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Sleep and the sleep electroencephalogram in C57BL/6 and C3H/HeN mice
被引:2
作者:
van Dorp, Rick
[1
]
Rolleri, Elisa
[1
]
Deboer, Tom
[1
,2
]
机构:
[1] Leiden Univ Med Ctr, Dept Cell & Chem Biol, Lab Neurophysiol, Leiden, Netherlands
[2] Leiden Univ Med Ctr, Dept Cell & Chem Biol, LUMC S-05-P,POB 9600, NL-2300 RC Leiden, Netherlands
关键词:
circadian rhythms;
electroencephalogram;
mouse strains;
sleep deprivation;
sleep homeostasis;
MELATONIN-PROFICIENT C3H;
CLOCK GENE-EXPRESSION;
CIRCADIAN PACEMAKER;
PROMOTING ACTION;
SYSTEM;
OSCILLATIONS;
DEPRIVATION;
AGONIST;
RHYTHMS;
NEURONS;
D O I:
10.1111/jsr.14062
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Different mouse strains used in biomedical research show different phenotypes associated with their genotypes. Two mouse strains commonly used in biomedical sleep research are C57Bl/6 and C3H/He, the strains differ in numerous aspects, including their ability to secrete melatonin as well as the expression of several sleep-related genes. However, sleep regulation has only limitedly been compared between C3H/HeN and C57Bl/6 mice. We therefore compared sleep-wake behaviour and EEG-measured spectral brain activity for C57bl/6 and C3H/HeN mice during a 12:12 h light: dark baseline and during and after a 6 h sleep deprivation. The C3H mice spent more time in NREM sleep around the light-dark transition and more time in REM sleep during the dark phase compared with C57bl/6 mice. The C3H mice also showed more EEG activity in the 4.5-7.5 Hz range during all stages and a stronger 24 h modulation of EEG power density in almost all EEG frequencies during NREM sleep. After the sleep deprivation, C3H mice showed a stronger recovery response, which was expressed in both a larger increase in EEG slow wave activity (SWA) and more time spent in NREM sleep. We show large differences regarding sleep architecture and EEG activity between C3H and C57bl/6 mice. These differences include the amount of waking during the late dark phase, the 24 h amplitude in EEG power density, and the amount of REM sleep during the dark phase. We conclude that differences between mouse strains should be considered when selecting a model strain to improve the generalisability of studies investigating biomedical parameters related to sleep and circadian rhythms.
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