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Chu, S. S.

Publications and source records attributed to Chu, S. S..

2 recordsLinked to original sources

Early life sleep disruption has long lasting, sex specific effects on later development of sleep in prairie voles

In mammals, sleep duration is highest in the early postnatal period of life and is critical for shaping neural circuits that control the development of complex behaviors. The prairie vole is a wild, highly social rodent that serves as a unique model for the study of complex, species-typical social behaviors. Previous work in our laboratory has found that early life sleep disruption (ELSD) in prairie voles during a sensitive window of postnatal development leads to long lasting changes in social and cognitive behaviors as well as structural changes in excitatory and inhibitory neural circuits in the brain. However, it is currently unknown how later sleep is impacted by ELSD, both shortly after ELSD and over the long term. Therefore, the aim of this study was to describe the effects of ELSD on later life sleep, compared to sleep in normally developing prairie voles. First, we conducted tethered electroencephalogram/electromyogram (EEG/EMG) recordings in juvenile prairie voles undergoing ELSD, compared to Control conditions. Second, we conducted 24 hours of home cage tethered EEG/EMG recordings in either adolescent or adult male and female prairie voles that had previously undergone ELSD or Control conditions as juveniles. We found that, as adults, male ELSD prairie voles showed persistently lower REM sleep duration and female ELSD prairie voles showed persistently higher NREM sleep duration compared to Controls, but no other sleep parameters differed. We concluded that 1) persistent effects of ELSD on sleep into adulthood may contribute to the social and cognitive deficits observed in adult voles, and 2) sleep disruption early in life can influence later sleep patterns in adulthood.

neuroscience↗

Computationally Guided Design of Two Novel Soluble Epoxide Hydrolase Inhibitors

The enzyme soluble epoxide hydrolase (sEH) has been found to play a role in many ailments such as inflammation, pain, renal function, pulmonary function, hypertension, and diabetes. Multiple sEH inhibitors have been developed to reduce the adverse effects of the ailments. Due to high inhibitory concentrations, there is urgent need for developing improved sEH inhibitors. In this study, two novel sEH inhibitors were designed via computational bioisosteric replacement and chemical intuition with the goal of increasing binding affinity, which can potentially decrease inhibitory concentration. The new drug candidates were found to have improved binding properties compared to existing drugs.

biochemistry↗