Zhang Qiu-jin, Shen Hong, Zhang Wei, Li Yin-ping, Li Tan-shi
Emergency Department, General Hospital of PLA, Beijing 100853, China.
Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2005 Jun;17(6):370-2.
To investigate the effects of a combination of naloxone and methylprednisolone on nuclear factor-kappaB (NF-kappaB) p65 expression in the lung tissue in lipopolysaccharide (LPS)-induced acute lung injury (ALI) in rats.
ALI models were reproduced by intratracheal instillation of LPS (3 mg/kg). Four hours after LPS instillation, rats were randomly divided into five groups: normal saline group, LPS group, methylprednisolone group, naloxone group (LPS+naloxone) and combined drug group (LPS+naloxone+methylprednisolone). The level of interleukin-8 (IL-8) in serum was measured by immunoassay. Meanwhile, the expression of NF-kappaB p65 in the lung tissue was determined with immunohistochemical staining.
Naloxone and methylprednisolone significantly reduced the LPS-induced increase in IL-8 concentrations in serum in vivo, and suppressed the activation of NF-kappaB p65 in the lung tissue.
NF-kappaB activation is involved in the LPS-induced ALI in rats. Combination of naloxone and methylprednisolone could suppress the increase of IL-8 content and NF-kappaB activation in the lung tissue of rat in vivo in our experiment.
探讨纳洛酮与甲泼尼龙联合应用对脂多糖(LPS)诱导的大鼠急性肺损伤(ALI)肺组织中核因子-κB(NF-κB)p65表达的影响。
通过气管内滴注LPS(3mg/kg)复制ALI模型。LPS滴注4小时后,将大鼠随机分为五组:生理盐水组、LPS组、甲泼尼龙组、纳洛酮组(LPS+纳洛酮)和联合用药组(LPS+纳洛酮+甲泼尼龙)。采用免疫分析法测定血清中白细胞介素-8(IL-8)水平。同时,用免疫组织化学染色法检测肺组织中NF-κB p65的表达。
纳洛酮和甲泼尼龙显著降低了LPS诱导的体内血清IL-8浓度升高,并抑制了肺组织中NF-κB p65的激活。
NF-κB激活参与了LPS诱导的大鼠ALI。在我们的实验中,纳洛酮与甲泼尼龙联合应用可抑制大鼠肺组织中IL-8含量的增加和NF-κB的激活。