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Neuroscience bulletin, 2012-12, Vol.28 (6), p.746-758
2012

Details

Autor(en) / Beteiligte
Titel
Sleep alterations in mammals: Did aquatic conditions inhibit rapid eye movement sleep
Ist Teil von
  • Neuroscience bulletin, 2012-12, Vol.28 (6), p.746-758
Ort / Verlag
Heidelberg: Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences
Erscheinungsjahr
2012
Link zum Volltext
Quelle
Free E-Journal (出版社公開部分のみ)
Beschreibungen/Notizen
  • Sleep has been studied widely in mammals and to some extent in other vertebrates. Higher vertebrates such as birds and mammals have evolved an inimitable rapid eye movement (REM) sleep state. During REM sleep, postural muscles become atonic and the temperature regulating machinery remains suspended. Although REM sleep is present in almost all the terrestrial mammals, the aquatic mammals have either radically reduced or completely eliminated REM sleep. Further, we found a significant negative correlation between REM sleep and the adaptation of the organism to live on land or in water. The amount of REM sleep is highest in terrestrial mammals, significantly reduced in semi-aquatic mammals and completely absent or negligible in aquatic mammals. The aquatic mammals are obligate swimmers and have to sur- face at regular intervals for air. Also, these animals live in thermally challenging environments, where the conductive heat loss is approximately -90 times greater than air. Therefore, they have to be moving most of the time. As an adaptation, they have evolved unihemispheric sleep, during which they can rove as well as rest. A condition that immobilizes muscle activity and suspends the thermoregulatory machinery, as happens during REM sleep, is not suitable for these animals. It is possible that, in accord with Darwin's theory, aquatic mammals might have abolished REM sleep with time. In this review, we discuss the possibility of the intrinsic role of aquatic conditions in the elimination of REM sleep in the aquatic mammals.
Sprache
Englisch
Identifikatoren
ISSN: 1673-7067
eISSN: 1995-8218
DOI: 10.1007/s12264-012-1285-8
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5561822

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