The involvement of amyloid-β in the central nervous system regulation underlying sleep deprivation-induced rapid ejaculation in rats.

IF 3.2 2区 医学 Q1 ANDROLOGY Andrology Pub Date : 2024-12-20 DOI:10.1111/andr.13826
Peng Yang, Tianle Zhu, Yukuai Ma, Zhi Cao, Pan Gao, Hui Jiang, Xiansheng Zhang
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Abstract

Background: Although some studies suggest that sleep deprivation may affect ejaculation regulation, related research is limited, and the mechanisms remain unclear.

Aim: This study aimed to explore whether sleep deprivation influences ejaculation regulation through amyloid-beta and to investigate its potential mechanisms.

Materials and methods: Normal ejaculating rats were randomly distributed into three separate groups for the study, and treated with sleep deprivation combined with saline gavage, sleep deprivation combined with sodium butyrate gavage, and control with saline gavage. The levels of amyloid-beta and 5-HT1A receptors were assessed through Western blotting, PCR, and immunohistochemical techniques. The levels of interleukin-4 and serotonin (5-hydroxytryptamine) in the brain were determined by enzyme-linked immunosorbent assay.

Results: The experiment showed that the rats in the sleep deprivation combined with saline gavage group rats had a significantly faster ejaculation compared to the control combined with saline gavage group rats. Meanwhile, sleep deprivation combined with saline gavage group had the highest levels of amyloid-beta oligomers in the brain tissue. Correlation results revealed that the levels of amyloid-beta oligomers in brain tissue were inversely related to ejaculation latency and positively associated with ejaculation frequency. Furthermore, we found that elevated levels of amyloid-beta oligomers in brain tissue led to upregulation of 5-HT1A receptor expression. Additionally, elevated levels of amyloid-beta oligomers in brain tissue were found to increase interleukin-4 levels, thereby reducing 5-hydroxytryptamine levels.

Discussion: Sleep deprivation indeed accelerates ejaculation, and this acceleration is closely related to amyloid-beta. Sleep deprivation can increase amyloid-beta levels in brain tissue, mediating a decrease in 5-hydroxytryptamine levels and overexpression of 5-HT1A receptors, thereby accelerating ejaculation.

Conclusion: There is a significant correlation between elevated amyloid-beta levels in brain tissue because of sleep deprivation and accelerated ejaculation. This study's main findings offer insights into the development of acquired premature ejaculation linked to poor sleep and establish a theoretical framework for investigating potential treatments for this condition.

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淀粉样蛋白β参与睡眠剥夺引起的大鼠快速射精的中枢神经系统调节。
背景:虽然一些研究表明睡眠不足可能影响射精调节,但相关研究有限,机制尚不清楚。目的:本研究旨在探讨睡眠剥夺是否通过淀粉样蛋白- β影响射精调节并探讨其潜在机制。材料与方法:将正常射精大鼠随机分为3组,分别给予剥夺睡眠联合生理盐水灌胃、剥夺睡眠联合丁酸钠灌胃和对照组生理盐水灌胃。通过Western blotting、PCR和免疫组织化学技术评估β淀粉样蛋白和5-HT1A受体的水平。采用酶联免疫吸附法测定脑内白细胞介素-4和血清素(5-羟色胺)水平。结果:实验显示,剥夺睡眠加生理盐水灌胃组大鼠射精速度明显快于对照组加生理盐水灌胃组大鼠。同时,睡眠剥夺联合生理盐水灌胃组脑组织中淀粉样蛋白低聚物水平最高。相关结果显示,脑组织中β淀粉样蛋白低聚物的水平与射精潜伏期呈负相关,与射精频率呈正相关。此外,我们发现脑组织中β淀粉样蛋白低聚物水平升高导致5-HT1A受体表达上调。此外,脑组织中淀粉样蛋白低聚物水平升高,可增加白细胞介素-4水平,从而降低5-羟色胺水平。讨论:睡眠不足确实会加速射精,而且这种加速与淀粉样蛋白密切相关。睡眠剥夺可以增加脑组织中淀粉样蛋白水平,介导5-羟色胺水平的降低和5-HT1A受体的过度表达,从而加速射精。结论:睡眠不足导致脑组织淀粉样蛋白水平升高与射精加速之间存在显著相关性。这项研究的主要发现为研究与睡眠不足有关的获得性早泄的发展提供了见解,并为研究这种情况的潜在治疗方法建立了理论框架。
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来源期刊
Andrology
Andrology ANDROLOGY-
CiteScore
9.10
自引率
6.70%
发文量
200
期刊介绍: Andrology is the study of the male reproductive system and other male gender related health issues. Andrology deals with basic and clinical aspects of the male reproductive system (gonads, endocrine and accessory organs) in all species, including the diagnosis and treatment of medical problems associated with sexual development, infertility, sexual dysfunction, sex hormone action and other urological problems. In medicine, Andrology as a specialty is a recent development, as it had previously been considered a subspecialty of urology or endocrinology
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