AI Article Synopsis

  • The suprachiasmatic nucleus (SCN) acts as the master clock for circadian rhythms and can adjust its activity based on metabolic and cardiovascular signals.
  • Disruption of the connection between the SCN and arcuate nucleus (ARC) in Wistar rats leads to loss of regular rhythms in activities such as locomotion, hormone levels, and body temperature in constant darkness.
  • The findings suggest that the SCN and ARC communication is vital for maintaining physiological rhythms, indicating potential links between circadian disruption and metabolic disorders.

Article Abstract

The suprachiasmatic nucleus (SCN) is generally considered the master clock, independently driving all circadian rhythms. We recently demonstrated the SCN receives metabolic and cardiovascular feedback adeptly altering its neuronal activity. In the present study, we show that microcuts effectively removing SCN-arcuate nucleus (ARC) interconnectivity in Wistar rats result in a loss of rhythmicity in locomotor activity, corticosterone levels, and body temperature in constant dark (DD) conditions. Elimination of these reciprocal connections did not affect SCN clock gene rhythmicity but did cause the ARC to desynchronize. Moreover, unilateral SCN lesions with contralateral retrochiasmatic microcuts resulted in identical arrhythmicity, proving that for the expression of physiological rhythms this reciprocal SCN-ARC interaction is essential. The unaltered SCN c-Fos expression following glucose administration in disconnected animals as compared to a significant decrease in controls demonstrates the importance of the ARC as metabolic modulator of SCN neuronal activity. Together, these results indicate that the SCN is more than an autonomous clock, and forms an essential component of a larger network controlling homeostasis. The present novel findings illustrate how an imbalance between SCN and ARC communication through circadian disruption could be involved in the etiology of metabolic disorders.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364589PMC
http://dx.doi.org/10.1523/ENEURO.0028-17.2017DOI Listing

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