目的:观察护心康对动脉粥样硬化兔动脉血管壁基质金属蛋白酶-9(MMP-9)及基质金属蛋白酶组织抑制剂-1(TIMP-1)表达的影响。方法:将家兔随机分4组:正常对照组(饲养普通饲料)、模型组、护心康组、辛伐他汀组,高脂饲料喂养16周,在12周造模...目的:观察护心康对动脉粥样硬化兔动脉血管壁基质金属蛋白酶-9(MMP-9)及基质金属蛋白酶组织抑制剂-1(TIMP-1)表达的影响。方法:将家兔随机分4组:正常对照组(饲养普通饲料)、模型组、护心康组、辛伐他汀组,高脂饲料喂养16周,在12周造模成功后护心康组给予护心康1.08 g/(kg·d)混悬液灌胃,辛伐他汀组给予辛伐他汀2.5 mg/(kg·d)混悬液灌胃干预4周。在16周后,取胸主动脉提取总RNA应用半定量逆转录多聚酶链式反应(RT-PCR)测定MMP-9和TIMP-1 m RNA的表达。结果:兔动脉粥样硬化中MMP-9 m RNA(m RNA/β-actin m RNA)表达,正常对照组、模型组、护心康组、辛伐他汀组分别为(0.36±0.18)、(0.85±0.15)、(0.71±0.19)、(0.57±0.13),与模型组比较,差异有统计学意义(P<0.01)。上述4组TIMP-1m RNA的相对值分别为(0.38±0.15)、(0.72±0.13)、(0.85±0.14)、(0.93±0.19),与模型组比较,护心康组和辛伐他汀组有所增加(P<0.05,P<0.01)。结论:护心康能降低斑块中MMP-9的水平,增高TIMP-1水平,抑制动脉粥样硬化的形成。展开更多
Background It is known that ultraviolet irradiation can affect cellular function through a number of signaling pathways ( ) epigallocatechin 3 gallate (EGCG) is the major effective component in green tea and can offer...Background It is known that ultraviolet irradiation can affect cellular function through a number of signaling pathways ( ) epigallocatechin 3 gallate (EGCG) is the major effective component in green tea and can offer protection from ultraviolet induced damage In this study, we investigated the protective mechanism of EGCG on human dermal fibroblasts damaged by ultraviolet A (UVA) in vitro Methods Transcription factor Jun protein levels were measured by Western blot Matrix metalloproteinase 1 (MMP 1) and tissue inhibitor of metalloproteinase 1 (TIMP 1) mRNA were studied by reverse transcription polymerase chain reaction (RT PCR) analysis in conjunction with computer assisted image analysis MMP 1 and TIMP 1 proteins were quantified by enzyme linked immunosorbent assay (ELISA) Results EGCG decreased transcription activity of Jun protein after induction by UVA Both the mRNA and protein levels of MMP 1 were increased by UVA irradiation, while no significant changes were observed in TIMP 1 levels The ratio of MMP 1 to TIMP 1 showed statistically significant differences compared with the control EGCG decreased the ratio of MMP 1 to TIMP 1 by inhibiting UVA induced MMP 1 expression ( P <0 05) Conclusion EGCG can protect human fibroblasts against UVA damage by downregulating the transcription activity of Jun protein and the expression of MMP 1 The ratio of MMP 1 to TIMP 1, rather than the levels of MMP 1 or TIMP 1 alone, may play a significant role in human skin photodamage展开更多
Small hairpin RNA （shRNA） was used to silence the HIF1α gene in human retinal pigment epithelial cells （RPE） under hypoxia in order to observe the effect of gene silencing on the expression of matrix metalloprote...Small hairpin RNA （shRNA） was used to silence the HIF1α gene in human retinal pigment epithelial cells （RPE） under hypoxia in order to observe the effect of gene silencing on the expression of matrix metalloproteinase tissue inhibitor 1 （TIMP1）. By using chemical hypoxic inducer CoCl2 to mimic RPE hypoxic environment, shRNA against the targeting region of HIF1α mRNA sequence was synthesized by a method of in vitro transcription, and the HIF1α was interfered in RPE cultured under hypoxia （induced by 150 μmol/L CoCl2 ）. RT-PCR was employed to detect the expression of HIF1α and TIMP1. The expression levels of HIF1α and TIMP1 were measured by using Western blotting. The results showed that after the RPE were transfected with specific shRNA against HIF1α mRNA, RT PCR revealed that under hypoxia, the efficacy of HIF1α gene silencing in RPE was 83.4 %. Western blotting revealed that the expression levels of HIF1α protein was dramatically dropped. In addition, RT-PCR results demonstrated that the expression of TIMP1 mRNA was decreased by 28.9 %, and the expression levels of TIMP1 protein were also significantly reduced by Western blotting. It was suggested that shRNA targeted against HIF1α mRNA could effectively silence the HIF1α gene, subsequently effectively inhibit the hypoxia-induced up-regulation of TIMP1.展开更多
文摘目的:观察护心康对动脉粥样硬化兔动脉血管壁基质金属蛋白酶-9(MMP-9)及基质金属蛋白酶组织抑制剂-1(TIMP-1)表达的影响。方法:将家兔随机分4组:正常对照组(饲养普通饲料)、模型组、护心康组、辛伐他汀组,高脂饲料喂养16周,在12周造模成功后护心康组给予护心康1.08 g/(kg·d)混悬液灌胃,辛伐他汀组给予辛伐他汀2.5 mg/(kg·d)混悬液灌胃干预4周。在16周后,取胸主动脉提取总RNA应用半定量逆转录多聚酶链式反应(RT-PCR)测定MMP-9和TIMP-1 m RNA的表达。结果:兔动脉粥样硬化中MMP-9 m RNA(m RNA/β-actin m RNA)表达,正常对照组、模型组、护心康组、辛伐他汀组分别为(0.36±0.18)、(0.85±0.15)、(0.71±0.19)、(0.57±0.13),与模型组比较,差异有统计学意义(P<0.01)。上述4组TIMP-1m RNA的相对值分别为(0.38±0.15)、(0.72±0.13)、(0.85±0.14)、(0.93±0.19),与模型组比较,护心康组和辛伐他汀组有所增加(P<0.05,P<0.01)。结论:护心康能降低斑块中MMP-9的水平,增高TIMP-1水平,抑制动脉粥样硬化的形成。
文摘Background It is known that ultraviolet irradiation can affect cellular function through a number of signaling pathways ( ) epigallocatechin 3 gallate (EGCG) is the major effective component in green tea and can offer protection from ultraviolet induced damage In this study, we investigated the protective mechanism of EGCG on human dermal fibroblasts damaged by ultraviolet A (UVA) in vitro Methods Transcription factor Jun protein levels were measured by Western blot Matrix metalloproteinase 1 (MMP 1) and tissue inhibitor of metalloproteinase 1 (TIMP 1) mRNA were studied by reverse transcription polymerase chain reaction (RT PCR) analysis in conjunction with computer assisted image analysis MMP 1 and TIMP 1 proteins were quantified by enzyme linked immunosorbent assay (ELISA) Results EGCG decreased transcription activity of Jun protein after induction by UVA Both the mRNA and protein levels of MMP 1 were increased by UVA irradiation, while no significant changes were observed in TIMP 1 levels The ratio of MMP 1 to TIMP 1 showed statistically significant differences compared with the control EGCG decreased the ratio of MMP 1 to TIMP 1 by inhibiting UVA induced MMP 1 expression ( P <0 05) Conclusion EGCG can protect human fibroblasts against UVA damage by downregulating the transcription activity of Jun protein and the expression of MMP 1 The ratio of MMP 1 to TIMP 1, rather than the levels of MMP 1 or TIMP 1 alone, may play a significant role in human skin photodamage
文摘Small hairpin RNA （shRNA） was used to silence the HIF1α gene in human retinal pigment epithelial cells （RPE） under hypoxia in order to observe the effect of gene silencing on the expression of matrix metalloproteinase tissue inhibitor 1 （TIMP1）. By using chemical hypoxic inducer CoCl2 to mimic RPE hypoxic environment, shRNA against the targeting region of HIF1α mRNA sequence was synthesized by a method of in vitro transcription, and the HIF1α was interfered in RPE cultured under hypoxia （induced by 150 μmol/L CoCl2 ）. RT-PCR was employed to detect the expression of HIF1α and TIMP1. The expression levels of HIF1α and TIMP1 were measured by using Western blotting. The results showed that after the RPE were transfected with specific shRNA against HIF1α mRNA, RT PCR revealed that under hypoxia, the efficacy of HIF1α gene silencing in RPE was 83.4 %. Western blotting revealed that the expression levels of HIF1α protein was dramatically dropped. In addition, RT-PCR results demonstrated that the expression of TIMP1 mRNA was decreased by 28.9 %, and the expression levels of TIMP1 protein were also significantly reduced by Western blotting. It was suggested that shRNA targeted against HIF1α mRNA could effectively silence the HIF1α gene, subsequently effectively inhibit the hypoxia-induced up-regulation of TIMP1.
