Histamine-1 receptor is not required as a downstream effector of orexin-2 receptor in maintenance of basal sleep/wake states

M. Hondo, K. Nagai, K. Ohno, Y. Kisanuki, J. T. Willie, T. Watanabe, Masashi Yanagisawa, T. Sakurai

Research output: Contribution to journalArticle

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Abstract

Aim: The effect of orexin on wakefulness has been suggested to be largely mediated by activation of histaminergic neurones in the tuberomammillary nucleus (TMN) via orexin receptor-2 (OX2R). However, orexin receptors in other regions of the brain might also play important roles in maintenance of wakefulness. To dissect the role of the histaminergic system as a downstream mediator of the orexin system in the regulation of sleep/wake states without compensation by the orexin receptor-1 (OX1R) mediated pathways, we analysed the phenotype of Histamine-1 receptor (H1R) and OX 1R double-deficient (H1R-/-;OX 1R-/-) mice. These mice lack OX1R-mediated pathways in addition to deficiency of H1R, which is thought to be the most important system in downstream of OX2R. Methods: We used H 1R deficient (H1R-/-) mice, H1R -/-;OX1R-/- mice, OX1R and OX 2R double-deficient (OX1R-/-;OX 2R-/-) mice, and wild type controls. Rapid eye movement (REM) sleep, non-REM (NREM) sleep and awake states were determined by polygraphic electroencephalographic/electromyographic recording. Results: No abnormality in sleep/wake states was observed in H1R-/- mice, consistent with previous studies. H1R-/-;OX 1R-/- mice also showed a sleep/wake phenotype comparable to that of wild type mice, while OX1R-/-; OX 2R-/- mice showed severe fragmentation of sleep/wake states. Conclusion: Our observations showed that regulation of the sleep/wake states is completely achieved by OX2R-expressing neurones without involving H1R-mediated pathways. The maintenance of basal physiological sleep/wake states is fully achieved without both H1 and OX1 receptors. Downstream pathways of OX2R other than the histaminergic system might play an important role in the maintenance of sleep/wake states.

Original languageEnglish (US)
Pages (from-to)287-294
Number of pages8
JournalActa Physiologica
Volume198
Issue number3
DOIs
StatePublished - Mar 2010

Fingerprint

Orexin Receptors
Histamine Receptors
Sleep
Maintenance
Wakefulness
Lateral Hypothalamic Area
Phenotype
Neurons
Histamine H1 Receptors
Sleep Deprivation
REM Sleep
Eye Movements

Keywords

  • Electroencephalography
  • Histamine H receptor
  • Orexin receptor-1
  • Orexin receptor-2
  • Sleep/wake states
  • Tuberomammillary nucleus

ASJC Scopus subject areas

  • Physiology

Cite this

Histamine-1 receptor is not required as a downstream effector of orexin-2 receptor in maintenance of basal sleep/wake states. / Hondo, M.; Nagai, K.; Ohno, K.; Kisanuki, Y.; Willie, J. T.; Watanabe, T.; Yanagisawa, Masashi; Sakurai, T.

In: Acta Physiologica, Vol. 198, No. 3, 03.2010, p. 287-294.

Research output: Contribution to journalArticle

Hondo, M. ; Nagai, K. ; Ohno, K. ; Kisanuki, Y. ; Willie, J. T. ; Watanabe, T. ; Yanagisawa, Masashi ; Sakurai, T. / Histamine-1 receptor is not required as a downstream effector of orexin-2 receptor in maintenance of basal sleep/wake states. In: Acta Physiologica. 2010 ; Vol. 198, No. 3. pp. 287-294.
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abstract = "Aim: The effect of orexin on wakefulness has been suggested to be largely mediated by activation of histaminergic neurones in the tuberomammillary nucleus (TMN) via orexin receptor-2 (OX2R). However, orexin receptors in other regions of the brain might also play important roles in maintenance of wakefulness. To dissect the role of the histaminergic system as a downstream mediator of the orexin system in the regulation of sleep/wake states without compensation by the orexin receptor-1 (OX1R) mediated pathways, we analysed the phenotype of Histamine-1 receptor (H1R) and OX 1R double-deficient (H1R-/-;OX 1R-/-) mice. These mice lack OX1R-mediated pathways in addition to deficiency of H1R, which is thought to be the most important system in downstream of OX2R. Methods: We used H 1R deficient (H1R-/-) mice, H1R -/-;OX1R-/- mice, OX1R and OX 2R double-deficient (OX1R-/-;OX 2R-/-) mice, and wild type controls. Rapid eye movement (REM) sleep, non-REM (NREM) sleep and awake states were determined by polygraphic electroencephalographic/electromyographic recording. Results: No abnormality in sleep/wake states was observed in H1R-/- mice, consistent with previous studies. H1R-/-;OX 1R-/- mice also showed a sleep/wake phenotype comparable to that of wild type mice, while OX1R-/-; OX 2R-/- mice showed severe fragmentation of sleep/wake states. Conclusion: Our observations showed that regulation of the sleep/wake states is completely achieved by OX2R-expressing neurones without involving H1R-mediated pathways. The maintenance of basal physiological sleep/wake states is fully achieved without both H1 and OX1 receptors. Downstream pathways of OX2R other than the histaminergic system might play an important role in the maintenance of sleep/wake states.",
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AU - Nagai, K.

AU - Ohno, K.

AU - Kisanuki, Y.

AU - Willie, J. T.

AU - Watanabe, T.

AU - Yanagisawa, Masashi

AU - Sakurai, T.

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N2 - Aim: The effect of orexin on wakefulness has been suggested to be largely mediated by activation of histaminergic neurones in the tuberomammillary nucleus (TMN) via orexin receptor-2 (OX2R). However, orexin receptors in other regions of the brain might also play important roles in maintenance of wakefulness. To dissect the role of the histaminergic system as a downstream mediator of the orexin system in the regulation of sleep/wake states without compensation by the orexin receptor-1 (OX1R) mediated pathways, we analysed the phenotype of Histamine-1 receptor (H1R) and OX 1R double-deficient (H1R-/-;OX 1R-/-) mice. These mice lack OX1R-mediated pathways in addition to deficiency of H1R, which is thought to be the most important system in downstream of OX2R. Methods: We used H 1R deficient (H1R-/-) mice, H1R -/-;OX1R-/- mice, OX1R and OX 2R double-deficient (OX1R-/-;OX 2R-/-) mice, and wild type controls. Rapid eye movement (REM) sleep, non-REM (NREM) sleep and awake states were determined by polygraphic electroencephalographic/electromyographic recording. Results: No abnormality in sleep/wake states was observed in H1R-/- mice, consistent with previous studies. H1R-/-;OX 1R-/- mice also showed a sleep/wake phenotype comparable to that of wild type mice, while OX1R-/-; OX 2R-/- mice showed severe fragmentation of sleep/wake states. Conclusion: Our observations showed that regulation of the sleep/wake states is completely achieved by OX2R-expressing neurones without involving H1R-mediated pathways. The maintenance of basal physiological sleep/wake states is fully achieved without both H1 and OX1 receptors. Downstream pathways of OX2R other than the histaminergic system might play an important role in the maintenance of sleep/wake states.

AB - Aim: The effect of orexin on wakefulness has been suggested to be largely mediated by activation of histaminergic neurones in the tuberomammillary nucleus (TMN) via orexin receptor-2 (OX2R). However, orexin receptors in other regions of the brain might also play important roles in maintenance of wakefulness. To dissect the role of the histaminergic system as a downstream mediator of the orexin system in the regulation of sleep/wake states without compensation by the orexin receptor-1 (OX1R) mediated pathways, we analysed the phenotype of Histamine-1 receptor (H1R) and OX 1R double-deficient (H1R-/-;OX 1R-/-) mice. These mice lack OX1R-mediated pathways in addition to deficiency of H1R, which is thought to be the most important system in downstream of OX2R. Methods: We used H 1R deficient (H1R-/-) mice, H1R -/-;OX1R-/- mice, OX1R and OX 2R double-deficient (OX1R-/-;OX 2R-/-) mice, and wild type controls. Rapid eye movement (REM) sleep, non-REM (NREM) sleep and awake states were determined by polygraphic electroencephalographic/electromyographic recording. Results: No abnormality in sleep/wake states was observed in H1R-/- mice, consistent with previous studies. H1R-/-;OX 1R-/- mice also showed a sleep/wake phenotype comparable to that of wild type mice, while OX1R-/-; OX 2R-/- mice showed severe fragmentation of sleep/wake states. Conclusion: Our observations showed that regulation of the sleep/wake states is completely achieved by OX2R-expressing neurones without involving H1R-mediated pathways. The maintenance of basal physiological sleep/wake states is fully achieved without both H1 and OX1 receptors. Downstream pathways of OX2R other than the histaminergic system might play an important role in the maintenance of sleep/wake states.

KW - Electroencephalography

KW - Histamine H receptor

KW - Orexin receptor-1

KW - Orexin receptor-2

KW - Sleep/wake states

KW - Tuberomammillary nucleus

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