Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Physical properties and structure  





2 Synthetic pathways  





3 Function  





4 Role in disease  





5 History  





6 References  














Neuromelanin






العربية
Català
Deutsch
Español
Français
Македонски
Português
Русский
 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


5,6-Dihydroxyindole, the monomer out of which neuromelanin polymers are formed

Neuromelanin (NM) is a dark pigment found in the brain which is structurally related to melanin. It is a polymerof5,6-dihydroxyindole monomers.[1] Neuromelanin is found in large quantities in catecholaminergic cells of the substantia nigra pars compacta and locus coeruleus, giving a dark color to the structures mostly found in Black or Brown pigmented skin.[2]

Physical properties and structure[edit]

Photomicrograph of neuromelanin (brown material) in a neuron of the substantia nigra. Hematoxylin and eosin stain. The scale bar is 20 microns (0.02mm) in length.

Neuromelanin gives specific brain sections, such as the substantia nigra or the locus coeruleus, distinct color. It is a type of melanin and similar to other forms of peripheral melanin. It is insoluble in organic compounds, and can be labeled by silver staining. It is called neuromelanin because of its function and the color change that appears in tissues containing it. It contains black/brown pigmented granules. Neuromelanin is found to accumulate during aging, noticeably after the first 2–3 years of life. It is believed to protect neurons in the substantia nigra from iron-induced oxidative stress. It is considered a true melanin due to its stable free radical structure and it avidly chelates metals.[3]

Synthetic pathways[edit]

Neuromelanin is directly biosynthesized from L-DOPA, precursor to dopamine, by tyrosine hydroxylase (TH) and aromatic acid decarboxylase (AADC). Alternatively, synaptic vesicles and endosomes accumulate cytosolic dopamine (via vesicular monoamine transporter 2 (VMAT2) and transport it to mitochondria where it is metabolized by monoamine oxidase. Excess dopamine and DOPA molecules are oxidized by iron catalysis into dopaquinones and semiquinones which are then phagocytosed and are stored as neuromelanin.[4]

Neuromelanin biosynthesis is driven by excess cytosolic catecholamines not accumulated by synaptic vesicles.[5]

Function[edit]

Neuromelanin is found in higher concentrations in humans than in other primates.[2] Neuromelanin concentration increases with age, suggesting a role in neuroprotection (neuromelanin can chelate metals and xenobiotics[6]) or senescence.[citation needed]

Role in disease[edit]

Neuromelanin-containing neurons in the substantia nigra degenerate during Parkinson's disease.[citation needed] Motor symptoms of Parkinson's disease are caused by cell death in the substantia nigra, which may be partly due to oxidative stress.[citation needed] This oxidation may be relieved by neuromelanin.[citation needed] Patients with Parkinson's disease had 50% the amount of neuromelanin in the substantia nigra as compared to similar patients of their same age, but without Parkinson's.[citation needed] The death of neuromelanin-containing neurons in the substantia nigra, pars compacta, and locus coeruleus have been linked to Parkinson's disease and also have been visualized in vivo with neuromelanin imaging.[7]

Neuromelanin has been shown to bind neurotoxic and toxic metals that could promote neurodegeneration.[5]

History[edit]

Dark pigments in the substantia nigra were first described in 1838 by Purkyně,[8] and the term neuromelanin was proposed in 1957 by Lillie,[9] though it has been thought to serve no function until recently. It is now believed to play a vital role in preventing cell death in certain parts of the brain. It has been linked to Parkinson's disease and because of this possible connection, neuromelanin has been heavily researched in the last decade.[10]

References[edit]

  1. ^ Charkoudian LK, Franz KJ (2006). "Fe(III)-coordination properties of neuromelanin components: 5,6-dihydroxyindole and 5,6-dihydroxyindole-2-carboxylic acid". Inorganic Chemistry. 45 (9): 3657–64. doi:10.1021/ic060014r. PMID 16634598.
  • ^ a b Fedorow, H; Tribl, F; Halliday, G; Gerlach, M; Riederer, P; Double, K. L. (2005). "Neuromelanin in human dopamine neurons: Comparison with peripheral melanins and relevance to Parkinson's disease". Progress in Neurobiology. 75 (2): 109–24. doi:10.1016/j.pneurobio.2005.02.001. PMID 15784302. S2CID 503902.
  • ^ "IBA in life sciences". Archived from the original on 2013-12-03. Retrieved 2013-11-30.
  • ^ Rabey, J.M.; Hefti, F. (1990). "Neuromelanin synthesis in rat and human substantia nigra". Journal of Neural Transmission. Parkinson's Disease and Dementia Section. 2 (1): 1–14. doi:10.1007/BF02251241. PMID 2357268. S2CID 6769760.
  • ^ a b Stepień, K; Dzierzega-Lecznar, A; Tam, I (2007). "The role of neuromelanin in Parkinson's disease--new concepts". Wiadomosci Lekarskie. 60 (11–12): 563–9. PMID 18540183.
  • ^ Tribl, F; Asan, E; Arzberger, T; Tatschner, T; Langenfeld, E; Meyer, H. E.; Bringmann, G; Riederer, P; Gerlach, M; Marcus, K (2009). "Identification of L-ferritin in neuromelanin granules of the human substantia nigra: A targeted proteomics approach". Molecular & Cellular Proteomics. 8 (8): 1832–8. doi:10.1074/mcp.M900006-MCP200. PMC 2722774. PMID 19318681.
  • ^ Sasaki M, Shibata E, Tohyama K, Takahashi J, Otsuka K, Tsuchiya K, Takahashi S, Ehara S, Terayama Y, Sakai A (July 2006). "Neuromelanin magnetic resonance imaging of locus ceruleus and substantia nigra in Parkinson's disease". NeuroReport. 17 (11): 1215–8. doi:10.1097/01.wnr.0000227984.84927.a7. PMID 16837857. S2CID 24597825.
  • ^ Usunoff, K. G.; Itzev, D. E.; Ovtscharoff, W. A.; Marani, E (2002). "Neuromelanin in the human brain: A review and atlas of pigmented cells in the substantia nigra". Archives of Physiology and Biochemistry. 110 (4): 257–369. doi:10.1076/apab.110.4.257.11827. PMID 12516659. S2CID 2735201.
  • ^ Lillie, R. D. (1957). "Metal reduction reactions of the melanins: Histochemical studies". Journal of Histochemistry and Cytochemistry. 5 (4): 325–33. doi:10.1177/5.4.325. PMID 13463306.
  • ^ Zecca, L; Tampellini, D; Gerlach, M; Riederer, P; Fariello, R. G.; Sulzer, D (2001). "Substantia nigra neuromelanin: Structure, synthesis, and molecular behaviour". Molecular Pathology. 54 (6): 414–8. PMC 1187132. PMID 11724917.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Neuromelanin&oldid=1229254375"

    Categories: 
    Biological pigments
    Neurochemistry
    Hidden categories: 
    Articles with short description
    Short description is different from Wikidata
    All articles with unsourced statements
    Articles with unsourced statements from August 2023
     



    This page was last edited on 15 June 2024, at 19:25 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki