网络首发:2013-01-20,
纸质出版:2013
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罗晨芳. NO吸入对肝移植急性肺损伤大鼠肺组织iNOS?IL-1β及IL-6的影响[J]. 中山大学学报(医学科学版), 2013,34(1).
Effects of Inhaled Nitric Oxide on iNOS, IL-1β, and IL-6 of Lung Tissue in Rats with Acute Lung Injury Post-Liver Transplantation[J]. Journal of Sun Yat-sen University (Medical Sciences), 2013, 34(1).
【目的】 观察一氧化氮(NO)吸入对肝移植急性肺损伤大鼠肺组织诱导型NO合酶(iNOS)?白细胞介素-1β(IL-1β)?白细胞介素-6(IL-6)水平的影响与意义?【方法】 选用SD大鼠24只
按随机数字表法分为对照组(C组)?自体原位肝移植组(M组)和NO吸入组(T组)
每组8只?对照组开腹游离肝叶后即关腹
后两组行大鼠自体原位肝移植?对照组及自体原位肝移植组术后于室内吸空气
NO吸入组术后即放入特制的密封盒内(NO体积分数为20 × 10-6)?手术结束后8 h行肺脏病理检查
测定肺组织干湿质量比(W/D)
并检测iNOS?IL-1β?IL-6水平?【结果】 ① C组肺组织结构基本正常
M组肺组织炎症损伤明显
T组肺组织炎症损伤较M组明显减轻?②M组肺组织W/D明显高于对照组
T组则低于M组
但仍高于对照组?③M组iNOS活性及蛋白表达?IL-1β?IL-6水平较C组明显升高
T组则较M组降低
但仍高于C组?【结论】 肝移植术后NO吸入可抑制肺组织iNOS活性及蛋白表达
降低IL-1β?IL-6水平
肺组织病理损伤减轻
干湿质量比下降?
【Objective】 To study the effects of inhaled nitric oxide (iNO) on iNOS (inducible nitric oxide synthase)
IL-1β (interleukin-1β) and IL-6 (interleukin-6) of lung tissue in rats with acute lung injury post liver transplantation. 【Methods】 Twenty-four SD rats were randomly divided into three groups: 1) a sham-operation control group (C group)
the abdomen was only opened and then closed besides the liver lobes were isolated
without NO inhalation. 2) an autologous OLT group (M group)
received autologous OLT
without NO inhalation. 3) an iNO group (T group)
received autologous OLT
with 20 × 10-6 NO inhalation. The lung was removed at 8 h after operation and pathological changes were observed. The concentration of iNOS
IL-1β
and IL-6 in lung tissue were respectively examined in each group
lung wet -to- dry weight ratio (W/D) were also measured. 【Results】 (1) The lung pathological section of C group was normal
but in M group it showed inflammatory injury. The lung inflammatory injury was improved in T group. (2) Lung dry-to-wet weight ratio in M group was higher than in C group. It decreased in T group
but still higher than in C group. (3) The levels of iNOS
IL-1β
and IL-6 in M group were higher than in C group. All decreased in T group
but still higher than in C group. The expression of iNOS showed the same change. 【Conclusion】 Inhaled NO after autologous OLT inhibits the activity of iNOS in lung
decreases the production of IL-1β and IL-6
attenuates pathological changes
and decreased lung wet -to- dry weight ratio.
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