中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
The Chinese Journal of Clinical Pharmacology
2015年
16期
1652-1655
,共4页
苏启表%韦桂宁%王来友%苏华%廖丽贞%赵杰%李国标%李卫东
囌啟錶%韋桂寧%王來友%囌華%廖麗貞%趙傑%李國標%李衛東
소계표%위계저%왕래우%소화%료려정%조걸%리국표%리위동
泛素-蛋白酶体系统%P-糖蛋白%表达下调
汎素-蛋白酶體繫統%P-糖蛋白%錶達下調
범소-단백매체계통%P-당단백%표체하조
ubiquitin -proteasome pathway%P -glycoprotein%down-regulation
目的:研究急性炎症状态下大鼠肝 P -糖蛋白翻译后修饰的机制。方法20只大鼠随机分成2组,模型组10只,对照组10只。模型组予以腹腔单次注射5 mg? kg-1脂多糖,对照组予以腹腔单次注射等体积0.9%氯化钠。24 h后,取肝组织,制备匀浆,分别用Western blot、免疫沉淀法和荧光法检测模型组和对照组的肝P-糖蛋白表达水平、P-糖蛋白泛素化水平和26S蛋白体活性的变化。结果与对照组相比,模型组肝 P -糖蛋白蛋白表达水平显著降低(P<0.01),肝P-糖蛋白泛素化水平显著升高(P<0.01),26S蛋白体的活性显著升高(P<0.01)。结论泛素-蛋白酶体途径参与急性炎症状态下大鼠肝P-糖蛋白的下调。
目的:研究急性炎癥狀態下大鼠肝 P -糖蛋白翻譯後脩飾的機製。方法20隻大鼠隨機分成2組,模型組10隻,對照組10隻。模型組予以腹腔單次註射5 mg? kg-1脂多糖,對照組予以腹腔單次註射等體積0.9%氯化鈉。24 h後,取肝組織,製備勻漿,分彆用Western blot、免疫沉澱法和熒光法檢測模型組和對照組的肝P-糖蛋白錶達水平、P-糖蛋白汎素化水平和26S蛋白體活性的變化。結果與對照組相比,模型組肝 P -糖蛋白蛋白錶達水平顯著降低(P<0.01),肝P-糖蛋白汎素化水平顯著升高(P<0.01),26S蛋白體的活性顯著升高(P<0.01)。結論汎素-蛋白酶體途徑參與急性炎癥狀態下大鼠肝P-糖蛋白的下調。
목적:연구급성염증상태하대서간 P -당단백번역후수식적궤제。방법20지대서수궤분성2조,모형조10지,대조조10지。모형조여이복강단차주사5 mg? kg-1지다당,대조조여이복강단차주사등체적0.9%록화납。24 h후,취간조직,제비균장,분별용Western blot、면역침정법화형광법검측모형조화대조조적간P-당단백표체수평、P-당단백범소화수평화26S단백체활성적변화。결과여대조조상비,모형조간 P -당단백단백표체수평현저강저(P<0.01),간P-당단백범소화수평현저승고(P<0.01),26S단백체적활성현저승고(P<0.01)。결론범소-단백매체도경삼여급성염증상태하대서간P-당단백적하조。
Objective To explore the expression of P -glycoprotein ( P-gp) in rat liver during acute inflammation ( AI ) and the possible mechanism involved.Methods Twenty rats were randomly divided into two groups:model group (n=10) and control group (n=10).The rats in model group were treated by a single 5 mg? kg -1 intraperitoneal injec-tion of lipopolysaccharide ( LPS).Control rats received equivalent injec-tion of sterile normal saline.The levels of P-gp, ubiquitinated P-gp and 26 S proteasome activity in both groups were analyzed by Western blot, immunoprecipitation and fluorescence detection, respectively. Results Compared to the control groups, ubiquitination levels of liver P-gp and 26S proteasome activity in model groups were significantly in-creased ( P<0.01 ) , accompanied by an decrease of liver P-gp protein expression level. Conclusion The participation of the ubiquitin -proteasome system in down-regulation of liver P-gp expression levels under AI conditions.