In vivo Electrophysiology Research Group, Department of Physiology and Neurobiology, Eötvös Loránd University, Hungary.
In vivo Electrophysiology Research Group, Department of Physiology and Neurobiology, Eötvös Loránd University, Hungary.
Pharmacol Biochem Behav. 2024 Jun;239:173754. doi: 10.1016/j.pbb.2024.173754. Epub 2024 Mar 25.
Pituitary lactotrophs are under tonic dopaminergic inhibitory control and bromocriptine treatment blocks prolactin secretion.
Sleep and local field potential were addressed for 72 h after bromocriptine treatments applied during the different stages of the estrus cycle and for 24 h in the early- and middle postpartum period characterized by spontaneously different dynamics of prolactin release in female rats.
Sleep changes showed strong dependency on the estrus cycle phase of the drug application. Strongest increase of wakefulness and reduction of slow wave sleep- and rapid eye movements sleep appeared during diestrus-proestrus and middle postpartum treatments. Stronger sleep-wake effects appeared in the dark phase in case of the estrus cycle treatments, but in the light phase in postpartum treatments. Slow wave sleep and REM sleep loss in case of estrus cycle treatments was not compensated at all and sleep loss seen in the first day post-injection was gained further later. In opposition, slow wave sleep loss in the light phase after bromocriptine injections showed compensation in the postpartum period treatments. Bromocriptine treatments resulted in a depression of local field potential delta power during slow wave sleep while an enhancement in beta and gamma power during wakefulness regardless of the treatment timing.
These results can be explained by the interplay of dopamine D2 receptor agonism, lack of prolactin release and the spontaneous homeostatic sleep drive being altered in the different stages of the estrus cycle and the postpartum period.
垂体催乳素细胞受到持续的多巴胺能抑制性控制,而溴隐亭治疗会阻断催乳素的分泌。
在雌性大鼠的发情周期的不同阶段应用溴隐亭治疗后,我们对睡眠和局部场电位进行了 72 小时的检测,并在产后早期和中期进行了 24 小时的检测,这两个阶段的催乳素释放具有自发的不同动力学特征。
睡眠变化显示出对药物应用发情周期阶段的强烈依赖性。在发情期-发情前期和产后中期治疗中,清醒时间明显增加,慢波睡眠和快速眼动睡眠减少。在发情周期治疗中,睡眠-觉醒效应在暗期更强,但在产后治疗中在光期更强。在发情周期治疗中,慢波睡眠和 REM 睡眠的缺失并没有得到完全补偿,并且在注射后的第一天丢失的睡眠进一步得到了恢复。相反,在产后治疗中,溴隐亭注射后光期的慢波睡眠缺失表现出补偿。溴隐亭治疗导致慢波睡眠期间局部场电位 delta 功率降低,而在觉醒期间 beta 和 gamma 功率增强,无论治疗时间如何。
这些结果可以用多巴胺 D2 受体激动作用、催乳素释放缺乏以及发情周期和产后阶段自发的稳态睡眠驱动的相互作用来解释。