局解手术学杂志
跼解手術學雜誌
국해수술학잡지
JOURNAL OF REGIONAL ANATOMY AND OPERATIVE SURGERY
2014年
6期
583-585,586
,共4页
王秀芹%王凯国%罗红敏%李浩%王宝胜%王培民
王秀芹%王凱國%囉紅敏%李浩%王寶勝%王培民
왕수근%왕개국%라홍민%리호%왕보성%왕배민
肺损伤%机械通气%过氧化体增殖物激活受体γ
肺損傷%機械通氣%過氧化體增殖物激活受體γ
폐손상%궤계통기%과양화체증식물격활수체γ
lung injury%mechanical ventilation%peroxisome proliferator activated receptor-γ(PPARγ)
目的:观察PPARγ在通气相关性肺损伤大鼠肺组织中的表达,探讨PPARγ在通气相关性肺损伤中的作用。方法清洁雄性SD大鼠,随机分为大潮气量( Tidal volume,VT)组,Vt=12 mL;小潮气量组,Vt=6 mL;自主呼吸组。每组又分为3个亚组:即通气1h、4h、8h组。于各时间段末放血处死动物,收集肺组织和肺灌洗液标本,测定肺灌洗液中蛋白总量、白细胞计数;测定肺组织湿/干重比( W/D);逆转录聚合酶链反应检测PPARγmRNA的表达;western blot检测PPARγ蛋白的变化。结果大潮气量组机械通气4 h、8 h后,与小潮气量组及自主呼吸组相比,肺灌洗液中白细胞计数、蛋白总量明显增加(P <0.01),肺 W/D 增加(P<0.01);肺组织出现明显病理组织学损伤;PPARγmRNA和PPARγ蛋白表达减少(P<0.01)。通气1 h时,各组之间比较无显著差异(P>0.05)。结论通气相关性肺损伤大鼠肺组织中PPARγ基因和蛋白表达下降,这可能与炎症损伤和持续有关。
目的:觀察PPARγ在通氣相關性肺損傷大鼠肺組織中的錶達,探討PPARγ在通氣相關性肺損傷中的作用。方法清潔雄性SD大鼠,隨機分為大潮氣量( Tidal volume,VT)組,Vt=12 mL;小潮氣量組,Vt=6 mL;自主呼吸組。每組又分為3箇亞組:即通氣1h、4h、8h組。于各時間段末放血處死動物,收集肺組織和肺灌洗液標本,測定肺灌洗液中蛋白總量、白細胞計數;測定肺組織濕/榦重比( W/D);逆轉錄聚閤酶鏈反應檢測PPARγmRNA的錶達;western blot檢測PPARγ蛋白的變化。結果大潮氣量組機械通氣4 h、8 h後,與小潮氣量組及自主呼吸組相比,肺灌洗液中白細胞計數、蛋白總量明顯增加(P <0.01),肺 W/D 增加(P<0.01);肺組織齣現明顯病理組織學損傷;PPARγmRNA和PPARγ蛋白錶達減少(P<0.01)。通氣1 h時,各組之間比較無顯著差異(P>0.05)。結論通氣相關性肺損傷大鼠肺組織中PPARγ基因和蛋白錶達下降,這可能與炎癥損傷和持續有關。
목적:관찰PPARγ재통기상관성폐손상대서폐조직중적표체,탐토PPARγ재통기상관성폐손상중적작용。방법청길웅성SD대서,수궤분위대조기량( Tidal volume,VT)조,Vt=12 mL;소조기량조,Vt=6 mL;자주호흡조。매조우분위3개아조:즉통기1h、4h、8h조。우각시간단말방혈처사동물,수집폐조직화폐관세액표본,측정폐관세액중단백총량、백세포계수;측정폐조직습/간중비( W/D);역전록취합매련반응검측PPARγmRNA적표체;western blot검측PPARγ단백적변화。결과대조기량조궤계통기4 h、8 h후,여소조기량조급자주호흡조상비,폐관세액중백세포계수、단백총량명현증가(P <0.01),폐 W/D 증가(P<0.01);폐조직출현명현병리조직학손상;PPARγmRNA화PPARγ단백표체감소(P<0.01)。통기1 h시,각조지간비교무현저차이(P>0.05)。결론통기상관성폐손상대서폐조직중PPARγ기인화단백표체하강,저가능여염증손상화지속유관。
Objective To observe the changes of PPARγ expression in ventilator-induced lung injury rats and explore the role of PPARγ in the pathogenesis of ventilator-induced lung injury. Methods Sixty male Sprague-Dawley rats were randomly divided into 3 groups ( n=21 each ):group N received large tidal volume with mechanical ventilation ( Vt=12 mL/kg);group C received lower tidal volume with mechanical ventilation ( Vt=6 mL/kg);group R received room air without mechanical ventilation. Rats in every group were randomly divided into 3 subgroups respectively by 1,4 and 8 h. The samples of lung were collected at 1,4 and 8 h after ventilation. Lung pathological examina-tion, total protein and white blood cells in bronchoalveolar fluid and wet-to-dry weight were detected. The exoressions of PPARγmRNA were detected by RTPCR;PPARγ protein in lung tissues was detected by western bolt. Result After 4 and 8 h ventilation in group N,total pro-tein and WBC in bronchoalvelor fluid,W/D were markedly higher than those of group C and R (P <0. 01). While PPARγ mRNA and PPARγ protein were decreased than those of group C and R (P<0. 01). There were no difference after 1 h ventilation in three group (P>0. 05). Conclusion PPARγmRNA and protein expressions in the rats lung tissue of ventilator-induced lung injury were decreased and as-sociated with inflammation and damage of lung tissue.