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本文引用的文献

1
Circulating adiponectin and adiponectin receptor expression in skeletal muscle: effects of exercise.循环脂联素及骨骼肌中脂联素受体的表达:运动的影响
Diabetes Metab Res Rev. 2007 Nov;23(8):600-11. doi: 10.1002/dmrr.778.
2
Cardiac expression of adiponectin and its receptors in streptozotocin-induced diabetic rats.链脲佐菌素诱导的糖尿病大鼠中脂联素及其受体的心脏表达
Metabolism. 2007 Oct;56(10):1363-71. doi: 10.1016/j.metabol.2007.05.005.
3
Evidence for adipose-muscle cross talk: opposing regulation of muscle proteolysis by adiponectin and Fatty acids.脂肪-肌肉相互作用的证据:脂联素和脂肪酸对肌肉蛋白水解的相反调节
Endocrinology. 2007 Dec;148(12):5696-705. doi: 10.1210/en.2007-0183. Epub 2007 Aug 30.
4
Total and high molecular weight but not trimeric or hexameric forms of adiponectin correlate with markers of the metabolic syndrome and liver injury in Thai subjects.在泰国受试者中,脂联素的总形式和高分子量形式(而非三聚体或六聚体形式)与代谢综合征及肝损伤标志物相关。
J Clin Endocrinol Metab. 2007 Nov;92(11):4313-8. doi: 10.1210/jc.2007-0890. Epub 2007 Aug 14.
5
Adiponectin and its receptors are expressed in adult ventricular cardiomyocytes and upregulated by activation of peroxisome proliferator-activated receptor gamma.脂联素及其受体在成人心室心肌细胞中表达,并通过过氧化物酶体增殖物激活受体γ的激活而上调。
J Mol Cell Cardiol. 2007 Jul;43(1):73-84. doi: 10.1016/j.yjmcc.2007.04.014. Epub 2007 Apr 27.
6
Mechanisms regulating energy metabolism by adiponectin in obesity and diabetes.脂联素在肥胖和糖尿病中调节能量代谢的机制。
Biochem Soc Trans. 2006 Nov;34(Pt 5):798-801. doi: 10.1042/BST0340798.
7
Adiponectin increases fatty acid oxidation in skeletal muscle cells by sequential activation of AMP-activated protein kinase, p38 mitogen-activated protein kinase, and peroxisome proliferator-activated receptor alpha.脂联素通过依次激活AMP活化蛋白激酶、p38丝裂原活化蛋白激酶和过氧化物酶体增殖物激活受体α来增加骨骼肌细胞中的脂肪酸氧化。
Diabetes. 2006 Sep;55(9):2562-70. doi: 10.2337/db05-1322.
8
Post-translational modifications of the four conserved lysine residues within the collagenous domain of adiponectin are required for the formation of its high molecular weight oligomeric complex.脂联素胶原结构域内四个保守赖氨酸残基的翻译后修饰对于其高分子量寡聚复合物的形成是必需的。
J Biol Chem. 2006 Jun 16;281(24):16391-400. doi: 10.1074/jbc.M513907200. Epub 2006 Apr 18.
9
Induction of adiponectin in skeletal muscle of type 2 diabetic mice: In vivo and in vitro studies.2型糖尿病小鼠骨骼肌中脂联素的诱导:体内和体外研究。
Diabetologia. 2006 Jun;49(6):1311-23. doi: 10.1007/s00125-006-0210-y. Epub 2006 Mar 29.
10
Changes of skeletal muscle adiponectin content in diet-induced insulin resistant rats.饮食诱导的胰岛素抵抗大鼠骨骼肌脂联素含量的变化
Biochem Biophys Res Commun. 2006 Mar 3;341(1):209-17. doi: 10.1016/j.bbrc.2005.12.172. Epub 2006 Jan 9.

脂联素由骨骼肌纤维表达,并影响肌肉表型和功能。

Adiponectin is expressed by skeletal muscle fibers and influences muscle phenotype and function.

作者信息

Krause Matthew P, Liu Ying, Vu Vivian, Chan Lawrence, Xu Aimin, Riddell Michael C, Sweeney Gary, Hawke Thomas J

机构信息

School of Kinesiology and Health Science, York University, Toronto, Ontario, Canada.

出版信息

Am J Physiol Cell Physiol. 2008 Jul;295(1):C203-12. doi: 10.1152/ajpcell.00030.2008. Epub 2008 May 7.

DOI:10.1152/ajpcell.00030.2008
PMID:18463233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2493546/
Abstract

Adiponectin (Ad) is linked to various disease states and mediates antidiabetic and anti-inflammatory effects. While it was originally thought that Ad expression was limited to adipocytes, we demonstrate here that Ad is expressed in mouse skeletal muscles and within differentiated L6 myotubes, as assessed by RT-PCR, Western blot, and immunohistochemical analyses. Serial muscle sections stained for fiber type, lipid content, and Ad revealed that muscle fibers with elevated intramyocellular Ad expression were consistently type IIA and IID fibers with detectably higher intramyocellular lipid (IMCL) content. To determine the effect of Ad on muscle phenotype and function, we used an Ad-null [knockout (KO)] mouse model. Body mass increased significantly in 24-wk-old KO mice [+5.5 +/- 3% relative to wild-type mice (WT)], with no change in muscle mass observed. IMCL content was significantly increased (+75.1 +/- 25%), whereas epididymal fat mass, although elevated, was not different in the KO mice compared with WT (+35.1 +/- 23%; P = 0.16). Fiber-type composition was unaltered, although type IIB fiber area was increased in KO mice (+25.5 +/- 6%). In situ muscle stimulation revealed lower peak tetanic forces in KO mice relative to WT (-47.5 +/- 6%), with no change in low-frequency fatigue rates. These data demonstrate that the absence of Ad expression causes contractile dysfunction and phenotypical changes in skeletal muscle. Furthermore, we demonstrate that Ad is expressed in skeletal muscle and that its intramyocellular localization is associated with elevated IMCL, particularly in type IIA/D fibers.

摘要

脂联素(Ad)与多种疾病状态相关,并介导抗糖尿病和抗炎作用。虽然最初认为Ad的表达仅限于脂肪细胞,但我们在此证明,通过逆转录聚合酶链反应(RT-PCR)、蛋白质印迹法和免疫组织化学分析评估,Ad在小鼠骨骼肌和分化的L6肌管中表达。对纤维类型、脂质含量和Ad进行染色的连续肌肉切片显示,细胞内Ad表达升高的肌纤维始终是IIA型和IID型纤维,其细胞内脂质(IMCL)含量明显更高。为了确定Ad对肌肉表型和功能的影响,我们使用了Ad基因敲除(KO)小鼠模型。24周龄的KO小鼠体重显著增加[相对于野生型小鼠(WT)增加了5.5±3%],而肌肉质量没有变化。IMCL含量显著增加(+75.1±25%),而附睾脂肪量虽然有所升高,但与WT相比,KO小鼠没有差异(+35.1±23%;P = 0.16)。纤维类型组成未改变,尽管KO小鼠的IIB型纤维面积增加(+25.5±6%)。原位肌肉刺激显示,与WT相比,KO小鼠的强直收缩峰值力较低(-47.5±6%),低频疲劳率没有变化。这些数据表明,Ad表达缺失会导致骨骼肌收缩功能障碍和表型变化。此外,我们证明Ad在骨骼肌中表达,其细胞内定位与IMCL升高有关,特别是在IIA/D型纤维中。