期刊文献+

大鼠肺内血管活性肠肽与支气管粘蛋白总量的相关性分析 被引量:2

Relevance of vasoactive intestinal peptide and total bronchial mucin in rat lung
原文传递
导出
摘要 本研究旨在观察臭氧应激不同时间,大鼠肺内血管活性肠肽(vasoactive intestinal peptide,VIP)含量和支气管粘蛋白总量的变化,分析两者之间的相关性。取64只Sprague-Dawley大鼠,臭氧应激不同时间后,用放射免疫方法检测肺组织匀浆VIP含量,过碘酸-希夫(periodic acid-Schiff,PAS)染色检测支气管粘蛋白总量的变化,分析两者之间的相关性。结果显示,呼吸道损伤初期,VIP变化不明显,支气管粘蛋白总量分泌增加,随着损伤加重,引起VIP代偿性分泌增加,支气管粘蛋白总量有所减少。随损伤时间的延长,损伤程度加重,肺内分泌VIP的阳性神经纤维及内分泌细胞数量减少,呼吸道对炎性介质的抗损伤作用下降,支气管粘蛋白总量逐渐增加。以上结果证实在气道高反应过程中,VIP分泌与支气管粘蛋白总量呈负相关。 Vasoactive intestinal peptide (VIP) is a neuropeptide with potent bronchodilator, immunomodulator, and anti-inflammatory properties, and thus has biological properties capable of counteracting all major features of the asthmatic response. However, the effect of VIP on bronchial mucin secretion remains unclear. In order to observe the influence of VIP on bronchial mucin, the present study was designed to observe the correlation between VIP and total bronchial mucin changes under different time of ozone stress in rat lung. Sixty-four Sprague-Dawley rats were used in the experiment. Under different time of ozone stress, VIP content in lung homogenate was analyzed by radioimmunoassay, and changes in total bronchial mucin in the lung were analyzed by calculating the goblet cell hyperplasia ratio and the epithelial cell mucus occupying ratio from the periodic acid-Schiff reaction (PAS) staining. The results showed that, at early stage of respiratory tract injury, VIP did not change significantly, while the total bronchial mucin secretion increased; with the development of damage, the secretion of VIP increased by compensation, followed by a decrease in total bronchial mucin; with further injury, the numbers of pulmonary endocrine VIP positive nerve fibers and endocrine cells decreased, but bronchial mucin volume gradually increased. It is concluded that the secretion of VIP is negatively correlated with the secretion of bronchial mucin during the development of inflammation.
出处 《生理学报》 CAS CSCD 北大核心 2009年第6期539-543,共5页 Acta Physiologica Sinica
基金 supported by the National Natural Science Foundation of China(No.30500227) the Natural Science Foundation of Hunan Province(No.04JJ3015) the Scientific Research Foundation of Health Department of Hunan Province China(No.B2007117)
关键词 血管活性肠肽 臭氧 支气管粘蛋白总量 vasoactive intestinal peptide ozone total bronchial mucin
  • 相关文献

参考文献14

  • 1Martinez-Anton A, Debolos C, Garrido M, Roca-Ferrer J, Barranco C, Alobid I, Xaubet A, Picado C, Mullol J. Mucin genes have different expression patterns in healthy and diseased upper airway mucosa. Clin Exp Allergy 2006; 36(4): 448-457.
  • 2Tesfaigzi Y. Regulation of mucous cell metaplasia in bronchial asthma. Curt Mol Med 2008; 8(5): 408-415.
  • 3Dakhama A, Park JW, Taube C, El Gazzar M, Kodama T, Miyahara N, Takeda K, Kanehiro A, Balhorn A, Joetham A, Loader JE, Larsen GL, Gelfand EW. Alteration of airway neuropeptide expression and development of airway hyperresponsiveness following respiratory syncytial virus infection. Am J Physiol Lung Cell Mol Physiol 2005; 288(4): L761-L770.
  • 4Groneberg DA, Rabe KF, Fischer A. Novel concepts of neuropeptide-based drug therapy: Vasoactive intestinal polypeptide and its receptors. Eur J Pharmacol 2006; 53(3): 182-194.
  • 5管茶香,张长青,秦晓群,罗自强,周伏文,孙秀泓.血管活性肠肽对支气管上皮细胞趋化迁移的影响及机制[J].生理学报,2002,54(2):103-106. 被引量:3
  • 6谭宇蓉,秦晓群,管茶香,张长青,向阳,任雁宏.肺内调节肽对兔支气管上皮细胞分泌白介素的影响[J].生理学报,2002,54(2):107-110. 被引量:10
  • 7彭丽花,秦晓群,谭宇蓉,向阳,刘惠君.肺内调节肽对人支气管上皮细胞HLA-DR、CD80、CD86表达的影响[J].生理学报,2008,60(6):723-729. 被引量:3
  • 8Said SI, Mutt V. Polypeptide with broad biological activity:isolation from small intestine. Science 1970; 169(951): 1217- 1218.
  • 9Miotto D, Boschetto P, Bononi I, Zeni E, Cavallesco G, Fabbri LM, Mapp CE. Vasoactive intestinal peptide receptors in the airways of smokers with chronic bronchitis. Eur Respir J 2004; 24(6): 958-963.
  • 10Gomariz RP, Leceta J, Garrido E, Garrido T, Delgado M. Vasoactive intestinal peptide (VIP) mRNA expression in rat T and B lymphocytes. Regul Pept 1994; 50(2): 177-184.

二级参考文献27

  • 1刘惠君,王悦,柒铭铭,屈飞,向阳,谭宇容,张长青,秦晓群.蛙皮素受体亚型-3对人支气管上皮细胞的抗损伤保护作用[J].中南大学学报(医学版),2006,31(2):178-183. 被引量:3
  • 2Holt PG. Antigen presentation in the lung. Am J Respir Crit Care Med 2000; 162: S151-S156.
  • 3Tan YR, Qi MM, Qin XQ, Xiang Y, Li X, Wang Y, Qu F, Liu HJ, Zhang JS. Wound repair and proliferation of bronchial epithelial cells enhanced by bombesin receptor subtype 3 activation. Peptides 2006; 27: 1852-1858.
  • 4Lanzavecchia A. Receptor mediated antigen uptake and its effect on antigen presentation to class2- restricted T lymphocytes. Annu Rev Immunol 1990; 8: 773-793.
  • 5Damle NK, Klussman K, Linsley PS, Aruffo A. Differential costimulatory effects of adhesion milecules B7, ICAM-1, LFA-3, and VCAM-1 on resting and antigen primed CD4+ T lymphocytes. J Immuunol 1992; 148: 1985-1992.
  • 6Kalb TH, Chuang MT, Marom Z, Mayer L. Evidence for accessory cell function by class Ⅱ MHC antigen-expressing airway epithelial cells. Am Respir Cell Mol B iol 1991; 4(4): 320-329.
  • 7Bugeon L, Dallman MJ. Costimulation of T cells. Am J Crit Care Med 2000; 162: S164-S168.
  • 8Salik E, Tyorkin M, Moban S, George I, Becker K, Oei E, Kalb T, Sperber K. Antigen trafficking and accessory cell function in respiratory epithelial cells. Am Respir Cell Mol Biol 1999; 21(3): 365-379.
  • 9Kurosawa S, Myers AC, Chen L, Wang S, Ni J, Plitt JR, Heller NM, Bochner BS, Schleimer RP. Expression of the costimulatory molecule B7-H2 by humam airway epithelial cells. Am Respir Cell Mol Biol 2003; 28: 563-573.
  • 10Takizawa R, Pawankar R, Yamagishi S, Takenaka H, Yaqi T. Increased expression of HLA-DR and CD86 in nasal epithelial cells in allergic rhinitics: antigen presentation to T cells and up-regulation by diesel exhaust particles. Clin Exp Allergy 2007; 37(3): 420-433.

共引文献12

同被引文献20

  • 1MORCILLO E J, CORTIJO J. Mucus and MUC in asthma[J]. Curr Opin Pulm Med, 2006,12(1) :1-6.
  • 2HATTRUP C L, GENDLER S J. Structure and function of the cell surface (tethered) mueins [ J ]. Annu Rev Physiol, 2008,70 : 431-457.
  • 3AGRE P. Clinical relevance of basic research on red cell membranes[J]. Clin Res,1992,40 (2) :176-86.
  • 4VERKMAN A S, MATTHAY M A, SONG Y. Aquapofin water channels and lung physiology[J]. Am J Physiol Lung Cell Mol Physiol, 2000,278 : L867-L879.
  • 5KING LS, NIELSEN S, AGRE P, et al. Decreased pulmonary vascular permeability in aquaporin-l-null humans [ J ]. Proc Natl Aead Sci USA, 2002,99:1059-1063.
  • 6SKIEPKO R, ZIETKOWSKI Z, TOMASIAK-LOZOWSKA M M, et al. Bronchial hyperresponsiveness and airway inflammation in patients with seasonal allergic rhinitis [ J ]. J Investig Allergol Clin Immunol, 2011,21 (7) :532-539.
  • 7SONG Y, VERKMAN A S. Aquapofin-5 dependent fluid secretion in airwaysubmueosal glands[ J]. J Biol Chem, 2001,276: 41288-41292.
  • 8TOWNE J E, HARROD K S, KRANE C M, et al. Decreased expression of aquaporin AQP1 and AQP5 in mouse lung after acute viral infection[ J]. Am J Respir Cell Mol Biol, 2000,22( 1 ) :34-44.
  • 9GABAZZA E C, KASPER M, OHTA K, et al. Decreased expression of aquapofin-5 in bleomycin-induced lung fibrosis in the mouse[ J]. Pathol Int, 2004,54(10) :774-780.
  • 10Ngoc LP, Gold DR, Tzianabos AO, et al. Cytokines, allergy, and asthma[J]. Curr Opin Allergy Clin Immunol, 2005, 5(2):161-166.

引证文献2

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部