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败血症下调骨骼肌中肌肉生长抑制素 mRNA 水平而不改变肌肉生长抑制素蛋白水平。

Sepsis downregulates myostatin mRNA levels without altering myostatin protein levels in skeletal muscle.

机构信息

Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.

出版信息

J Cell Biochem. 2010 Nov 1;111(4):1059-73. doi: 10.1002/jcb.22796.

Abstract

Myostatin is a negative regulator of muscle mass and has been reported to be upregulated in several conditions characterized by muscle atrophy. The influence of sepsis on myostatin expression and activity is poorly understood. Here, we tested the hypothesis that sepsis upregulates the expression and downstream signaling of myostatin in skeletal muscle. Because sepsis-induced muscle wasting is at least in part regulated by glucocorticoids, we also determined the influence of glucocorticoids on myostatin expression. Sepsis was induced in rats by cecal ligation and puncture and control rats were sham-operated. In other experiments, rats were injected intraperitoneally with dexamethasone (10 mg/kg) or corresponding volume of vehicle. Surprisingly, myostatin mRNA levels were reduced and myostatin protein levels were unchanged in muscles from septic rats. Muscle levels of activin A, follistatin, and total and phosphorylated Smad2 (p-Smad2) were not influenced by sepsis, suggesting that myostatin downstream signaling was not altered during sepsis. Interestingly, total and p-Smad3 levels were increased in septic muscle, possibly reflecting altered signaling through pathways other than myostatin. Similar to sepsis, treatment of rats with dexamethasone reduced myostatin mRNA levels and did not alter myostatin protein levels. Fasting, an additional condition characterized by muscle wasting, reduced myostatin mRNA and activin A protein levels, increased myostatin protein, and did not influence follistatin and p-Smad2 levels. Of note, total and p-Smad3 levels were reduced in muscle during fasting. The results suggest that sepsis and glucocorticoids do not upregulate the expression and activity of myostatin in skeletal muscle. The role of myostatin may vary between different conditions characterized by muscle wasting. Downstream signaling through Smad2 and 3 is probably regulated not only by myostatin but by other mechanisms as well.

摘要

肌肉生长抑制素是肌肉质量的负调控因子,已在多种肌肉萎缩症中报道其表达上调。脓毒症对肌肉生长抑制素表达和活性的影响知之甚少。在这里,我们检验了这样一个假设,即脓毒症上调骨骼肌中肌肉生长抑制素的表达和下游信号。由于脓毒症引起的肌肉消耗至少部分受糖皮质激素调节,我们还确定了糖皮质激素对肌肉生长抑制素表达的影响。通过盲肠结扎和穿刺术诱导大鼠脓毒症,而假手术组大鼠接受假手术。在其他实验中,大鼠腹腔内注射地塞米松(10mg/kg)或相应体积的载体。令人惊讶的是,脓毒症大鼠肌肉中的肌肉生长抑制素 mRNA 水平降低,而肌肉生长抑制素蛋白水平不变。肌肉中的激活素 A、卵泡抑素、总和磷酸化 Smad2(p-Smad2)水平不受脓毒症影响,表明脓毒症期间肌肉生长抑制素下游信号未改变。有趣的是,总和 p-Smad3 水平在脓毒症肌肉中增加,可能反映了通过肌肉生长抑制素以外的途径改变的信号转导。类似于脓毒症,用地塞米松治疗大鼠降低了肌肉生长抑制素 mRNA 水平,而不改变肌肉生长抑制素蛋白水平。禁食,另一种以肌肉消耗为特征的状态,降低了肌肉生长抑制素 mRNA 和激活素 A 蛋白水平,增加了肌肉生长抑制素蛋白水平,而不影响卵泡抑素和 p-Smad2 水平。值得注意的是,禁食期间肌肉中的总和 p-Smad3 水平降低。结果表明,脓毒症和糖皮质激素不会上调骨骼肌中肌肉生长抑制素的表达和活性。肌肉生长抑制素在不同以肌肉消耗为特征的状态下的作用可能不同。Smad2 和 3 的下游信号不仅受肌肉生长抑制素调节,还受其他机制调节。

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