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本文引用的文献

1
Aging sustains the hypertrophy-associated elevation of apoptotic suppressor X-linked inhibitor of apoptosis protein (XIAP) in skeletal muscle during unloading.衰老维持了卸载过程中骨骼肌中与肥大相关的凋亡抑制因子X连锁凋亡抑制蛋白(XIAP)的升高。
J Gerontol A Biol Sci Med Sci. 2005 Aug;60(8):976-83. doi: 10.1093/gerona/60.8.976.
2
Subcellular responses of p53 and Id2 in fast and slow skeletal muscle in response to stretch-induced overload.p53和Id2在快、慢肌中对拉伸诱导过载的亚细胞反应。
J Appl Physiol (1985). 2005 Nov;99(5):1897-904. doi: 10.1152/japplphysiol.00374.2005. Epub 2005 Jul 7.
3
Apoptotic responses to hindlimb suspension in gastrocnemius muscles from young adult and aged rats.年轻成年大鼠和老年大鼠腓肠肌对后肢悬吊的凋亡反应。
Am J Physiol Regul Integr Comp Physiol. 2005 Oct;289(4):R1015-26. doi: 10.1152/ajpregu.00198.2005. Epub 2005 May 26.
4
Age-related differences in apoptosis with disuse atrophy in soleus muscle.比目鱼肌废用性萎缩时细胞凋亡的年龄相关差异。
Am J Physiol Regul Integr Comp Physiol. 2005 May;288(5):R1288-96. doi: 10.1152/ajpregu.00576.2004. Epub 2005 Jan 13.
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Id2 and p53 participate in apoptosis during unloading-induced muscle atrophy.Id2和p53在卸载诱导的肌肉萎缩过程中参与细胞凋亡。
Am J Physiol Cell Physiol. 2005 May;288(5):C1058-73. doi: 10.1152/ajpcell.00495.2004. Epub 2004 Dec 15.
6
Aging influences cellular and molecular responses of apoptosis to skeletal muscle unloading.衰老影响细胞凋亡对骨骼肌卸载的细胞和分子反应。
Am J Physiol Cell Physiol. 2005 Feb;288(2):C338-49. doi: 10.1152/ajpcell.00239.2004. Epub 2004 Oct 13.
7
Splitting the apoptosome.裂解凋亡小体
Cell Cycle. 2004 Apr;3(4):446-8. Epub 2004 Apr 1.
8
Coupling of caspase-9 to Apaf1 in response to loss of pRb or cytotoxic drugs is cell-type-specific.响应pRb缺失或细胞毒性药物时,半胱天冬酶-9与凋亡蛋白酶激活因子1的偶联具有细胞类型特异性。
EMBO J. 2004 Jan 28;23(2):460-72. doi: 10.1038/sj.emboj.7600039. Epub 2004 Jan 8.
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Skeletal muscle function and hypertrophy are diminished in old age.骨骼肌功能和肥大在老年时会减弱。
Muscle Nerve. 2003 Mar;27(3):339-47. doi: 10.1002/mus.10314.
10
Gravitational unloading effects on muscle fiber size, phenotype and myonuclear number.重力卸载对肌纤维大小、表型和肌核数量的影响。
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老年大鼠快肌型跖肌中细胞凋亡的分子调控

Molecular regulation of apoptosis in fast plantaris muscles of aged rats.

作者信息

Pistilli Emidio E, Siu Parco M, Alway Stephen E

机构信息

Laboratory of Muscle biology and Sarcopenia, Division of Exercise Physiology, West Virginia University School of Medicine, Morgantown, WV 26506-9227, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2006 Mar;61(3):245-55. doi: 10.1093/gerona/61.3.245.

DOI:10.1093/gerona/61.3.245
PMID:16567372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2778222/
Abstract

This study tested the hypothesis that aging exacerbates apoptotic signaling in rat fast plantaris muscle during muscle unloading. Plantaris muscle mass was 22% lower in aged animals and the apoptotic index was 600% higher, when compared to those in young adult animals. Following 14 days of hind-limb unloading, absolute plantaris muscle mass was 20% lower in young adult animals with a corresponding 200% higher elevation of the apoptotic index. Unloading had no affect on muscle weight or apoptotic index of aged plantaris muscles. The changes in pro-apoptotic messenger RNA (mRNA) for apoptotic protease activating factor-1 (Apaf-1), Bax, and inhibitor of differentiation protein-2 (Id2) were exacerbated with aging. Bax and Bcl-2 protein levels were also altered differently in aged muscle, compared to young. Significant positive correlations were observed between the changes in Id2 and Bax mRNA, and Id2 and caspase-9 mRNA. These data suggest that a pro-apoptotic environment may contribute to aging-associated atrophy in fast skeletal muscle, but apoptotic signaling differs by age.

摘要

本研究检验了这样一个假设

衰老会加剧大鼠比目鱼肌在肌肉卸载过程中的凋亡信号。与年轻成年动物相比,老年动物的比目鱼肌质量降低了22%,凋亡指数高出600%。在进行14天的后肢卸载后,年轻成年动物的比目鱼肌绝对质量降低了20%,相应地凋亡指数升高了200%。卸载对老年比目鱼肌的肌肉重量或凋亡指数没有影响。随着衰老,凋亡蛋白酶激活因子-1(Apaf-1)、Bax和分化抑制蛋白-2(Id2)等促凋亡信使核糖核酸(mRNA)的变化加剧。与年轻肌肉相比,老年肌肉中Bax和Bcl-2蛋白水平的变化也有所不同。在Id2与Bax mRNA的变化之间,以及Id2与半胱天冬酶-9 mRNA的变化之间,观察到显著的正相关。这些数据表明,促凋亡环境可能导致快速骨骼肌中与衰老相关的萎缩,但凋亡信号因年龄而异。