» Articles » PMID: 38461157

Sleep- and Sleep Deprivation-related Changes of Vertex Auditory Evoked Potentials During the Estrus Cycle in Female Rats

Overview
Journal Sci Rep
Specialty Science
Date 2024 Mar 9
PMID 38461157
Authors
Affiliations
Soon will be listed here.
Abstract

The estrus cycle in female rodents has been shown to affect a variety of physiological functions. However, little is known about its presumably thorough effect on auditory processing during the sleep-wake cycle and sleep deprivation. Vertex auditory evoked potentials (vAEPs) were evoked by single click tone stimulation and recorded during different stages of the estrus cycle and sleep deprivation performed in metestrus and proestrus in female rats. vAEPs showed a strong sleep-dependency, with the largest amplitudes present during slow wave sleep while the smallest ones during wakefulness. Higher amplitudes and longer latencies were seen in the light phase during all vigilance stages. The largest amplitudes were found during proestrus (light phase) while the shortest latencies were seen during estrus (dark phase) compared to the 2nd day diestrus baseline. High-amplitude responses without latency changes were also seen during metestrus with increased homeostatic sleep drive. More intense and faster processing of auditory information during proestrus and estrus suggesting a more effective perception of relevant environmental cues presumably in preparation for sexual receptivity. A 4-h sleep deprivation resulted in more pronounced sleep recovery in metestrus compared to proestrus without difference in delta power replacement suggesting a better tolerance of sleep deprivation in proestrus. Sleep deprivation decreased neuronal excitability and responsiveness in a similar manner both during metestrus and proestrus, suggesting that the negative consequences of sleep deprivation on auditory processing may have a limited correlation with the estrus cycle stage.

Citing Articles

Post-conditioning sleep deprivation facilitates delay and trace fear memory extinction.

Miyamoto D, Mahmoud M Mol Brain. 2024; 17(1):90.

PMID: 39614358 PMC: 11605955. DOI: 10.1186/s13041-024-01163-w.


On the basis of sex and sleep: the influence of the estrous cycle and sex on sleep-wake behavior.

Swift K, Gary N, Urbanczyk P Front Neurosci. 2024; 18:1426189.

PMID: 39268035 PMC: 11390649. DOI: 10.3389/fnins.2024.1426189.

References
1.
Moayedi M, Liang M, Sim A, Hu L, Haggard P, Iannetti G . Laser-Evoked Vertex Potentials Predict Defensive Motor Actions. Cereb Cortex. 2015; 25(12):4789-98. PMC: 4635919. DOI: 10.1093/cercor/bhv149. View

2.
Jeffreys D, Tukmachi E . The vertex-positive scalp potential evoked by faces and by objects. Exp Brain Res. 1992; 91(2):340-50. DOI: 10.1007/BF00231668. View

3.
Campbell K, Kalmbacher C, Specht C, Gregg T . Dependence of rat vertex auditory evoked potentials on central muscarinic receptor activation. Brain Res. 1995; 702(1-2):110-6. DOI: 10.1016/0006-8993(95)01027-4. View

4.
Haberham Z, van den Brom W, Venker-van Haagen A, De Groot H, Baumans V, Hellebrekers L . The rat vertex-middle latency auditory-evoked potential as indicator of anaesthetic depth: a comparison with evoked-reflex testing. Brain Res. 2000; 873(2):287-90. DOI: 10.1016/s0006-8993(00)02504-x. View

5.
Schaap M, van Oostrom H, Doornenbal A, Baars A, Arndt S, Hellebrekers L . Predictability of painful stimulation modulates the somatosensory-evoked potential in the rat. PLoS One. 2013; 8(4):e61487. PMC: 3629015. DOI: 10.1371/journal.pone.0061487. View