Night and day

Abstract

How does the brain develop differently to support nocturnality in some mammals, but diurnality in others? To answer this question, one might look to the suprachiasmatic nucleus (SCN), the pacemaker of the mammalian brain, which is required for all circadian biological and behavioral rhythms. Light arriving at the retina entrains the SCN to the daily light-dark cycle via the retinohypothalamic tract (RHT). However, in all mammals studied thus far, whether nocturnal or diurnal, the SCN exhibits a rhythm of increased activity during the day and decreased activity at night. Therefore, structures downstream of the SCN are likely to determine whether a species is nocturnal or diurnal. From an evolutionary perspective, nocturnality appears to be the primitive condition in mammals, with diurnality having reemerged independently in some lineages. However, it is unclear what mechanisms underlie the development of one or the other circadian phase preference. In adult Norway rats (Rattus norvegicus), which are nocturnal, the RHT also projects to the ventral subparaventricular zone (vSPVZ), an adjacent region that expresses an in-phase pattern of SCN-vSPVZ neuronal activity (in other words, activity in the SCN and vSPVZ increase and decrease together). In contrast, in adult Nile grass rats (Arvicanthis niloticus), a diurnal species that is closely related to Norway rats, an anti-phase pattern of SCN-vSPVZ neuronal activity is expressed (in other words, activity in the SCN increases as activity in the vSPVZ decreases, and vice versa). We hypothesized that these species differences in activity pattern result in part from a weak or absent RHTvSPVZ projection in grass rats.