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首页> 外文期刊>American Journal of Physiology >Effect of pioglitazone treatment on endoplasmic reticulum stress response in human adipose and in palmitate-induced stress in human liver and adipose cell lines
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Effect of pioglitazone treatment on endoplasmic reticulum stress response in human adipose and in palmitate-induced stress in human liver and adipose cell lines

机译:吡格列酮对人脂肪内质网应激反应以及棕榈酸酯诱导的人肝和脂肪细胞系应激的影响

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First published June 10, 2008; doi: 10.1152/ajpendo.90355.2008.-Obesity and elevated cytokine secretion result in a chronic inflammatory state and may cause the insulin resistance observed in type 2 diabetes. Recent studies suggest a key role for endoplasmic reticulum stress in hepatocytes and adipocytes from obese mice, resulting in reduced insulin sensitivity. To address the hypothesis that thiazolidinediones, which improve peripheral insulin sensitivity, act in part by reducing the endoplasmic reticulum stress response, we tested subcutaneous adipose tissue from 20 obese volunteers treated with pioglitazone for 10 wk. We also experimentally induced endoplasmic reticulum stress using palmitate, tunicamycin, and thapsigargin in the human HepG2 liver cell line with or without pioglitazone pretreatment. We quantified endoplasmic reticulum stress response by measuring both gene expression and phosphorylation. Pioglitazone significantly improved insulin sensitivity in human volunteers (P = 0.002) but did not alter markers of endoplasmic reticulum stress. Differences in pre- and posttreatment endoplasmic reticulum stress levels were not correlated with changes in insulin sensitivity or body mass index. In vitro, palmitate, thapsigargin, and tunicamycin but not oleate induced endoplasmic reticulum stress in HepG2 cells, including increased transcripts CHOP, ERN1, GADD34, and PERK, and increased XBP1 splicing along with phosphorylation of eukaryotk initiation factor eIF2a, JNK1, and c-jun. Although patterns of endoplasmic reticulum stress response differed among palmitate, tunicamycin, and thapsigargin, pioglitazone pretreatment had no significant effect on any measure of endoplasmic reticulum stress, regardless of the inducer. Together, our data suggest that improved insulin sensitivity with pioglitazone is not mediated by a reduction in endoplasmic reticulum stress.
机译:首次发布于2008年6月10日; doi:10.1152 / ajpendo.90355.2008.-肥胖和细胞因子分泌升高会导致慢性炎症,并可能导致2型糖尿病患者出现胰岛素抵抗。最近的研究表明,内质网应激在肥胖小鼠的肝细胞和脂肪细胞中起关键作用,导致胰岛素敏感性降低。为了解决以下假设:提高外周胰岛素敏感性的噻唑烷二酮部分地通过减少内质网应激反应而起作用,我们测试了来自20名接受吡格列酮治疗的肥胖志愿者皮下脂肪组织的作用,剂量为10周。我们还使用或不使用吡格列酮对人类HepG2肝细胞系进行了实验性诱导,使用棕榈酸酯,衣霉素和thapsigargin诱导了内质网应激。我们通过测量基因表达和磷酸化来量化内质网应激反应。吡格列酮显着改善了人类志愿者的胰岛素敏感性(P = 0.002),但并未改变内质网应激的标志物。治疗前后内质网应激水平的差异与胰岛素敏感性或体重指数的变化无关。在体外,棕榈酸酯,毒胡萝卜素和衣霉素,但不是油酸酯诱导的HepG2细胞内质网应激,包括增加的转录本CHOP,ERN1,GADD34和PERK,以及增加的XBP1剪接以及真核生物起始因子eIF2a,JNK1和c-的磷酸化俊尽管棕榈酸酯,衣霉素和毒胡萝卜素中内质网应激反应的模式有所不同,但吡格列酮预处理对内质网应激的任何测量均无显着影响,而与诱导剂无关。总之,我们的数据表明吡格列酮对胰岛素敏感性的提高不是由内质网应激的降低引起的。

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