| First Author | Sun Y | Year | 2020 |
| Journal | eNeuro | Volume | 7 |
| Issue | 2 | PubMed ID | 32303567 |
| Mgi Jnum | J:289474 | Mgi Id | MGI:6431353 |
| Doi | 10.1523/ENEURO.0017-20.2020 | Citation | Sun Y, et al. (2020) Hypothalamic MCH Neuron Activity Dynamics during Cataplexy of Narcolepsy. eNeuro 7(2):ENEURO.0017-20.2020 |
| abstractText | Hypothalamic orexin (hypocretin, HCRT) deficiency causes sleep disorder narcolepsy with cataplexy in humans and murine. As another integral group of sleep/wake-regulating neurons in the same brain area, the melanin-concentrating hormone (MCH) neurons' involvement in cataplexy remains ambiguous. Here we used the live animal deep-brain calcium (Ca(2+)) imaging tool to record MCH neuron dynamics during cataplexy by expressing calcium sensor GCaMP6s into genetically defined MCH neurons in orexin knock-out mice, which are a model of human narcolepsy. Similar to wild-type mice, MCH neurons of the narcoleptic mice displayed significantly higher Ca(2+) transient fluorescent intensity during rapid eye movement (REM) sleep and active waking (AW) episodes compared with non-REM (NREM) sleep. Moreover, MCH neurons displayed significantly lower Ca(2+) signals during cataplexy. Importantly, a pre-cataplexy elevation of Ca(2+) signals from MCH neurons was not a prerequisite for cataplexy initiation. Our results demonstrated the inactivation status of MCH neurons during cataplexy and suggested that MCH neurons are not involved in the initiation and maintenance of cataplexy in orexin knock-out mice. |
