绘制在体大鼠在整个发情周期内子宫电特性的变异性。

IF 2.8 4区 医学 Q2 PHYSIOLOGY
Mathias W Roesler, Amy S Garrett, Leo K Cheng, Alys R Clark
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引用次数: 0

摘要

性成熟后,子宫功能是由激素水平的周期性变化驱动的。在月经周期中,子宫内的电和机械活动会发生变化,为精子运输和月经内膜脱落等基本功能做出贡献。然而,缺乏量化的变化在子宫功能发生在整个周期的过程中。用雌性Wistar大鼠在体内量化子宫电活动随发情周期的变化。在麻醉状态下,将子宫外化,电极放置在子宫的背侧和腹侧,记录浆膜的自发活动。根据频率将电事件分为慢速和快速两部分。使用高空间分辨率电极阵列测量了事件之间的持续时间和间隔,并沿子宫绘制了传播方向和速度。发情周期的所有阶段均表现为卵巢-子宫颈繁殖,但在发情前期和发情中期也存在子宫颈-卵巢繁殖。在发情期和退发情期,卵巢-子宫颈繁殖占优势。发情期和退发情期的事件间隔分别为40.2±5.6 s(1.51±0.25 cpm)和60.5±2.6 s(1.02±0.05 cpm),差异有统计学意义(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mapping the variability of in vivo rat uterine electrical properties throughout the oestrous cycle.

After reaching sexual maturity, uterine function is driven by cyclical variations in hormone levels. The electrical and mechanical activity in the uterus varies during the menstrual cycle, contributing to essential functions such as sperm transport and shedding the menstrual lining. However, there is a lack of quantification of the variation in uterine function occurring over the course of the cycle. Female Wistar rats were used to quantify the changes in uterine electrical activity in vivo with respect to the oestrous cycle. Under anaesthesia, the uterus was exteriorised, and electrodes were placed on the dorsal and ventral sides of the organ to record spontaneous activity from the serosa. Electrical events were separated into slow and fast components based on frequency. The duration and interval between events were measured and propagation directions and velocities were mapped along the uterus using high spatial resolution electrode arrays. All stages of the oestrous cycle showed ovarian-cervical propagation, but cervical-ovarian propagation was also present in pro-oestrus and metoestrus. Ovarian-cervical propagation was dominant in oestrus and metoestrus. The interval between events showed significant differences with 40.2 ± 5.6 s (1.51 ± 0.25 cpm) and 60.5 ± 2.6 s (1.02 ± 0.05 cpm) during the dioestrus and metoestrus phases, respectively (P < 0.001). The slow and fast component durations were similar across the oestrous cycle (19.9 ± 2.2 s and 10.2 ± 3.0 s, respectively). This emphasizes the role of the oestrous cycle in guiding uterine function through modulation of the electrical activity and shows potential for estimating the oestrous cycle phases based on electrical characteristics.

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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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