Post by melaninman on Mar 27, 2008 15:34:25 GMT -5
The Many Benefits of Melanin Print E-mail
Tuesday, 08 January 2008
It has also been shown that Caucasians have higher concentrations of a more deleterious form of melanin known as “Pheomelanin.” The type of melanin that causes blonde and red hair actually increases the risk for cell death. Melanin filters out UV radiation, but it also increases UV harmful effects and causes cell death, particularly when the melanin is the kind found in light hair or skin (Brash et al., 2004).The resulting sunlight sensitivity of individuals with any particular melanin type would reflect the balance between protection and damage, with pheomelanin contributing 3-fold greater damage than eumelanin and perhaps less efficient protection (ibid). In this scenario, when a pheomelanin-containing individual visits the beach, his melanosomes act as microscopic x-ray sources to generate superoxide and OH_ radicals. Pheomelanin also produces almost five times as much superoxide as eumelanin after UV exposure (Persad et al, 1983).
Blonde Hair & Blue Eyes, bad for you??
By Bernie Douglas (January 8, 2008)
Although it is well known that Caucasians suffer from higher rates of skin cancer than do those with more skin pigment -- for example, In the U.S., rates of basal and squamous cell carcinomas are 50 times higher in Caucasians than in African Americans and African Americans have a 13-fold lower incidence of melanoma than do Caucasians (Tadokoro et al, 2003) – many are unaware of skin pigment’s (melanin) other beneficial properties. For example, calcium regulation in melanocytes (cells that produce pigment) affects numerous biological pathways including protecting the redox (oxidation and reduction) balance in the cell (William, 2007). Melanin has also been implicated in maintaining calcium homeostasis (mechanism by which the body maintains adequate calcium levels), acts as a free radical scavenger (Norris et al, 2005), and is known to be involved with calcium ion regulation in the inner ear (William, 2007).
Recent research has shown that four genes involved in skin pigmentation show clear evidence of selection in Europeans (OCA2, MYO5A, DTNBP1, TYRP1). All four genes are associated with Mendelian disorders that cause lighter pigmentation or albinism, and all are in different genomic locations, indicating the action of separate selective events (Voight et al, 2006). One of these genes, “OCA2”, is associated with the third longest haplotype on a high frequency SNP anywhere in the genome for Europeans. A fifth gene, “SLC24A5”, has recently been shown by another group to impact skin pigmentation and to have a derived, selected allele near fixation in Europeans (Lamason et al., 2005).
It has also been shown that Caucasians have higher concentrations of a more deleterious form of melanin known as “Pheomelanin.” The type of melanin that causes blonde and red hair actually increases the risk for cell death. Melanin filters out UV radiation, but it also increases UV harmful effects and causes cell death, particularly when the melanin is the kind found in light hair or skin (Brash et al., 2004). The resulting sunlight sensitivity of individuals with any particular melanin type would reflect the balance between protection and damage, with pheomelanin contributing 3-fold greater damage than eumelanin and perhaps less efficient protection (ibid). In this scenario, when a pheomelanin-containing individual visits the beach, his melanosomes act as microscopic x-ray sources to generate superoxide and OH_ radicals. Pheomelanin also produces almost five times as much superoxide as eumelanin after UV exposure (Persad et al, 1983).
Melanin is also said to play an important role in vision. James Norris Jr., Professor in Chemistry, and retina surgeon Kourous Rezaei, Director of the Vitreoretinal Service in Ophthalmology & Visual Science, combined resources to show that melanin, a pigment found throughout the human body, acts like a neutralizing sponge inside cells in the retina to soak up and destroy reactive oxygen species. Reactive oxygen species, or free radicals, which are energized by light, are thought to play a major role in “macular degeneration”, the leading cause of blindness in people over the age of 60. The disorder is far more prevalent among whites than among African-Americans. It causes gradual loss of central vision by damaging the RPE (retinal pigment epithelial) cells that lie underneath the macula, the small region of the retina responsible for fine detail at the center of the field of vision (See, Norris et al, 2005).
Dark eyes, “in general”, are known to absorb UV better than blue or green (common among Europeans). Melanin provides protection to the lens of the eye from UV damage- decreasing the risks of cataracts. It also provides near optimum protection to the retina and reduces the risk of macular degeneration, as mentioned above. Glare is reduced in dark eyes; and, thus, vision is enhanced.
TADOKORO et al. (2003) for the first time reported the effects of melanin on UV responses in different racial/ethnic groups. DNA damage in all subjects was greatest immediately after UV exposure and was gradually repaired thereafter. Rates and efficiencies of removal of DNA lesions differed dramatically between subjects in all groupings, but DNA damage was most severe in the light skin. The overall finding was that melanin affords significant protection against DNA damage in underlying skin cells, a concept previously supported by tissue culture and organ model systems. They also found that Melanin can absorb UV efficiently at most wavelengths; an important consideration was whether the protective benefits of melanin derive solely from its function as an optical filter.
References
Brash D.E., Takeuchi S., Zhang W., Wakamatsu K, Ito S., Hearing V.J. Kraemer K.H., (2004).
Melanin acts as a potent UVB photosensitizer to cause an atypical mode of cell death in murine skin. PNAS October 19, 2004 vol. 101 no. 42.
Lamason RL, Mohideen M, Mest JR, Wong AC, Norton HL, et al. (2005) SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science 310:1782–1786.
Norris J. R. , Brandon-Luke L. Seagle, Kourous A. Rezai, Yasuhiro Kobori, Elzbieta M. Gasyna, and Kasra A. Rezaei (2005) Melanin photoprotection in the human retinal pigment epithelium and its correlation with light-induced cell apoptosis. PNAS June 21, 2005 vol. 102 no. 25.
Persad, S., Menon, I. A. & Haberman, H. F. (1983) Photochem. Photobiol. 37, 63–68.
TADOKORO T., KOBAYASHI N., ZMUDZKA B.Z., ITO S., WAKAMATSU K., YAMAGUCHI Y., KOROSSY
K. S., MILLER S. A., BEER J.Z., AND HEARING V. J.(2003). UV-induced DNA damage and melanin content in human skin differing in racial/ethnic origin. The FASEB Journal Vol. 17 June 2003 pages 1177-1179.
Voight BF, Kudaravalli S, Wen X, Pritchard JK (2006) A map of recent positive selection in the human genome. PLoS Biol 4(3): e72.
William B. (2007). Quantification of Ca2+ binding to melanin supports the hypothesis that melanosomes serve a functional role in regulating calcium homeostasis. Pigment Cell Research. 20(2):134-139, April 2007.
Tuesday, 08 January 2008
It has also been shown that Caucasians have higher concentrations of a more deleterious form of melanin known as “Pheomelanin.” The type of melanin that causes blonde and red hair actually increases the risk for cell death. Melanin filters out UV radiation, but it also increases UV harmful effects and causes cell death, particularly when the melanin is the kind found in light hair or skin (Brash et al., 2004).The resulting sunlight sensitivity of individuals with any particular melanin type would reflect the balance between protection and damage, with pheomelanin contributing 3-fold greater damage than eumelanin and perhaps less efficient protection (ibid). In this scenario, when a pheomelanin-containing individual visits the beach, his melanosomes act as microscopic x-ray sources to generate superoxide and OH_ radicals. Pheomelanin also produces almost five times as much superoxide as eumelanin after UV exposure (Persad et al, 1983).
Blonde Hair & Blue Eyes, bad for you??
By Bernie Douglas (January 8, 2008)
Although it is well known that Caucasians suffer from higher rates of skin cancer than do those with more skin pigment -- for example, In the U.S., rates of basal and squamous cell carcinomas are 50 times higher in Caucasians than in African Americans and African Americans have a 13-fold lower incidence of melanoma than do Caucasians (Tadokoro et al, 2003) – many are unaware of skin pigment’s (melanin) other beneficial properties. For example, calcium regulation in melanocytes (cells that produce pigment) affects numerous biological pathways including protecting the redox (oxidation and reduction) balance in the cell (William, 2007). Melanin has also been implicated in maintaining calcium homeostasis (mechanism by which the body maintains adequate calcium levels), acts as a free radical scavenger (Norris et al, 2005), and is known to be involved with calcium ion regulation in the inner ear (William, 2007).
Recent research has shown that four genes involved in skin pigmentation show clear evidence of selection in Europeans (OCA2, MYO5A, DTNBP1, TYRP1). All four genes are associated with Mendelian disorders that cause lighter pigmentation or albinism, and all are in different genomic locations, indicating the action of separate selective events (Voight et al, 2006). One of these genes, “OCA2”, is associated with the third longest haplotype on a high frequency SNP anywhere in the genome for Europeans. A fifth gene, “SLC24A5”, has recently been shown by another group to impact skin pigmentation and to have a derived, selected allele near fixation in Europeans (Lamason et al., 2005).
It has also been shown that Caucasians have higher concentrations of a more deleterious form of melanin known as “Pheomelanin.” The type of melanin that causes blonde and red hair actually increases the risk for cell death. Melanin filters out UV radiation, but it also increases UV harmful effects and causes cell death, particularly when the melanin is the kind found in light hair or skin (Brash et al., 2004). The resulting sunlight sensitivity of individuals with any particular melanin type would reflect the balance between protection and damage, with pheomelanin contributing 3-fold greater damage than eumelanin and perhaps less efficient protection (ibid). In this scenario, when a pheomelanin-containing individual visits the beach, his melanosomes act as microscopic x-ray sources to generate superoxide and OH_ radicals. Pheomelanin also produces almost five times as much superoxide as eumelanin after UV exposure (Persad et al, 1983).
Melanin is also said to play an important role in vision. James Norris Jr., Professor in Chemistry, and retina surgeon Kourous Rezaei, Director of the Vitreoretinal Service in Ophthalmology & Visual Science, combined resources to show that melanin, a pigment found throughout the human body, acts like a neutralizing sponge inside cells in the retina to soak up and destroy reactive oxygen species. Reactive oxygen species, or free radicals, which are energized by light, are thought to play a major role in “macular degeneration”, the leading cause of blindness in people over the age of 60. The disorder is far more prevalent among whites than among African-Americans. It causes gradual loss of central vision by damaging the RPE (retinal pigment epithelial) cells that lie underneath the macula, the small region of the retina responsible for fine detail at the center of the field of vision (See, Norris et al, 2005).
Dark eyes, “in general”, are known to absorb UV better than blue or green (common among Europeans). Melanin provides protection to the lens of the eye from UV damage- decreasing the risks of cataracts. It also provides near optimum protection to the retina and reduces the risk of macular degeneration, as mentioned above. Glare is reduced in dark eyes; and, thus, vision is enhanced.
TADOKORO et al. (2003) for the first time reported the effects of melanin on UV responses in different racial/ethnic groups. DNA damage in all subjects was greatest immediately after UV exposure and was gradually repaired thereafter. Rates and efficiencies of removal of DNA lesions differed dramatically between subjects in all groupings, but DNA damage was most severe in the light skin. The overall finding was that melanin affords significant protection against DNA damage in underlying skin cells, a concept previously supported by tissue culture and organ model systems. They also found that Melanin can absorb UV efficiently at most wavelengths; an important consideration was whether the protective benefits of melanin derive solely from its function as an optical filter.
References
Brash D.E., Takeuchi S., Zhang W., Wakamatsu K, Ito S., Hearing V.J. Kraemer K.H., (2004).
Melanin acts as a potent UVB photosensitizer to cause an atypical mode of cell death in murine skin. PNAS October 19, 2004 vol. 101 no. 42.
Lamason RL, Mohideen M, Mest JR, Wong AC, Norton HL, et al. (2005) SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science 310:1782–1786.
Norris J. R. , Brandon-Luke L. Seagle, Kourous A. Rezai, Yasuhiro Kobori, Elzbieta M. Gasyna, and Kasra A. Rezaei (2005) Melanin photoprotection in the human retinal pigment epithelium and its correlation with light-induced cell apoptosis. PNAS June 21, 2005 vol. 102 no. 25.
Persad, S., Menon, I. A. & Haberman, H. F. (1983) Photochem. Photobiol. 37, 63–68.
TADOKORO T., KOBAYASHI N., ZMUDZKA B.Z., ITO S., WAKAMATSU K., YAMAGUCHI Y., KOROSSY
K. S., MILLER S. A., BEER J.Z., AND HEARING V. J.(2003). UV-induced DNA damage and melanin content in human skin differing in racial/ethnic origin. The FASEB Journal Vol. 17 June 2003 pages 1177-1179.
Voight BF, Kudaravalli S, Wen X, Pritchard JK (2006) A map of recent positive selection in the human genome. PLoS Biol 4(3): e72.
William B. (2007). Quantification of Ca2+ binding to melanin supports the hypothesis that melanosomes serve a functional role in regulating calcium homeostasis. Pigment Cell Research. 20(2):134-139, April 2007.