Neurotoxic N-methyl-D-aspartate lesion of the ventral midbrain and mesopontine junction alters sleep-wake organization.

TitleNeurotoxic N-methyl-D-aspartate lesion of the ventral midbrain and mesopontine junction alters sleep-wake organization.
Publication TypeJournal Article
Year of Publication1999
AuthorsLai YY, Shalita T, Hajnik T, Wu JP, Kuo JS, Chia LG, Siegel JM
JournalNeuroscience
Volume90
Issue2
Pagination469-83
Date Published1999 May
ISSN0306-4522
KeywordsAnimals, Brain Mapping, Brain Stem, Cats, Electroencephalography, Electromyography, Electrooculography, Female, Male, Mesencephalon, Motor Activity, N-Methylaspartate, Nerve Degeneration, Neurons, Neurotoxins, Organ Specificity, Pons, Prosencephalon, Sleep, Sleep, REM, Wakefulness
Abstract

The dorsal regions of the midbrain and pons have been found to participate in sleep regulation. However, the physiological role of the ventral brainstem in sleep regulation remains unclear. We used N-methyl-D-aspartate-induced lesions of the ventral midbrain and pons to address this question. Unlike dorsal mesencephalic reticular formation lesions, which produce somnolence and electroencephalogram synchronization, we found that ventral midbrain lesions produce insomnia and hyperactivity. Marked increases in waking and decreases in slow wave sleep stage 1 (S1), stage 2 (S2) and rapid eye movement sleep were found immediately after the lesion. Sleep gradually increased, but never returned to baseline levels (baseline/month 1 post-lesion: waking, 30.6 +/- 4.58%/62.3 +/- 10.1%; S1, 5.1 +/- 0.74/3.9 +/- 1.91%; S2, 46.2 +/- 4.74%/23.1 +/- 5.47%; rapid eye movement sleep, 14.1 +/- 3.15%/7.2 +/- 5.42%). These changes are comparable in magnitude to those seen after basal forebrain lesions. Neuronal degeneration was found in the ventral rostral pons and midbrain, including the substantia nigra, ventral tegmental area, retrorubral nucleus, and ventral mesencephalic and rostroventral pontine reticular formation. We conclude that nuclei within the ventral mesencephalon and rostroventral pons play an important role in sleep regulation.

DOI10.1016/s0306-4522(98)00429-1
Alternate JournalNeuroscience
PubMed ID10215152
Grant ListHL41370 / HL / NHLBI NIH HHS / United States