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作 者:彭雪梅[1] 席露[1] 李雅兰[1] 王仲红[1] 王华东[2]
机构地区:[1]暨南大学附属第一医院麻醉科,广东广州510632 [2]暨南大学医学院病理生理学系,国家中医药管理局病理生理学重点实验室,广东广州510632
出 处:《中国病理生理杂志》2010年第1期112-115,共4页Chinese Journal of Pathophysiology
基 金:2006年广东省中医药管理局资助项目(No.1060108);2007年广东省科技计划资助项目(No.2007B031402008)
摘 要:目的:探讨乳化氟碳结合川芎嗪对肝肺综合征(HPS)猪肝移植围手术期肺部炎症的影响及其机制。方法:采用慢性胆管结扎复制猪肝肺综合征模型,随机分为2组:(1)乳化氟碳结合川芎嗪(PFCL)组:肺内灌以20mL/kg的全氟碳乳剂(PFC)及川芎嗪(20mg/kg,气管内滴注),机械通气下进行原位肝移植;(2)机械通气对照(MV)组:常规MV下,进行原位肝移植。实验观察5h,实验结束后处死动物,取肺脏进行分析。结果:PFCL组肺脏的湿/干比值、肺通透指数及支气管肺泡灌洗液中白细胞计数均显著降低,与MV组比较差异显著(P<0.05);PFCL组肺组织及支气管肺泡灌洗液中肿瘤坏死因子α(TNF-α)、干扰素(IFN)-γ含量均显著低于MV组(P<0.05)。免疫组化染色发现,PFCL组肺组织炎症和上皮细胞核内NF-κBp65的含量明显低于MV组。结论:乳化氟碳结合中药川芎嗪可以有效地减少中性粒细胞浸润,抑制炎性细胞NF-κB的活化和细胞因子TNF-α与IFN-γ的表达,减轻HPS引起的肺损伤。AIM : To investigate the effects of perfluorocarbon and ligustrazine on lung injury during liver transplantation in pigs with hepatopulmonary syndrome. METHODS : A hepatopulmonary syndrome (HPS) model of pig was established by chronic bile duct ligation. The animals were assigned randomly to 2 groups : ( 1 ) Perfluorocarbon in combination with ligustrazine treatment groups ( PFCL group) : the pigs were treated with intratracheal instillation of perfluorocarban and ligustrazine; (2) The conventional mechanical ventilation group (MV group) : all animals were subjected to mechanical ventilation and orthotopic liver transplantation. After 5 h the lungs were harvested for further analysis. RESULTS: The lung wet to dry weight radio, puhnonary permeation index and leukocyte count in bronchoalveolar lavage fluids (BALF) in PFCL group significantly decreased compared to MV group ( P 〈 0. 05 ). Contents of tumor necrosis factor- α (TNF -α) and interferon-γ(IFN -γ) in the lung tissue, plasma and BALF of pigs in PFCL group were significantly lower than those in MV group (P 〈 0. 05). Moreover, the activation of NF -κB was inhibited markedly by PFCL. CONCLUSION: Perfluorocarbon in combination with ligustrazine effectively reduces the PMN accumulation in the lungs, inhibits TNF -or and IFN -γproduction and protects against lung injury during liver transplantation in pigs with hepatopulmonary syndrome.
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