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  • Melanophore stimulating hormone  (1)
  • melanogenesis  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 104 (1970), S. 282-294 
    ISSN: 1432-0878
    Keywords: Pigment cells ; Melanophore stimulating hormone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The skin of the lizard, Anolis carolinensis, changes rapidly from bright green to a dark brown color in response to melanophore stimulating hormone (MSH). Chromatophores responsible for color changes of the skin are xanthophores which lie just beneath the basal lamina containing pterinosomes and carotenoid vesicles. Iridophores lying immediately below the xanthophores contain regularly arranged rows of reflecting platelets. Melanophores containing melanosomes are present immediately below the iridophores. The ultrastructural features of these chromatophores and their pigmentary organelles are described. The color of Anolis skin is determined by the position of the melanosomes within the melanophores which is regulated by MSH and other hormones such as norepinephrine. Skins are green when melanosomes are located in a perinuclear position within melanophores. In response to MSH, they migrate into the terminal processes of the melanophores which overlie the xanthophores above, thus effectively preventing light penetration to the iridophores below, resulting in skins becoming brown. The structural and functional characteristics of Anolis chromatophores are compared to the dermal chromatophore unit of the frog.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-904X
    Keywords: Melanotan-I ; poly (D,L-Lactide-co-glycolide) ; pharmacologic response ; controlled-release ; melanogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. The objective of this study was to evaluate in vitro and invivo the melanogenic activity of one-month duration Melanotan-I(MT-I) implants prepared using poly (D,L lactide-co-glycolide) polymer. Methods. The biological activity of the samples of MT-I released invitro from the non-irradiated or gamma irradiated implants wasmeasured using a frog skin bioassay. The effect of MT-I on skinpigmentation was measured using a Chroma meter (reflectometer) aftersubcutaneous administration of implants containing 4 mg MT-I toguinea pigs. Eumelanin, the black/brown melanin pigment, wasquantified in skin biopsies as pyrrole-2, 3, 5-tricarboxylic acid using HPLC. Results. The MT-I released in vitro from implants after 24 hoursexhibited 100% melanotropic activity in frog skins compared to an identicalconcentration of a freshly prepared MT-I standard. The reflectancereadings demonstrated a prolonged skin darkening for up to threemonths as evidenced by the decrease in the luminance values from 0to −4.82. A 2.5-fold increase in eumelanin levels was observed afterone month and the increased pigmentation lasted for 3 months. Conclusions. The melanogenic response to MT-I implants persisted forthree months and the increase in pigmentation, especially the increasedeumelanin levels, could provide protection from ultraviolet radiation.
    Type of Medium: Electronic Resource
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