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      프락셔널 레이저(Er:glass) 조사한 무모생쥐에서 교원질의 합성 및 TGF-β1의 발현 = Collagen Synthesis and Expression of TGF-β1 in Er:glass Fractional Laser Treated Hairless Mice프락셔널 레이저(Er:glass) 조사한 무모생쥐에서 교원질의 합성 및 TGF-β1의 발현

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      https://www.riss.kr/link?id=A77009297

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      다국어 초록 (Multilingual Abstract)

      Background: Non-ablative dermal remodeling and ablative skin resurfacing are currently well-established skin treatment modalities. Fractional laser was recently introduced as a new concept for laser skin rejuvenation, and is characterized by creation of a dense pattern of epidermal and dermal microthermal treatment zones (MTZs). However, the precise mechanisms of dermal remodeling by Er:glass fractional laser treatment are largely unknown. Objective: The purpose of this study was to investigate the effect of 1,550 nm Er:glass fractional laser treatment on dermal collagen synthesis and expression of TGF-β1, a potent cytokine involved in collagen synthesis. Methods: We treated hairless mice with several power densities (5 W 5 mJ∼20 W 20 mJ), and examined the tissue samples on days 1, 30, and 90 after treatment. We analyzed the penetrating depth of laser treatment by determining dermal response through assessment of type I collagen synthesis and TGF-β1 expression by H&E, Masson-trichrome staining, western blot analysis and immunohistochemistry staining. Results: We observed, through H&E staining, that increasing the pulse energy of fractional laser treatment correlated with increasing depth of MTZ. Also, fractional laser treatment increased type 1 collagen synthesis on days 30 and 90, energy dependently. Immunohistochemical study showed that fractional laser treatment increased expression of type I collagen and TGF-β1, energy dependently, with TGF-β1 expression peaking on day 1. In addition, according to western blot analysis, expressions of TGF-β1 and type I collagen were up-regulated in an energy-dependent manner. Conclusion: Er:glass fractional laser induced dermal remodeling by up-regulation of TGF-β1 and type I collagen synthesis, and may be a promising modality for skin rejuvenation. (Korean J Dermatol 2010;48(2):79∼86)
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      Background: Non-ablative dermal remodeling and ablative skin resurfacing are currently well-established skin treatment modalities. Fractional laser was recently introduced as a new concept for laser skin rejuvenation, and is characterized by creation ...

      Background: Non-ablative dermal remodeling and ablative skin resurfacing are currently well-established skin treatment modalities. Fractional laser was recently introduced as a new concept for laser skin rejuvenation, and is characterized by creation of a dense pattern of epidermal and dermal microthermal treatment zones (MTZs). However, the precise mechanisms of dermal remodeling by Er:glass fractional laser treatment are largely unknown. Objective: The purpose of this study was to investigate the effect of 1,550 nm Er:glass fractional laser treatment on dermal collagen synthesis and expression of TGF-β1, a potent cytokine involved in collagen synthesis. Methods: We treated hairless mice with several power densities (5 W 5 mJ∼20 W 20 mJ), and examined the tissue samples on days 1, 30, and 90 after treatment. We analyzed the penetrating depth of laser treatment by determining dermal response through assessment of type I collagen synthesis and TGF-β1 expression by H&E, Masson-trichrome staining, western blot analysis and immunohistochemistry staining. Results: We observed, through H&E staining, that increasing the pulse energy of fractional laser treatment correlated with increasing depth of MTZ. Also, fractional laser treatment increased type 1 collagen synthesis on days 30 and 90, energy dependently. Immunohistochemical study showed that fractional laser treatment increased expression of type I collagen and TGF-β1, energy dependently, with TGF-β1 expression peaking on day 1. In addition, according to western blot analysis, expressions of TGF-β1 and type I collagen were up-regulated in an energy-dependent manner. Conclusion: Er:glass fractional laser induced dermal remodeling by up-regulation of TGF-β1 and type I collagen synthesis, and may be a promising modality for skin rejuvenation. (Korean J Dermatol 2010;48(2):79∼86)

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      참고문헌 (Reference)

      1 Fonder MA, "Treating the chronic wound:a practical approach th the care of nonhealing wounds and wound care dressings" 58 : 185-206, 2008

      2 Kinbara T, "Transforming growth factor-β isoforms differently simulate Proα2(I)collagen gene expression during wound healing process in transgenic mice" 190 : 375-381, 2002

      3 Manolis EN, "Tissue concentration of transforming growth factor beta1 and basic fibroblast growth factor in skin wounds created with a CO2 laser and scalpel" 15 : 252-257, 2007

      4 Alexiades-Armenakas MR, "The spectrum of laser skin resurfacing:nonablative,fractional,and ablative laser resurfacing" 58 : 719-737, 2008

      5 Laubach HJ, "Skin responses to fractional photothermolysis" 38 : 142-149, 2006

      6 Lee KS, "Regulation of the collagen gene expression" 33 : 1005-1013, 1995

      7 Lupton JR, "Nonablatvie laser skin resurfacing using a 1540 nm erbium glass laser:a clinical and histologic analysis" 28 : 833-835, 2002

      8 Ross EV, "Nonablative skin remodeling:selective dermal heating with a mid-infrared laser and contact cooling combination" 26 : 186-195, 2000

      9 Hantash BM, "In vivo histological evaluation of a novel ablative fractional resurfacing device" 39 : 96-107, 2007

      10 Lessa S, "Histologic stydy of the structural changes in fine paplebral skin following selective photothermolysis with CO2 laser" 33 : 66-71, 2009

      1 Fonder MA, "Treating the chronic wound:a practical approach th the care of nonhealing wounds and wound care dressings" 58 : 185-206, 2008

      2 Kinbara T, "Transforming growth factor-β isoforms differently simulate Proα2(I)collagen gene expression during wound healing process in transgenic mice" 190 : 375-381, 2002

      3 Manolis EN, "Tissue concentration of transforming growth factor beta1 and basic fibroblast growth factor in skin wounds created with a CO2 laser and scalpel" 15 : 252-257, 2007

      4 Alexiades-Armenakas MR, "The spectrum of laser skin resurfacing:nonablative,fractional,and ablative laser resurfacing" 58 : 719-737, 2008

      5 Laubach HJ, "Skin responses to fractional photothermolysis" 38 : 142-149, 2006

      6 Lee KS, "Regulation of the collagen gene expression" 33 : 1005-1013, 1995

      7 Lupton JR, "Nonablatvie laser skin resurfacing using a 1540 nm erbium glass laser:a clinical and histologic analysis" 28 : 833-835, 2002

      8 Ross EV, "Nonablative skin remodeling:selective dermal heating with a mid-infrared laser and contact cooling combination" 26 : 186-195, 2000

      9 Hantash BM, "In vivo histological evaluation of a novel ablative fractional resurfacing device" 39 : 96-107, 2007

      10 Lessa S, "Histologic stydy of the structural changes in fine paplebral skin following selective photothermolysis with CO2 laser" 33 : 66-71, 2009

      11 Yang L, "Healing of burn wounds in transgenic mice overexpressing transforming growth factor-1 in the epidermis" 159 : 2147-2157, 2001

      12 Wanner M, "Fractional photothermolysis:treatment of facial and nonfacial cutaneous photodamage with a 1550-nm erbium-doped fiber laser" 33 : 23-28, 2007

      13 Cohen SR, "Fractional photothermolysis for skin rejuvenation" 124 : 281-290, 2009

      14 Manstein D, "Fractional photodermolysis:a new concept for cutaneous remodeling using microscopid patterns of thermal injury" 34 : 426-438, 2004

      15 Orringer JS, "Connective tissue remodeling induced by carbon dioxide laser resurfacing of photodamaged human skin" 140 : 1326-1332, 2004

      16 Timonthy K, "Collagen thermal damage and collagen synthesis after cutaneous laser resurfacing" 23 : 66-71, 1998

      17 Riggs K, "Ablative laser resurfacing:high-energy pulsed carbon dioxide and erbium:yttrium-aluminum-garnet" 25 : 462-473, 2007

      18 Berlin AL, "A prospective study of fractional scanned nonsequential carbon dioxide laser resurfacing:a clinical and histopathologic evaluation" 35 : 222-228, 2009

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      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-06-29 학술지명변경 외국어명 : 미등록 -> Korean Journal of Dermatology KCI등재
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      2002-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2000-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.11 0.11 0.13
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.13 0.14 0.254 0.01
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