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噻唑烷二酮类药物可急性刺激大鼠骨骼肌中解偶联蛋白-3 mRNA的表达:一种类似运动的效应?

Expression of uncoupling protein-3 mRNA in rat skeletal muscle is acutely stimulated by thiazolidinediones: an exercise-like effect?

作者信息

Brunmair B, Gras F, Wagner L, Artwohl M, Zierhut B, Waldhäusl W, Fürnsinn C

机构信息

Department of Medicine III, Division of Endocrinology & Metabolism, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.

出版信息

Diabetologia. 2004 Sep;47(9):1611-4. doi: 10.1007/s00125-004-1488-2. Epub 2004 Sep 2.

Abstract

AIMS/HYPOTHESIS: We examined whether thiazolidinediones (TZDs) acutely affect uncoupling protein-3 ( UCP-3) expression in skeletal muscle and plasma NEFA in Sprague-Dawley rats.

METHODS

Expression of UCP-3 mRNA in hindlimb muscles and plasma NEFA were measured after a single intraperitoneal injection of TZDs in healthy male rats.

RESULTS

Independent of which TZD was injected (50 micromol/kg), UCP-3 expression in gastrocnemius muscle was distinctly increased after 6 h (increase vs vehicle-injected control: pioglitazone, 10.3+/-3.2-fold, p=0.03; rosiglitazone, 8.7+/-1.2-fold, p=0.001; RWJ241947, 9.5+/-2.7-fold, p=0.03). This was accompanied by elevated plasma NEFA (control 158+/-13 micromol/l; pioglitazone, 281+/-40 micromol/l, p=0.03; rosiglitazone, 276+/-27 micromol/l, p=0.005; RWJ241947, 398+/-51 micromol/l, p=0.004). The increase in plasma NEFA could in part have mediated TZD-induced UCP-3 expression, but increased UCP-3 mRNA was also found in isolated muscle after 2 h of TZD exposure in vitro (25 micromol/l pioglitazone, 1.7+/-0.3-fold, p=0.046), suggesting that TZDs act directly and independently of NEFA on skeletal muscle.

CONCLUSIONS/INTERPRETATION: In healthy rats, a single dose of TZDs rapidly increases UCP-3 mRNA in skeletal muscle and plasma NEFA. This effect resembles the acute response to a bout of exercise.

摘要

目的/假设:我们研究了噻唑烷二酮类药物(TZDs)是否会对Sprague-Dawley大鼠的骨骼肌解偶联蛋白-3(UCP-3)表达和血浆非酯化脂肪酸(NEFA)产生急性影响。

方法

对健康雄性大鼠单次腹腔注射TZDs后,测量其下肢肌肉中UCP-3 mRNA的表达及血浆NEFA水平。

结果

无论注射哪种TZDs(50微摩尔/千克),6小时后腓肠肌中UCP-3的表达均显著增加(与注射溶媒的对照组相比增加倍数:吡格列酮,10.3±3.2倍,p = 0.03;罗格列酮,8.7±1.2倍,p = 0.001;RWJ241947,9.5±2.7倍,p = 0.03)。同时血浆NEFA水平升高(对照组158±13微摩尔/升;吡格列酮,281±40微摩尔/升,p = 0.03;罗格列酮,276±27微摩尔/升,p = 0.005;RWJ241947,398±51微摩尔/升,p = 0.004)。血浆NEFA的增加可能部分介导了TZDs诱导的UCP-3表达,但在体外将肌肉暴露于TZDs 2小时后(25微摩尔/升吡格列酮),分离的肌肉中也发现UCP-3 mRNA增加(1.7±0.3倍,p = 0.046),这表明TZDs直接作用于骨骼肌且独立于NEFA。

结论/解读:在健康大鼠中,单次剂量的TZDs可迅速增加骨骼肌中UCP-3 mRNA和血浆NEFA水平。这种效应类似于一次运动后的急性反应。

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