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glutathione

 Glutathione molecule

Glutathione is a ubiquitous compound found in our bodies. Aside from its many ascribed biologic functions, it has also been implicated in skin lightening. Glutathione induced inhibition of tyrosinase glycosylation, blocks the maturation and transfer of tyrosinase from GERL (Golgi-endoplasmic reticulum-lysosome)-coated vesicles to the pre-melanosome. Other mechanisms of action proposed for glutathione include :

  • Direct inactivation of the enzyme tyrosinase by binding and chelating copper within the enzyme’s active site
  • Mediating the switch mechanism from eumelanogenesis to phaeomelanogenesis, as glutathione participates in the conversion of dopaquinone to pheomelanin. The observed differences in the glutathione and glutathione-related enzyme content between black and yellow (or red) skin provide evidence that the increase of glutathione-reductase activity in the environment of the melanocytes may stimulate the pigment cells to produce phaeomelanin instead of eumelanin pigment. As expected, the lowest levels of reduced glutathione (GSH) were found associated with eumelanin type pigmentation, whereas the highest ones were found in the skin with phaeomelanin producing melanocytes;
  • Quenching of free radicals and peroxides that contribute to tyrosinase activation and melanin formation;
  • Modulation of depigmenting abilities of melanocytotoxic agents.
  • Research results also indicate that glutathione inhibits the synthesis and agglutination of melanin by interrupting the function of L-DOPA. The balance between CysH and GSH, which is partly determined by the rate of utilization of CysH for GSH biosynthesis, regulates not only the levels of 5-S-CD and DOPA but also the melanogenic activity of pigment cells. Since DOPA functions as a cofactor in the monophenolase reaction of tyrosinase, it is proposed that the ratio of 5-S-CD to DOPA may be an important factor in the regulation of tyrosinase activity in situ.

These concepts supported by the various experimental evidence presented form basis for future research in the use of glutathione in the treatment of pigmentary disorders.

 

 


 
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TYROSINASE INHIBITORS
Polyphenols
Benzaldehyde and Benzoate Derivatives
Gallic Acid and Derivatives
Long-Chain Lipids and Steroids

INHIBITORS OF MELANOSOMAL TRANSFER
Centaureidin and Methylophiopogonanone B
Niacinamide
PAR-2 Inhibitors
Lectins and Neoglycoproteins

ANTIOXIDANTS
Glutathione
Vitamin C
Alpha Tocopherol and Alpha Tocopherol Ferulate

ACCELERATORS OF EPIDERMAL TURNOVER AND DESQUAMATORS
α-Hydroxyacids
Salicylic Acid
Linoleic Acid
Retinoids

TRANSCRIPTIONAL REGULATION OF MELANOGENIC ENZYMES
The MAPK Pathway
MC1R
cAMP Pathway and MITF

UV ABSORVERS (SUN SCREEN)

a-MSH BLOCKERS

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