Imperial College London
Portrait Picture

Prof. William Wisden F. Med. Sci.

Faculty of Natural Sciences, Department of Life Sciences

Chair in Molecular Neuroscience
 
 
 
//

Contact

 

+44 (0)20 7594 9744w.wisden Website CV

 
 
//

Location

 

401BSir Ernst Chain BuildingSouth Kensington Campus

//

Summary

 

Publications

Citation

BibTex format

@unpublished{Harding:2021:10.1101/2021.05.14.444161,
author = {Harding, EC and Ba, W and Zahir, R and Yu, X and Yustos, R and Hsieh, B and Lignos, L and Vyssotski, AL and Constandinou, T and Franks, NP and Wisden, W},
doi = {10.1101/2021.05.14.444161},
publisher = {Cold Spring Harbor Laboratory},
title = {Nitric oxide synthase neurons in the preoptic hypothalamus are sleep-active and contribute to regulating NREM and REM sleep and lowering body temperature},
url = {http://dx.doi.org/10.1101/2021.05.14.444161},
year = {2021}
}
Download

RIS format (EndNote, RefMan)

TY  - UNPB
AB  - When mice are exposed to external warmth, nitric oxide synthase (NOS1) neurons in the median and medial preoptic (MnPO/MPO) hypothalamus induce sleep and concomitant body cooling. However, how these neurons regulate baseline sleep and body temperature is unknown. Using calcium photometry, we show that NOS1 neurons in MnPO/MPO are predominantly NREM active. This is the first instance of a predominantly NREM-active population in the PO area, or to our knowledge, elsewhere in the brain. In addition to releasing nitric oxide, NOS1 neurons in MnPO/MPO can release GABA, glutamate and peptides. We expressed tetanus-toxin light-chain in MnPO/MPO NOS1 cells to reduce vesicular release of transmitters. This induced changes in sleep structure: over 24 hours, mice had less NREM sleep in their dark (active) phase, and more NREM sleep in their light (sleep) phase. REM sleep episodes in the dark phase were longer, and there were fewer REM transitions between other vigilance states. REM sleep had less theta power. Mice with synaptically blocked MnPO/MPO NOS1 neurons were also warmer. In particular, mice were warmer than control mice at the dark-light transition (ZT0), as well as during the dark phase siesta (ZT16-20), where there is usually a body temperature dip. Also, at this siesta point of cooled body temperature, mice usually have more NREM, but mice with synaptically blocked MnPO/MPO NOS1 cells showed reduced NREM sleep at this time. Overall, MnPO/MPO NOS1 neurons promote both NREM and REM sleep and contribute to chronically lowering body temperature, particularly at transitions where the mice normally enter NREM sleep.
AU  - Harding,EC
AU  - Ba,W
AU  - Zahir,R
AU  - Yu,X
AU  - Yustos,R
AU  - Hsieh,B
AU  - Lignos,L
AU  - Vyssotski,AL
AU  - Constandinou,T
AU  - Franks,NP
AU  - Wisden,W
DO  - 10.1101/2021.05.14.444161
PB  - Cold Spring Harbor Laboratory
PY  - 2021///
TI  - Nitric oxide synthase neurons in the preoptic hypothalamus are sleep-active and contribute to regulating NREM and REM sleep and lowering body temperature
UR  - http://dx.doi.org/10.1101/2021.05.14.444161
UR  - http://hdl.handle.net/10044/1/90627
ER  -
Download