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雷公藤甲素对体外培养大鼠气道平滑肌细胞增殖及原癌基因的影响 被引量:1

Study on effects of triptolide on proliferation of airway smooth muscle cells and expression of oncogene in vitro
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摘要 目的 探讨雷公藤甲素 (triptolide ,TL)对培养的大鼠气道平滑肌细胞 (ASMC)增生及原癌基因c fos与c jun表达的影响。方法 按不同药物分为 6组 ,TL组 (浓度分别为 5 ,2 0 ,80 ,32 0 ,12 80 μg·L-1)及地塞米松 1mg·L-1组 ,采用MTT法检测不同浓度药物对ASMC增殖的影响 ,同时进行逆转录 聚合酶链反应 (RT PCR)检测各组c fos ,c jun的mRNA表达水平。 结果 MTT方法显示TL对ASMC增殖有明显抑制作用 ,并呈剂量依赖性 ,TL的IC50 为 5 1.5 2mg·L-1;RT PCR方法显示TL浓度分别为 80 ,32 0 ,12 80 μg·L-1和地塞米松 1mg·L-1能显著抑制c fos ,c junmRNA表达。 结论 TL有抑制ASMC增生的作用 ,其机制可能与下调c fos和c jun表达有关。 OBJECTIVE: To investigate the effects of triptolide on airway smooth muscle cells (ASMC) proliferation and expressions of oncogene c-fos and c-jun in culturing ASMC. METHODS: The primary ASMC from rat were collected and cultured and studied. The effects of triptolide at different doses (5,20,80,320 and 1 280 μg&middotL-1) and dexamethasone (1 mg&middotL-1) on ASMC proliferation were studied by MTT method. The mRNA expressions of c-fos and c-jun form ASMC were examined by RT-PCR. RESULTS: The ASMC proliferation was inhibited at the dose (IC50 = 51.52 mg&middotL-1). The mRNA expression of c-fos and c-jun in ASMC was also inhibited by triptolide (80,320 and 1 280 μg&middotL-1)and dexamethasone. CONCLUSIONS: It suggested that triptolide remarkably inhibited ASMC proliferation probably by suppressing the expression of c-fos and c-jun.
出处 《中国药学杂志》 EI CAS CSCD 北大核心 2003年第5期348-350,共3页 Chinese Pharmaceutical Journal
基金 广东省高教厅课题 (973 5 )
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  • 1王长征,王春霞,金运林,钱桂生.哮喘豚鼠IL-5、IL-3、GM-CSF mRNA表达及雷公藤内酯醇的影响[J].中华微生物学和免疫学杂志,1998,18(2):145-148. 被引量:17
  • 2Redington AE, Howarth PH. Airway wall remodeling in asthma[J]. Thorax ,1997,52(4) :310.
  • 3Bento AM, Hershenson MB. Airway remodeling: potential contribu-tions of subepithelial fibrosis and airway smooth muscle hcpertrophy/hyperplasia to airway narrowing in asthma[J]. Allergy Asthma Proc, 1998,19(6) :353.
  • 4Fryer A, Huang YC, Rao G, et al. Selective O-desulfation producesnonanticoagulant heparin that retains pharmacological activity in the lung[J]. J Pharmacol Exp Ther, 1997,282(1) : 208.
  • 5Demoly P, Basset SN, Chanez P, et al. c-fos proto-oncogene expression in brochial biopsies of asthmatics[J]. Aim J Respir Cell Mol Biol, 1992,7( 1 ) : 128.
  • 6Panettieri RA, Goldie RG, Rigby PJ, et al. Endothelin-l-induced potentiation of human airway smooth muscle proliferation: an ETA receptor mediated phenomenon[J]. Br J Pharmacol, 1996,118(1) :191.
  • 7Mckay S,de Jongste JC,Saxena PR, et al. Angiotensin Ⅱ induces hyperteophy of human airway smooth muscle cells expression of transcription factor and transforming growth factor-betal[J]. Am J Respir Cell Mol Biol, 1998,18( 6 ) :823.
  • 8Walker TR, Moore SM, Lawson MF, et al. Platelet-derived growth factor-BB and thrombin activate phosphatidylinositol 3-Kinase and protein Kinase B: role in mediating airway smooth muscle proliferation[ J ]. Mol Pharmacol, 1998,54 (6) : 1007.
  • 9Kelleher MD,Abe MK, Chao TS, et al. Role of MAP klnase activationin bovine tracheal smooth muscle mitogenesis [ J ]. Am J Physiol, 1995,268 (6 Pt 1 ) : 894.
  • 10De S,Zelazny ET,Souhrada JF, et al. Interleukin -1 beta stimuhates the proliferation of cultured airway smooth muscle cells via phatdet-derived growth factor[J]. Am J Respir Cell Mol Biol,1993,9(6) :645.

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