期刊文献+

一氧化氮吸入对新生鼠高氧肺损伤时表面活性蛋白A和肺甘露糖结合力的影响 被引量:2

Effect of inhaled nitric oxide on surfactant protein A and mannose binding ability in the lung of neonatal rats with hyperoxia-induced lung injury
下载PDF
导出
摘要 目的通过观察吸入一氧化氮(iNO)对新生大鼠高氧肺损伤时表面活性蛋白A(SP-A)和肺组织甘露糖结合力(MBA)的影响,探讨iNO对高氧肺损伤保护作用的可能机制。方法新生大鼠随机分为对照组(空气);高氧组(>95%O2,6d);NO组(空气+10ppmNO,24h);高氧+NO组(>95%O2,6d+10ppmNO,24h)。观察暴露后2d和6d肺组织病理变化,肺SP-AmRNA基因表达、蛋白含量和MBA的变化。结果高氧组病理损伤明显,暴露后2d时SP-A的mRNA含量(0.81±0.04vs1.53±0.25)和蛋白表达(59.45±18.37vs89.77±16.41)比对照组减少,6d时分别比对照组增加(0.81±0.02vs0.63±0.03),(93.57±13.71vs47.73±21.69),(P<0.05)。高氧+NO组暴露后2d时病理损伤比高氧组明显减轻,SP-AmRNA(0.55±0.91)比对照组和高氧组降低,SP-A蛋白表达(55.12±17.53)比对照组降低(P<0.01);6d时SP-A蛋白表达(67.33±18.59)比高氧组降低(P<0.05)。甘露糖结合力在暴露后2d时NO组比对照组增加(0.821±0.133vs0.580±0.158)、高氧+NO组比高氧组增加(0.430±0.175vs0.738±0.141)(P<0.05)。结论小剂量NO吸入可降低高氧肺组织SP-A蛋白表达的升高,增加肺组织的MBA,减轻肺组织的病理损伤。 Objective To investigate the effect of inhaled nitric oxide (NO) on surfactant protein A (SP-A) and mannose binding ability (MBA) in neonatal rats with hyperoxia-induced lung injury.. Methods Sixty-four neonatal rats were randomly exposed to room air ( Control group) , 〉 95% oxygen for 6 days ( Hyperoxia group) , 10 ppm NO for 24 hrs (NO group) , and 〉95% oxygen for 6 days along with 10 ppm NO for 24 hrs ( Hyperoxia + NO group). After 2 and 6 days of exposure, the lung pathologic changes, gene and protein expressions of SP-A and MBA were measured. Results The rats from the Hyperoxia group presented with obvious lung injuries. The SP-A expressions of mRNA (0.81 ±0.04 vs 1.53 ±0. 25 ) and protein (59.45± 18.37 vs 89.77±16.41 ) in the Hyperoxia group decreased significantly 2 days after exposure but increased significantly 6 days after exposure ( SP-A mRNA 0.81 ± 0.02 vs 0.63 ± 0.03 ; SP-A protein 93.57±13.71 vs 47.73 ±21,69) compared with those of the Control group (P 〈 0. 05 ). NO treatment alleviated the hyperoxla-indueed pathologic injuries 2 days after exposure. The SP-A mRNA expression (0.55 ±0.91 ) in the Hyperoxia + NO group was significantly reduced as compared to both the Control and Hyperoxia groups ( P 〈 0. 05 ) , and the SP-A protein expression (55. 12 ± 17.53) in the Hyperoxia + NO group was noticeably lower than that of the Control group (P 〈0.01) 2 days after exposure. The SP-A protein expression in the Hyperoxia + NO group (67.33 ± 18.59) was significantly lower than that of the Hyperoxia group 6 days after exposure ( P 〈 0.05 ). Two days after exposure, the NO group had significantly higher MBA than the Control group (0.821 0. 133 vs 0. 58 ±0. 158) ; the Ilyperoxia + NO group had significantly higher MBA than the Hyperoxla group (0. 43 ± 0. 175 vs 0. 738 ± 0. 141 ) (P 〈 0. 05). Conclusions Inhaled low dose NO may decrease SP-A protein expression and increase MBA of the lung tissue. This lessens the pathologic lung injury in neonatal rats with hyperoxia.
出处 《中国当代儿科杂志》 CAS CSCD 2006年第6期486-490,共5页 Chinese Journal of Contemporary Pediatrics
基金 国家自然科学基金资助(No:31371498)。
关键词 高氧肺损伤 表面活性蛋白A 甘露糖结合力 吸入一氧化氮 新生大鼠 Hyperoxia-indueed lung injury Surfactant protein A Mannose binding ability Inhaled nitrie oxide Neonatal rats
  • 相关文献

参考文献19

  • 1Stuart LM,Henson PM,Vandivier RW.Collectins:opsonins for apoptotic cells and regulators of inflammation[J].Curr Dir Autoimmun,2006,9(9):143-161.
  • 2Turner MW.The role of mannose-binding lectin in health and disease[J].Mol Immunol,2003,40 (7):423-429.
  • 3Preanis JS,Kojima M,Sim RB.Biochemistry and genetics of mannan-binding Iectin (MBL)[J].Biochem Soc Trans,2003,31 (Pt4):748-752.
  • 4Konishi M,Nishitani C,Mitsuzawa H,Shimizu T,Sano H,Harimaya A,et al.Alloiococcus otitidis is a ligand for collectins and Toll-like receptor 2,and its phagocytosis is cnhanced by collectins[J].Eur J Immunol,2006,36 (6):1527-1536.
  • 5Narasaraju TA,Jin N,Narcndranath CR,Chen Z,Gou D,Liu L.Protein nitration in rat lungs during hyperoxia exposure:a possible role of myeloperoxidase[J].Am J Physiol Lung Cell Mol Physiol,2003,285 (5):L1037-1045.
  • 6Cotton RB,Sundell HW,Zeldin DC,Morrow JD,Roberts LJ,Hazinski TA,et al.Inhaled nitric oxide attenuates hyperoxic lung injury in lambs[J].Pediatr Res 2006,59 (1):142-146.
  • 7Davis IC,Zhu S,Sampson JB,Crow JP,Matalon S.Inhibition of human surfactant protein A function by oxidation intermediates of nitrite[J].Free Radic Biol Med,2002,33 (12):1703-1713.
  • 8Saugatad OD.Bronchopulmonary dysplasia and oxidative stress:are we closer to an understanding of the pathogenesis of BPD[J].Acta Paeditr,1997,86(12):1277-1287.
  • 9Nelin LD,Morrisey JF,Effros RM,Dawson CA,Schapira RM.The effect of inhaled nitric oxide and oxygen on the hydroxylation of salicylate in rat lungs[J].Pediatr Res,2003,54 (3):337-343.
  • 10Sano H,Kuroki Y.The lung collcetins,SP-A and SP-D,modulate pulmonary innate immunity[J].Mol Immunol,2005,42 (3):279 -287.

同被引文献31

  • 1富建华,薛辛东.慢性肺疾病早产鼠BALF及肺组织中脂质过氧化的同步研究[J].中国优生与遗传杂志,2004,12(6):32-33. 被引量:6
  • 2刘雪雁,吴捷,薛辛东.高氧致新生鼠肺损伤时肾组织一氧化氮及氧自由基的变化[J].中国当代儿科杂志,2005,7(1):71-74. 被引量:16
  • 3富建华,薛辛东.慢性肺疾病早产鼠肺组织转化生长因子β_1基因及蛋白表达的动态变化(英文)[J].中国当代儿科杂志,2005,7(3):207-211. 被引量:4
  • 4杨群,邵肖梅,王晓宁,郭春宝,孙波.吸入一氧化氮对早产猪未成熟肺的作用[J].中国当代儿科杂志,2006,8(1):54-58. 被引量:8
  • 5Abman SH . Bronchopulmonary dysplasia: “a vascular hypothesis.” [J]. AmJ Respir Crit Care Med, 2001, 164(10 Pt 1): 1755-1756.
  • 6Bhatt AJ, Pryhuber GS, Huyck H, Watkins RH, Metlay LA, Maniscalco WM. Disrupted pulmonary vasculature and decreased vascular endothelial growth factor, Fh-1, and TIE-2 in human infants dying with bronchopulmonary dysplasia [ J ]. Am J Respir Crit Care Med, 2001, 164( 10 Pt 1 ) :1971-1980.
  • 7Han RN, Babaei S, Robb M, Lee T, Ridsdale R, Ackerley C, et al. Defective lung vascular development and fatal respiratory distress in endothelial NO synthase deficient mice: a model of alveolar capillary dysplasia? [ J ]. Circ Res, 2004, 94 ( 8 ) : 1115- 1123.
  • 8Tang JR, Markham NE, Lin YJ, McMurtry IF, Maxey A, Kinsella JP, et al. Inhaled nitric oxide attenuates pulmonary hypertension and improves lung growth in infant rats after neonatal treatment with a VEGF receptor inhibitor[ J]. Am J Physiol Lung Cell Mol Physiol. 2004. 287(2) : L344-L351.
  • 9Cudmore M, Ahmad S, AI-Ani B, Hewett P, Ahmed S, Ahmed A. VEGF-E activates endothelial nitric oxide synthase to induce angiogenesis via cGMP and PKG-independent pathways[ J]. Biochem Biophys Res Commun, 2006, 345(4) : 1275-1282.
  • 10Bland RD, Albertine KH, Carlton DP, Kullama L, Davis P, Cho SC, et al. Chronic lung injury in preterm lambs: abnormalities of the pulmonary circulation and lung fluid balance [ J ]. Pediatr Res, 2000, 48 ( 1 ) : 64-74.

引证文献2

二级引证文献4

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