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首页> 外文期刊>Clinical Science >Hyperglycemia-induced transcriptional regulation of ROCK1 and TGM2 expression is involved in small artery remodeling in obese diabetic Gottingen Minipigs
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Hyperglycemia-induced transcriptional regulation of ROCK1 and TGM2 expression is involved in small artery remodeling in obese diabetic Gottingen Minipigs

机译:高血糖诱导的ROCK1和TGM2表达的转录调节涉及肥胖糖尿病菌毒素MINIPIG的小动脉重塑

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Obesity and diabetes in humans are associated with hypertrophic remodeling and increased media:lumen ratio of small resistance arteries, which is an independent predictor of cardiovascular events. In order to minimize increases in media:lumen ratio, hypertrophic remodeling should be accompanied by outward remodeling. We aimed to investigate the mechanisms of structural remodeling in small pial arteries (PAs) and terminal mesenteric arteries (TMAs) from obese Gottingen Minipigs with or without diabetes. Gottingen Minipigs received either control diet (lean control (LC)), high fat/high fructose/high cholesterol diet (FFC), or FFC diet with streptozotocin (STZ)-induced diabetes (FFC/STZ) for 13 months. At the end of the study (20 months), we assessed body weight, fasting plasma biochemistry, passive a vessel dimensions, mRNA expression (matrix metallopeptidases 2/9 (MMP2, MMP9), tissue inhibitor of metallopeptidase 1 (TIMP1), transglutaminase 2 (TGM2), Rho-kinase 1 (ROCK1), TGF beta-receptor 2 (TGFBR2), and IGF1-receptor (IGFR1) genes), and immunofluorescence in PAs and TMAs. We performed multiple linear correlation analyses using plasma values, structural data, and gene expression data. We detected outward hypertrophic remodeling in TMAs and hypertrophic remodeling in PAs from FFC/STZ animals. ROCK1 and TGM2 genes were up-regulated in PAs and TMAs from the FFC/STZ group. Passive lumen diameter (PLD) of TMAs was correlated with plasma values of glucose (GLU), fructosamine (FRA), total cholesterol (TC), and triglycerides (TGs). ROCK1 and TGM2 expressions in TMAs a were correlated with PLD, plasma GLU, fructosamine, and TC. ROCK1 and TGM2 proteins a were immunolocalized in the media of PAs and TMAs, and their fluorescence levels were increased in the FFC/STZ group. Hyperglycemia/hyperlipidemia is involved in regulation of ROCK1 and TGM2 expression leading to outward remodeling of small resistance arteries in obese diabetic Gottingen Minipigs.
机译:人类肥胖症和糖尿病与肥厚性重塑和增加的培养基:小抵抗动脉的腔比,这是心血管事件的独立预测因子。为了最小化培养基的增加:腔比,肥厚重塑应伴有外部重塑。我们旨在调查小型动脉(PAS)和末端肠系膜动脉(TMA)的结构重塑机制来自肥胖的Gottingen Minipigs或没有糖尿病。 Gottingen Minips接受了控制饮食(LEN控制(LC)),高脂肪/高果糖/高胆固醇饮食(FFC),或用链脲佐菌素(STZ)诱导糖尿病(FFC / STZ)的FFC饮食13个月。在研究结束时(20个月),我们评估了体重,禁食血浆生物化学,被动血管尺寸,mRNA表达(基质金属肽酶2/9(MMP2,MMP9),金属肽酶1(TIMP1)的组织抑制剂,转谷氨酸酶2 (TGM2),RHO-激酶1(ROCK1),TGFβ受体2(TG​​FBR2)和IGF1-受体(IGFR1)基因)和PAS和TMA中的免疫荧光。我们使用等离子体值,结构数据和基因表达数据进行多种线性相关分析。我们在FFC / STZ动物中检测到TMA中的肥厚性和肥厚性重塑。来自FFC / STZ组的PAS和TMA中的Rock1和TGM2基因上调。 TMA的被动腔直径(PLD)与葡萄糖(Glu),果糖胺(FRA),总胆固醇(TC)和甘油三酯(TGS)的血浆值相关。 TMAS A中的Rock1和TGM2表达与PLD,血浆Glu,果糖胺和TC相关。 Rock1和TGM2蛋白A在PAS和TMA的培养基中被免疫化,并且在FFC / STZ组中增加了它们的荧光水平。高血糖/高脂血症涉及ROCK1和TGM2表达的调节,导致肥胖糖尿病菌毒素的小型耐药动脉的外出重塑。

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