Age‐Related Effects on the Biological Clock and its Behavioral Output in a Primate

References

• Aujard F., Perret M. Age‐related effects on reproductive function and sexual competition in the male prosimian primate, Microcebus murinus. Physiol. Behav. 1998; 64: 513–519
   PubMed Web of Science ®Google Scholar
• Aujard F., Perret M., Vannier G. Thermoregulatory responses to variations of photoperiod and ambient temperature in the male lesser mouse lemur: a primitive or an advanced adaptive character?. J. Comp. Physiol. B. 1998; 168: 540–548
   PubMedGoogle Scholar
• Aujard F., Dkhissi‐Benyahya O., Fournier I., Claustrat B., Schilling A., Cooper H. M., Perret M. Artificially accelerated aging by shortened photoperiod alters early gene expression (FOS) in the suprachiasmatic nucleus and sulfatoxymelatonin excretion in a small primate, Microcebus murinus. Neurosci. 2001; 105: 403–412
   Google Scholar
• Bliwise D. L. Sleep apnea and cognitive function: where do we stand now?. Sleep 1993; 16: S72–873
   PubMedGoogle Scholar
• Bons N., Mestre N., Petter A. Senile plaques and neurofibrillary changes in the brain of an aged lemurian primate Microcebus murinus. Neurobiol. Aging 1991; 13: 99–105
   Google Scholar
• Brock M. A. Chronobiology, and aging. J. Am. Geriatric Soc. 1991; 39: 74–91
   PubMed Web of Science ®Google Scholar
• Cayetanot F., Van Someren E. J.W., Perret M., Aujard F. Shortened seasonal photoperiodic cycles accelerate aging of the diurnal and circadian locomotor activity rhythms in a primate. J. Biol. Rhythms. 2005a; 20(5)461–469
   PubMedGoogle Scholar
• Cayetanot F., Bentivoglio M., Aujard F. Arginine‐vasopressin and vasointestinal polypeptide rhythms in the suprachiasmatic nucleus of the mouse lemur reveal aging‐related alterations of circadian pacemaker neurons in a non‐human primate. Eur. J. Neurosci. 2005b; 22: 902–910
   PubMed Web of Science ®Google Scholar
• Chou T. C., Scammell T. E., Gooley J. J., Gaus S. E., Saper C. B., Lu J. Critical role of dorsomedial hypothalmus nucleus in a wide range of behavioral circadian rhythms. J. Neurosci. 2003; 23: 10691–10702
   PubMed Web of Science ®Google Scholar
• Dardente H., Menet J. S., Challet E., Tournier B. B., Pevet P., Masson‐Pevet M. Daily and circadian expression of neuropeptides in the suprachiasmatic nuclei of nocturnal and diurnal rodents. Mol. Brain Res. 2004; 124: 143–151
   PubMedGoogle Scholar
• Dhenain M., Michot J. L., Privat N., Picq J. L., Boller F., Duyckaerts C., Volk A. MRI description of cerebral atrophy in mouse lemur primates. Neurobiol. Aging 2000; 21: 81–88
   PubMedGoogle Scholar
• Duncan M. J., Herron J. M., Hill S. A. Aging selectively supresses vasoactive intestinal peptide messenger RNA expression in the suprachiasmatic nucleus of Syrian hamster. Mol. Brain Res. 2001; 87: 196–203
   PubMedGoogle Scholar
• Hofman M. A., Swaab D. F. Alterations in circadian rhythmicity of the vasopressin‐producing neurons of the human suprachiasmatic nucleus (SCN) with aging. Brain Res. 1994; 651: 134–142
   PubMed Web of Science ®Google Scholar
• Hofman M. A., Zhou J. N., Swaab D. F. No evidence for a diurnal vasoactive intestinal polypeptide (VIP) rhythm in the human suprachiasmatic nucleus. Brain Res. 1996; 722: 78–82
   PubMed Web of Science ®Google Scholar
• Huang Y. L., Liu R. Y., Wang Q. S., Van Someren E. J.W., Xu H., Zhou J. N. Age associated difference in circadian sleep‐wake and rest‐activity rhythms. Physiol. Behav. 2002; 76: 597–603
   PubMed Web of Science ®Google Scholar
• Ibata Y., Takahashi Y., Okamura H., Kawakami F., Terubayashi H., Kubo T., Yanaihara N. Vasoactive intestinal peptide (VIP)‐like immunoreactive neurons located in the rat suprachiasmatic nucleus receive a direct retinal projection. Neurosci. Lett. 1989; 97: 1–5
   PubMedGoogle Scholar
• Kalamatianos T., Kallo I., Coen C. W. Ageing and the diurnal expression of the mRNAs for vasopressin and for the V1a and V1b vasopressin receptors in the suprachiasmatic nucleus of male rats. J. Neuroendocrinol. 2004; 16: 493–501
   PubMedGoogle Scholar
• Kallo I., Kalamatianos T., Piggins H. D., Coen C. W. Ageing and the diurnal expression of mRNAs for vasoactive intestinal polypeptide and for the VPAC2 and VPAC1 receptors in the suprachiasmatic nucleus of male rats. J. Neuroendocrinol. 2004; 16: 758–766
   PubMedGoogle Scholar
• Kawakami F., Okamura H., Tamada Y., Maebayashi Y., Fukui K., Ibata Y. Loss of day‐night differences in VIP mRNA levels in the suprachiasmatic nucleus of aged rats. Neurosci. Lett. 1997; 222: 99–102
   PubMed Web of Science ®Google Scholar
• Krajnak K., Kashon M. L., Rosewell K. L., Wise P. M. Aging alters the rhythmic expression of vasoactive intestinal polypeptide mRNA but not arginine vasopressin mRNA suprachiasmatic nuclei of female rats. J. Neurosci. 1998; 18: 4767–4774
   PubMed Web of Science ®Google Scholar
• Lucassen P. J., Hofman M. A., Swaab D. F. Increased light intensity prevents the age related loss of vasopressin expressing neurons in the rat suprachiasmatic nucleus. Brain Res. 1995; 693: 261–266
   PubMed Web of Science ®Google Scholar
• Moore R. Y. Entrainment pathways and the functional organization of the circadian system. Prog. Brain. Res. 1996; 111: 103–119
   PubMed Web of Science ®Google Scholar
• Némoz‐Bertholet F., Aujard F. Physical activity and balance performance as a function of age in a prosimian primate (Microcebus murinus). Exp. Gerontol. 2003; 38: 407–414
   PubMed Web of Science ®Google Scholar
• Penev P. D., Zee P. C., Turek F. W. Quantitative analysis of the age‐related fragmentation of hamster 24‐h activity rhythms. Am. J. Physiol. 1997; 273: R2132–R2137
   PubMedGoogle Scholar
• Perret M. Environmental and social determinants of sexual function in the male lesser mouse lemur (Microcebus murinus). Folia Primatol. 1992; 59: 1–25
   PubMedGoogle Scholar
• Perret M. Change in photoperiodic cycle affects life span in a prosimian primate (Microcebus murinus). J. Biol. Rhythms. 1997; 12: 136–145
   PubMed Web of Science ®Google Scholar
• Perret M., Aujard F., Vannier G. Influence of daylength on metabolic rate and daily water loss in the male prosimian primate Microcebus murinus. Comp. Biochem. Physiol. A. 1998; 119: 981–989
   PubMedGoogle Scholar
• Piggins H. D., Antle M. C., Rusak B. Neuropeptides phase shift the mammalian circadian pacemaker. J. Neurosci. 1995; 15: 5612–5622
   PubMed Web of Science ®Google Scholar
• Reed H. E., Meyer‐Spasche A., Cutler D. J., Coen C. W., Piggins H. D. Vasoactive intestinal polypeptide (VIP) phase‐shifts the rat suprachiasmatic nucleus clock in vitro. Eur. J. Neurosci. 2001; 13: 839–843
   PubMed Web of Science ®Google Scholar
• Shinohara K., Tominaga K., Isobe Y., Inouye S. I. Photic regulation of peptides located in the ventrolateral subdivision of the suprachiasmatic nucleus of the rat: daily variations of vasoactive intestinal polypeptide, gastrin‐releasing peptide, and neuropeptide Y. J. Neurosci. 1993; 13: 793–800
   PubMed Web of Science ®Google Scholar
• Touitou Y., Portaluppi F., Smolensky M. H., Rensing L. Ethical principles and standards for the conduct of human and animal biological rhythm research. Chronobiol. Int. 2004; 21: 161–170
   PubMed Web of Science ®Google Scholar
• Valentinuzzi V. S., Scarbrough K., Takahashi J. S., Turek F. W. Effects of aging on the circadian rhythm of wheel‐running activity in C57BL/6 mice. Am. J. Physiol. 1997; 273: R1957–1964
   PubMed Web of Science ®Google Scholar
• Van Esseveldt L. K.E., Lehman M. N., Boer G. J. The suprachiasmatic nucleus and the circadian time‐keeping system revisited. Brain Res. Rev. 2000; 33: 34–77
   PubMedGoogle Scholar
• Van Someren E. J.W., Swaab D. F., Colenda C. C., Cohen W., Vaughn McCall W., Rosenquist P. B. Bright light therapy: improved sensitivity to its effects on rest‐activity rhythms in Alzheimer patients by application of nonparametric methods. Chronobiol. Int. 1999; 16: 505–518
   PubMed Web of Science ®Google Scholar
• Zhou J. N., Hofman M. A., Swaab D. F. VIP neurons in the SCN in relation to sex, age, and Alzheimer's disease. Neurobiol. Aging 1995; 16: 571–576
   PubMed Web of Science ®Google Scholar