Circadian variations in rat liver gene expression: Relationships to drug actions

被引:47
作者
Almon, Richard R. [1 ,2 ,3 ]
Yang, Eric [4 ]
Lai, William [1 ]
Androulakis, Ioannis P. [4 ]
DuBois, Debra C. [1 ,2 ]
Jusko, William J. [2 ,3 ]
机构
[1] SUNY Buffalo, Dept Biol Sci, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Dept Pharmaceut Sci, Buffalo, NY 14260 USA
[3] New York State Ctr Excellence Bioinformat & Life, Buffalo, NY USA
[4] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ USA
基金
美国国家卫生研究院;
关键词
D O I
10.1124/jpet.108.140186
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chronopharmacology is an important but under-explored aspect of therapeutics. Rhythmic variations in biological processes can influence drug action, including pharmacodynamic responses, due to circadian variations in the availability or functioning of drug targets. We hypothesized that global gene expression analysis can be useful in the identification of circadian-regulated genes involved in drug action. Circadian variations in gene expression in rat liver were explored using Affymetrix gene arrays. A rich time series involving animals analyzed at 18 time points within the 24-h cycle was generated. Of the more than 15,000 probe sets on these arrays, 265 exhibited oscillations with a 24-h frequency. Cluster analysis yielded five distinct circadian clusters, with approximately two thirds of the transcripts reaching maximal expression during the dark/active period of the animal. Of the 265 probe sets, 107 were identified as having potential therapeutic importance. The expression levels of clock genes were also investigated in this study. Five clock genes exhibited circadian variation in the liver, and data suggest that these genes may also be regulated by corticosteroids.
引用
收藏
页码:700 / 716
页数:17
相关论文
共 39 条
[1]   A microarray analysis of the temporal response of liver to methylprednisolone: A comparative analysis of two dosing regimens [J].
Almon, Richard R. ;
DuBois, Debra C. ;
Jusko, William J. .
ENDOCRINOLOGY, 2007, 148 (05) :2209-2225
[2]   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
[3]   Genetic clock of biologic rhythms [J].
Badiu, C .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2003, 7 (04) :408-416
[4]   Emerging concepts in targeting the polyamine metabolic pathway in epithelial cancer chemoprevention and chemotherapy [J].
Basuroy, UK ;
Gerner, EW .
JOURNAL OF BIOCHEMISTRY, 2006, 139 (01) :27-33
[5]   Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment [J].
Binder, EB ;
Salyakina, D ;
Lichtner, P ;
Wochnik, GM ;
Ising, M ;
Pütz, B ;
Papiol, S ;
Seaman, S ;
Lucae, S ;
Kohli, MA ;
Nickel, T ;
Künzel, HE ;
Fuchs, B ;
Majer, M ;
Pfennig, A ;
Kern, N ;
Brunner, J ;
Modell, S ;
Baghai, T ;
Deiml, T ;
Zill, P ;
Bondy, B ;
Rupprecht, R ;
Messer, T ;
Köhnlein, O ;
Dabitz, H ;
Brückl, T ;
Müller, N ;
Pfister, H ;
Lieb, R ;
Mueller, JC ;
Lohmussaar, E ;
Strom, TM ;
Bettecken, T ;
Meitinger, T ;
Uhr, M ;
Rein, T ;
Holsboer, F ;
Muller-Myhsok, B .
NATURE GENETICS, 2004, 36 (12) :1319-1325
[6]  
Canaple L, 2003, CANCER RES, V63, P7545
[7]   Molecular basis of intrahepatic cholestasis [J].
Carlton, VEH ;
Pawlikowska, L ;
Bull, LN .
ANNALS OF MEDICINE, 2004, 36 (08) :606-617
[8]   Synchronization of the molecular clockwork by light- and food-related cues in mammals [J].
Challet, E ;
Caldelas, I ;
Graff, C ;
Pévet, P .
BIOLOGICAL CHEMISTRY, 2003, 384 (05) :711-719
[9]   eIF4A3 is a novel component of the exon junction complex [J].
Chan, CC ;
Dostie, J ;
Diem, MD ;
Feng, WQ ;
Mann, M ;
Rappsilber, J ;
Dreyfuss, G .
RNA, 2004, 10 (02) :200-209
[10]   Squalene epoxidase as hypocholesterolemic drug target revisited [J].
Chugh, A ;
Ray, A ;
Gupta, JB .
PROGRESS IN LIPID RESEARCH, 2003, 42 (01) :37-50