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罗格列酮和二甲双胍对2型糖尿病患者肝脏脂肪含量、肝脏胰岛素抵抗、胰岛素清除率及脂肪组织基因表达的影响。

Effects of rosiglitazone and metformin on liver fat content, hepatic insulin resistance, insulin clearance, and gene expression in adipose tissue in patients with type 2 diabetes.

作者信息

Tiikkainen Mirja, Häkkinen Anna-Maija, Korsheninnikova Elena, Nyman Tuulikki, Mäkimattila Sari, Yki-Järvinen Hannele

机构信息

Department of Medicine, University of Helsinki, Helsinki, Finland.

出版信息

Diabetes. 2004 Aug;53(8):2169-76. doi: 10.2337/diabetes.53.8.2169.

Abstract

Both rosiglitazone and metformin increase hepatic insulin sensitivity, but their mechanism of action has not been compared in humans. The objective of this study was to compare the effects of rosiglitazone and metformin treatment on liver fat content, hepatic insulin sensitivity, insulin clearance, and gene expression in adipose tissue and serum adiponectin concentrations in type 2 diabetes. A total of 20 drug-naive patients with type 2 diabetes (age 48 +/- 3 years, fasting plasma glucose 152 +/- 9 mg/dl, BMI 30.6 +/- 0.8 kg/m2) were treated in a double-blind randomized fashion with either 8 mg rosiglitazone or 2 g metformin for 16 weeks. Both drugs similarly decreased HbA1c, insulin, and free fatty acid concentrations. Body weight decreased in the metformin (84 +/- 4 vs. 82 +/- 4 kg, P < 0.05) but not the rosiglitazone group. Liver fat (proton spectroscopy) was decreased with rosiglitazone by 51% (15 +/- 3 vs. 7 +/- 1%, 0 vs. 16 weeks, P = 0.003) but not by metformin (13 +/- 3 to 14 +/- 3%, NS). Rosiglitazone (16 +/- 2 vs. 20 +/- 1 ml.kg(-1).min(-1), P = 0.02) but not metformin increased insulin clearance by 20%. Hepatic insulin sensitivity in the basal state increased similarly in both groups. Insulin-stimulated glucose uptake increased significantly with rosiglitazone but not with metformin. Serum adiponectin concentrations increased by 123% with rosiglitazone but remained unchanged during metformin treatment. The decrease of serum adiponectin concentrations correlated with the decrease in liver fat (r = -0.74, P < 0.001). Rosiglitazone but not metformin significantly increased expression of peroxisome proliferator-activated receptor-gamma, adiponectin, and lipoprotein lipase in adipose tissue. In conclusion, rosiglitazone but not metformin decreases liver fat and increases insulin clearance. The decrease in liver fat by rosiglitazone is associated with an increase in serum adiponectin concentrations. Both agents increase hepatic insulin sensitivity, but only rosiglitazone increases peripheral glucose uptake.

摘要

罗格列酮和二甲双胍均可提高肝脏胰岛素敏感性,但二者在人体中的作用机制尚未得到比较。本研究的目的是比较罗格列酮和二甲双胍治疗对2型糖尿病患者肝脏脂肪含量、肝脏胰岛素敏感性、胰岛素清除率、脂肪组织基因表达以及血清脂联素浓度的影响。共有20例未接受过药物治疗的2型糖尿病患者(年龄48±3岁,空腹血糖152±9mg/dl,体重指数30.6±0.8kg/m²)以双盲随机方式接受8mg罗格列酮或2g二甲双胍治疗16周。两种药物均同样降低了糖化血红蛋白、胰岛素和游离脂肪酸浓度。二甲双胍组体重下降(84±4 vs. 82±4kg,P<0.05),而罗格列酮组体重未下降。罗格列酮使肝脏脂肪(质子磁共振波谱法)减少51%(15±3% vs. 7±1%,0周vs. 16周,P = 0.003),而二甲双胍未使其减少(13±3%至14±3%,无显著性差异)。罗格列酮使胰岛素清除率提高20%(16±2 vs. 20±1ml·kg⁻¹·min⁻¹,P = 0.02),而二甲双胍未使其提高。两组基础状态下的肝脏胰岛素敏感性均同样增加。罗格列酮使胰岛素刺激的葡萄糖摄取显著增加,而二甲双胍未使其增加。罗格列酮使血清脂联素浓度增加123%,而二甲双胍治疗期间血清脂联素浓度保持不变。血清脂联素浓度的降低与肝脏脂肪的减少相关(r = -0.74,P<0.001)。罗格列酮而非二甲双胍显著增加脂肪组织中过氧化物酶体增殖物激活受体γ、脂联素和脂蛋白脂肪酶的表达。总之,罗格列酮而非二甲双胍可降低肝脏脂肪并提高胰岛素清除率。罗格列酮所致的肝脏脂肪减少与血清脂联素浓度增加相关。两种药物均增加肝脏胰岛素敏感性,但只有罗格列酮增加外周葡萄糖摄取。

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