当前位置: 首页 > 期刊 > 《第四军医大学学报》 > 2006年第14期
编号:11177053
先天性心脏病合并肺动脉高压一氧化氮合酶mRNA表达及临床意义
http://www.100md.com 《第四军医大学学报》 2006年第14期
心脏缺损,先天性;高血压,肺性;一氧化氮合酶;RNA,信使,,心脏缺损,先天性;高血压,肺性;一氧化氮合酶;RNA,信使,【摘要】
     FENG JiaTao1, SU YanLing1, GONG GuangFu2, HU DongXu2, CAOYa2

    1Department of Cardiovascular Surgery, First Peoples Hospital of Foshan City, Foshan 528000, China, 2Department of Cardiovascular Surgery, Xiangya Hospital, Zhongnan University, Changsha 410011, China

    【Abstract】 AIM: To explore the pathophysiological significance of nitric oxide(NO) and nitric oxide synthase(NOS) in congenital heart defects with pulmonary hypertension. METHODS: Twentyfour patients with congenital heart defects were divided into 3 groups: mild pulmonary hypertension group(n=8), moderate or severe pulmonary hypertension group(n=9), and nonpulmonary hypertension group(n=7). NOS mRNA expression was detected in lung tissues with reverse transcriptase polymerase chain reaction (RTPCR). RESULTS: The NOS mRNA expression levels in the patients with moderate or severe pulmonary hypertension were much lower than those in the ones with mildpulmonary hypertension or nonpulmonary hypertension (P<0.05). There was an inverse correlation between the NOS mRNA expression level and the pulmonary arteriopathy in the patients with pulmonary hypertension (r=-0.833, P<0.01). CONCLUSION: In patients with congenital heart defects associated with pulmonary hypertension, NO and NOS play a role in pathological process of pulmonary arteriopathy, and the NOS mRNA expression level was proportional to the severity of pulmonary hypertension or pulmonary arteriopathy. ......

您现在查看是摘要页,全文长 11087 字符