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艾拉光动力治疗对兔耳增生性瘢痕组织中MMP-2、MMP-9、MMP-13及TIMP-1的mRNA水平的影响 被引量:3

The effects of ALA-PDT on the expression of mRNA of MMP-9,MMP-13 and TIMP-1 of hypertrophic scar model in rabbit ears
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摘要 目的:研究艾拉光动力治疗对兔耳增生性瘢痕中基质金属蛋白酶-2信使核糖核酸(MMP-2mRNA)、基质金属蛋白酶-9信使核糖核酸(MMP-9mRNA)、基质金属蛋白酶-13信使核糖核酸(MMP-13mRNA)和基质金属蛋白酶组织抑制剂-1信使核糖核酸(TIMP-1mRNA)的变化,探讨艾拉光动力治疗对兔耳增生性瘢痕的初步治疗机制。方法:将实验动物分为正常组、阴性对照组、高浓度艾拉光动力治疗组、低浓度艾拉光动力治疗组、光动力治疗组,对高浓度艾拉光动力治疗组、低浓度艾拉光动力治疗组、光动力治疗组分别进行干预治疗,1次/周,共3次,于治疗后1月、2月和3月采集样本,进行RT-PCR实验。结果:治疗组中MMP-2、MMP-9、MMP-13的mRNA表达水平在艾拉光动力治疗后1月、2月和3月的增生性瘢痕表达要明显高于阴性对照组,差异具有显著性(P?0.01),而治疗组中TIMP-1的mRNA表达水平要明显低于阴性对照组,差异具有显著性(P?0.01);高浓度治疗组与低浓度治疗组之间比较有差异(P?0.05)。结论:艾拉光动力治疗可改变兔耳增生性瘢痕中的MMP-2mRNA、MMP-9mRNA、MMP-13mRNA和TIMP-1mRNA的表达,使MMPs/TIMP-1之间的比例上调。 Objective: To investigate the effects of ALA-PDT treatment on the expression of mRNA of MMP-2, MMP-9, MMP-13 and TIMP-1 of hypertrophic scar model of rabbits' ears, and analysis the treatment mechanism of ALA-PDT treatment to HS of rabbit ears. Methods: We divided the test animals into normal control, negative control, high concentration ALA-PDT, low concentration ALA-PDT and PDT groups. The latter three groups received PDT treatment once a week for 3 weeks. The specimens were collected respectively 1, 2 and 3 months after PDT to used for RT-PCR test. Results: 1, 2 and 3 months after PDT, the mRNA of MMP-2 MMP-9 and MMP-13 level in HS tissue of three treatment groups were significantly higher than those in the negative group (P〈0.01), and the mRNA of TIMP-1 level of three treatment groups were significantly lower than those in the negative group (P〈0.01). There were also significant difference between high concentration group and low concen- tration group (P〈0.05). Conclusion: ALA-PDT treatment can change the expression of the mRNA of MMP-2, MMP-9, MMP-13 and TIMP-1 of the tissues of hypertrophic scar of rabbits' ears, resulting in the proportion be- tween the MMPs/TIMP-1 be up-regulated.
出处 《陕西医学杂志》 CAS 2013年第8期939-942,共4页 Shaanxi Medical Journal
基金 国家自然科学基金资助项目(30901298)
关键词 瘢痕 增生 基质金属蛋白酶 核糖核酸 动物 实验 Cicatrix Hyperplasia metalloproteinases Ribonucleic acid Animals,laboratoryRabbits
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  • 1牛扶幼,牛永敢,陈言汤.兔耳增生性瘢痕模型的建立[J].中国医学工程,2004,12(5):12-14. 被引量:15
  • 2滕雯,郝立君,任丽虹,肖志波,王敏,李芍华.595nm Vbeam激光对兔耳增生性瘢痕成纤维细胞增殖的影响[J].中国临床康复,2006,10(24):120-123. 被引量:7
  • 3郭丽丽,陈言汤,牛扶幼,刘林嶓.病理性瘢痕组织中基质金属蛋白酶-1、金属蛋白酶组织抑制剂-1、血小板源性生长因子、增殖细胞核抗原的表达[J].郑州大学学报(医学版),2006,41(6):1027-1030. 被引量:4
  • 4Akasaka Y,Ito K,Fujita K,et al.Aetivated easpase expression and apoptosis increase in keloids:eytoehrom~ c release and easpase-9 activation during the apoptosis of keliod fibroblast lines [J].Wound Repair Regen,2005,13:373-382.
  • 5Huang Z,Chen Q,Luek D,et al.Studies of a vascular acting photo2 Sensitizer,Pd-bacteriopheophorbide (Tookad),in normal canine prostate and spontaneous canine prostate cancer[J].Lasers Surg Med,2005,36 (5):390-397.
  • 6Reid RR,Mogford JE,Butt R,et al.Inhibition of proeollagen C2 proteinase reduces scar hypertrophy in a rabbit model of cutaneous searring[J].Wound Repair Regen,2006,14:138-141.
  • 7[1]Robb EC, Waymack JP, Warden GD, et al. A new modal for studying the development of human hypertrophic burn scar formation[J]. J Burn Care Rehabil, 1987, 8: 371.
  • 8[2]Morris DE, WU L, ZHAO LL, et al. Acute and chronic animal models for excessive dermal scarring: quantitaative studies [J].Plast Reconstr Surg, 1997, 100: 674-681.
  • 9[3]Marcenac N. Cheloides cicatricielles du cheval[J]. Recueil. Med.Veterinaire, 1951, 127: 385.
  • 10[4]Abdulkader M,Vasudevan DM, Leena Devi KR, Nair VJ. Experimental production of keloids[J]. Int. J. Cancer, 1983, 20: 27.

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