan M, Jurič DM (2010). "Regulatory role of monoamine neurotransmitters in astrocytic NT-3 synthesis". International Journal of Developmental Neuroscience. 28 (1): 13–9. doi:10.1016/j.ijdevneu.2009.10.003. PMID 19854260. S2CID 25734591.
  2. ^ Kurian MA, Gissen P, Smith M, Heales SJ, Clayton PT (2011). "The monoamine neurotransmitter disorders: An expanding range of neurological syndromes". The Lancet Neurology. 10 (8): 721–33. doi:10.1016/S1474-4422(11)70141-7. PMID 21777827. S2CID 32271477.
  3. ^ Broadley KJ (March 2010). "The vascular effects of trace amines and amphetamines". Pharmacology & Therapeutics. 125 (3): 363–375. doi:10.1016/j.pharmthera.2009.11.005. PMID 19948186.
  4. ^ Lindemann L, Hoener MC (May 2005). "A renaissance in trace amines inspired by a novel GPCR family". Trends in Pharmacological Sciences. 26 (5): 274–281. doi:10.1016/j.tips.2005.03.007. PMID 15860375.
  5. ^ Wang X, Li J, Dong G, Yue J (February 2014). "The endogenous substrates of brain CYP2D". European Journal of Pharmacology. 724: 211–218. doi:10.1016/j.ejphar.2013.12.025. PMID 24374199.
  6. ^ Romero-Calderón R, Uhlenbrock G, Borycz J, Simon AF, Grygoruk A, Yee SK, Shyer A, Ackerson LC, Maidment NT, Meinertzhagen IA, Hovemann BT, Krantz DE (November 2008). "A glial variant of the vesicular monoamine transporter is required to store histamine in the Drosophila visual system". PLOS Genet. 4 (11): e1000245. doi:10.1371/journal.pgen.1000245. PMC 2570955. PMID 18989452. Unlike other monoamine neurotransmitters, the mechanism by which the brain's histamine content is regulated remains unclear. In mammals, vesicular monoamine transporters (VMATs) are expressed exclusively in neurons and mediate the storage of histamine and other monoamines.
  7. ^ a b c d e f g Broadley KJ (March 2010). "The vascular effects of trace amines and amphetamines". Pharmacol. Ther. 125 (3): 363–375. doi:10.1016/j.pharmthera.2009.11.005. PMID 19948186. Trace amines are metabolized in the mammalian body via monoamine oxidase (MAO; EC 1.4.3.4) (Berry, 2004) (Fig. 2) ... It deaminates primary and secondary amines that are free in the neuronal cytoplasm but not those bound in storage vesicles of the sympathetic neurone ... Similarly, β-PEA would not be deaminated in the gut as it is a selective substrate for MAO-B which is not found in the gut ...
    Brain levels of endogenous trace amines are several hundred-fold below those for the classical neurotransmitters noradrenaline, dopamine and serotonin but their rates of synthesis are equivalent to those of noradrenaline and dopamine and they have a very rapid turnover rate (Berry, 2004). Endogenous extracellular tissue levels of trace amines measured in the brain are in the low nanomolar range. These low concentrations arise because of their very short half-life ...
  8. ^ a b Miller GM (January 2011). "The emerging role of trace amine-associated receptor 1 in the functional regulation of monoamine transporters and dopaminergic activity". J. Neurochem. 116 (2): 164–176. doi:10.1111/j.1471-4159.2010.07109.x. PMC 3005101. PMID 21073468.
  9. ^ a b c d e f g h i j k Khan MZ, Nawaz W (October 2016). "The emerging roles of human trace amines and human trace amine-associated receptors (hTAARs) in central nervous system". Biomed. Pharmacother. 83: 439–449. doi:10.1016/j.biopha.2016.07.002. PMID 27424325.
  10. ^ a b c d e Lindemann L, Hoener MC (May 2005). "A renaissance in trace amines inspired by a novel GPCR family". Trends Pharmacol. Sci. 26 (5): 274–281. doi:10.1016/j.tips.2005.03.007. PMID 15860375. In addition to the main metabolic pathway, TAs can also be converted by nonspecific N-methyltransferase (NMT) [22] and phenylethanolamine N-methyltransferase (PNMT) [23] to the corresponding secondary amines (e.g. synephrine [14], N-methylphenylethylamine and N-methyltyramine [15]), which display similar activities on TAAR1 (TA1) as their primary amine precursors...Both dopamine and 3-methoxytyramine, which do not undergo further N-methylation, are partial agonists of TAAR1 (TA1). ...
    The dysregulation of TA levels has been linked to several diseases, which highlights the corresponding members of the TAAR family as potential targets for drug development. In this article, we focus on the relevance of TAs and their receptors to nervous system-related disorders, namely schizophrenia and depression; however, TAs have also been linked to other diseases such as migraine, attention deficit hyperactivity disorder, substance abuse and eating disorders [7,8,36]. Clinical studies report increased β-PEA plasma levels in patients suffering from acute schizophrenia [37] and elevated urinary excretion of β-PEA in paranoid schizophrenics [38], which supports a role of TAs in schizophrenia. As a result of these studies, β-PEA has been referred to as the body's 'endogenous amphetamine' [39]
  11. ^ Wainscott DB, Little SP, Yin T, Tu Y, Rocco VP, He JX, Nelson DL (January 2007). "Pharmacologic characterization of the cloned human trace amine-associated receptor1 (TAAR1) and evidence for species differences with the rat TAAR1". The Journal of Pharmacology and Experimental Therapeutics. 320 (1): 475–85. doi:10.1124/jpet.106.112532. PMID 17038507. S2CID 10829497.
  12. ^ Callier S, Snapyan M, Le Crom S, Prou D, Vincent JD, Vernier P (2003). "Evolution and cell biology of dopamine receptors in vertebrates". Biology of the Cell. 95 (7): 489–502. doi:10.1016/s0248-4900(03)00089-3. PMID 14597267. S2CID 18277786. This "evolvability" of dopamine systems has been instrumental to adapt the vertebrate species to nearly all the possible environments.
  13. ^ Vincent JD, Cardinaud B, Vernier P (1998). "[Evolution of monoamine receptors and the origin of motivational and emotional systems in vertebrates]". Bulletin de l'Académie Nationale de Médecine (in French). 182 (7): 1505–14, discussion 1515–6. PMID 9916344. These data suggest that a D1/beta receptor gene duplication was required to elaborate novel catecholamine psychomotor adaptive responses and that a noradrenergic system specifically emerged at the origin of vertebrate evolution.
  14. ^ Goulty M, Botton-Amiot G, Rosato E, Sprecher SG, Feuda R (2023-06-06). "The monoaminergic system is a bilaterian innovation". Nature Communications. 14 (1): 3284. Bibcode:2023NatCo..14.3284G. doi:10.1038/s41467-023-39030-2. ISSN 2041-1723. PMC 10244343. PMID 37280201.

External links

This page was last edited on 11 March 2024, at 21:17
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