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作 者:孙晓霞[1] 王健春[1] 唐笑迪[2] 赵雪俭[3]
机构地区:[1]吉林大学基础医学院机能科学实验中心,吉林长春130021 [2]吉林大学中日联谊医院放疗科,吉林长春130031 [3]吉林大学基础医学院病理生理教研室,吉林长春130021
出 处:《中国现代医学杂志》2006年第15期2298-2300,2305,共4页China Journal of Modern Medicine
基 金:吉林省自然科学基金资助项目(20030501)
摘 要:目的观察人参二醇组皂苷(PDS)对感染性休克大鼠血清中一氧化氮合酶(NOS)活性及一氧化氮(NO)含量的影响,探讨其抗感染性休克的作用机制。方法大鼠舌下静脉注射PDS进行预治疗,10min后注射细菌内毒素(LPS5mg/kg)复制感染性休克模型。实验动物随机分为对照(Control)组;内毒素休克(LPS)组;地塞米松(LPS+Dex)组;人参二醇组皂苷(LPS+PDS)组。颈动脉插管记录平均动脉压(MAP)。分别于休克后2h和4h腹主动脉取血,用硝酸还原酶法测定血清中NOS活性和NO2-/NO3-的含量,间接反映NO的水平。结果注射内毒素后,模型组的MAP迅速下降,在低水平维持,LPS+Dex组和LPS+PDS组的MAP未见明显下降,优于模型组(P<0.01);注射内毒素2h后模型组的血清NOS和NO明显升高,LPS+Dex组和LPS+PDS组NOS活性、NO2-/NO3-含量显著低于LPS组(P<0.05)。结论PDS能够明显改善内毒素休克大鼠的低血压状态,降低NOS活性、NO含量,并对其NO的生成具有抑制作用。[Objective] To study the effects of PDS on the endotoxic shock rats and its mechanism by analyzing serum NOS activity and NO levels. [Methods] PDS was injected into ranine vein and ten minutes later septic shock model was induced by injecting LPS 4 mg/kg. Rats were randomly divided into LPS, LPS+Dex, LPS+PDS and control groups respectively. MAP was measured through carotid arterial cannula and blood was collected through abdominal aorta 2 h and 4 h after shock. NOS activity, content of NO2^-/NO3^- in serum were assayed by nitrate reductase method to indirectly reflect NO content. [Results] MAP of model decreased signdficantly after injection of ETX and maintained at lower level. While MAP of LPS+Dex, LPS+PDS showed obvious decrease. NOS activity and NO con- tent of model increased significantly 2 h after injection of ETX while NOS activity and content of NO2^-/NO3^- of LPS+ Dex and LPS+PDS groups decreased obviously with compared with LPS group. [Conclusion] PDS can improve hypotension in septic shock rats, inhibit NOS activity and reduce NO content by inhibiting its production.
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