摘要
目的:观察己酮可可碱(PTX)对创伤性急性肺损伤(ALI)家兔肺组织肿瘤坏死因子 α基因(TNF αm RNA)表达的影响,探讨PTX在创伤性ALI治疗中的作用机制。方法:采用创伤性ALI模型,实验动物随机分为正常对照组(8 只)、创伤性ALI模型组(24 只)和PTX治疗组(24 只),用ELISA 和逆转录聚合酶链反应(RT PCR)方法分别检测不同时间点血浆TNF α含量及肺组织TNF αm RNA表达水平。结果:血浆TNF α含量创伤性ALI模型组于创伤后1.5 小时达峰值〔(1.27±0.26)μg/L〕,肺组织TNF αm RNA表达于创伤后8 小时达高峰(2.67±0.18),二者在时间上不完全平行。PTX治疗组肺组织TNF αm RNA 的表达和外周血TNF α含量均低于创伤性ALI模型组(P均< 0.05)。结论:PTX能有效抑制创伤性ALI家兔肺组织TNF αm RNA表达;本研究为PTX治疗创伤性ALI提供了实验依据。
Objective:To investigate the effects of pentoxifylline (PTX) on pulmonary expression of tumor necrosis factorα (TNFα) in rabbits with acute lung injury (ALI),and explore the mechanism underlying PTX on the treatment of ALI.Methods:Traumatic ALI models were used in this study.Rabbits were randomly divided into three groups as follows:normal control group ( n =8),ALI model group ( n =24),and PTX treatment group ( n =24).ELISA and reversetranscription polymerase chain reaction methods were used to detect the TNFα contents in plasma and TNFα mRNA levels in lung tissues at various intervals.Results:Peak value of TNFα in plasma was found at 1 5 hours after trauma 〔(1 27±0 26)μg/L〕,while the peak value of TNFα mRNA in lung tissues was presented at 8 hours after trauma (2 67±0 18),no parallel pattern was found between plasma TNFα and pulmonary TNFα mRNA levels.Treatment with PTX could markedly inhibit the expression of pulmonary TNFα mRNA and decrease plasma TNFα contents following traumatic ALI (both P <0 05).Conclusions:PTX can effectively inhibit the expression of pulmonary TNFα mRNA in rabbits with traumatic ALI.The present study may provide the experimental basis for use of PTX in treating traumatic ALI.
出处
《中国危重病急救医学》
CSCD
1999年第11期643-645,共3页
Chinese Critical Care Medicine
基金
国家自然科学基金
关键词
创伤
肺损伤
急性
己酮可可碱
基因表达
治疗
trauma
acute lung injury
pentoxifylline
gene expression
tumor necrosis factor