Ionomycin, but not physiologic doses of epinephrine, stimulates skeletal muscle interleukin-6 mRNA expression and protein release

被引:32
作者
Holmes, AG [1 ]
Watt, MJ [1 ]
Carey, AL [1 ]
Febbraio, MA [1 ]
机构
[1] RMIT Univ, Sch Med Sci, Skeletal Muscle Res Lab, Bundoora, Vic 3038, Australia
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2004年 / 53卷 / 11期
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.metabol.2004.05.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It has been hypothesized that epinephrine may stimulate interleukin (IL)-6 gene expression in skeletal muscle. The aim of the present study was to examine the effect of epinephrine on IL-6 gene expression within, and protein release from, skeletal muscle. We hypothesized that physiologic epinephrine would neither result in an increase in IL-6 mRNA nor protein release from skeletal muscle. Soleus muscle was excised from 4-week-old anesthetized Sprague Dawley rats and incubated in a Krebs buffer with the addition of either saline (CON), epinephrine, at concentrations of 1,000 nmol/L (EPI 1,000), 100 nmol/L (EPI 100), or 10 nmol/L (EPI 10), or the calcium ionophore, ionomycin (IONO), a positive control. After a 1-hour incubation, muscle was collected and extracted for RNA, reverse transcribed, and IL-6 gene expression was determined by real-time polymerase chain reaction (PCR). An aliquot of incubation medium was also collected and analyzed for IL-6 protein by enzyme-linked immunosorbent (ELISA). EPI 1,000 and IONO increased (P < .05) IL-6 mRNA, whereas EPI 100 and EPI 10 were without effect. IL-6 protein release from skeletal muscle was increased in IONO (P < .05), but not in CON or EPI at any concentration. These data demonstrate that while pharmacologic concentrations of epinephrine activate IL-6 mRNA, supraphysiologic and highphysiologic doses appear to have little, if any, effect on IL-6 gene transcription in skeletal muscle. In addition, ionomycin can stimulate IL-6 gene expression and protein release after only 1 hour of exposure. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1492 / 1495
页数:4
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