Sleep and local field potential effect of the D2 receptor agonist bromocriptine during the estrus cycle and postpartum period in female rats

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Attila Tóth , Dóra Keserű , Máté Pethő , László Détári , Norbert Bencsik , Árpád Dobolyi , Tünde Hajnik
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引用次数: 0

Abstract

Background

Pituitary lactotrophs are under tonic dopaminergic inhibitory control and bromocriptine treatment blocks prolactin secretion.

Methods

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.

Results

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.

Conclusions

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.

D2受体激动剂溴隐亭在雌性大鼠发情周期和产后期间对睡眠和局部场电位的影响
背景:垂体泌乳素受强直性多巴胺能抑制控制,溴隐亭治疗可阻止泌乳素分泌:垂体泌乳素受强直性多巴胺能抑制控制,溴隐亭治疗可阻断泌乳素分泌:方法:在雌性大鼠发情周期的不同阶段使用溴隐亭治疗72小时后,以及在产后早期和中期使用溴隐亭治疗24小时后,对睡眠和局部场电位进行了研究:结果:睡眠变化与用药的发情周期阶段有很大关系。在发情-发情期和产后中期用药期间,大鼠的清醒度增加最多,慢波睡眠和眼球快速运动睡眠减少最多。在发情周期用药的黑暗阶段,睡眠-觉醒效应更强,而在产后用药的光明阶段,睡眠-觉醒效应更强。在发情周期治疗中,慢波睡眠和快速动眼期睡眠的损失完全没有得到补偿,注射后第一天的睡眠损失在之后会进一步增加。与此相反,注射溴隐亭后,光照阶段的慢波睡眠损失在产后治疗中得到了补偿。溴隐亭治疗导致慢波睡眠时局部场电位δ功率下降,而清醒时β和γ功率增强,与治疗时间无关:这些结果可以解释为多巴胺 D2 受体激动、催乳素释放不足以及自发的同态睡眠驱动力在发情周期的不同阶段和产后发生了改变。
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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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