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. 2024 Nov 1;5(1):zpae074.
doi: 10.1093/sleepadvances/zpae074. eCollection 2024.

How did I come to sleep research and stay there?

Craig Heller  1
Affiliations

How did I come to sleep research and stay there?

Craig Heller. Sleep Adv. .
No abstract available

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Figures

Figure 1.
Figure 1.
Thermosensitivity of the hypothalamic thermostat of kangaroo rats (Dipodomys ingens) is lower during NREM sleep than during wake and is canceled during REM sleep. (From Glotzbach and Heller. 1976. Science).
Figure 2.
Figure 2.
The loss of neural structure is reflected in the loss of MAP2 (a microtubule marker) staining in the hippocampus during bouts of hibernation. (From Von der Ohe et al., 2006, J. Neuroscience).
Figure 3.
Figure 3.
Disruptive phase shift (DPS) in entrained Siberian hamsters induced by exposure to an extra 5 hours of light on one day produces permanent arrhythmia and eliminates the capacity for memory formation as measured by the novel object recognition test (long-term memory) and the spontaneous alternation test (working memory). Arrhythmia induced by SCN lesions does not disrupt these forms of recognition memory. In animals made arrhythmic by the DPS, complete SCN lesion restores their capacity to form object memories. Open circles represent sham-operated animals, gray circles represent animals with partial SCN lesions, and black circles represent the behavior of animals with complete SCN lesions. The first data set in part C is entrained animals, the second data set comes from arrhythmic DPS animals, and the third data set is animals that received complete SCN lesions (black), partial SCN lesions (gray), or sham lesion operations (white; from Fernandez et al. 2014, Science).
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References

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