The neural subtrate of biological rhythms

被引:3
作者
Aréchiga, H [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Med, Div Estudios Posgrad & Invest, Mexico City 04510, DF, Mexico
关键词
biological clocks; biological rhythms; chronobiology; circadian rhythms;
D O I
10.33588/rn.3601.2002585
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction and method. The various bodily functions vary rhythmically along the 24-hour cycle. These circadian rhythms, display common properties and are generated by common cellular and molecular mechanisms. The basic rhythm is endogenously produced in cellular pacemakers in various regions; the most conspicuous are located in the central nervous system. They are composed by cells endowed with the molecular substrate necessary to generate rhythmicity, and to send the circadian time signal to the effectors of the overt rhythms. The rhythmicity in the pacemaker cells is generated by specific genes integrated in a negative feedback double loop. The structure of the genes responsible for the rhythmicity is phylogenetically well preserved. The circadian pacemakers are in turn synchronized by environmental stimuli, being light the best characterized, but other external agents, such as food and some homeostatic factors and products of metabolic activity are also effective. These synchronizing signals are conveyed to the pacemakers via specific receptors and pathways. The role of some neurotransmitters in the synchronizing action has been demonstrated Conclusion. The functional integrity of this complex biochronometrical system is necessary for the maintenance of health. Its alteration results in specific ailments, and enhances the vulnerability to certain diseases.
引用
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页码:49 / 60
页数:12
相关论文
共 266 条
[91]   Melanopsin-containing retinal. ganglion cells: Architecture, projections, and intrinsic photosensitivity [J].
Hattar, S ;
Liao, HW ;
Takao, M ;
Berson, DM ;
Yau, KW .
SCIENCE, 2002, 295 (5557) :1065-1070
[92]   CLONING OF A FACTOR REQUIRED FOR ACTIVITY OF THE AH (DIOXIN) RECEPTOR [J].
HOFFMAN, EC ;
REYES, H ;
CHU, FF ;
SANDER, F ;
CONLEY, LH ;
BROOKS, BA ;
HANKINSON, O .
SCIENCE, 1991, 252 (5008) :954-958
[93]  
HOFFMAN K, 1965, CIRCADIAN CLOCKS
[94]   Circadian periods of single suprachiasmatic neurons in rats [J].
Honma, S ;
Shirakawa, T ;
Katsuno, Y ;
Namihira, M ;
Honma, K .
NEUROSCIENCE LETTERS, 1998, 250 (03) :157-160
[95]   VASOPRESSIN FIBER PATHWAYS IN THE RAT-BRAIN FOLLOWING SUPRACHIASMATIC NUCLEUS LESIONING [J].
HOORNEMAN, EMD ;
BUIJS, RM .
BRAIN RESEARCH, 1982, 243 (02) :235-241
[96]   PAS IS A DIMERIZATION DOMAIN COMMON TO DROSOPHILA PERIOD AND SEVERAL TRANSCRIPTION FACTORS [J].
HUANG, ZJ ;
EDERY, I ;
ROSBASH, M .
NATURE, 1993, 364 (6434) :259-262
[97]   Regulation of the Drosophila protein timeless suggests a mechanism for resetting the circadian clock by light [J].
HunterEnsor, M ;
Ousley, A ;
Sehgal, A .
CELL, 1996, 84 (05) :677-685
[98]   Immortalized suprachiasmatic nucleus cells express components of multiple circadian regulatory pathways [J].
Hurst, WJ ;
Earnest, D ;
Gillette, MU .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 292 (01) :20-30
[99]  
INOUYE SIT, 1996, HYPOTHALAMIC INTEGRA, V3
[100]   PERSISTENCE OF CIRCADIAN RHYTHMICITY IN A MAMMALIAN HYPOTHALAMIC ISLAND CONTAINING THE SUPRACHIASMATIC NUCLEUS [J].
INOUYE, ST ;
KAWAMURA, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (11) :5962-5966