摘要
目的研究西替利嗪对P物质诱导表皮角质形成细胞系HaCaT细胞和真皮成纤维细胞表达单核细胞趋化蛋白-1(MCP-1)的影响。方法采用MTT法考察西替利嗪对两种皮肤细胞生存性的影响;ELISA方法测定P物质诱导两种皮肤细胞分泌MCP-1的时效关系与量效关系。以P物质刺激HaCaT细胞和真皮成纤维细胞,加入不同剂量的西替利嗪共孵育24h,测定西替利嗪对MCP-1表达的影响。结果以10-8mol·L-1P物质刺激HaCaT细胞24h可以显著增加HaCaT细胞和真皮成纤维细胞MCP-1的分泌量,不同浓度的西替利嗪均可以抑制皮肤细胞MCP-1的分泌。结论西替利嗪可能通过抑制趋化因子MCP-1的表达而发挥抗皮肤过敏作用。
Abstract
OBJECTIVE To study the effect of cetirizine on the expression of moncyte chemoattractant protein-1(MCP-1) induced by substance P(SP)in keratinocytes line HaCaT cells and fibroblasts.METHODS The time-and dose-response relationships of MCP-1 release of HaCaT cells and fibrobalsts stimulated by SP were determinated by ELISA method. The effect of cetirizine on the release of MCP-1 in HaCaT cells and fibrobalsts was also measured by using ELISA kit.RESULTS The expression of MCP-1 in HaCaT cells and fibrobalsts stimulated by SP (10-8mol·L-1) for 24 h was significantly increased. Cetirizine significantly decreased the production of MCP-1 in HaCaT cells and fibroblasts stimulated by SP.CONCLUSION The role of cetirizine on the cutaneous allergy may be related to inhibiting the expression of MCP-1.
关键词
西替利嗪 /
P物质 /
HaCaT细胞 /
真皮成纤维细胞 /
皮肤过敏 /
单核细胞趋化蛋白-1
{{custom_keyword}} /
Key words
cetirizine /
substance P /
HaCaT cells /
fibroblasts /
cutaneous allergy /
moncyte chemoattractant protein-1(MCP-1)
{{custom_keyword}} /
刘继勇;胡晋红;朱全刚;孙华君;彭程.
西替利嗪对P物质诱导皮肤细胞单核细胞趋化蛋白-1表达的影响[J]. 中国药学杂志, 2007, 42(14): 1067-1070
LIU Ji-yong;HU Jin-hong;ZHU Qun-gng;SUN Hu-jun;PENG Cheng.
Effect of Cetirizine on Expression of MCP-1 Induced by Substance P in HaCaT Cells and FiBroblasts [J]. Chinese Pharmaceutical Journal, 2007, 42(14): 1067-1070
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1] SCHOLZEN T,ARMSTRONG C A,BUNNETT N W,et al. Neuropeptides in the skin: interaction between the neuroendocrine and the skin immune system [J] .Exp Dermatol,1998,7(2-3):81-96.
[2] LIU J Y,HU J H,ZHU Q G. Expression and regulation characteristics of the substance P receptor in human skin keratinocytes and fibroblasts[J] .Chin Pharmacol Bull(中国药理学通报),2005,21(6):667-670.
[3] ZHU Q G,HU J H,FAN G R,et al. Metabolism of ketoprofen isopropyl ester in HaCaT cells[J] .Chin Pharm J(中国药学杂志),2003,38(1):22-25.
[4] ZHU Q G,HU J H,FAN G R,et al.Metabolism of ketoprofen isopropyl ester in skin cells[J] .Chin Hosp Pharm J(中国医院药学杂志),2002,22(4):195-197.
[5] ROMAGNANI S. Cytokines and chemoattractants in allergic inflammation[J] .Molecular Immunol,2001,38(5):881-885.
[6] FUJKURA T,SHIMOSAWA T,YAKUO I.Regulatory effect of histamine H1 receptor antagonist on the expression of messenger RNA encoding CC chemokines in the human nasal mucosa[J] .J Allergy Clin Immunol,2001,107(1):123-128.
[7] HOLGATE S T,BODEY K S,JANEZIC A,et al.Release of RANTES,MIP-1alpha,and MCP-1 into asthmatic airways following endobronchial allergen challenge[J] .Am J Respir Crit Care Med,1997,156(5):1377-1383.
[8] ZWEIMAN B,KAPLAN A P,TONG L,et al. Cytokine levels and inflammatory responses in developing late-phase allergic reactions in the skin[J] .J Allergy Clin Immunol,1997,100(1):104-109.
[9] KIM K H,PARK K C,CHUNG J H,et al. The effect of substance P on peripheral blood mononuclear cells in patients with atopic dermatitis[J] .J Dermatol Sci,2003,32(1):115-124.
{{custom_fnGroup.title_cn}}
脚注
{{custom_fn.content}}
基金
军队医药卫生十五重点项目基金(01Z66);上海市科委重大专项基金(04DZ19846)
{{custom_fund}}