期刊文献+

光动力疗法抑制兔耳增生性瘢痕形成的实验研究

The experiment study of photodynamic therapy in the inhibition of hypertrophic scars formation in rabbit ears
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摘要 目的:探讨光动力疗法(PDT)对兔耳增生性瘢痕(HS)的治疗作用及其机制。方法:构建兔耳HS模型,将模型分为高浓度光敏剂、低浓度光敏剂、无光敏剂、阴性对照、正常对照5组,观察了PDT对其外观的影响,通过Masson染色观察对HS病理形态的影响,同时通过RT-PCR和ELISA法观察了各组样本MMP-2、MMP-3、MMP-9和TIMP-1蛋白的表达以及!-gal浓度改变。结果:PDT可通过诱导MMPs/TIMPs比例上调,引起成纤维细胞老化,促进胶原蛋白和ECM降解,从而抑制HS的形成,效果持久达60d,适当高浓度的光敏剂疗效更佳。结论:PDT可通过诱导成纤维细胞老化抑制HS的形成,PDT或许成为将来治疗病理性瘢痕的一种理想手段。 Objective: This study sought to investigate the effect of photodynamic on the rabbit ear HS model and its specific mechanism of action. Methods: We constructed the rabbit ear HS model and divided them into 5 groups as high concentration aminolevulinic acid (ALA), low concentration ALA, without ALA, negative and normal control. Then observed the appearance of rabbit ear HS model, investigated its pathological morphology by Masson stain. Furthermore, the mRNA levels of MMP-2, -3, -9, and TIMP-1 in HS tissue were investigated by RT-PCR, and the β-gal concentration were detected by ELISA to confirm the cell senescence. Results: Our data indicated that by increasing the ratio of MMP to TIMP, PDT could accelerate the aging of fibroblasted and promote the degradation of collagen and the extraeellular matrix, thereby inhibiting HS formation with an effect that lasted up to 60 days. The efficacy of the treatment could be maximized by applying an appropriately high concentration of ALA. Conclusions: PDT can induce fibroblasts senescence and might become an ideal treatment for pathological scar.
出处 《陕西医学杂志》 CAS 2013年第7期774-776,共3页 Shaanxi Medical Journal
基金 国家自然科学基金项目(30901298)
关键词 瘢痕 病理生理学 增生 @光动力疗法 基质金属蛋白酶 金属蛋白酶类 组织抑制剂 耳兔 Cicatrix/physiopathology Hyperplasia @Photodynamic therapy Matrix metalloproteinase Tissue inhibitor of metalloproteinase Ear Rabbits
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参考文献11

  • 1吴红娟,刘晓梅,朱秀梅.烧伤后瘢痕畸形病人的社会支持状况分析[J].陕西医学杂志,2009,38(6):760-761. 被引量:4
  • 2Nicholas RS, Falvey H, Lemonas P, et al. Patient-relat- ed keloid scar assessment and outcome measures [J]. Plast Reconstr Surg, 2012, 129(3): 648-656. 被引量:1
  • 3Lee Y, Baron ED. Photodynamic therapy: current evi- dence and applications in dermatology[J]. Semin Cutan Med Surg, 2011, 30(4): 199-209. 被引量:1
  • 4Kloeters O, Tandara A, Mustoe TA. Hypertrophic scar model in the rabbit ear: a reproducible model for studying scar tissue behavior with new observations on silicone gel sheeting for scar reduction[J]. Wound Repair Regen, 2007, 15 Suppl 1:S40-5. 被引量:1
  • 5Blazic TM, Brajac I. Defective induction of senescence during wound healing is a possible mechanism of keloid formation[J]. Med Hypotheses, 2006, 66(3): 649-652. 被引量:1
  • 6Wang Q, Peng Z, Xiao S, et al. RNAi-mediated inhibi- tion of COL1A1 and COL3A1 in human skin fibroblasts [J]. ExpDermatol, 2007, 16(7): 611-617. 被引量:1
  • 7Ulrich D, Ulrich F, Unglaub F, et al. Matrix metallo proteinases and tissue inhibitors of metalloproteinases in patients with different types of scars and keloids[J]. J Plast Reconstr Aesthet Surg, 2010, 63(6) : 1015-1021. 被引量:1
  • 8Yeh FL, Shen HD, Tai HY. Decreased production of MCP-1 and MMP-2 by keloid-derived fibroblasts [J]. Burns, 2009, 35(3): 348-351. 被引量:1
  • 9Quan T, Qin Z, Xia W, etal. Matrix-degrading metallo- proteinases in photoaging[J]. J Investig Dermatol Symp Proc, 2009, 14(1): 20-24. 被引量:1
  • 10李伟,方婷,于叔麒,杨谦,王倩,陈岩,郭生龙.基质金属蛋白酶及其抑制剂与脑出血预后的关系[J].陕西医学杂志,2012,41(4):401-404. 被引量:3

二级参考文献21

  • 1Steiner T,Bosel J.Options to restrict hematoma expan-sion after spontaneous intracerebral hemorrhage[J].Stroke,2010,41(2):402-409. 被引量:1
  • 2Leira R,Davalos A,Silva Y,et al.Early neurologic de-terioration in intracerebral hemorrhage:predictors and as-sociated factors[J].Neurology,2004,63(3):461-467. 被引量:1
  • 3Manso H,Krug T,Sobral J,et al.Variants of the Ma-trix Metalloproteinase-2but not the Matrix Metalloprotei-nase-9genes significantly influence functional outcome af-ter stroke[J].BMC Medical Genetics,2010,11(1):40. 被引量:1
  • 4Castellanos M,Leira R,Serena J,et al.Plasma metalo-porteinase-9concenrtration predicts hemorrhagic transfor-mation in acute ischemic storke[J].Storke,2003,34(1):40-46. 被引量:1
  • 5Abilleira S,Montaner J,Molina CA,et al.Matrix met-alloproteinase-9concentration after spontaneous intracere-bral hemorrhage[J].J Neurosurg,2003,99(1):65–70. 被引量:1
  • 6Khotari RU,Brott T,Broderick JP,et al.The ABCs of measuring intracerebral hemorrhage volume[J].Stroke,1996,27(8):1304–1305. 被引量:1
  • 7Sansing LH,Kaznatcheeva EA,Perkins CJ,et al.Ede-ma after intracerebral hemorrhage:correlations with co-agulation parameters and treatment[J].J Neurosurg,2003,98(5):985–992. 被引量:1
  • 8Rosell A,Ortega-Aznar A,Alvarez-Sabin J,et al.In-creased brain expression of matrix metalloproteinase-9af-ter ischemic and hemorrhagic human stroke[J].Stroke,2006,37(6):1399–1406. 被引量:1
  • 9Lee JM,Yin KJ,Hsin I,et al.Matrix metalloproteinase-9and spontaneous hemorrhage in an animal model of cerebral amyloid angiopathy[J].Ann Neurol,2003,54(3):379–382. 被引量:1
  • 10Horstmann S,Kalb P,Koziol J,et al.Profiles of ma-trix metalloproteinases,their inhibitors,and laminin in stroke patients:influence of different therapies[J].Stroke,2003,34(9):2165-2170. 被引量:1

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