Search bioRxiv⌕ Search

Biology subjects

Yamaguchi, S. T.

Publications and source records attributed to Yamaguchi, S. T..

2 recordsLinked to original sources

Sleep homeostasis in lizards and the role of cortex

Although their phenotypes are diverse, slow-wave sleep (SWS) and rapid eye movement sleep (REMS) are the two primary components of electrophysiological sleep (e-sleep) in mammals and birds. Slow waves in the cortex not only characterize SWS but are also used as biological markers for sleep homeostasis, given their rebound after sleep deprivation (SD). Recently, it has been reported that the Australian dragon Pogona vitticeps exhibits two-stage sleep pattern in the dorsal ventricular ridge (DVR), which includes a homologue of the mammalian claustrum (CLA). It remains unclear whether reptilian e-sleep, which has been characterized by activity outside the cortex, compensates for sleep loss, as observed in mammals. We here report a significant rebound in the local field potential (LFP) after 7 hours of SD, during both SWS and REMS. Meanwhile, the cycle and mean bout length of SWS/REMS remained unaffected. We further investigated a possible role of the cortex in e-sleep regulation and homeostasis in Pogona and found that, although a corticotomy had no obvious effect on the LFP features investigated, it abolished LFP power rebound in the CLA/DVR after SD. These findings suggest that e-sleep homeostasis is a common feature in amniotes, and that cortex is involved in regulating activity rebounds in reptiles and mammals.

neuroscience↗

The regulation of circadian rhythm by insulin signaling in Drosophila

Circadian rhythm is well conserved across species and relates to numerous biological functions. Circadian misalignment impairs metabolic function. Insulin signaling is a key modulator of metabolism in the fruit fly as well as mammals and its defects cause metabolic disease. Daily diet timing affects both circadian rhythmicities of behavior and metabolism. However, the relationship between circadian clock and insulin signaling is still elusive. Here, we report that insulin signaling regulates circadian rhythm in Drosophila melanogaster. We found the insulin receptor substrate mutant, chico1, showed a shorter free-running circadian period. The knockdown of insulin receptor (InR), or another signaling molecule downstream of InR, dp110, or the expression of a dominant-negative form of InR resulted in the shortening of the circadian period and diminished its amplitude. The impairment of insulin signaling both in all neurons and restricted circadian clock neurons altered circadian period length, indicating the insulin signaling plays a role in the regulation of circadian rhythm in clock cells. Among 3 insulin-like ligands expressed in the brain, dilp5 showed the largest effect on circadian phenotype when deleted. These results suggested that insulin signaling contributes to the robustness of the circadian oscillation and coordinates metabolism and behavior. HighlightsO_LIInsulin receptor substrate mutant, chico1, displayed circadian rhythm phenotype. C_LIO_LIPan-neuronal inhibition of insulin receptor signaling shortened circadian cycle. C_LIO_LIInhibition of insulin signaling only in clock neurons altered circadian cycle. C_LIO_LIDilp5 is a major insulin receptor ligand for circadian effects. C_LI

animal behavior and cognition↗