Hairless 마우스에서 LED 광 조사의 피부주름 개선효과
Inhibitory Effect of LED Light Irradiation on the Wrinkle Formation in Hairless Mouse
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초록
To induce the skin aging in hairless mouse, UVB irradiation and squalene monohydroperoxide (Sq-OOH) were applied to the back region. Then, light emitting diode (LED) irradiation was applied to the same region 6 days a week for 4 weeks 2(wavelength: 635 nm, quantity of light=3.5 mW/cm , group E1: 30 minutes a day, group E2: 60 minutes a day). According to gross observation of wrinkle formation on skin tissues, experimental groups (E1 and E2) showed thinner ridge line, narrower ridge spacing, and shallower wrinkle formation than control (C group). In quantitative analysis, E1 and E2 groups showed a significant improvement in wrinkle parameters than C group. Positive control (PC group), E1, and E2 groups showed higher density of intradermal collagen fiber and higher regularity of its arrangement than C group. E1 and E2 groups showed lower degenerated elastic fiber than C group. On the other hand, PC, E1, and E2 groups showed significantly lower dermal xanthine oxidase (XO) activity than C group. And E1 and E2 groups showed higher dermal superoxide dismutase (SOD) activity than C and PC groups. In comparison with N group, E1 and E2 groups showed similar level of dermal catalase (CAT) activity and matrix metalloproteinase-3 (MMP-3) expression. Summing up, it is concluded that LED irradiation is effective in control or improving skin wrinkle formation by inhibiting generation of reactive oxygen species (ROS) and facilitating elimination of generated ROS. And E2 group is more effective than E1 group, which indicates that the effects of LED irradiation depend on irradiation time.
Abstract
To induce the skin aging in hairless mouse, UVB irradiation and squalene monohydroperoxide (Sq-OOH) were applied to the back region. Then, light emitting diode (LED) irradiation was applied to the same region 6 days a week for 4 weeks 2(wavelength: 635 nm, quantity of light=3.5 mW/cm , group E1: 30 minutes a day, group E2: 60 minutes a day). According to gross observation of wrinkle formation on skin tissues, experimental groups (E1 and E2) showed thinner ridge line, narrower ridge spacing, and shallower wrinkle formation than control (C group). In quantitative analysis, E1 and E2 groups showed a significant improvement in wrinkle parameters than C group. Positive control (PC group), E1, and E2 groups showed higher density of intradermal collagen fiber and higher regularity of its arrangement than C group. E1 and E2 groups showed lower degenerated elastic fiber than C group. On the other hand, PC, E1, and E2 groups showed significantly lower dermal xanthine oxidase (XO) activity than C group. And E1 and E2 groups showed higher dermal superoxide dismutase (SOD) activity than C and PC groups. In comparison with N group, E1 and E2 groups showed similar level of dermal catalase (CAT) activity and matrix metalloproteinase-3 (MMP-3) expression. Summing up, it is concluded that LED irradiation is effective in control or improving skin wrinkle formation by inhibiting generation of reactive oxygen species (ROS) and facilitating elimination of generated ROS. And E2 group is more effective than E1 group, which indicates that the effects of LED irradiation depend on irradiation time.
참고문헌 (29)
- 고미경, "사람 피부세포에서 UV-A에 의해 생성되는 활성산소와 MMP-1, -2, -3 발현에 대한 저출력 광조사의 영향", 석사, pp.2006
- 김혜영, "노화 치은섬유아세포에서 LED 광 조사의 효과", 석사, pp.2006
- 정 권, "사람 피부 섬유아세포에서 H2O2로 유도한 노화세포에 LED 조사가 미치는 영향", 석사, pp.2006
- 정진호, "피부는 왜 늙는가", 녹십자의보, 32(1), pp.23~27 (2004)
- 조규승, "사람 SH-SY5Y 신경아세포종에서 CoCl2에 의한 세포고사에 LED 조사의 영향", 박사, pp.2006
- Aebi H, "Catalase. In Methods of Enzymatic Analysis", pp.673~684 (1974), Academic Press
- Baez F, "The use of light-emitting diode therapy in the treatment of photoaged skin", Journal of Cosmetic Dermatology, 6(3), pp.189~196 (2007)
- Beauvoit B, "Correlation between the light scattering and the mitochondrial content of normal tissues and transplantable rodent tumors", Analytical Biochemistry, 226(1), pp.167~174 (1995)
- Brenneisen P, "Hydrogen peroxide increases the steady mRNA levels of collagenase", MMP-1 in human dermal fibroblasts, 1997, pp.22(3), 515~524
- Cadenas E, "Biochemistry of oxygen toxicity", Annual Review of Biochemistry, 58, pp.79~110 (1989)
- Cha SH, "Oxidation of skin tissue proteins by ultraviolet-B irradiation", Korean Journal of Gerontology, 1, pp.82~86 (1991)
- Chance B, "Time-resolved spectroscopy of hemoglobin and myoglobin in resting and ischemic muscle", Analytical Biochemistry, 174(2), pp.698~707 (1988)
- Chiba K, "Characteristics of skin wrinkling and dermal changes induced by repeated application of squalene monohydroperoxide to hairless mouse skin", Skin Pharmacology and Applied Skin Physiology, 16(4), pp.242~251 (2003)
- Chung JH, "The effects of sunlight on the skin of asians", Comprehensive Series in Photomedicines, 3, pp.69~90 (2001)
- Fisher GJ, "Mechanisms of photoaging and chronological skin aging", Archives of Dermatology, 138(11), pp.1462~1470 (2002)
- Fisher GJ, "Pathophysiology of premature skin aging induced by ultraviolet light", New England Journal of Medicine, 337(20), pp.1419~1428 (1997)
- Fuchs J, "Impairment of enzymic and nonenzymic antioxidants in skin by UVB irradiation", Journal of Investigative Dermatology, 93(6), pp.769~773 (1989)
- Hasegawa T, "Changes in lipid peroxide levels and activity of reactive oxygen scavenging enzymes in skin, serum and liver following UVB irradiation in mice", Life Sciences, 50(24), pp.1893~1903 (1992)
- Kligman LH, "The hairless mouse model for photoaging", Clinics in Dermatology, 14(2), pp.185~195 (1996)
- Lowry OH, "Protein measurement with the folin phenol reagent", Journal of Biological Chemistry, 193(1), pp.265~275 (1951)
- MacNaul KL, "Discoordinate expression of stromelysin, collagenase, and tissue inhibitor of metalloproteinases-1 in rheumatoid human synovial fibroblast. Synergistic effects of interleukin-1 and tumor necrosis factor-alpha on stromelysin expression", Journal of Biological Chemistry, 265(28), pp.17238~17245 (1990)
- Martin JP, "Negative and positive assays of superoxide dismutase based on hematoxylin autooxidation", Archives of Biochemistry and Biophysics, 225(2), pp.329~336 (1987)
- Miyachi Y, "Decreased skin superoxide dismutse activity by a single exposure of ultrviolet radiation is reduced by liposomal suporoxide dismutase pretreatment", Journal of Investigative Dermatology, 89, pp.111~112 (1987)
- Montagna W, "Histology of sun-damaged skin", Journal of the American Academy of Dermatology, 21(1), pp.907~918 (1989)
- Murphy G, "Matrix metalloproteinases in arthritic disease", Arthritis Research and Therapy, 4(3), pp.39~49 (2002)
- Nagase H, "Design and characterization of the fluorogenic substrate selectively hydrolyzed by stromelysin-1 (matrix meralloproteinase-3)", Journal of Biological Chemistry, 269(33), pp.20952~20957 (1994)
- Sternlicht M, "The stromal proteinase MMP3", stromelysin-1 promotes mammary carcinogenesis, 1999, pp.98(2), 137~146
- Stripe F, "The regulation of rat liver xanthine oxidase. conversion in vitro of the enzyme activity from dehydrogenase (type D) oxidase (type O)", Journal of Biological Chemistry, 244(14), pp.3855~3863 (1969)
- Wlaschek M, "Scharffetter-Kochanek K: Singlet oxygen may mediate the ultraviolet A-induced synthesis of interstitial collagenase", Journal of Investigative Dermatology, 104(2), pp.194~198 (1995)
