N-Acetylserotonin

N-Acetylserotonin
Names
IUPAC name
N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]acetamide
Other names
N-acetyl-5-hydroxytryptamine, N-acetyl-5-HT
Identifiers
1210-83-9 N
ChEBI CHEBI:17697 YesY
ChEMBL ChEMBL33103 YesY
ChemSpider 879 YesY
5451
Jmol 3D model Interactive image
MeSH N-Acetylserotonin N-Acetylserotonin
PubChem 903
Properties
C12H14N2O2
Molar mass 218.252 g/mol
Density 1.268 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

N-Acetylserotonin (NAS), also known as normelatonin, is a naturally occurring chemical intermediate in the endogenous production of melatonin from serotonin.[1][2] It is produced from serotonin by the enzyme aralkylamine N-acetyltransferase (AANAT) and is converted to melatonin by acetylserotonin O-methyltransferase (ASMT). Like melatonin, NAS is an agonist at the melatonin receptors MT1, MT2, and MT3, and may be considered to be a neurotransmitter.[3][4][5][6] In addition, NAS is distributed in some areas of the brain where serotonin and melatonin are not, suggesting that it may have unique central duties of its own instead of merely functioning as a precursor in the synthesis of melatonin.[3] NAS is able to penetrate the blood–brain barrier, unlike serotonin.[7] NAS is known to have anti-depressant, neurotrophic and cognition-enhancing effects [8][9] and has been proposed to be a target for the treatment of aging-associated cognitive decline and depression [9]

NAS may play a role in the antidepressant effects of selective serotonin reuptake inhibitors (SSRIs) and monoamine oxidase inhibitors (MAOIs).[3] The SSRI fluoxetine and the MAO-A inhibitor clorgyline upregulate AANAT indirectly through serotonergic mechanisms and thereby increase NAS levels after chronic administration, and this correlates with the onset of their antidepressant effects.[3][10] Furthermore, light exposure inhibits the synthesis of NAS and reduces the antidepressant effects of MAOIs.[3] In addition, AANAT knockout mice display significantly greater immobility times versus control mice in animal models of depression.[3] These data support a potential role for NAS in mood regulation and in antidepressant-induced therapeutic benefits.

Through a currently unidentified mechanism, NAS may be the cause of the orthostatic hypotension seen with clinical treatment of MAOIs.[10][11] It reduces blood pressure in rodents, and pinealectomy (the pineal gland being a major site of NAS and melatonin synthesis) abolishes the hypotensive effects of clorgyline.[10][11] Why orthostatic hypotension is commonly seen with MAOIs but not SSRIs (both of which increase NAS levels) however, is unknown.

The TrkB receptor

NAS has been shown to act as a potent TrkB receptor agonist, while serotonin and melatonin do not.[3] Subchronic and chronic administration of NAS to adult mice induces proliferation of neural progenitor cells (NPC)s, blockage of TrkB abolished this effect suggesting that it is TrkB-dependent.[12] NAS was also found to significantly enhance NPC proliferation in sleep-deprived mice.[12] It is thought that the anti-depressant and neurotrophic effects of NAS are in part due to its role as a TrkB agonist.[8]

Antioxidant properties

NAS acts as a potent anti-oxidant, NAS effectiveness as an anti-oxidant has been found to be different depending on the experimental model used, it has been described as being between 5 to 20 times more effect than melatonin at protecting against oxidant damage.[13] NAS has been shown to protect against lipid peroxidation in microsomes and mitochondria.[14] NAS has also been reported to lower resting levels of ROS in peripheral blood lymphocytes and to exhibit anti-oxidant effects against t-butylated hydroperoxide- and diamide-induced ROS.[15] NAS has also been observed to inhibit nitric oxide synthase.[16]

Anti-inflammatory effects

NAS has been reported to have anti-inflammatory effects. NAS has been shown to inhibit LPS-stimulated production of the proinflammatory cytokine TNF-alpha in differentiated THP-1-derived human monocytes.[17]

See also

References

  1. ↑ AXELROD J, WEISSBACH H (April 1960). "Enzymatic O-methylation of N-acetylserotonin to melatonin". Science 131 (3409): 1312. doi:10.1126/science.131.3409.1312. PMID 13795316.
  2. ↑ WEISSBACH H, REDFIELD BG, AXELROD J (September 1960). "Biosynthesis of melatonin: enzymic conversion of serotonin to N-acetylserotonin". Biochimica et Biophysica Acta 43: 352–3. doi:10.1016/0006-3002(60)90453-4. PMID 13784117.
  3. 1 2 3 4 5 6 7 Jang SW, Liu X, Pradoldej S, et al. (February 2010). "N-acetylserotonin activates TrkB receptor in a circadian rhythm". Proceedings of the National Academy of Sciences of the United States of America 107 (8): 3876–81. doi:10.1073/pnas.0912531107. PMC: 2840510. PMID 20133677.
  4. ↑ Zhao H, Poon AM, Pang SF (March 2000). "Pharmacological characterization, molecular subtyping, and autoradiographic localization of putative melatonin receptors in uterine endometrium of estrous rats". Life Sciences 66 (17): 1581–91. doi:10.1016/S0024-3205(00)00478-1. PMID 11261588.
  5. ↑ Nonno R, Pannacci M, Lucini V, Angeloni D, Fraschini F, Stankov BM (July 1999). "Ligand efficacy and potency at recombinant human MT2 melatonin receptors: evidence for agonist activity of some mt1-antagonists". British Journal of Pharmacology 127 (5): 1288–94. doi:10.1038/sj.bjp.0702658. PMC: 1566130. PMID 10455277.
  6. ↑ Paul P, Lahaye C, Delagrange P, Nicolas JP, Canet E, Boutin JA (July 1999). "Characterization of 2-[125I]iodomelatonin binding sites in Syrian hamster peripheral organs". The Journal of Pharmacology and Experimental Therapeutics 290 (1): 334–40. PMID 10381796.
  7. ↑ http://www.drugbank.ca/drugs/DB04275
  8. 1 2 Tosini G., Ye K. & Iuvone PM. (2012) neuroprotection, neurogenesis, and the sleepy brain. Neuroscientist, 18(6):645-53.
  9. 1 2 Oxenkrug G. & Ratner R. (2012) N-acetylserotonin and aging-associated cognitive impairment and depression. Aging Dis., 3(4):330-8.
  10. 1 2 3 Oxenkrug GF (1999). "Antidepressive and antihypertensive effects of MAO-A inhibition: role of N-acetylserotonin. A review". Neurobiology (Budapest, Hungary) 7 (2): 213–24. PMID 10591054.
  11. 1 2 Oxenkrug GF (1997). "[N-acetylserotonin and hypotensive effect of MAO-A inhibitors]". Voprosy Meditsinskoi Khimii (in Russian) 43 (6): 522–6. PMID 9503569.
  12. 1 2 Sompol P., Liu X., Baba K., Paul KN., Tosini G., Iuvone PM., Ye K. (2011). "N-acetylserotonin promotes hippocampal neuroprogenitor cell proliferation in sleep-deprived mice". Proc. Natl. Acad. Sci. U.S.A 108 (21): 8844–9. doi:10.1073/pnas.1105114108.
  13. ↑ Oxenkrug G (2005). "Antioxidant effects of N-acetylserotonin: possible mechanisms and clinical implications". Ann. N. Y. Acad. Sci. 1053: 334–47. doi:10.1111/j.1749-6632.2005.tb00042.x.
  14. ↑ Gavazza MB., Català A. (2004). "Protective effect of N-acetyl-serotonin on the nonenzymatic lipid peroxidation in rat testicular microsomes and mitochondria". J. Pineal Res. 37 (3): 153–60. doi:10.1111/j.1600-079x.2004.00150.x.
  15. ↑ Wölfler A., Abuja PM., Schauenstein K., Liebmann PM. (1999). "N-acetylserotonin is a better extra- and intracellular antioxidant than melatonin". FEBS Lett 449 (2-3): 206–10. doi:10.1016/s0014-5793(99)00435-4.
  16. ↑ Peter Klemm, Markus Hecker, Hannelore Stockhausen, Chin Chen Wu & Christoph Thiemermann (Aug 1995). "Inhibition by N-acetyl-5-hydroxytryptamine of nitric oxide synthase expression in cultured cells and in the anaesthetized rat.". Br J Pharmacol 115 (7): 1175–1181. doi:10.1111/j.1476-5381.1995.tb15021.x. PMID 7582541.
  17. ↑ Perianayagam MC., Oxenkrug GF., Jaber BL. (2005). "Immune-modulating effects of melatonin, N-acetylserotonin, and N-acetyldopamine". Ann. N. Y. Acad. Sci. 1053: 386–93. doi:10.1111/j.1749-6632.2005.tb00046.x.
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