机构地区:[1]复旦大学附属金山医院烧伤整形科,上海市200540 [2]复旦大学附属中山医院整形外科,上海市200032
出 处:《中国临床康复》2006年第37期78-80,i0004,共4页Chinese Journal of Clinical Rehabilitation
摘 要:目的:探讨哺乳动物细胞源性生长激素抗皮肤老化的作用机制。方法:实验于2004-03/12在复旦大学附属金山医院动物实验室完成。选择18~20月龄健康SD大鼠90只,随机数字表法分为3组,重组人生长激素0.08U/kg组,重组人生长激素0.12U/kg组,生理盐水对照组,每组30只。每组又分为用药前及用药后4,6,8,10,12周6个时间点,每个时间点5只。重组人生长激素0.08,0.12U/kg组:0.02U/mL重组人生长激素悬液分别行皮下注射0.08,0.12U/kg,3次/周,共12周。生理盐水对照组:以生理盐水皮下注射。另选取10只2~3月龄正常SD大鼠为空白对照组。于各时间点切取大鼠背部标记区的皮肤组织,行Masson染色并测定皮肤胶原厚度,反转录-聚合酶链反应检测皮肤转化生长因子βⅠ型和Ⅱ型受体mRNA的表达。结果:纳入动物100只,均进入结果分析。①大鼠皮肤胶原厚度:重组人生长激素0.08U/kg组注射8周胶原开始增厚,重组人生长激素0.12U/kg组第6周胶原开始增厚,厚度明显大于生理盐水对照组犤分别为(787±18),(766±20),(649±50)μm,P<0.05犦,与空白对照组比较差异无显著性意义(P>0.05)。②重组人生长激素0.08,0.12U/kg组转化生长因子βⅠ型和Ⅱ型受体mRNA的表达高于生理盐水对照组(以注射4周为例,转化生长因子βⅠ型受体分别为0.321±0.011,0.534±0.013,0.000±0.000;转化生长因子βⅡ型受体分别为0.297±0.009,0.541±0.025,0.000±0.000,P<0.05)。结论:重组人生长激素可上调皮肤转化生长因子βⅠ型和Ⅱ型受体mRNA的表达,促进胶原增殖而发挥抗皮肤老化作用。AIM: To investigate the action mechanism of recombinant human growth hormone (rhGH) on the collagen metabolism of senile skins. METHODS: The experiment was conducted in the Animal Laboratory of Jinshan Hospital, Fudan University from March to December 2004. Ninety healthy 18-20-month-old SD rats were selected and randomly divided into 3 groups: 0.08 U/kg rhGH group, 0.12 U/kg rhGH group and saline control group with 30 rats in each group. Every group was subdivided into 6 subgroups according to 6 time points: before and 4, 6, 8, 10 and 12 weeks after administration with 5 rats at each time point. The 0.08 U/kg and 0.12 U/kg rhGH groups: The rats were injected subcutaneously 0.08 and 0.12 U/kg rhGH (0.02 U/mL) suspension, respectively, three times a week for 12 weeks. The saline control group: The rats were injected. Another ten normal 2-3-month-old SD rats were selected as blank control group. The skin graft was incised from each rat for Masson staining and the thickness of collagen was detected. RT-PCR was used to detect the expression of transforming growth factor of TβR Ⅰ and TβR Ⅱ respectively. RESULTS; All the 100 rats were involved in the result analysis. ①Collagen thickness: From the 8th week, the collagen of the 0.08 U/kg rhGH group began to thicken, and the collagen of the 0.12 U/kg rhGH group began to thicken from the 6th week, which were higher than the saline control group [(787±18), (766±20), (649±50)μm, P 〈 0.05], and had no significant difference compared with the blank control group (P 〉 0.05). ②The expression of TβR Ⅰ and TβR Ⅱ of 0.08 and 0.12 U/kg rhGH groups were higher than the saline control group (at the 4^th week: TβR Ⅰ 0.321±0.011, 0534±0.013, 0.000±0.000; TβR Ⅱ 0.297±0.009, 0.541±0.025, 0.000±0.000, P 〈 0.05). CONCLUSION: rhGH can accelerate the collagen proliferation by upregulating the expressions of TβR Ⅰ and TβR Ⅱ in the skin to play a key role in the anti-aging process.
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