Sleeping Sickness Disrupts the Sleep-Regulating Adenosine System.
Filipa Rijo-FerreiraTheresa E BjornessKimberly H CoxAlex SonnebornRobert W GreeneJoseph S TakahashiPublished in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2020)
Patients with sleeping sickness, caused by the parasite Trypanosoma brucei, have disruptions in both sleep timing and sleep architecture. However, the underlying cause of these sleep disturbances is not well understood. Here, we assessed the sleep architecture of male mice infected with T. brucei and found that infected mice had drastically altered sleep patterns. Interestingly, T. brucei-infected mice also had a reduced homeostatic sleep response to sleep deprivation, a response modulated by the adenosine system. We found that infected mice had a reduced electrophysiological response to an adenosine receptor antagonist and increased adenosine receptor gene expression. Although the mechanism by which T. brucei infection causes these changes remains to be determined, our findings suggest that the symptoms of sleeping sickness may be because of alterations in homeostatic adenosine signaling.SIGNIFICANCE STATEMENT Sleeping sickness is a fatal disease that disrupts the circadian clock, causes disordered temperature regulation, and induces sleep disturbance. To examine the neurologic effects of infection in the absence of other symptoms, in this study, we used a mouse model of sleeping sickness in which the acute infection was treated but brain infection remained. Using this model, we evaluated the effects of the sleeping sickness parasite, Trypanosoma brucei, on sleep patterns in mice, under both normal and sleep-deprived conditions. Our findings suggest that signaling of adenosine, a neuromodulator involved in mediating homeostatic sleep drive, may be reduced in infected mice.
Keyphrases
- sleep quality
- physical activity
- gene expression
- mouse model
- depressive symptoms
- high fat diet induced
- multiple sclerosis
- type diabetes
- metabolic syndrome
- protein kinase
- acute respiratory distress syndrome
- functional connectivity
- brain injury
- newly diagnosed
- binding protein
- white matter
- extracorporeal membrane oxygenation