Daily rhythms of physiology and behavior are governed by an endogenous timekeeping mechanism (a circadian """"""""clock""""""""). In addition to photic signals, social cues may play an important role in the function of the circadian system. The efficacy of social cues may require that cohabitants be in direct physical contact for a relatively long period of time, but the experimental problem has been that the usual methods of recording daily activity fail to distinguish the activities of individual animals housed together in the same cage. We present preliminary data that we believe open new opportunities to pose questions and address mechanisms at this social level of temporal organization. We have found that co-housing pairs of golden hamsters or female laboratory mice can result in a change in a circadian clock property (the free-running circadian period, D). We have also developed and tested miniature implantable devices for longitudinally recording body temperature and general locomotor activity in individual rodents. In this application, we wish to exploit these advances by proposing three specific aims.
In Aim 1, we propose to develop a chronobiology of cohabitation in hamsters, asking if the cohabitation-associated change in D is a function of the phase relationship between cohabitants, depends on wheel running, exhibits a sex difference, and leads to an altered phase or distribution of activity during photic entrainment.
In Aim 2, we seek to implicate two likely factors - olfaction and gonadal hormones - as candidate neuroendocrine elements in the pathways involved in transducing social cues into signals that ultimately affect the oscillation of the master circadian pacemaker in the suprachiasmatic nucleus (SCN).
In Aim 3, we begin to investigate a social clock in female laboratory mice, asking if group synchronization can be a consequence of cohabitation-associated changes in D and how cohabitation outcome is affected by co- housing wild type mice with behaviorally-defective, mutant cage-mates (Clock ?19/?19, Avpr1atm1Dgen).

Public Health Relevance

What we learn from our experiments should enrich our understanding of the circadian clock and the chronobiology of animal communities, perhaps providing future insights into the adaptive function of the circadian system for cooperation and/or competition in the temporal domain. Notably, humans, including blind individuals, suffer from circadian disorders, and our investigation of the effects of social cues on the circadian system could eventually lead to the development of non-photic approaches to help these individuals adjust to a daily schedule or more easily shift to a new one, thereby reducing the physiological and psychological consequences of these disorders.

National Institute of Health (NIH)
National Institute of General Medical Sciences (NIGMS)
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Biological Rhythms and Sleep Study Section (BRS)
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Tompkins, Laurie
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University of Massachusetts Medical School Worcester
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Castillo-Ruiz, Alexandra; Indic, Premananda; Schwartz, William J (2018) Time management in a co-housed social rodent species (Arvicanthis niloticus). Sci Rep 8:1202
Wang, Shuo; Herzog, Erik D; Kiss, István Z et al. (2018) Inferring dynamic topology for decoding spatiotemporal structures in complex heterogeneous networks. Proc Natl Acad Sci U S A 115:9300-9305
Paul, Matthew J; Indic, Premananda; Schwartz, William J (2015) Social synchronization of circadian rhythmicity in female mice depends on the number of cohabiting animals. Biol Lett 11:20150204
Paul, Matthew J; Indic, Premananda; Schwartz, William J (2014) Social forces can impact the circadian clocks of cohabiting hamsters. Proc Biol Sci 281:20132535
Bloch, Guy; Herzog, Erik D; Levine, Joel D et al. (2013) Socially synchronized circadian oscillators. Proc Biol Sci 280:20130035
Leise, Tanya L; Indic, Premananda; Paul, Matthew J et al. (2013) Wavelet meets actogram. J Biol Rhythms 28:62-8
Gu, Changgui; Liu, Zonghua; Schwartz, William J et al. (2012) Photic desynchronization of two subgroups of circadian oscillators in a network model of the suprachiasmatic nucleus with dispersed coupling strengths. PLoS One 7:e36900
Castillo-Ruiz, Alexandra; Paul, Matthew J; Schwartz, William J (2012) In search of a temporal niche: social interactions. Prog Brain Res 199:267-80
Paul, Matthew J; Indic, Premananda; Schwartz, William J (2011) A role for the habenula in the regulation of locomotor activity cycles. Eur J Neurosci 34:478-88
Schwartz, William J; Tavakoli-Nezhad, Mahboubeh; Lambert, Christopher M et al. (2011) Distinct patterns of Period gene expression in the suprachiasmatic nucleus underlie circadian clock photoentrainment by advances or delays. Proc Natl Acad Sci U S A 108:17219-24

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