摘要
目的:确定钴原卟啉(CoPP)诱导血红素氧合酶-1(heme oxygenase-1,HO-1)对豚鼠银屑病样皮损的影响。方法:普萘洛尔外涂构建豚鼠的银屑病样模型,豚鼠腹腔内注射钴原卟啉(HO-1特异性诱导剂)或锌原卟啉(HO-1特异性抑制剂),磷酸盐缓冲液(phosphate buffered saline,PBS)作为对照,每周1次,共6周。记录皮损的动态评分和组织病理学评分。RT-PCR和Western-blot法检测动物耳部标本中的HO-1 mRNA和蛋白的表达。免疫组化染色方法检测标本中增殖细胞核抗原(proliferatingcell nuclear antigen,PCNA)蛋白的表达和定位。结果:CoPP腹腔内注射显著诱导了HO-1 mRNA和蛋白的表达,CoPP治疗组银屑病样皮损的组织病理学评分和临床皮肤评分显著降低,与PBS对照组相比有显著性差异(P<0.05),同时CoPP治疗组的PCNA表达也显著低于PBS对照组(P<0.05)。结论:钴原卟啉通过诱导血红素氧合酶-1的过表达对银屑病样皮损有治疗作用。
Objective: To determine the effect of heme - oxygenase - 1 (HO - 1 ) induced by cobalt proporphyrin (CoPP) on psoriasislike skin lesions. Methods: After a psoriasiform model of guinea pig was established using topical propranolol, cobalt proporphyrin (a HO- 1 inducer) or zinc proporphyrin (ZnPP), a HO- 1 inhibitor was intraperitoneally injected, once a week for six weeks. Phosphate buffered saline (PBS) was used as control. The clinical skin score and the histopathological score were noted. The level of HO - 1 mRNA and protein was assessed by RT - PCR and Western - blot. The expression of proliferating cell nuclear antigen (PCNA) protein was measured by immunohistochemical staining. Results: The expression of HO - 1 mRNA and protein was significantly increased, and the clinical and pathological scores of psoriasiform skin lesions was significantly decreased in CoPP group, when compared with PBS group ( Ps 〈 0.05). The expression of PCNA in the CoPP group was significantly less than that in PBS group. Conclusion: PPCoPP can resolve psoriasiform skin lesions by inducing HO- 1 over- expression.
出处
《中国麻风皮肤病杂志》
2010年第10期689-693,共5页
China Journal of Leprosy and Skin Diseases
基金
哈尔滨市科技创新人才研究专项资金项目(RFQQS2232009)