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Visceral signals reach visual cortex during slow wave sleep: study in monkeys
Ivan Pigarev1, Helena Almirall, Marina L Pigareva
1Institute for Information Transmission Problems, Russian Academy of Sciences, Bol'shoy Karetniy 19, 127994 Moscow, Russia.
Acta Neurobiologiae Experimentalis
|April 19, 2006
Summary
Visceral signals travel from the gut to the brain
Area of Science:
- Neuroscience
- Gastroenterology
- Sleep Science
Background:
- Parkinson's disease models involve motor deficits and sleep disturbances.
- The connection between gastro-intestinal signals and brain activity during sleep is not fully understood.
- Primate models offer insights into complex physiological processes.
Purpose of the Study:
- To investigate the propagation of gastro-intestinal signals to the occipital cortex during the sleep-wake cycle in primates.
- To determine if visceral information transfer to the cortex occurs during sleep, particularly slow-wave sleep.
- To compare signal propagation in animals with varying degrees of motor impairment and sleep structure alterations.
Main Methods:
- Utilized a chronic MPTP model of parkinsonism in three monkeys with differing motor and sleep phenotypes.
- Implanted screw electrodes over the occipital cortex for sleep level evaluation and cortical evoked response recording.
- Administered intraperitoneal electrical stimulation via implanted gut electrodes during slow-wave sleep and wakefulness.
Main Results:
- Cortical evoked responses to visceral stimulation were observed during sleep in monkeys with normal sleep patterns (M1 and M2).
- No complete sleep cycles were observed in one severely motor-affected monkey (M3).
- Visceral information transfer to the cerebral cortex during slow-wave sleep was confirmed in primates with normal sleep.
Conclusions:
- Visceral signals are transmitted to the cerebral cortex during slow-wave sleep in primates with normal sleep patterns.
- This pathway remains functional even in the context of parkinsonism models, though sleep architecture may be affected.
- The study highlights a conserved mechanism for interoception during sleep across different physiological states.
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