1. 广州中医药大学
2. 广州中医药大学第一附属医院
3. 深圳市龙岗区中医院/北京中医药大学深圳医院
纸质出版:2018
移动端阅览
[1]刘靖,涂绍忠,何亚男,陈智斌,陈梦雅,查旭山.银屑1号对Trappin-2刺激下肿瘤坏死因子α干预造模的HaCaT细胞分泌NE、Trappin-2的影响[J].中医杂志,2018,59(17):1498-1502.
LIU Jing, TU Shaozhong, HE Ya’nan, et al. Effects of Yinxie Yihao Prescription(银屑 1 号) on Neutrophil Elastase and Trappin-2 Secreted by HaCaT Cells Interfered and Modeled by Tumor Necrosis Factor α Stimulated by Trappin-2[J]. Journal of Traditional Chinese Medicine2018, 59(17): 1498-1502.
[1]刘靖,涂绍忠,何亚男,陈智斌,陈梦雅,查旭山.银屑1号对Trappin-2刺激下肿瘤坏死因子α干预造模的HaCaT细胞分泌NE、Trappin-2的影响[J].中医杂志,2018,59(17):1498-1502. DOI: 10.13288/j.11-2166/r.2018.17.014.
LIU Jing, TU Shaozhong, HE Ya’nan, et al. Effects of Yinxie Yihao Prescription(银屑 1 号) on Neutrophil Elastase and Trappin-2 Secreted by HaCaT Cells Interfered and Modeled by Tumor Necrosis Factor α Stimulated by Trappin-2[J]. Journal of Traditional Chinese Medicine2018, 59(17): 1498-1502. DOI: 10.13288/j.11-2166/r.2018.17.014.
目的探讨银屑1号治疗银屑病的可能作用机制。方法 24只大鼠随机分为银屑1号组、雷公藤组、空白组
每组8只。银屑1号组大鼠给予银屑1号煎煮浓缩液196 g/(kg·d)灌胃
雷公藤组给予雷公藤多甙片混悬液6 mg/(kg·d)灌胃
空白组给予生理盐水灌胃
均每日2次
每次5 ml
连续5天
制备含药血清。体外培养Ha Ca T细胞
以肿瘤坏死因子α(TNF-α)刺激Ha Ca T细胞建立银屑病细胞模型。实验设置空白组、雷公藤组、抑制剂组、银屑1号组、抑制剂+银屑1号组。空白组、雷公藤组、银屑1号组分别加入基础培养基3.8 ml与相应含药血清
抑制剂组、抑制剂+银屑1号组分别加入空白含药血清和银屑1号含药血清
同时均加入Trappin-2(0.3μg/ml)培养基3.8 ml。体外培养48 h
检测Ha Ca T细胞中中性粒细胞弹性蛋白酶(NE)、Trappin-2含量及NE、Trappin-2 mRNA表达。结果与空白组比较
雷公藤组、抑制剂组、银屑1号组、抑制剂+银屑1号组NE、Trapppin-2含量及mRNA含量明显降低(P<0.05或P<0.01)。与雷公藤组比较
抑制剂组、银屑1号组、抑制剂+银屑1号组NE、Trapppin-2含量及mRNA表达明显升高(P<0.01)。与抑制剂组比较
银屑1号组、抑制剂+银屑1号组NE、Trapppin-2表达明显降低(P<0.05或P<0.01);银屑1号组NE mRNA表达明显升高(P<0.01);抑制剂+银屑1号组Trapppin-2mRNA表达降低(P<0.05)。与银屑1号组比较
抑制剂+银屑1号组NE、Trapppin-2含量及mRNA表达明显降低(P<0.05或P<0.01)。结论银屑1号可降低Ha Ca T细胞中NE、Trappin-2含量及基因表达水平
从而减轻炎症反应
可能是其治疗银屑病的作用机制之一。
Objective To explore the possible mechanism of Yinxie Yihao Prescription(YXYHP)(银屑 1 号) on psoriasis. Methods A total of 24 rats were randomly divided into YXYHP group
Leigongteng group and blank group
with 8 rats in each group. The rats in YXYHP group were given concentrate decoction of YXYHP 196 g/(kg·d) in gavage. Rats in Leigongteng group were given suspension liquid of Triperygium wilfordii multiglucoside tablet6 mg/(kg·d) in gavage. Rats in the blank group were given normal saline in gavage
twice a day
5 ml each time for continuous 5 days. The serum containing medicine from each group was prepared. The psoriatic cell model was established stimulating HaCaT cell cultivated in vitro with tumor necrosis factor α(TNF-α). The experiment set blank group
Leigongteng group
inhibitor group
Chinese medicine group
and inhibitor + Chinese medicine group. The blank group
Leigongteng group
and Chinese medicine group were added basal culture medium 3. 8 ml
Trappin-2 culture medium and serum containing Chinese medicine respectively. The inhibitor group
and inhibitor + Chinese medicine group were added Trappin-2(0. 3 μg/ml) culture medium 3. 8 ml and Trappin-2 culture medium serum containing related medicine. After culturing in vitro for 48 h
the neutrophil elastase(NE)
Trapinin-2 and expression of NE
Trappin-2 mRNA in HaCaT cells were detected. Results Compared with the control group
the contents of NE
Trappin-2 and mRNA expression in Leigongteng group
inhibitor group
Chinese medicine group
and inhibitor +Chinese medicine group were significantly decreased(P < 0. 05 or P < 0. 01). Compared with Leigongteng group
the contents of NE
Trappin-2 and mRNA expression in inhibitor group
Chinese medicine group
and inhibitor + Chinese medicine group were significantly increased(P < 0. 01). Compared with the inhibitor group
the expression of NE and Trappin-2 in the Chinese medicine group
inhibitor + Chinese medicine group was significantly decreased(P <0. 05 or P < 0. 01). The NE and mRNA expression in the Chinese medicine group was significantly increased(P <0. 01). The expression of Trappin-2 mRNA was decreased in inhibitor + Chinese medicine group(P < 0. 05). Compared with the Chinese medicine group
NE and Trappin-2 contents and mRNA expression in the inhibitor + Chinese medicine group were significantly decreased(P < 0. 05 or P < 0. 01). Conclusion YXYHP can reduce the contents of NE
Trappin-2 and the gene expression level in HaCaT cells
thus reducing inflammatory response
which may be one of the action mechanisms in treating psoriasis.
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