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È÷¾Ë·ç·Ð»ê / Hyaluronic Acid

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D-Glucuronic acid¿Í N-acetyl-D-glucosamineÀÇ °áÇÕÀÌ ¹Ýº¹µÈ ±¸Á¶ÀÌ´Ù.

Hyaluronic acid, also called hyaluronan, is an anionic, nonsulfated glycosaminoglycan distributed widely throughout connective, epithelial, and neural tissues. It is unique among glycosaminoglycans in that it is nonsulfated, forms in the plasma membrane instead of the Golgi apparatus, and can be very large:

The fourth class of GAG, hyaluronic acid, is not sulfated and is synthesized by three transmembrane synthase proteins HAS1, HAS2, and HAS3.

(Âü°í) https://en.wikipedia.org/wiki/Hyaluronic_acid
2 INCI Hyaluronic Acid
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4 µ¿ÀǾîhyaluronan
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Hyaluronic acid (HA) is a high molecular weight biopolysacharide, discovered in 1934, by Karl Meyer
and his assistant, John Palmer in the vitreous of bovine eyes. Hyaluronic acid is a naturally occurring biopolymer,
which has important biological functions in bacteria and higher animals including humans. It is found in most
connective tissues and is particularly concentrated in synovial fluid, the vitreous fluid of the eye, umbilical cords
and chicken combs. It is naturally synthesized by a class of integral membrane proteins called hyaluronan synthases,
and degraded by a family of enzymes called hyaluronidases.
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https://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.513.5936&rep=rep1&type=pdf
14 Àοë³í¹®1. Chen WYJ, Abatangelo G (1999). "Functions of hyaluronan in wound repair". Wound Repair Regen. 7 (2): 79–89. doi:10.1046/j.1524-475x.1999.00079.x. PMID 10231509. S2CID 2382548.

Raszeja- Kotelba B., Neumann E., Bowszyc J.: Kwas hialuronowy i skóra.
Polish Journal of Cosmetology 2002, 1, 21-25.

Jaszczuk A., Ostrowska J., Kleszczewska E.: Kwas hialuronowy- jego
w©©aściwości oraz wykorzystanie w kosmetyce i medycynie. Polish
Journal of Cosmetology 2009, 12(3), 185-189.

Jóźwiak- Bębenista M., Nowak J. Z.: Hialuronian: charakterystyka
i praktyczne zastosowanie w medycynie. Farmacja Polska 2010, 66(12),
882-893.

Pavicic T., Gauglitz G.G., Lersch P., Schwach-Abdellaoui K., Malle B.,
Korting H.C., Farwick M.: Efficacy of Cream-Based Novel Formulations of
Hyaluronic Acid of Different Molecular Weights in Anti-Wrinkle Treatment.
Journal of Drugs Dermatology 2011, 10(9), 990-1000.

* À̹ÌÁöÃâó : ÀÌÁî¾ØÆ®¸®, ´ÚÅÍ¿À¶óŬ


Skin healing
HA plays an important role in the normal epidermis. HA also has crucial functions in the reepithelization process due to several of its properties. These include being an integral part of the extracellular matrix of basal keratinocytes, which are major constituents of the epidermis; its free-radical scavenging function, and its role in keratinocyte proliferation and migration.[18]

In normal skin, HA is found in relatively high concentrations in the basal layer of the epidermis where proliferating keratinocytes are found.[24] CD44 is collocated with HA in the basal layer of epidermis where additionally it has been shown to be preferentially expressed on plasma membrane facing the HA-rich matrix pouches.[18][25] Maintaining the extracellular space and providing an open, as well as hydrated, structure for the passage of nutrients are the main functions of HA in epidermis. A report found HA content increases in the presence of retinoic acid (vitamin A).[24] The proposed effects of retinoic acid against skin photo-damage and photoaging may be correlated, at least in part, with an increase of skin HA content, giving rise to increased tissue hydration. It has been suggested that the free-radical scavenging property of HA contributes to protection against solar radiation, supporting the role of CD44 acting as a HA receptor in the epidermis.[18]

Epidermal HA also functions as a manipulator in the process of keratinocyte proliferation, which is essential in normal epidermal function, as well as during reepithelization in tissue repair. In the wound healing process, HA is expressed in the wound margin, in the connective tissue matrix, and collocating with CD44 expression in migrating keratinocytes.[18][26] Kaya et al. found suppression of CD44 expression by an epidermis-specific antisense transgene resulted in animals with defective HA accumulation in the superficial dermis, accompanied by distinct morphologic alterations of basal keratinocytes and defective keratinocyte proliferation in response to mitogen and growth factors. Decrease in skin elasticity, impaired local inflammatory response, and impaired tissue repair were also observed.[18] Their observations are strongly supportive of the important roles HA and CD44 have in skin physiology and tissue repair.[18]