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斑秃患者血浆和皮损中降钙素基因相关肽、血管活性肠肽的研究 被引量:1

Calcitonin Gene-related peptides and Vasoactive Intestinal Peptide in Plasma and Lesion of Patients with Alopecia Areata
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摘要 目的探讨降钙素基因相关肽(CGRP)和血管活性肠肽(VIP)在斑秃发病中的作用。方法利用放射免疫分析法检测30例斑秃患者和20例正常人血浆中的CGRP和VIP水平,利用免疫组化方法检测21例斑秃患者皮损和16例正常人头皮中的CGRP和VIP表达情况。结果①斑秃活动期患者血浆中的CGRP水平为(142.63±67.95)pg/mL,低于稳定期(197.33±67.15)pg/mL和正常人(188.40±72.95)pg/mL,差异均有显著性。②斑秃活动期血浆中的VIP水平为(105.94±55.42)pg/mL,低于斑秃稳定期(156.86±47.37)pg/mL和正常人(176.44±84.70)pg/mL,差异均有显著性。③CGRP和VIP在斑秃皮损及其周围的表达明显低于正常人,差异有显著性。结论CGRP和VIP在斑秃发病中起一定的作用。 Objective To study the role of calcitonin gene-related peptide(CGRP)and vasoactive intestinal peptide(VIP)in the pathogenesis of alopecia areata(AA).Methods Radioimmunoassay(RIA)was used to measure the levels of CGRP and VIP in plasma from30patients with AA and20normal controls.Immunohistochemistry was employed to detect the expression of CGRP and VIP in lesions of21patients with AA and16normal scalps.Results①The plasma levels of CGRP in progressing stage of AA(142.63±67.95pg/mL)were significantly lower than those in stable stage of AA(197.33±67.15pg/mL)and in normal controls(188.40±72.95pg/mL).②The plasma levels of VIP in progressing stage of AA(105.94±55.42pg/mL)were significantly lower than those in stable stage of AA(156.86±47.37pg/mL)and in normal controls(176.44±84.70pg/mL).③The expression of CGRP and VIP was significanly decreased in lesions of AA than that in normal scalps.Conclusion These findings indicate that CGRP and VIP may play a role in the pathogenesis of alopecia areata.
出处 《中华皮肤科杂志》 CAS CSCD 北大核心 2003年第2期79-81,共3页 Chinese Journal of Dermatology
基金 河北省科技厅科技攻关项目资助(00276190D)
关键词 血浆 皮损 斑秃 降钙素基因相关肽 血管活性肠肽 CGRP VIP 放射免疫分析法 Alopecia areata Calcitonin gene-related peptide Vasoactive intestinal peptide
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  • 1AnselJC,ArmstrongCA,SongI,etal.In-teractionoftheskinandnervoussystem[].JInvestigDermatolSympProc.1997

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  • 1周静,杨勤萍,黄岚.斑秃毛囊器官特异性自身免疫发病机制和治疗研究进展[J].中国皮肤性病学杂志,2007,21(6):368-370. 被引量:7
  • 2Gilhar A,Kalish RS. Alopecia areata:atissue specific autoimmune disease of the hair follicle [ J ]. Autoimmun Rev,2006,5 ( 1 ) :64 - 69.
  • 3Bertolini M, Gilhar A, Paus R. Alopecia areata as a model for T cell- dependentautoimmune diseases[ J-. Exp Dermatol, 2012,21(6) :477- 479.
  • 4Siebenhaar F,Sharov AA, Petors EM, et al. Substance P as animmunomodulatory neuropeptide in a mouse model forautoimmune hair loss ( alopecia areata) [ J ]. J Invest Dermatol, 2007,127 (6) : 1489 - 1497.
  • 5Zhang X, Yu M, Yu W, et al. Development of alopeciaareatais associated with highercentral and peripheral hypothalamic-pituitary-adrenal tone in the skin graftinduced C3H /HeJ mouse model [ J]. J Invest Dermatol, 2009,129(6) : 1527 - 1538.
  • 6Gilhar A, Etzioni A, Paus R. Alopecia areata[J]. N Engl J Med, 2012,366(16) :1515 - 1525.
  • 7Toyoda M, makino T, Kagoura M, et al. Expression of neuropeptide- degrading enzymes in alopecia areata:an immunohistochemical Study [ J ]. Br J Dermatol,2001,144 ( 1 ) :46 - 54.
  • 8Meyronet D, Jaber K, Gentil-Perret A, et al. Decreased CGRP staining in alopecia areata[J]. Br J Dermatol,2003,149(2) :422.
  • 9Daly TJ. Alopecia areata has low plasma levels of the vasodilator/immunomodulator calcitonin gene-related peptide [ J ]. Arch Dermatol, 1998,134(9) :1164 - 1165.
  • 10Samuelov L, Kinori M, Bertolini M, et al. Neural controls of human hair ; growth : calcitoningene-related peptide (CGRP) induces catagen [J]. J Dermatol Sci,2012,67(2) :153 - 155.

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