Microarray analysis of the temporal response of skeletal muscle to methylprednisolone: comparative analysis of two dosing regimens

被引:46
作者
Almon, Richard R.
DuBois, Debra C.
Yao, Zhenling
Hoffman, Eric P.
Ghimbovschi, Svetlana
Jusko, William J.
机构
[1] SUNY Buffalo, Dept Sci Biol, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Dept Pharmaceut Sci, Buffalo, NY 14260 USA
[3] Childrens Natl Med Ctr, Washington, DC 20010 USA
关键词
glucocorticoids; corticosteroids; affymetrix gene chips; gene expression; time series;
D O I
10.1152/physiolgenomics.00242.2006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
The transcriptional response of skeletal muscle to chronic corticosteroid exposure was examined over 168 h and compared with the response profiles observed following a single dose of corticosteroid. Male adrenalectomized Wistar rats were given a constant- rate infusion of 0.3 mg center dot kg(-1)center dot h(-1) methylprednisolone for up to 7 days via subcutaneously implanted minipumps. Four control and forty drug- treated animals were killed at ten different time points during infusion. Liver total RNAs were hybridized to 44 individual Affymetrix REA230A gene chips. Previously, we described a filtration approach for identifying genes of interest in microarray data sets developed from tissues of rats treated with methylprednisolone ( MPL) following acute dosing. Here, a similar approach involving a series of three filters was applied sequentially to identify genes of interest. These filters were designed to eliminate probe sets that were not expressed in the tissue, not regulated by the drug, or did not meet defined quality control standards. Filtering eliminated 86% of probe sets, leaving a remainder of 2,316 for further consideration. In a previous study, 653 probe sets were identified as MPL regulated following administration of a single ( acute) dose of the drug. Comparison of the two data sets yielded 196 genes identified as regulated by MPL in both dosing regimens. Because of receptor downregulation, it was predicted that genes regulated by receptor- glucocorticoid response element interactions would exhibit tolerance in chronic profiles. However, many genes did not exhibit steroid tolerance, indicating that present perspectives on the mechanism of glucocorticoid action cannot entirely explain all temporal profiles.
引用
收藏
页码:282 / 299
页数:18
相关论文
共 48 条
[1]
Almon R R, 1985, Physiologist, V28, pS69
[2]
ADRENALECTOMY ELIMINATES BOTH FIBER-TYPE DIFFERENCES AND STARVATION EFFECTS ON DENERVATED MUSCLE [J].
ALMON, RR ;
DUBOIS, DC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (06) :E850-E856
[3]
Pharmacogenomic responses of rat liver to methylprednisolone: An approach to mining a rich microarray time series [J].
Almon, RR ;
Dubois, DC ;
Jin, JY ;
Jusko, WJ .
AAPS JOURNAL, 2005, 7 (01) :E156-E194
[4]
Corticosteroid-regulated genes in rat kidney: mining time series array data [J].
Almon, RR ;
Lai, W ;
DuBois, DC ;
Jusko, WJ .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2005, 289 (05) :E870-E882
[5]
Temporal profiling of the transcriptional basis for the development of corticosteroid-induced insulin resistance in rat muscle [J].
Almon, RR ;
DuBois, DC ;
Jin, JY ;
Jusko, WJ .
JOURNAL OF ENDOCRINOLOGY, 2005, 184 (01) :219-232
[6]
The genomic response of skeletal muscle to methylprednisolone using microarrays: tailoring data mining to the structure of the pharmacogenomic time series [J].
Almon, RR ;
DuBois, DC ;
Piel, WH ;
Jusko, WJ .
PHARMACOGENOMICS, 2004, 5 (05) :525-552
[7]
ALMON RR, 1990, MED SCI SPORT EXER, V22, P304
[8]
ANDROULAKIS IP, 2005, P FDN SYSTEMS BIOL E
[9]
Intrahepatic amino acid and glucose metabolism in a D-galactosamine-induced rat liver failure model [J].
Arai, K ;
Lee, K ;
Berthiaume, F ;
Tompkins, RG ;
Yarmush, ML .
HEPATOLOGY, 2001, 34 (02) :360-371
[10]
Expression of mRNAs encoding uncoupling proteins in human skeletal muscle - Effects of obesity and diabetes [J].
Bao, S ;
Kennedy, A ;
Wojciechowski, B ;
Wallace, P ;
Ganaway, E ;
Garvey, WT .
DIABETES, 1998, 47 (12) :1935-1940