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艾迪注射液对小鼠放射性肺损伤的防治作用 被引量:6

Preventive and Therapeutic Effect of Aidi Injection on Radiation-Induced Lung Injury
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摘要 目的 观察艾迪注射液在放射性肺损伤中的防治作用,并探讨其相关机制.方法 将SPF级C57BL/6小鼠120只随机分为4组:空白对照组,照射+艾迪组,照射+甲泼尼龙组和照射组,每组30只.给予小鼠单次12 Gy胸部照射以建立放射性肺损伤模型,照射前2 h及以后每日腹腔注射艾迪及甲泼尼龙.分别于照射后1,24,72 h及1,2,4,8,16和24周处死小鼠,取左肺固定做组织切片,行苏木精-伊红(HE)染色观察病理变化、Masson染色观察胶原形成和免疫组化检测转化生长因子β1(TGF-β1)蛋白含量,取右肺行Western-blot测定TGF-β1蛋白含量,Real-time 聚合酶链反应(PCR)测定TGF-β1mRNA含量.结果 小鼠在接受照射后于1~2周出现放射性肺炎表现,TGF-β1mRNA和蛋白含量升高,但在给予艾迪注射液和甲泼尼龙处理组中TGF-β1mRNA和蛋白相对含量较照射组少,差异有统计学意义(P<0.05),照射+艾迪组和照射+甲泼尼龙组差异无统计学意义.在照射后16及24周观察到纤维形成增加,但照射+艾迪组和照射+甲泼尼龙组较照射组少.结论 艾迪注射液和甲泼尼龙可以下调因照射引起的TGF-β1mRNA和蛋白含量上升,二者在此作用上未观察到差别,这可能是其减轻放射性肺损伤的关键. Objective To study the effect of aidi injection on radiation-induced lung injury and the probable Mechanism. Methods One hundred and twenty C57BL/6 mice were exposed to either sham radiation or single fraction of12 Gy delivered to the thorax. Four groups were defined as follows:in normal control group,the mice received neither radiation nordrug;in aidi injection+radiation group,the mice received radiation and aidi injection;in Solu Medrol+radiation group,the micereceived Solu Medrol;in radiation group,the mice were exposed to radiation. Aidi or Solu Medrol were injected intraperitoneally 2hbefore the radiation and daily after the radiation. Mice were sacrificed 1,24,72 hours,1 ,2 ,4,8,16 and 24 weeks after radiation.The left lungs were fixed and sectioned. The sections were stained by haematoxylin and eosin, masson stain andimmunohistochemical stain for transforming growth factor β1(TGF-β1 ). The right lungs were collected to detect TGF-β1 mRNAexpression by reverse transcipiase quantitative real-time polymerase chain reaction (RT-PCR) and TGF-β1 protein expression byWestern blotting. Results Pneumonitis developed 1 to 2 weeks after radiation. Their TGF-β1 mRNA and protein expressionlevels in radiation-treated mice were significantly higher than those in normal control group (both P〈0. 05). But the effects werereversed by aidi and Solu Medrol treatment (P〈0. 05). The TGF-β1 mRNA and protein expression levels were not significantlydifferent between aidi and Solu Medrol treatment. Conclusion Both aidi injection and Solu Medrol can significantly down-regulate TGF-β1 mRNA and protein expression levels in the lungs of mice with radiation-induced lung injury. There is nosignificant difference in the effect between aidi injection and Solu Medrol.
出处 《医药导报》 CAS 北大核心 2014年第2期184-188,共5页 Herald of Medicine
关键词 艾迪注射液 肺损伤 放射性 转化生长因子Β1 Aidi injection Radiation-induced lung injury Transforming growth factor-1
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  • 1PAUL R G,FARZAN S,MITCHELL S A. Radiation pulm-onary toxicity: from mechanisms to management [ J ].Seminars Radiation Oncology,2010,20(3):201-207.
  • 2PAIMAN G,LAWRENCE B M,ZELJKO V,et al. Radiation-induced lung injury: assessment, management, andprevention[J]. Oncology,2008,22(1):37-47.
  • 3王景娜,刘莉.中药在放射性肺损伤防护中的作用[J].现代肿瘤医学,2008,16(10):1800-1803. 被引量:7
  • 4CLAUDIA E R,FALK W,CHRISTIAN R,et al. Modulationof radiation-induced tumour necrosis factor a ( TNF-琢)expression in the lung tissue by pentoxifylline [ J ].Radiotherapy Oncology,2002,64(2):177-187.
  • 5FRICDRICHS K,GLUBA S,EIDTMANN H,et al. Overex-pression of P53 and prognosis in breast cancer[J]. Cancer,1993,72(12):3641-3647.
  • 6ZHAO W,ROBBINS M E. Inflammation and chronic oxida-tive stress in radiation-induced late normal tissue injury[J]. Curr Med Chem,2009,16(2):130-143.
  • 7M A,VAN DYKJ,YEUNG I W,et al. Partial volume ratlung irradiation ; assessment of early DNA damage indifferent lung regions and effect of radical scavengers[J ].Radio ther Oncol,2003 ,66 (1) :95-102.
  • 8TSOU TSOU P G,KOU KOURA KIS M I. Radiation pneu-monitis and fibrosis:mechanisms underlying its pathogenesisand implications for future research[J]. Int J Radiat OncolBiol Phys,2006,66(5):1281-1293.
  • 9WILSON M S,WYNN T A. Pulmonary fibrosis:pathogen-esis,etiology and regulation[J]. Mucosal Immunol,2009 ,2(2):103-121.
  • 10RUBIN P,JOHNSTON C J,WILLIAMS J P,et al. A per-petual cascade of cytokines post irradiation leads topulmonary fibrosis[J]. Int J Radiat Oncol Biol Phys,1995,33(1):99-109.

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  • 1喻杰,汪步海,张西志,曹文淼.苦参碱对放射性肺炎转化生长因子β_1表达水平影响的研究[J].云南医药,2013,34(6):464-468. 被引量:4
  • 2ZARIC B, STOJSIC V, TEPAVAC A, et al. Adjuvant chemo- therapy and radiotherapy in the treatment of non-small cell lung cancer ( NSCLC ) [ J ]. J Thorac Dis,2013,5 ( Suppl 4 ) : S371 -S377.
  • 3MURPHY J O, SACCHINI V S. New innovative techniques in radiotherapy for breast cancer [J].Minerva Chir,2013, 68(2) :139-154.
  • 4FOKAS E, WEISS C, RODEL C. The role of radiotherapy in the multimodal management of esophageal cancer [ J ]. Dig Dis,2013,31 ( 1 ) :30-37.
  • 5FAY M, POOLE C M, PRATT G. Recent advances in radiotherapy for thoracic tumours [ J]. J Thorac Dis, 2013,5 (Suppl 5) :S551-S555.
  • 6CANNON D M, MEHTA M P, ADKISON J B, et al. Doselimiting toxicity after hypofractionated dose-escalated radiotherapy in non-small-cell lung cancer [ J ]. J Clin Oncol,2013,31 (34) :4343-4348.
  • 7DING N H, LI J J, SUN L Q. Molecular mechanisms and treatment of radiation-induced lung fibrosis [ J ]. Curr Drug Targets ,2013,14 ( 11 ) : 1347-1356.
  • 8MARTINEZ C O, MCHALE M J, WELLS J T, et al. Regulation of skeletal muscle regeneration by CCR2-activating chemokines is directly related to macrophage recruitment [ J]. Am J Physiol Regul Integr Comp Physiol, 2010,299 ( 3 ) : R832-842.
  • 9CHO Y J, YI C O, JEON B T, et al. Curcnmin attenuates radiation-induced inflammation and fibrosis in rat lungs [J]. Korean J Physiol Pharmacol,2013,17(4) :267-274.
  • 10LEPRIEUR E G, FERNANDE Z D, CHATELLIER G, et al. Acute radiation pneumonitis after conformational radiotherapy for nonsmall cell lung cancer: clinical, dosimetric, and associated-treatment risk factors [ J ]. J Cancer Res Ther,2013,9(3) :447-451.

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