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Pharmacodynamic/Pharmacogenomic Modeling of Insulin Resistance Genes in Rat Muscle After Methylprednisolone Treatment: Exploring Regulatory Signaling Cascades

机译:甲基强的松龙治疗后大鼠肌肉中胰岛素抵抗基因的药效动力学/药物基因组学建模:探索调控信号通路。

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摘要

Corticosteroids (CS) effects on insulin resistance related genes in rat skeletal muscle were studied. In our acute study, adrenalectomized (ADX) rats were given single doses of 50 mg/kg methylprednisolone (MPL) intravenously. In our chronic study, ADX rats were implanted with Alzet mini-pumps giving zero-order release rates of 0.3 mg/kg/h MPL and sacrificed at various times up to 7 days. Total RNA was extracted from gastrocnemius muscles and hybridized to Affymetrix GeneChips. Data mining and literature searches identified 6 insulin resistance related genes which exhibited complex regulatory pathways. Insulin receptor substrate-1 (IRS-1), uncoupling protein 3 (UCP3), pyruvate dehydrogenase kinase isoenzyme 4 (PDK4), fatty acid translocase (FAT) and glycerol-3-phosphate acyltransferase (GPAT) dynamic profiles were modeled with mutual effects by calculated nuclear drug-receptor complex (DR(N)) and transcription factors. The oscillatory feature of endothelin-1 (ET-1) expression was depicted by a negative feedback loop. These integrated models provide testable quantitative hypotheses for these regulatory cascades.
机译:研究了皮质类固醇(CS)对大鼠骨骼肌胰岛素抵抗相关基因的影响。在我们的急性研究中,对肾上腺切除术(ADX)大鼠进行静脉单剂量50 mg / kg甲基强的松龙(MPL)给药。在我们的长期研究中,向ADX大鼠植入Alzet微型泵,零级释放速率为0.3 mg / kg / h MPL,并在长达7天的不同时间处死。从腓肠肌提取总RNA,并与Affymetrix GeneChips杂交。数据挖掘和文献检索确定了6种与胰岛素抵抗相关的基因,这些基因表现出复杂的调节途径。建立了胰岛素受体底物1(IRS-1),解偶联蛋白3(UCP3),丙酮酸脱氢酶激酶同工酶4(PDK4),脂肪酸转位酶(FAT)和甘油3磷酸酰基转移酶(GPAT)动力学模型,并具有相互影响的模型通过计算核药物受体复合物(DR(N))和转录因子。内皮素-1(ET-1)表达的振荡特征由负反馈回路描绘。这些集成模型为这些调节级联提供了可检验的定量假设。

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