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5-ALA-纳米金光动力治疗小鼠光老化的初步研究 被引量:1

Experimental Research of the Treatment of Mouse Photaging by the ALA-gold Nanoparticles
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摘要 目的:初步探讨5-ALA-纳米金光动力治疗小鼠皮肤光老化的作用。方法:48只雄性健康ICR小鼠分为正常对照组(8只)、光老化组(40只),正常组不予特殊处理,光老化组照射紫外线,肉眼观察和HE染色验证光老化模型。40只光老化组小鼠分为B组光老化对照组,C组红光组、D组纳米金组、E组5-ALA组、F组5-ALA-纳米金组,C、D、E、F组小鼠背部分别涂抹不同溶液0.5ml(分别为生理盐水、纳米金溶液、5-ALA溶液和5-ALA-纳米金组溶液)避光封包3h,红光照射10min,2周治疗1次,共治疗2次,A组为正常组对照组不予任何处理。观察各组小鼠皮肤表现和组织病理改变。结果:与A组比较,紫外线照射后,B组小鼠皮肤皮肤增厚,出现皮屑、深皱纹、缺乏弹性等光老化特征;组织切片显示,B组小鼠表皮厚度[(168.235±13.665)μm]较A组[表皮(87.165±2.627)μm]增厚(P<0.05),而胶原纤维面积密度[(7.390±2.5)%]均较A组[(40.114±3.0)%]明显减少(P<0.05)。与B组相比,C、D、E和F组小鼠的表皮变薄[分别为(154.458±2.942)μm,(114.958±2.229)μm,(50.623±4.203)μm和(31.694±1.970)μm,P<0.05],胶原纤维面积密度增加[分别为(15.840±3.0)%,(27.320±2.5)%,(60.812±2.0)%和(70.024±3.0)%,P<0.05],其中以F组效果最显著。结论:5-ALA结合体能提高光动力疗法治疗小鼠光老化的疗效,同时纳米金的光热作用可能用于治疗光老化。 Objective To primarily discuss the effects of using 5-ALA- nanogold for the treatment of photoaged mice irradiated with 640nm red light. Methods 48 ICR male mice are randomly divided into normal control group (8 mice) and photoaging group (40 mice) with ultraviolet irradiation,then we verify the success of photoaging mice models utilizing HE staining and gross inspection.Second A total of 40 photoaging mice are equally devided in fve groups: photoaging control group(group B) receiving no treatment, red laser group (group C),nanogolds group (group D),5-ALA group (group E)and 5-ALA-nanogold group(group F).The dorsal skin of group C,D,E and F’ mice are applied 0.5ml different kinds of solutions (respectively normal saline, nanogald, 5-ALA and 5-ALA-nanogold), then receiving red light irradiation for 10min after covering with plastic mulch for 3 hours, and received a second treatment after two weeks. The normal control group without treatment is named as group A. The dorsal skin of each group mice are analysed by clinical manifestations and histopathologic changes. Results Compared with group A, the mice skin of group B shows the photoaging charactristics such as thickened and hardened skin, loss of resilience, deep winkles and dandruffs affter irradiation from UV. HE staining show the epidermis thickness of group B[(168.235±13.665)μm] is significantly thickener than group A[(87.165±2.627)μm] (P〈0.05), and the collagen fiber area density of group B [(7.390±2.5)%] is signifcantly reduction than group A [(40.114±3.0)%] (P〈0.05). The epidermis thickness of group C, D, E, F are respectively thinner than group B[respectivly (154.458±2.942)μm,(114.958±2.229)μm,(50.623±4.203)μm and (31.694±1.970)μm,P〈0.05] and the collagen fber area density of group C, D, E, F are signifcantly on the increase [respectively (15.840±3.0)%, (27.320±2.5)%, (60.812±2.0)% and (70.024±3.0)%, P〈0.05] than group B, of which the most signifcant effect is group F. Conclusion 5-ALA and nanogold can cooperativly effect photodynamic therapy for photoaging mice skin and the photothermal effect of nanogold may be able to treat skin photoaging.
作者 葛芹 刘亚乐 李张军 刘彦婷 耿松梅 姚翠萍 张镇西 曾维惠 GE Qin;LIU Ya-le;LI Zhang-jun;LIU Yan-ting;GENG Song-mei;YAO Cui-ping;ZHANG Zhen-xi;ZENG Wei-hui(Department of Dermatology,the Second Affliated Hospital of Xi'an Jiaotong University,Xi'an 710004,Shaanxi,China;Department of Dermatology,Jingmen First People's Hospital,Jingmen 448000,Hubei,China;School of Life Science and Technology,Xi'an Jiaotong University,Xi'an 710004,Shaanxi,China)
出处 《中国美容医学》 CAS 2018年第11期137-141,共5页 Chinese Journal of Aesthetic Medicine
基金 陕西省自然科学基础研究计划(2016JM8114) 高等学校博士学科点专项科研基金(20130201110068) 西安交通大学学科综合交叉项目(xjj20100201)
关键词 皮肤 光老化 光动力 纳米金 5-氨基乙酰丙酸 HE染色 胶原纤维 小鼠 skin photoaging photodynamic therapy nanogold 5-ALA HE staining collagen fbers mice
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  • 1王宏伟,王秀丽,过明霞,虞叶风.5-氨基酮戊酸乳膏光动力疗法治疗皮肤癌前病变和皮肤原位癌[J].中华皮肤科杂志,2006,39(3):137-139. 被引量:49
  • 2Rabe JH,Mamelak A J,McElguun PJ,etal.Photoaging:mechanisms and repair.J Am Acad Dermatol,2006,55(1):1-19.
  • 3Wang XL,Wang HW,Huang Z,et al.Study of protoporphyrin Ⅸ (PpⅨ) pharmacokineticsafter topical application of 5-aminolevulinic acid in urethral condylomataacuminata.Photochem Photobiol,2007,83(5):1069-1073.
  • 4Ruiz-Rodríguez R,Sanz-Sánchez T,Códoba S.Photodynamicphotorejuvenation.Dermatol Surg,2002,28(8):742-744.
  • 5Chen Z,Seo JY,Kim YK,et al.Heat modulation of tropoelastin,fibrillin-1,and matrixmetalloproteinase-12 in human skin in vivo.J Invest Dermatol,2005,124(1):70-78.
  • 6Goldberg DJ.Lasers for facial rejuvenation.Am J Clin Dermatol,2003,4(4):225-234.
  • 7Bjerring P.Photorejuvenation-an overview.Med Laser Appl,2004,19(4):186-195.
  • 8Marmur ES,Phelps R,Goldberg DJ.Ultrastructural changes seen after ALA-IPLphotorejuvenation:a pilot study.J Cosmet Laser Ther,2005,7(1):21-24.
  • 9Zane C,Capezzera R,Sala R,et al.Clinical and echographic analysis of photodynamictherapy using methylaminolevulinate as sensitizer in the treatment of photoclamaged facialskin.Lasers Surg Med,2007,39(3):203-209.
  • 10Jayasree RS,Gupta AK,Rathinam K,et al.The influence of photodynamic therapy on thewound healing process in rats.J Biomater Appl,2001,15(3):176-186.

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