No loss of orexin/hypocretin, melanin‐concentrating hormone or locus coeruleus noradrenergic neurons in a rat model of chronic sleep restriction

التفاصيل البيبلوغرافية
العنوان: No loss of orexin/hypocretin, melanin‐concentrating hormone or locus coeruleus noradrenergic neurons in a rat model of chronic sleep restriction
المؤلفون: Andrew Baldin, Kazue Semba, Samuel Deurveilher, Michael Antonchuk, Brock St C Saumure
المصدر: European Journal of Neuroscience. 54:6027-6043
بيانات النشر: Wiley, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Adrenergic Neurons, Male, medicine.medical_specialty, Lateral hypothalamus, Melanin-concentrating hormone, chemical and pharmacologic phenomena, Stereology, Biology, Mice, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Internal medicine, medicine, Animals, Effects of sleep deprivation on cognitive performance, Rats, Wistar, Axon, 030304 developmental biology, Sleep restriction, Melanins, Orexins, 0303 health sciences, Hypothalamic Hormones, General Neuroscience, Rats, Orexin, Pituitary Hormones, medicine.anatomical_structure, Endocrinology, nervous system, chemistry, Locus coeruleus, Locus Coeruleus, Sleep, 030217 neurology & neurosurgery
الوصف: Chronic sleep restriction (CSR) is common in modern society, adversely affecting cognitive performance and health. Yet how it impacts neurons regulating sleep remains unclear. Several studies using mice reported substantial losses of wake-active orexin/hypocretin and locus coeruleus (LC) noradrenergic neurons, but not rapid eye movement sleep-active melanin-concentrating hormone (MCH) neurons, following CSR. Here, we used immunohistochemistry and stereology to examine orexin, MCH and LC noradrenergic neurons in a rat model of CSR that uses programmed wheel rotation (3 h on/1 h off; '3/1' protocol). Adult male Wistar rats underwent one or four cycles of the 4-day 3/1 CSR protocol, with 2-day recovery between cycles in home cages. Time-matched control rats were housed in locked wheels/home cages. We found no significant differences in the numbers of orexin, MCH and LC noradrenergic neurons following either one- or four-cycle CSR protocol compared to respective controls. Similarly, the four-cycle CSR protocol had no effect on the densities of orexin axon terminals in the LC, noradrenergic dendrites in the LC and noradrenergic axon terminals in the frontal cortex. Body weights, however, decreased after one cycle of CSR and then increased with diminishing slope over the next three cycles. Thus, we found no evidence for loss of orexin or LC noradrenergic neurons following one and four cycles of the 4-day 3/1 CSR protocol in rats. Differences in CSR protocols and/or possible species differences in neuronal vulnerability to sleep loss may account for the discrepancy between the current results in rats and previous findings in mice.
تدمد: 1460-9568
0953-816X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a390e4b575be90b14537f4eab45f17bTest
https://doi.org/10.1111/ejn.15412Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....0a390e4b575be90b14537f4eab45f17b
قاعدة البيانات: OpenAIRE