Circadian rhythms in mouse blood coagulation

被引:19
作者
Bertolucci, C
Pinotti, M
Colognesi, I
Foà, A
Bernardi, F
Portaluppi, F
机构
[1] Univ Ferrara, Dipartimento Biol, I-44100 Ferrara, Italy
[2] Univ Ferrara, Ctr Neurosci, I-44100 Ferrara, Italy
[3] Univ Ferrara, Dept Biochem & Mol Biol, I-44100 Ferrara, Italy
[4] Univ Ferrara, Hypertens Ctr, Dept Clin & Expt Med, I-44100 Ferrara, Italy
关键词
circadian rhythms; clocks; blood coagulation; factor Xa generation; thrombin generation;
D O I
10.1177/0748730405275654
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The circadian clock, influencing many biological processes, has been demonstrated to modulate levels of specific coagulation factors, but its impact on the coagulation efficiency is unknown. In a mouse model, the authors evaluated the temporal variations in the initial rate of activated factor X (FXa) and thrombin generation. Upon coagulation activation through the FVIIa-TF pathway (extrinsic activation), both parameters showed rhythmic variations with a significant peak at ZT 12, the light-to-dark transition. In mice subjected to a 6-h delayed light-dark cycle, the peak was shifted as expected. These cyclic oscillations were also observed in constant darkness, thus demonstrating, for the first time, the existence of strong circadian rhythms of the initial rate of either FXa or thrombin generation activity levels. These circadian variations overlapped with those that have been recently described in factor VII (FVII) activity. The peak of FXa generation activity was simulated by the addition of purified human FVII, thus indicating that circadian variations in FVII activity are important determinants of the circadian rhythm of the procoagulant cascade efficiency. These findings help to elucidate the complex control on the coagulation process and might contribute in explaining the temporal variations in the frequency of cardiovascular events observed in humans.
引用
收藏
页码:219 / 224
页数:6
相关论文
共 36 条
[1]   Circadian cycling of the mouse liver transcriptome, as revealed by cDNA microarray, is driven by the suprachiasmatic nucleus [J].
Akhtar, RA ;
Reddy, AB ;
Maywood, ES ;
Clayton, JD ;
King, VM ;
Smith, AG ;
Gant, TW ;
Hastings, MH ;
Kyriacou, CP .
CURRENT BIOLOGY, 2002, 12 (07) :540-550
[2]   The mammalian circadian clock: A network of gene expression [J].
Albrecht, U .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :48-55
[3]   The mammalian circadian clock [J].
Albrecht, U ;
Eichele, G .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (03) :271-277
[4]   DIURNAL-VARIATION OF TISSUE-TYPE PLASMINOGEN-ACTIVATOR AND ITS RAPID INHIBITOR (PAI-1) [J].
ANGLETON, P ;
CHANDLER, WL ;
SCHMER, G .
CIRCULATION, 1989, 79 (01) :101-106
[5]   Timing the cell cycle [J].
Cardone, L ;
Sassone-Corsi, P .
NATURE CELL BIOLOGY, 2003, 5 (10) :859-861
[6]  
Daan S., 1982, P305
[7]   Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus [J].
Damiola, F ;
Le Minh, N ;
Preitner, N ;
Kornmann, B ;
Fleury-Olela, F ;
Schibler, U .
GENES & DEVELOPMENT, 2000, 14 (23) :2950-2961
[8]   Circadian programs of transcriptional activation, signaling, and protein turnover revealed by microarray analysis of mammalian cells [J].
Duffield, GE ;
Best, JD ;
Meurers, BH ;
Bittner, A ;
Loros, JJ ;
Dunlap, JC .
CURRENT BIOLOGY, 2002, 12 (07) :551-557
[9]  
FURIE B, 1992, NEW ENGL J MED, V326, P800
[10]   The mammalian circadian timing system: from gene expression to physiology [J].
Gachon, F ;
Nagoshi, E ;
Brown, SA ;
Ripperger, J ;
Schibler, U .
CHROMOSOMA, 2004, 113 (03) :103-112