雄性大鼠在接受或不接受艾司西酞普兰治疗的情况下,从周岁开始诱发的慢性轻度应激对其性行为的影响。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-11-01 Epub Date: 2024-03-14 DOI:10.1111/andr.13620
Leonardo Wensing Fischer, Marina Nunes, Talita Biude Mendes, Joana Noguères Simas, Maria Martha Bernardi, Samara Urban de Oliva, Sandra Maria Miraglia
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引用次数: 0

摘要

背景:冠状病毒病大流行后,抑郁症的发病率越来越高,其中包括青少年。艾司西酞普兰是一种选择性血清素再摄取抑制剂,2009 年被批准用于治疗儿童和青少年的重度抑郁症。抗抑郁药对性功能障碍的不良影响通常被低估。目的:在一项转化研究中,以大鼠为实验模型,研究从青春期到成年期诱发的慢性轻度压力对男性性行为参数的影响,无论是否使用艾司西酞普兰治疗:将 44 只青春期雄性大鼠分为四组:材料:44 只青春期前雄性大鼠被分为四组:假对照组、艾司西酞普兰组、应激组和应激 + 艾司西酞普兰组。慢性轻度应激包括九种不同的应激源,每天随机施加一种,持续八周(从产后 41 天到 97 天)。依西酞普兰灌胃疗法(10 毫克/千克)从产后 70 天开始,持续 4 周。雄性性行为参数在产后114天进行评估。之后,进行安乐死以采集血液和睾丸。对睾丸和浆液睾酮水平进行了组织病理学检查:结果:无论是否服用艾司西酞普兰,接受应激方案的大鼠的性活动和性冲动都有所减少,而接受应激方案并服用艾司西酞普兰的动物的阉割总数则有所增加。接受或未接受艾司西酞普兰治疗(应激和应激+艾司西酞普兰)的动物睾酮水平较低。暴露于应激和/或接受艾司西酞普兰治疗(艾司西酞普兰、应激和应激+艾司西酞普兰)的动物,其生精小管切片组织学正常的频率较低:结论:从青春期开始诱发的慢性轻度应激,无论是否与艾司西酞普兰治疗相关,都会改变睾酮水平和睾丸组织结构,而且似乎与雄性性欲减退有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of chronic mild stress induced from peripuberty on sexual behavior in male rats, with or without escitalopram treatment.

Background: After the Coronavirus Disease pandemic, depression became more present, including in adolescents. Escitalopram, a selective serotonin reuptake inhibitor, was approved in 2009 for treatment of the major depressive disorder, both in children and adolescents. The undesirable effects of antidepressants on sexual dysfunction are usually underestimated.

Aims: To investigate the effects of chronic mild stress, induced from peripuberty up to adulthood, on male sexual behavior parameters, with or without the escitalopram treatment, using rats as experimental model in a translational study.

Materials and methods: Forty-four peripubertal male rats were distributed into four groups: Sham control, escitalopram, stress, and stress + escitalopram. The chronic mild stress consisted of nine different stressors randomly applied one per day, for 8 weeks (from 41 to 97 days postpartum). Escitalopram therapy by gavage (10 mg/kg) started at 70 days postpartum and lasted for 4 weeks. The male sexual behavior parameters were evaluated at 114 days postpartum. After that, euthanasia was performed for blood and testis collection. Histopathology of the testes and plasmatic testosterone level were carried out.

Results: There was a reduction in sexual activity and motivation in rats exposed to the stress protocol, which were treated or not with escitalopram, as well as an increase in the total number of mounts in animals exposed to the stress and treated with escitalopram. The testosterone levels were lower in animals exposed to the stress, which were or not treated with escitalopram (stress and stress + escitalopram). The frequency of histologically normal seminiferous tubule sections was lower in animals that were exposed to the stress and/or received escitalopram (escitalopram, stress, and stress + escitalopram).

Conclusion: Chronic mild stress induced from peripuberty, associated or not to escitalopram treatment, altered the testosterone levels and testicular histoarchitecture and seems to be related to the reduction in male sexual motivation.

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