过氧化物酶体

茶多酚对酒精性肝病过氧化物酶体增殖物激活受体α及核因子-κB的调节作用

Regulatory Effects of Tea Polyphenols on Peroxisome Proliferator-Activated Receptor α and Nuclear Factor - κ B in Alcoholic Liver Disease Models

罗格列酮对日本血吸虫病肝纤维化小鼠肝组织核因子-κB和过氧化物酶体增殖物激活受体γ表达的影响

Effect of rosiglitazone on the activity of hepatic nuclear factor-kappa B and expression of peroxisome proliferator-activated receptor - γ in mice with liver fibrosis due to schistosoma japonicum infection

复方茯苓制剂对大鼠前脂肪细胞增殖分化以及过氧化物酶体增生物激活受体γmRNA表达的影响

Effect of compound poria prescription on proliferation and differentiation and expression of PPAR γ mRNA in rat preadipocytes

靶向过氧化物酶体增殖活化受体-γ基因siRNA载体的构建

Construction of target siRNA vector to PPAR - γ gene

生长激素、胰岛素以及过氧化物酶体增殖物活化受体（PPAR）α、PPARγ和肝X受体激动剂等可影响脂联素受体的表达。

Growth hormone , insulin and agonists of PPAR α, PPAR γ and LXR affect the expression of adiponectin receptors .

过氧化物酶体增殖剂活化受体γ（PPARγ）是一个由配体激活的核转录因子，属于核激素受体（nuclearhormonereceptor）超家族。

Peroxisome proliferator activated receptor γ ( PPAR γ ) is a very important ligand activated nuclear transcription factor , belonging to nuclear hormone receptor superfamily .

目的构建靶向过氧化物酶体增殖活化受体-γ（PPAR-γ）基因的siRNA载体。

Objective To construct the target siRNA vector to peroxisome proliferator-activated receptor - γ( PPAR - γ) .

调控过氧化物酶体生物合成和增殖的microRNA的计算机分析

Computational Analyses of MicroRNA Involved in Peroxisome Biogenesis and Proliferation

菠菜叶过氧化物酶体转变甘油酸为丝氨酸的NAD供应

Supplement of NAD for the glycerate to serine conversion in intact spinach leaf Peroxisomes

目的：探讨动脉粥样硬化病变组织中过氧化物酶体增殖激活受体γ（PPARγ）的表达。

Objective To investigate the expression of peroxisome proliferator activated receptor γ ( PPAR γ) in atherosclerosis .

综述了过氧化物酶体增殖激活受体（PPAR）中α亚型的结构、功能和配体研究的最新进展。

The peroxisome proliferators - actived receptors ( PPAR ) are a member of the nuclear receptors .

叶过氧化物酶体在NAD和丙氨酸存在时，转变甘油酸成为丝氨酶。

Leaf peroxisomes convert glyceric acid to serine in the presence of NAD and alanine .

过氧化物酶体增殖剂PFOA对小鼠免疫系统的影响

Effects of peroxisome proliferators PFOA on immune system of mice

目的在大肠杆菌中表达过氧化物酶体增殖物激活受体γ共激活因子-1（PPARγC1）与谷胱甘肽-S转移酶（GST）的融合蛋白，并制备抗PPARγC1的多克隆抗体。

Objective To express the fusion protein of glutathione S-transferase ( GST ) and peroxisome proliferator-activated receptor-gamma coactivator-1 ( PPAR γ C1 ) in E.

目的初步探讨过氧化物酶体增殖体活化受体γ（PPARγ）之配体能否抑制人胆囊上皮细胞的炎症反应。

Objective To study the regulatory ability of peroxisome proliferator-activated receptor γ( PPAR γ) ligands to the inflammatory response in human gallbladder epithelial cells .

目的：观察溃疡性结肠炎（Ulcerativecolitis，UC）大鼠肠黏膜中过氧化物酶体增殖物激活受体γ（PPARγ）的表达。

Objective : To observe the expression of the peroxisome proliferators_ activated receptor γ( PPAR γ) in colonic mucosa of rat with ulcerative colitis ( UC ) .

用双2乙基己基酚酞酸酯（DEHP）诱导大鼠肝过氧化物酶体增殖，然后用蔗糖密度梯度离心法分离大鼠肝线粒体，用毛细管气相色谱法测定肝线粒体中的脂肪酸含量。

Mitochondria from rat liver were isolated with sucrose density gradient centrifugation , and their fatty acids were assayed by gas chromatography .

RS在植物细胞中的细胞核、线粒体基质空间、微体（过氧化物酶体）、叶绿体类囊体膜中的分布概率分别为：88%、36%、31.3%、28%。

The distribution probability of RS was respectively 88 % , 36 % , 31.3 % , 28 % in nucleus , mitochondrial matrix space , microbody ( peroxisome ) , chloroplast thylakoid membrane .

化疗药物联合过氧化物酶体增殖物激活受体（PPAR）的配体能够协同抑制肺细胞癌及卵巢癌细胞。

Chemotherapy given in combination with ligands for the peroxisome proliferator-activated receptor - ( PPAR ) synergistically inhibits the growth of lung and ovarian cancer cell lines .

PPAR（peroxisomeproliferator-activatedreceptor），即过氧化物酶体增殖剂激活受体，是一类由配体激活的核转录因子，为核受体家族的一员。PPAR在调节脂类代谢及机体能量代谢平衡方面有重要作用。

PPAR ( Peroxisome proliferator-activated receptors ), are ligand-activated transcription factors belonging to the nuclear hormone receptor superfamily that functions as critical regulators of lipid and energy homeostasis .

目的：观察过氧化物酶体增生物激活受体（PPAR）-r配体罗格列酮治疗葡聚糖硫酸钠（DSS）诱导小鼠结肠炎的疗效。

Aims : To investigate the effect of peroxisome proliferator-activated receptor ( PPAR ) - r li-gand rosiglitazone on dextran sulfate sodium ( DSS ) - induced colitis of mice .

过氧化物酶体增殖物活化受体γ激动剂对肾病大鼠肾组织nephrin表达的调控

Transcriptional Regulation of nephrin Gene by Peroxisome Proliferator-Activated Receptor γ Agonist in Nephridial Tissue in Nephropathy Rats

罗格列酮是过氧化物酶体增殖激活受体γ（PPARγ）激动剂，它能够诱导非小细胞肺癌凋亡并抑制非小细胞肺癌细胞侵袭及转移。

Rosiglitazone is a peroxisome proliferator-activated receptor γ( PPAR γ) agonists , which can induce apoptosis in non-small cell lung cancer and inhibit non-small cell lung cancer cell invasion and metastasis .

目的研究肺癌细胞上过氧化物酶体增生物激活受体γ（PPARγ）的表达及其经配体（激动剂）活化后抑制肺癌细胞生长的机制。

AIM To study the expression peroxisome proliferator activated receptor γ( PPAR γ) in lung cancer cell and the mechnism of PPAR γ activated by ligands inhibiting human lung cancer cell growth .

基于报告基因检测技术和过氧化物酶体增殖体激活受体γ（PPARγ）信号通路，建立PPARγ信号通路的筛选模型，并应用于初筛具有胰岛素增敏活性的小分子化合物。

Second , another drug screening model based on reporter gene and the signal transduction of PPAR γ system was established for finding new small molecular compounds with activity of improving insulin sensitivity .

目的：观察日本血吸虫病肝纤维化小鼠肝脏肝组织核因子-κB（NF-κB）的活性和过氧化物酶体增殖物激活受体γ（PPARγ）的表达，及PPARγ配体罗格列酮对其表达的影响。

AIM : To investigate the effect of rosiglitazone on the binding activity of hepatic nuclear factor-kappa B ( NF - κ B ) and the expression of peroxisome proliferator-activated receptor gamma ( PPAR γ) in mice with liver fibrosis caused by schistosoma japonicum infection .

研究背景和目的：过氧化物酶体增殖物激活受体（PPARs）是一类由配体激活的核转录因子，属于核内受体超家族成员。

Background and Objective : Peroxisome proliferator-activated receptors ( PPARs ) are a class of ligand-activated nuclear transcription factor belonging to the nuclear receptor superfamily .

目的：用贵州小香猪建立动脉粥样硬化（As）动物模型，探讨该模型中B类I型清道夫受体（SR-BI）和过氧化物酶体增殖物激活受体γ（PPARγ）表达的变化。

Aim : To study the expressions of scavenger receptor class B type I ( SR-BI ) and peroxisome proliferator-activated receptor γ( PPAR γ) in atherosclerotic mini swine and provide a new mechanism for investigating the pathogenesis of atherosclerosis .

目的探讨过氧化物酶体增殖物激活受体-γ（PPAR-γ）经其配体吡咯列酮（pioglitazone，PGZ）激活后，对胆管癌细胞体外侵袭力的影响及机制。

Objective To explore the effect and mechanism of ligand pioglitazone ( PGZ ) activating PPAR - γ on the invasiveness of cholangiocarcinoma cell in vitro .

目的：观察化痰活血方对高脂血症大鼠肝脏过氧化物酶体增殖物激活受体α（PPARα）、乙酰辅酶A氧化酶（ACO）表达的影响。

Objective : To observe effects of Huatan Huoxue Prescription on expressions of peroxisome proliferation substance activating receptor α ( PPAR α) and the target gene acetyl-CoA oxidase ( ACO ) in the liver of the rat with hyperlipemia .